Lediga jobb Ardena Södertälje AB i Södertälje

Introduction to Ardena
As a leading Contract Development and Manufacturing Organization (CDMO), Ardena partners with pharmaceutical companies of all sizes—from emerging biotech to global industry leaders—united by the mission to help biopharma innovators navigate drug development with precision, quality, and speed, bringing their molecules from discovery to the clinic and market. Our fully integrated services span drug substance and drug product development, manufacturing, nanomedicine, clinical logistics, bioanalytical services, state research, fill & finish, and CMC regulatory support.
With a rapidly growing international footprint, Ardena is home to over 750 professionals across six strategic locations—Belgium (Ghent), the Netherlands (Oss and Assen), Sweden (Södertälje), Spain (Pamplona), and Somerset, New Jersey (the US). Our open and transparent culture is built on collaboration, ownership, and innovation, guided by our We CARE values. We foster a communicative environment where mutual respect, accountability, and excellence empower our team.
We are looking for skilled and motivated professionals eager to grow their careers in an exciting and fast-paced environment. Whether you’re an experienced expert or just starting out, Ardena provides a dynamic workplace where you can contribute to meaningful drug development projects, expand your knowledge, and be part of a global team committed to making a difference. As an international organization, we help you navigate a career path that expands your possibilities beyond borders, opening doors to personal and professional growth without limits. Your potential to grow is limitless with us.
If you are ready to take on new opportunities, work alongside industry experts, and contribute to the future of medicine, Ardena is the place for you.  
For the Ardena Business Unit based in Södertälje, we are looking for a Project Manager.

WHAT YOU WILL WORK ON
YOUR ROLE
As a Project Manager, you will play a pivotal role at Ardena Södertälje, ensuring seamless execution of projects and good customer relations. You will work closely with process development, analytical development, manufacturing, quality control and quality assurance to deliver API:s for clinical studies.
YOUR KEY RESPONSIBILITIES
You will have the responsibility for projects concerning manufacturing of APIs for clinical studies
You will be the contact person towards our customers
A typical project team consists of colleagues from process development, analytical development, manufacturing, quality control and quality assurance
You will report to the Business Unit director
You will be responsible for planning, coordination, communication and timeline throughout the project


YOUR PROFILE
You have a masters degree or equivalent within the science/technology field, preferably chemistry, biotechnology or equivalent
You have at least 3 years of experience
You have experience from working with GMP
You feel comfortable in a dynamic and changing environment
You like to learn and develop yourself
You are flexible, a problem solver and a team player
You have an analytical mindset and you can handle multiple projects at the same time
You have good communication skills and are fluent in both Swedish and English (written as well as spoken)
We love creative thinking and pro-activeness


WHAT WE OFFER
At Ardena, we recognize that our people drive our success. We offer:
A true learning environment where you will have the ability to grow your skills A rapidly developing and growing international company with an attractive services, product and customer portfolio A dynamic working environment with nice colleagues Open straightforward but also caring culture We are true to our values An attractive remuneration package Flexible working hours
  
Please submit your application no later than the 6th of October. We will hold interviews continuously, so do not wait with your application.
Ready to start your career path with Ardena? Click the application button and join us in shaping the future of drug development!
Only candidates eligible to work in the EU will be considered for the position. Agency calls will not be appreciated. Visa mindre

Introduktion till Ardena
Som en ledande kontraktsutvecklings- och tillverkningsorganisation (CDMO) samarbetar Ardena med läkemedelsföretag av alla storlekar – från framväxande bioteknik till globala branschledare – förenade av uppdraget att hjälpa biofarmainnovatörer att navigera läkemedelsutveckling med precision, kvalitet och snabbhet, och föra sina molekyler från upptäckt till klinik och marknad. Våra helt integrerade tjänster spänner över utveckling av läkemedelssubstanser och läkemedelsprodukter, tillverkning, nanomedicin, klinisk logistik, bioanalytiska tjänster, statlig forskning, fyllning och finish samt CMC-regulatoriskt stöd.
Med ett snabbt växande internationellt fotavtryck är Ardena hem för över 750 yrkesverksamma på sex strategiska platser – Belgien (Gent), Nederländerna (Oss och Assen), Sverige (Södertälje), Spanien (Pamplona) och Somerset, New Jersey (USA). Vår öppna och transparenta kultur bygger på samarbete, ägarskap och innovation, vägledd av våra We CARE-värderingar. Vi främjar en kommunikativ miljö där ömsesidig respekt, ansvarstagande och excellens stärker vårt team.
Vi letar efter skickliga och motiverade proffs som är ivriga att utveckla sina karriärer i en spännande och fartfylld miljö. Oavsett om du är en erfaren expert eller precis har börjat, erbjuder Ardena en dynamisk arbetsplats där du kan bidra till meningsfulla läkemedelsutvecklingsprojekt, utöka dina kunskaper och vara en del av ett globalt team som är engagerat i att göra skillnad. Som en internationell organisation hjälper vi dig att navigera en karriärväg som utökar dina möjligheter över gränserna och öppnar dörrar till personlig och professionell tillväxt utan gränser. Din potential att växa är gränslös hos oss.
Om du är redo att ta dig an nya möjligheter, arbeta tillsammans med branschexperter och bidra till medicinens framtid är Ardena platsen för dig.
För vårbusiness unit baserad iSödertälje, letar vi nu efter en:
Senior Material and Logistics Officer (Föräldravikariat)
DIN ROLL
Som Senior Material and Logistics Officer kommer du att spela en nyckelroll i hanteringen av kvalitetsdokument och logistik. Du kommer att arbeta självständigt men i nära samarbete med dina kollegor och avdelningschef. Din roll innebär att säkerställa att alla kvalitetsdokument är korrekt hanterade och att alla in- och utleveranser av gods sker effektivt och i enlighet med interna krav. OBS! Tjänsten är ett föräldravikariat på 6 månader.
DINA PRIMÄRA ARBETSUPPGIFTER
Ansvara för avdelningens kvalitetsdokument, inklusive säkerställa att alla dokument hanteras enligt gällande rutiner
Säkerställa att dokumentation och spårbarhet är i ordning för alla produkter som hanteras, och följa upp på att alla kvalitetskrav efterlevs
Säkerställa korrekt hantering av lagerflöden, inklusive inkommande och utgående varor
Utföra inventeringar och kontrollera att lagerstatusen är korrekt och att lagernivåerna hålls på en optimal nivå
Ha tät kontakt med leverantörer och partners
Provtagning av råmaterial

DIN PROFIL
Har gymnasieutbildning
Erfarenhet av administrativt arbete och stöd till ledning.
God organisatorisk förmåga och förmåga att hantera flera projekt samtidigt.
Starka kommunikationsfärdigheter i svenska samt engelska, både skriftligt och muntligt.
Förmåga att arbeta självständigt såväl som i nära samarbete med andra.
Positiv inställning och god förmåga att bygga relationer inom organisationen
MERITERANDE Erfarenhet inom läkemedelsindustri
Erfarenhet av att arbeta med kvalitetsdokumentation och följa regulatoriska krav
Truckkort enligt TLP10, minsta krav: B1 (motviktstruck).

VAD VI ERBJUDER
På Ardena är vi medvetna om att det är våra medarbetare som driver vår framgång. Vi erbjuder:
Flexibel arbetstid En dynamiskinternationell arbetsmiljö med möjligheter till karriärutveckling Tillgångtill Ardena Academy, vår interna lärplattform för professionell utvecklingEn chans att bidra till banbrytande läkemedelsutvecklingsprojekt som gör verklig skillnad
SÅ HÄR ANSÖKER DU
Vill du veta mer? Kontakta avdelningschef: Stefanie Olsson på [email protected].
Tjänsten är ett föräldravikariat från juni till november 2025.
Är du redo att börja din karriär med Ardena? Klicka på ansökningsknappen och var med och forma framtidens läkemedelsutveckling! Visa mindre

Introduction to Ardena
As a leading Contract Development and Manufacturing Organization (CDMO), Ardena partners with pharmaceutical companies of all sizes—from emerging biotech to global industry leaders—united by the mission to help biopharma innovators navigate drug development with precision, quality, and speed, bringing their molecules from discovery to the clinic and market. Our fully integrated services span drug substance and drug product development, manufacturing, nanomedicine, clinical logistics, bioanalytical services, state research, fill & finish, and CMC regulatory support.
With a rapidly growing international footprint, Ardena is home to over 750 professionals across six strategic locations—Belgium (Ghent), the Netherlands (Oss and Assen), Sweden (Södertälje), Spain (Pamplona), and Somerset, New Jersey (the US). Our open and transparent culture is built on collaboration, ownership, and innovation, guided by our We CARE values. We foster a communicative environment where mutual respect, accountability, and excellence empower our team.
We are looking for skilled and motivated professionals eager to grow their careers in an exciting and fast-paced environment. Whether you’re an experienced expert or just starting out, Ardena provides a dynamic workplace where you can contribute to meaningful drug development projects, expand your knowledge, and be part of a global team committed to making a difference. As an international organization, we help you navigate a career path that expands your possibilities beyond borders, opening doors to personal and professional growth without limits. Your potential to grow is limitless with us.
If you are ready to take on new opportunities, work alongside industry experts, and contribute to the future of medicine, Ardena is the place for you.
For the Ardena Business Unit based in Sweden, Södertälje, we are looking for a process development chemist in a role as Scientist or Senior Scientist for a temporary position (6 months) with the possibility of extension.
WHAT YOU WILL WORK ON
Organic chemist (skilled in organic synthesis) in Process Development laboratory
YOUR ROLE
As a Scientist/ Senior Scientist in Process Development laboratory, you will play a pivotal role in process development, ensuring execution of projects in compliance with Ardenas manufacturing capabilities and regulations. You will work closely with analytical development and manufacturing teams to deliver high-quality solutions that align with Ardena’s mission.
YOUR KEY RESPONSIBILITIES
Development of chemical processes, bringing them from lab scale to multi-kilogram scale
Ensure compliance with latest development trends and insights, API manufacturing industry regulations, e.g., GMP
Support technology transfers of the processes into our manufacturing facilities
Participate in making process safety risk assessments for the lab and scale-up
Writing scientific reports

YOUR PROFILE
You have a MSc or PhD degree in organic chemistry or similar
You have a few years of experience from similar work
You have strong problem-solving skills with a collaborative and solution-driven mindset
You feel comfortable in a dynamic and changing environment
You have good communication skills and are fluent in English (written as well as spoken)
Soft skills that align with our CARE values- Communicative, Accountable, Reliable, and Excellent.

WHAT WE OFFER
At Ardena, we recognize that our people drive our success. We offer:
A true learning environment where you will have the ability to grow your skills
An attractive wellness allowance
Flexible working hours
A dynamic, international work environment with nice colleagues and caring culture
A chance to contribute to groundbreaking drug development projects that make a real impact
HOW TO APPLY
Please submit your application no later than the 23rd of April 2025
Ready to start your career path with Ardena? Click the application button and join us in shaping the future of drug development!
Only candidates eligible to work in the EU will be considered for the position. Unfortunately, given the high volume of applications we receive for our vacancies, these professionals (not entitled to work in the European Union) will not be given a status update. Agency calls will not be appreciated. Visa mindre

We are looking for a skilled organic chemist to our production team in Södertälje.

Ardena Södertälje AB is part of the Ardena Drug Substance team, and is responsible for producing active pharmaceutical ingredients (API) for use in clinical trials. Additionally we produce adjuvances and excipients for the Life Science market.

We are looking for the right person to join us in the production team.

Your day-to-day tasks will be to do the first large-scale synthesis of new potential drug substances according to internally developed processes according to Good manufacturing practice, investigate deviations and other project activities.

Primary tasks will be :

- Production of intermediates and end products/APIs in our reactor systems according to pre-approved procedures following cGMP.

- Performing in-process controls.

- General maintenance of equipment.

- Writing and updating batch production record.

You will be working in a group with 6 colleagues.

All work is expected to be performed independently, but in close collaboration with colleagues within and outside of the department.

Apart from work in the production facilities, scientists in the team also develop, design, implement and optimize process systems and process support systems.

The equipment you will be working with is mainly reactors (50 - 2000 L) and filters of varying sizes, but could also be preparatory liquid chromatography and distillation plants.

When joining our team, we will provide you with the relevant training and knowledge to independantly operate equipment and processes, and once fully trained, we expect you to take responsibility for the project you are assigned to - from start to finish.

Furthermore, work is being performed in collaboration with colleagues from our site at Biovation park in Södertälje.

The position is full-time permanent, with a 6 month trial period, with starting date as soon as possible.

Who are you?

We believe that you:

- Hold a MSc in Organic chemistry or equivalent

- Fluent in English (Written and verbal)

- Enjoy working in a group

- Are flexible and can work in more than one project simultaneously

- Are structured and able to follow written routines

Furthermore, it is good if you:

- Speak Swedish fluently

- Have experience in HPLC analysis

- Have knowledge of GMP

- Have prior experience with large scale manufacturing equipments

We offer a workplace with a good social environment and high individual responsibility. Everyone at Ardena Södertälje has different background, both educational and cultural, where each individual contribution is equally important.

You will be able to influence items in your day-to-day work, and suggestions for improvement are always appreciated.

You will be joining the company in a very interesting and expansive and interesting phase.

Ardena Södertälje AB is a contract development and manufacturing organization (CDMO) located within walking distance from Södertälje Hamn train station. We are currently around 62 employees divided into 6 departments: Production-API, Production-Commercial, Quality Control, Quality Assurance, IT & Facility and Logistics.
Since the start in 1998 we brought more than 50 APIs from early lead molecules to clinical studies, including scale-up of processes from the laboratory into pilot plant.

Ardena is a reputed contract partner delivering drug development, manufacturing, logistics and bioanalytical services to pharmaceutical customers globally. In parallel, we work with compiling regulatory dossier and to fast track products towards compliance. Every day, we guide companies through the hurdles and challenges of drug development. Our integrated service offering helps to streamline the drug’s progress to clinic and beyond, to reduce risk and timelines, and to facilitate a seamless flow of information.

We have several dedicated teams with over 300 professionals divided over 6 sites in Belgium, The Netherlands, Sweden and Spain.

Please submit your application before 17th of November 2023.
For questions regarding this recruitment, please contact Wangchuk Rabten: [email protected]; Telephone +46(0)728904391 Visa mindre

About us

Ardena is a leading contract development organization for the pharmaceutical industry. We assist pharmaceutical companies, from virtual biotech to big pharma, in bringing their valued molecule(s) to the clinic and market. We provide a comprehensive and integrated portfolio of drug substance and drug product development, manufacturing, logistics and bioanalytical services.

Ardena is a rapidly growing international orientated organization with a dedicated team of over 500 professionals operating from 7 sites in Belgium, The Netherlands, Sweden, Latvia and Spain. Ardena has an open and transparent culture: team-spirit, an open mindset and ownership are important values in our company.

We are a dynamic drug developer offering exciting career opportunities to skilled and motivated people who want to work in a fast-growing market within the global pharmaceutical industry. Do you want to work in a challenging contract research and development environment, where experts come together to develop innovative drugs for unmet medical needs? Do you want to further develop Ardena and grow with us by becoming our next colleague? Then we might have the right opportunity for you.



For the Ardena Business Unit based in Södertälje, we are looking for an Analytical Chemist with experience from method development for the role as Senior Scientist in Analytical Development.



WHAT YOU WILL WORK ON

YOUR KEY RESPONSIBILITIES


- You will be working as a senior team member in the analytical development team.

- You will independently develop analytical methods for testing of raw materials, intermediates and API:s.

- You will validate analytical methods to be used for GMP analysis of material for clinical studies.

- You will independently generate precise, reliable and reproducible data.

- You will independently prepare analytical methods or reports on the result from analytical method development.

- You will write and review validation protocols, data and reports.

- You will write and review specifications.

- You will approve and transfer analytical methods to the Quality Control group.

- You will qualify and implement pharmacopeia methods.

- You will collaborate with customers and other colleagues from R&D, manufacturing, quality control and quality assurance as to advance projects through development.

- You will be responsible to assure delivery against project timelines.

- You will be involved laboratory design, method transfer and instrument relocation in the team expansion.

YOUR PROFILE LOOKS LIKE/ RESEMBLES

- You have a university degree in Analytical Chemistry, Chemical Engineering, Biotechnology or similar.

- You have at least 2 years of experience from method development with chromatography.

- You have a minimum of 2 years experience from working in a cGMP/GLP environment.

- You have good knowledge/experience of working with analytical instrumentation, qualification procedures and troubleshooting.

- Experience with Chromeleon Chromatography Data Software is a merit.

- Previous experience with IR, KF, titration and/or pharmacopeia analysis is a merit.

- You feel comfortable in a dynamic and changing environment.

- You have strong analytical and problem solving ability.

- You like to learn and develop yourself.

- You are flexible, a problem solver and a team player.

- You have an analytical mindset and you can handle multiple projects at the same time.

WHAT WE OFFER

- A true learning environment where you will have the ability to grow your skills.

- A rapidly developing and growing international company with an attractive services, product and customer portfolio.

- A dynamic working environment with nice colleagues.

- Open, straightforward but also caring culture.

- We are true to our values.

- An attractive remuneration package.

- Flexible working hours.

- A generous wellness allowance (Friskvård).

Please submit your application no later than the 29th of March.

Ready to apply? Please click on the application button

Only candidates eligible to work in the EU will be considered for the position. Unfortunately, given the high volume of applications we receive for our vacancies, these professionals (not entitled to work in the European Union) will not be given a status update. Agency calls will not be appreciated. Visa mindre

About us

Ardena is a leading contract development organization for the pharmaceutical industry. We assist pharmaceutical companies, from virtual biotech to big pharma, in bringing their valued molecule(s) to the clinic and market. We provide a comprehensive and integrated portfolio of drug substance and drug product development, manufacturing, logistics and bioanalytical services.

Ardena is a rapidly growing international orientated organization with a dedicated team of about 480 professionals operating from 7 sites in Belgium, The Netherlands, Sweden, Latvia and Spain. Ardena has an open and transparent culture: team-spirit, an open mindset and ownership are important values in our company.

We are a dynamic drug developer offering exciting career opportunities to skilled and motivated people who want to work in a fast-growing market within the global pharmaceutical industry. Do you want to work in a challenging contract research and development environment, where experts come together to develop innovative drugs for unmet medical needs? Do you want to further develop Ardena and grow with us by becoming our next colleague? Then we might have the right opportunity for you.

For the Ardena Business Unit based in Södertälje, we are looking for an Associate Scientist within QC.

WHAT YOU WILL WORK ON

Are you working in Quality Control today and want to join a great team with varied QC tasks? In Ardena Södertälje we work in all phases of pharmaceutical development, which provides a dynamic work environment with a great variety of projects.

YOUR KEY RESPONSIBILITIES

- You will run analyses by HPLC/UPLC, GC, IR and Karl-Fisher.

- You will perform quality control of raw materials, intermediates and end products.

- You will perform in-process control analyses.

- You will independently generate precise, reliable and reproducible data in a timely manner.

- You will perform out of specification investigations and writing analytical errors.

- You will issue Certificate of Analysis for non-GMP and GMP materials.

- You will write GMP documentation such as SOP:s, CAPA:s and deviations.

- You will actively identify items of improvement and participate in implementation.

- You will be responsible to assure delivery against project timelines.

YOUR PROFILE LOOKS LIKE

- You have a university degree in Analytical Chemistry, Chemical Engineering, Biotechnology or similar.

- You feel comfortable in a dynamic and changing environment.

- You like to learn and develop yourself.

- You are flexible, a problem solver and a team player.

- You have an analytical mindset, and you can handle multiple projects at the same time.

- You have good communication skills and are fluent in English (written as well as spoken).

IT IS BENEFICIAL IF

- You have previous experience from work in a cGMP environment.

- You have a couple of years of relevant experience from the pharmaceutical industry.

- You have previous experience from LC and/or GC analyses and analytical instrumentation.

- You are a creative thinking and pro-active person.

WHAT WE OFFER

- A true learning environment where you will have the ability to grow your skills.

- A rapidly developing and growing international company with an attractive services, product and customer portfolio.

- A dynamic working environment with nice colleagues.

- Open, straightforward but also caring culture.

- We are true to our values.

- An attractive remuneration package.

- Flexible working hours.

- A generous wellness allowance (Friskvård).

Please submit your application no later than the 21st of November. We will hold interviews continuously, so do not wait with your application.

Ready to apply? Please click on the application button

Only candidates eligible to work in the EU will be considered for the position. Unfortunately, given the high volume of applications we receive for our vacancies, these professionals (not entitled to work in the European Union) will not be given a status update. Agency calls will not be appreciated. Visa mindre

Ardena Södertälje AB är en del av Ardenas Drug Substance grupp. Vi tillverkar aktiva farmaceutiska ingredienser (API) till kliniska studier. Dessutom tillverkar vi adjuvanser och excipienter till Life Science marknaden.

Vi är i en expansiv fas och söker rätt personer att bli en del av vårt team.

Därför söker vi nu lab support till vår site i Södertälje. Arbetet kommer att utföras självständigt, men i nära samarbete med kollegor inom och utanför avdelningen. Vi ser att du är ansvarstagande och ordningsam, samt bekväm med fysiskt arbete. Arbete med truck kommer att vara en del av din vardag.

Dina primära arbetsuppgifter kommer att vara:

- Stötta avdelningar administrativt

- Diverse enkla laborativa arbetsuppgifter, så som mobilfasberedning samt analyser av prover från produktionen

- Blanda kemikalielösningar

- Hantering av inkommande samt utgående gods

Vem är du?

Vi ser att du:

- Har gymnasieutbildning

- Har goda kunskaper i engelska, både i tal och skrift.

- Trivs med att arbeta självständigt

- Är flexibel och kan arbeta med flera arbetsuppgifter parallellt

- Är strukturerad och kan följa skriftliga instruktioner

Vad vi erbjuder

- En tydlig lönestruktur

- En dynamisk arbetsplats med trevliga kollegor

- Öppen, rak och omhändertagande kultur

- Flexibla arbetstider

- 25 dagars semester

- Friskvårdsbidrag (400 SEK/månad)

Tjänsten är på heltid och arbetstiderna är 8-17 inklusive 1 timmes lunch.

Vi erbjuder en arbetsplats med god social miljö, där individuellt ansvar är mycket viktigt. Alla medarbetare hos oss är från olika bakgrunder, både utbildningsmässigt och kulturellt, och allas bidrag är lika viktigt för att nå våra mål.

Du kommer att kunna påverka detaljer som rör ditt arbete och förslag på förbättringar uppmuntras.

Du kommer att ansluta till ett företag i en väldigt expansiv och spännande period.

Ansökningstiden är satt till 21 Januari!

För frågor gällande rekryteringen, kontakta Stefanie Olsson: [email protected] (mailto:[email protected]) Telefon: 070 935 09 07 Visa mindre

About us

Ardena is a leading contract development organization for the pharmaceutical industry. We assist pharmaceutical companies, from virtual biotech to big pharma, in bringing their valued molecule(s) to the clinic and market. We provide a comprehensive and integrated portfolio of drug substance and drug product development, manufacturing, logistics and bioanalytical services.

Ardena is a rapidly growing international orientated organization with a dedicated team of over 500 professionals operating from 7 sites in Belgium, The Netherlands, Sweden, Latvia and Spain. Ardena has an open and transparent culture: team-spirit, an open mindset and ownership are important values in our company.

We are a dynamic drug developer offering exciting career opportunities to skilled and motivated people who want to work in a fast-growing market within the global pharmaceutical industry. Do you want to work in a challenging contract research and development environment, where experts come together to develop innovative drugs for unmet medical needs? Do you want to further develop Ardena and grow with us by becoming our next colleague? Then we might have the right opportunity for you.

For the Ardena Business Unit based in Södertälje, we are looking for a for a Team Manager for the Analytical Development/Quality Control Team. You will be responsible for the day-to-day management, delivery and organization of the analytical team. You manage the capacity and growth of your team in terms of people, equipment, quality and science. You lead by example, and you provide assistance to your team. You enable and facilitate the professional development of your team members.



WHAT YOU WILL WORK ON

YOUR KEY RESPONSIBILITIES

- You’re responsible for the scientific quality of your department for the analytical development projects. You make sure the know-how of your team is and remains up to date. You identify training needs and ensure proper training. You support your people in technically challenging discussions and discussions with customer where necessary.

- You balance and optimize short and long-term planning in terms of people, equipment and infrastructure. You have the responsibility for team delivery on time and to the right quality.

- You’re a people manager. You create a harmonious working environment by streamlining all activities, encouraging teamwork and promoting effective communication. You coach, develop and mentor scientists within the laboratory. You perform Development plans in line with HR procedures.

- You’re responsible for the quality system, GMP and SHE (Safety, Health and Environment) compliance of your team. You make sure the know-how and expertise for these areas are and remain up to date.

- You are actively contributing to team deliveries by working as analytical lead on development projects and by reviewing and approving documents for Analytical Development/Quality Control.

- You team will deliver process development support, analytical method development, analytical method validation, batch release, stability studies etc.

- You lead improvements and efficiency drives within the analytical team and you make sure your team stays project and customer focused.

- You facilitate effecive coordination and communication with other departments such as process development, QC and business development.

- You recruit and train new team members within Analytical Development/Quality Control.

- You will be part of the department management team.

- You will report to the Director Analytical Science.

YOUR PROFILE LOOKS LIKE/ RESEMBLES

- You have a university degree in Analytical Chemistry, Chemical Engineering, Biotechnology or similar. Experience in analytical chemistry is a must.

- You have at least 3-6 years of pharma working experience.

- You have experience in the development of API’s and you understand the challenges and risks in early-phase development projects from pre-clinical to phase I/II/III. You’re familiar with early phase GMP, quality and regulatory standards.

- You have several years of experience in analytical development activities such as method development and method validation.

- You have extensive knowledge in use and operation of all commonly used laboratory equipment, especially for chromatography.

- You have experience from working in a GMP environment.

- You are a solid communicator, ready to face up to challenges and to solve complex problems.

- You are a people manager able to lead and motivate an experienced team of analytical chemists.

- You feel comfortable in a dynamic and changing environment.

- You have strong analytical and problem solving ability.

- You are flexible, a problem solver and a team player.

- You have good communication skills and are fluent in English (written as well as spoken).



WHAT WE OFFER

- A true learning environment where you will have the ability to grow your skills.

- A rapidly developing and growing international company with an attractive services, product and customer portfolio.

- A dynamic working environment with nice colleagues.

- Open straightforward but also caring culture.

- We are true to our values.

- An attractive remuneration package.

- Flexible working hours.

- A generous wellness allowance (Friskvård).



Please submit your application no later than the 19th January.

Ready to apply? Please click on the application button

Only candidates eligible to work in the EU will be considered for the position. Unfortunately, given the high volume of applications we receive for our vacancies, these professionals (not entitled to work in the European Union) will not be given a status update. Agency calls will not be appreciated. Visa mindre

About us

Ardena is a leading contract development organization for the pharmaceutical industry. We assist pharmaceutical companies, from virtual biotech to big pharma, in bringing their valued molecule(s) to the clinic and market. We provide a comprehensive and integrated portfolio of drug substance and drug product development, manufacturing, logistics and bioanalytical services.

Ardena is a rapidly growing international orientated organization with a dedicated team of over 500 professionals operating from 7 sites in Belgium, The Netherlands, Sweden, Latvia and Spain. Ardena has an open and transparent culture: team-spirit, an open mindset and ownership are important values in our company.

We are a dynamic drug developer offering exciting career opportunities to skilled and motivated people who want to work in a fast-growing market within the global pharmaceutical industry. Do you want to work in a challenging contract research and development environment, where experts come together to develop innovative drugs for unmet medical needs? Do you want to further develop Ardena and grow with us by becoming our next colleague? Then we might have the right opportunity for you.



For the Ardena Business Unit based in Södertläje, we are looking for a organic chemist to join our development team.



WHAT YOU WILL WORK ON

YOUR KEY RESPONSIBILITIES

- You will develop chemical processes for our customers, bringing them from lab scale to multi-kilogram scale

- You keep yourself up to date with the latest developments and insights
- You will assist in tech transfer of the processes into our manufacturing facilities

- You will participate in making risk assessments for the lab and scale-up
- You will issue batch production records
- You will write development reports


YOUR PROFILE LOOKS LIKE/ RESEMBLES

- You have a PhD degree in organic chemistry or similar
- You are newly examined, have a few years of experience from similar work or maybe did a postdoc or two
- You feel comfortable in a dynamic and changing environment
- You like to learn and develop yourself
- You are flexible, a problem solver and a team player
- You have an analytical mindset
- You have good communication skills and are fluent in English (written as well as spoken)
- We love creative thinking and pro-activeness


WHAT WE OFFER

- A true learning environment where you will have the ability to grow your skills
- A rapidly developing and growing international company with an attractive services, product and customer portfolio
- A dynamic working environment with nice colleagues
- Open straightforward but also caring culture
- An attractive wellness allowance
- Flexible working hours
- 28 days of holiday per year


Ready to apply? Please click on the application button

Only candidates eligible to work in the EU will be considered for the position. Unfortunately, given the high volume of applications we receive for our vacancies, these professionals (not entitled to work in the European Union) will not be given a status update. Agency calls will not be appreciated. Visa mindre

About us

Ardena is a leading contract development organization for the pharmaceutical industry. We assist pharmaceutical companies, from virtual biotech to big pharma, in bringing their valued molecule(s) to the clinic and market. We provide a comprehensive and integrated portfolio of drug substance and drug product development, manufacturing, logistics and bioanalytical services.

Ardena is a rapidly growing international orientated organization with a dedicated team of about 480 professionals operating from 7 sites in Belgium, The Netherlands, Sweden, Latvia and Spain. Ardena has an open and transparent culture: team-spirit, an open mindset and ownership are important values in our company.

We are a dynamic drug developer offering exciting career opportunities to skilled and motivated people who want to work in a fast-growing market within the global pharmaceutical industry. Do you want to work in a challenging contract research and development environment, where experts come together to develop innovative drugs for unmet medical needs? Do you want to further develop Ardena and grow with us by becoming our next colleague? Then we might have the right opportunity for you.

For the Ardena Business Unit based in Södertälje, we are looking for an Analytical Chemist for the role as Senior Scientist Quality Control.

WHAT YOU WILL WORK ON

YOUR KEY RESPONSIBILITIES

- You will be working as a team member in the quality control team with GMP related deliveries and problem solving.
- You will act as project coordinator from QC in pharmaceutical projects.
- You will perform and review analyses by HPLC/UPLC, GC, IR and Karl-Fisher.
- You will perform deviation investigations, write and implement change controls and CAPAs.
- You will write and review GMP documentation such as SOP:s.
- You will perform quality control of raw materials, intermediates and end products.
- You will issue Certificate of Analysis for non-GMP and GMP materials.
- You will perform out of specification investigations and writing analytical errors.
- You will be responsible to assure delivery against project timelines.


YOUR PROFILE LOOKS LIKE

- You have a university degree in Analytical Chemistry, Chemical Engineering, Biotechnology or similar.
- You have at least 2 years of previous experience from work in a cGMP environment, including writing and reviewing GMP documentation.
- You have knowledge of work in the GMP quality system.
- You feel comfortable in a dynamic and changing environment.
- You are a proactive person and like to learn and develop yourself.
- You are flexible, a problem solver and a team player.
- You have an analytical mindset, and you can handle multiple projects at the same time.
- You have good communication skills and are fluent in English (written as well as spoken).


WHAT WE OFFER

- A true learning environment where you will have the ability to grow your skills.
- A rapidly developing and growing international company with an attractive services, product and customer portfolio.
- A dynamic working environment with nice colleagues.
- Open, straightforward but also caring culture.
- We are true to our values.
- An attractive remuneration package.
- Flexible working hours.
- A generous wellness allowance (Friskvård).


Please submit your application no later than the 21th of November. We will hold interviews continuously, so do not wait with your application.

Ready to apply? Please click on the application button

Only candidates eligible to work in the EU will be considered for the position. Unfortunately, given the high volume of applications we receive for our vacancies, these professionals (not entitled to work in the European Union) will not be given a status update. Agency calls will not be appreciated. Visa mindre

scroll down for Swedish description"

About us

Ardena is a leading contract development organization for the pharmaceutical industry. We assist pharmaceutical companies, from virtual biotech to big pharma, in bringing their valued molecule(s) to the clinic and market. We provide a comprehensive and integrated portfolio of drug substance and drug product development services.

Ardena is a rapidly growing international orientated organization in the industry, with 7 company sites in 5 countries. (Belgium, the Netherlands, Spain, Latvia and Sweden). Each Business Unit has its specialization, but we are One Ardena Group. We currently have over 500 people working for us and have realized an average growth of 15% on annual basis over the past 3 years. We are ambitious! For you the possibility to expand and transfer your knowledge, grow and develop with us.

For the Ardena Business Unit based in Sodertalje, we are looking for a

HR officer ( 32-40 hr)

WHAT YOU WILL WORK ON

Our company is growing and the dedicated function of the HR officer is a new position for this Business Unit. API SE/LV is based in Sodertalje and Riga. We are currently working on professionalization of HR Management in the Nordics. This means that there is a lot to develop and room for initiative but that the administrative tasks and processes need to be done properly. Recruitment support will be in your hands for both countries. We have rolled out personal development planning, Learning & development needs are known and initiatives for Corporate trainings are being set up. Policies need to be drafted and communicated. We have done an Engagement survey in March and we need to continue with improvements. A role is cut out for you. You will be part of all of this and more.

YOUR KEY RESPONSIBILITIES

- Posting vacancies in our ATS and keeping track of the process
- Drafting employment contracts for the Swedish and the Latvian organization
- General HR and payroll administration for both countries
- Making new employees feel welcome, you will make sure their induction runs smoothly
- Reporting sick employees, keeping track of re-integration
- Provide answers to questions of employees
- Work closely with the other members of the International HR team who are based in the Netherlands, Belgium and Spain. We will work together on numerous HR projects, such as Employer Branding, HR policies, Internal communication and Learning & Development and Social events.
- You will report to BU director of Sweden & Latvia, with a dotted line to the Head of People
- You will closely work together with the General support team of Ardena Sodertalje
- You will have frequent contact with the payroll provider, Pension & insurances provider, and other external suppliers
- You keep yourself up to date with the latest developments and insights in Swedish social and labor legislation


YOUR PROFILE LOOKS LIKE/ RESEMBLES

- You have a Bachelor degree in HRM/ Business administration or similar
- You have several years experience in Swedish HR administration and payroll administration.
- You are used to work with an ATS and HRIS
- You have experience working with high qualified people in an International organization
- You feel comfortable in a dynamic and changing environment. Experience with organization development and chance management is a benefit
- You like to learn and develop yourself
- You are flexible, a problem solver and a team player
- You are accurate and consistent in your work and you are stress resistant
- You have good communication skills and are fluent in both Swedish & English (written as well as spoken).
- We love creative thinking and pro-activeness


WHAT WE OFFER

- A good remuneration package
- A true learning environment where you will have the ability to grow your skills
- A rapidly International developing and growing company with an interesting services, product and customer portfolio
- A dynamic working environment with nice colleagues
- Open straightforward but also caring culture
- We are true to our values
- Flexible working hours

- 28 days holiday a year


HR Officer Swedish

VAD DU KOMMER ATT ARBETA MED

Vårt företag växer och den dedikerade funktionen som HR Officer hos oss på Ardena Södertälje är en ny roll för denna affärsenhet. Affärsenheten API SE/LV är baserat i Södertälje och Riga. Vi arbetar för närvarande med professionalisering av HR Management i Norden och det innebär att det finns mycket att utveckla och utrymme för initiativ men att de administrativa uppgifterna och processerna behöver även utföras. Rekryteringsstöd kommer att ligga i dina händer för båda länderna. Vi har rullat ut personlig utvecklingsplanering, lärande & utvecklingsbehov är kända och initiativ för företagsutbildningar sätts upp. Policyer behöver utarbetas och kommuniceras. Vi har gjort en Engagemangsundersökning i mars och vi fortsätter jobba med förbättringar.

En roll klippt för dig! Du kommer att vara en del av allt detta och mer därtill.

DINA VIKTIGASTE ANSVARSOMRÅDEN

- Lägga ut lediga tjänster i vårt ATS och hålla reda på processen

- Upprättande av anställningsavtal för den svenska och den lettiska organisationen

- Allmän HR- och löneadministration för båda länderna

- Genom att få nyanställda att känna sig välkomna kommer du att se till att deras introduktion går smidigt

- Rapportera sjuka medarbetare, hålla koll på återintegrering

- Ge svar på frågor från anställda

- Arbeta nära de andra medlemmarna i det internationella HR-teamet som är baserade i Nederländerna, Belgien och Spanien. Vi kommer att arbeta tillsammans i många HR-projekt, såsom Employer Branding, HR-policyer, intern kommunikation och lärande och utveckling och sociala evenemang.

- Du kommer att rapportera till BU-chef för Sverige och Lettland, med en prickad linje till HR chefen

- Du kommer att arbeta nära tillsammans med Ardena Södertäljes ledning

- Du kommer att ha täta kontakter med löneleverantören, Pensions- och försäkringsgivaren och andra externa leverantörer

- Du håller dig uppdaterad med den senaste utvecklingen och insikterna inom svensk social- och arbetsmarknadslagstiftning

DIN PROFIL SER UT SOM/LIKNAR

- Du har en kandidatexamen i HRM/ Företagsekonomi eller liknande

- Du har flera års erfarenhet av svensk HR-administration och löneadministration.

- Du är van att arbeta med en ATS och HRIS

- Du har erfarenhet av att arbeta med högkvalificerade personer i en internationell organisation

- Du känner dig bekväm i en dynamis... Visa mindre

Ardena Södertälje AB är en del av Ardenas Drug Substance grupp. Vi tillverkar aktiva farmaceutiska ingredienser (API) till kliniska studier. Dessutom tillverkar vi adjuvanser och excipienter till Life Science marknaden.

Vi är i en expansiv fas och söker rätt personer att bli en del av vårt team.

Därför söker vi nu materialassistent till vår site i Södertälje. Arbetet kommer att utföras självständigt, men i nära samarbete med kollegor inom och utanför avdelningen. Vi ser att du är ansvarstagande och ordningsam.


Dina primära arbetsuppgifter kommer att vara:

- Inköp av material
- Hantera och följa upp ordererkännanden
- Leveransbevakning och säkerställning av hemtagning av material
- Rapportera eventuella avvikelser i inflödet av material
- Register och material-underhåll
- Prisuppdateringar och skapande av nya produktnummer
- Diverse administrativa och övrigt förekommande arbetsuppgifter


Vem är du?

Vi ser att du:

- Har gymnasieutbildning
- Tidigare erfarenhet inom inköp
- Har goda kunskaper i engelska, både i tal och skrift
- Trivs med att arbeta självständigt
- Är flexibel och kan arbeta med flera arbetsuppgifter parallellt
- Är strukturerad och kan följa skriftliga instruktioner
- Har god förmåga att prioritera och att kunna lösa problem som uppstår


Det är meriterande om:

- Du har arbetat inom läkemedelsbranschen

Vad vi erbjuder

- En tydlig lönestruktur
- En dynamisk arbetsplats med trevliga kollegor
- Öppen, rak och omhändertagande kultur
- Flexibla arbetstider
- 25 dagars semester
- Friskvårdsbidrag (400 SEK/månad)


Tjänsten är på heltid och börjar med en 6 månaders provanställning och övergår därefter i en tillsvidareanställning. Arbetstiderna är 8-17 inklusive 1 timmes lunch.

Vi erbjuder en arbetsplats med god social miljö, där individuellt ansvar är mycket viktigt. Alla medarbetare hos oss är från olika bakgrunder, både utbildningsmässigt och kulturellt, och allas bidrag är lika viktigt för att nå våra mål.

Du kommer att kunna påverka detaljer som rör ditt arbete och förslag på förbättringar uppmuntras.

Du kommer att ansluta till ett företag i en väldigt expansiv och spännande period.

Ansökningstiden är satt till 9 September, men vi kan komma att hålla intervjuer tidigare än så, så vänta inte med din ansökan!

För frågor gällande rekryteringen, kontakta Stefanie Olsson: [email protected] (mailto:[email protected]) Telefon 070 935 09 07 Visa mindre

About us

Ardena is a leading contract development organization for the pharmaceutical industry. We assist pharmaceutical companies, from virtual biotech to big pharma, in bringing their valued molecule(s) to the clinic and market. We provide a comprehensive and integrated portfolio of drug substance and drug product development, manufacturing, logistics and bioanalytical services.

Ardena is a rapidly growing international orientated organization with a dedicated team of over 500 professionals operating from 7 sites in Belgium, The Netherlands, Sweden, Latvia and Spain. Ardena has an open and transparent culture: team-spirit, an open mindset and ownership are important values in our company.

We are a dynamic drug developer offering exciting career opportunities to skilled and motivated people who want to work in a fast-growing market within the global pharmaceutical industry. Do you want to work in a challenging contract research and development environment, where experts come together to develop innovative drugs for unmet medical needs? Do you want to further develop Ardena and grow with us by becoming our next colleague? Then we might have the right opportunity for you.



For the Ardena Business Unit based in Södertälje, we are looking for an Analytical Chemist for the role as Scientist in Analytical Development.



WHAT YOU WILL WORK ON

YOUR KEY RESPONSIBILITIES

- You will develop analytical methods for testing of raw materials, intermediates and API:s.
- You will validate analytical methods to be used for GMP analysis of material for clinical studies.
- You will prepare analytical methods or reports on the result from analytical method development.
- You will write and review validation protocols, data and reports.
- You will participate in writing specifications.
- You will transfer analytical methods to the Quality Control group.
- You will qualify and implement pharmacopeia methods.
- You will collaborate with customers and other colleagues from R&D, manufacturing, quality control and quality assurance as to advance projects through development.
- You will be responsible to assure delivery against project timelines.
- You will be involved laboratory design, method transfer and instrument relocation in the team expansion.


YOUR PROFILE LOOKS LIKE/ RESEMBLES

- You have a university degree in Analytical Chemistry, Chemical Engineering, Biotechnology or similar.
- You have previous experience from method development and/or method validation.
- You have a minimum of 2 years of experience from work with chromatography.
- You have good knowledge/experience of working with analytical instrumentation, qualification procedures and troubleshooting.
- Experience with Chromeleon Chromatography Data Software is a merit.
- Previous experience with IR or KF analysis is a merit.
- You have experience from working in a cGMP/GLP environment.
- You feel comfortable in a dynamic and changing environment.
- You have strong analytical and problem solving ability.
- You like to learn and develop yourself.
- You are flexible, a problem solver and a team player.
- You have an analytical mindset and you can handle multiple projects at the same time.
- You have good communication skills and are fluent in English (written as well as spoken).


WHAT WE OFFER

- A true learning environment where you will have the ability to grow your skills.
- A rapidly developing and growing international company with an attractive services, product and customer portfolio.
- A dynamic working environment with nice colleagues.
- Open, straightforward but also caring culture.
- We are true to our values.
- An attractive remuneration package.
- Flexible working hours.
- A generous wellness allowance (Friskvård).


Please submit your application no later than the 22nd of August.



Ready to apply? Please click on the application button

Only candidates eligible to work in the EU will be considered for the position. Unfortunately, given the high volume of applications we receive for our vacancies, these professionals (not entitled to work in the European Union) will not be given a status update. Agency calls will not be appreciated. Visa mindre

Ardena Södertälje AB är en del av Ardenas Drug Substance grupp. Vi tillverkar aktiva farmaceutiska ingredienser (API) till kliniska studier. Dessutom tillverkar vi adjuvanser och excipienter till Life Science marknaden.

Vi är i en expansiv fas och söker rätt personer att bli en del av vårt team.

Därför söker vi nu fastighetsskötare till vår site i Södertälje. Arbetet kommer att utföras självständigt, men i nära samarbete med kollegor inom och utanför avdelningen. Vi ser att du är ansvarstagande, händig och ordningsam, samt bekväm med fysiskt och tyngre arbete.

Dina primära arbetsuppgifter kommer att vara:

- Inre och yttre skötseln av fastigheten
- Mindre reparationer och underhåll av faciliteter och viss utrustning
- Byte av glödlampor och lysrör
- Mottagning och hantering av felanmälningar
- Kontakt med och mottagande av externa hantverkare etc
- Hantering av passersystem


Vem är du?

Vi ser att du:

- Har gymnasieutbildning
- Har goda kunskaper i engelska, både i tal och skrift
- Trivs med att arbeta självständigt
- Är flexibel och kan arbeta med flera arbetsuppgifter parallellt
- Är strukturerad och kan följa skriftliga instruktioner
- Har goda kunskaper i officepaketet


Det är meriterande om:

- Du har erfarenhet från yrken inom bygg, el, VVS eller likvärdigt.

Vad vi erbjuder

- En tydlig lönestruktur
- En dynamisk arbetsplats med trevliga kollegor
- Öppen, rak och omhändertagande kultur
- Flexibla arbetstider
- 25 dagars semester
- Friskvårdsbidrag (400 SEK/månad)


Tjänsten är på heltid och börjar med en 6 månaders provanställning och övergår därefter i en tillsvidareanställning. Arbetstiderna är 8-17 inklusive 1 timmes lunch.

Vi erbjuder en arbetsplats med god social miljö, där individuellt ansvar är mycket viktigt. Alla medarbetare hos oss är från olika bakgrunder, både utbildningsmässigt och kulturellt, och allas bidrag är lika viktigt för att nå våra mål.

Du kommer att kunna påverka detaljer som rör ditt arbete och förslag på förbättringar uppmuntras.

Du kommer att ansluta till ett företag i en väldigt expansiv och spännande period.

Ansökningstiden är satt till 13 Maj, men vi kan komma att hålla intervjuer tidigare än så, så vänta inte med din ansökan!

För frågor gällande rekryteringen, kontakta Stefanie Olsson: [email protected] (mailto:[email protected]); Telefon 070 935 09 07 Visa mindre

Ardena Södertälje AB är en del av Ardenas Drug Substance grupp. Vi tillverkar aktiva farmaceutiska ingredienser (API) till kliniska studier. Dessutom tillverkar vi adjuvanser och excipienter till Life Science marknaden.

Vi är i en expansiv fas och söker rätt personer att bli en del av vårt team.

Därför söker vi nu lagerarbetare till vår site i Södertälje. Arbetet kommer att utföras självständigt, men i nära samarbete med kollegor inom och utanför avdelningen. Vi ser att du är ansvarstagande och ordningsam, samt bekväm med fysiskt arbete. Arbete med truck kommer att vara en del av din vardag.

Dina primära arbetsuppgifter kommer att vara:

- Hantering av inkommande samt utgående gods
- Provtagning av råvaror
- Hantering av råvaror och material på lagret
- Underhåll av faciliteter och viss utrustning
- Hantering av avfall


Vem är du?

Vi ser att du:

- Har gymnasieutbildning
- Har truckkort enligt TLP10, minsta krav: B1 (motviktstruck).
- Har goda kunskaper i engelska, både i tal och skrift.
- Trivs med att arbeta självständigt
- Är flexibel och kan arbeta med flera arbetsuppgifter parallellt
- Är strukturerad och kan följa skriftliga instruktioner


Det är meriterande om:

- Du har arbetat på lager inom läkemedelsbranschen

Vad vi erbjuder

- En tydlig lönestruktur
- En dynamisk arbetsplats med trevliga kollegor
- Öppen, rak och omhändertagande kultur
- Flexibla arbetstider
- 25 dagars semester
- Friskvårdsbidrag (400 SEK/månad)


Tjänsten är på heltid och börjar med en 6 månaders provanställning och övergår därefter i en tillsvidareanställning. Arbetstiderna är 8-17 inklusive 1 timmes lunch.

Vi erbjuder en arbetsplats med god social miljö, där individuellt ansvar är mycket viktigt. Alla medarbetare hos oss är från olika bakgrunder, både utbildningsmässigt och kulturellt, och allas bidrag är lika viktigt för att nå våra mål.

Du kommer att kunna påverka detaljer som rör ditt arbete och förslag på förbättringar uppmuntras.

Du kommer att ansluta till ett företag i en väldigt expansiv och spännande period.

Ansökningstiden är satt till 17 Augusti!

För frågor gällande rekryteringen, kontakta Stefanie Olsson: [email protected] (mailto:[email protected]) Telefon: 070 935 09 07

Under veckorna 29-32 är tillgängligheten begränsad, skicka därför ett mail med dina frågor så besvaras dessa snarast möjligast. Visa mindre