Receptarie - Lediga jobb

Välkommen till Apoteket, nummer ett sedan 1971. Med visioner för framtiden och kvalitet i varje detalj, skapar vi förutsättningar för ett liv i hälsa. Hos oss utvecklas du i en kultur där din röst alltid blir hörd. Och allt vi får över ger vi tillbaka till samhället. Det är så vi gör skillnad på riktigt.

Vill du vara med från start och samtidigt utvecklas i din roll som farmaceut? I höst öppnar vi ett nytt apotek i Väsby Centrum – och söker dig som vill bidra, påverka och ta initiativ.

Väsby Centrum är lättillgängligt och erbjuder ett brett utbud av handel och service. Det gör det till en naturlig destination för många – vilket skapar ett jämnt flöde av kunder och en varierad arbetsdag.

Här är du med och bygger upp både arbetssätt och teamkänsla. Du möter kunder med olika behov och bidrar med din service, ditt driv och din vilja att hjälpa.

Vardagen präglas av variation, många kundmöten och ett nära samarbete med kollegor. Tillsammans skapar vi en arbetsplats där det är enkelt att samarbeta, dela kunskap och hjälpa varandra.

Du får möjlighet att påverka hur vi jobbar – och vara med och sätta tonen för både teamet och kundupplevelsen.

Apotekets öppettider kommer att vara: Måndag-fredag 9-19, lördag 10-18, söndag 11-18.

Som farmaceut hos oss arbetar du alltid med omtanke, kvalitet och kundens behov i fokus. Du bidrar till en trygg, professionell och välkomnande upplevelse för alla som besöker apoteket. I ditt uppdrag ingår rådgivning, receptexpedition och egenvård, där du tar ansvar för hög service och trygghet i varje kundmöte.

För dig som vill utvecklas finns möjlighet att ta extra ansvar, exempelvis som läkemedelsansvarig eller farmaciledare.

• Ge professionell rådgivning och skapa mervärde i varje kundmöte, med omtanke och förståelse för människors olika behov.

• Bidra till patientsäkerhet och kvalitet i allt du gör, så att våra kunder kan känna sig trygga med oss.

• Dela kunskap och erfarenhet med dina kollegor – vi växer och utvecklas tillsammans.

• Hålla dig uppdaterad kring vårt sortiment och våra kampanjer, för att ge kunderna bästa möjliga hjälp.

• Bidra med idéer och initiativ för att utveckla både arbetsvardagen och kundupplevelsen på vårt apotek.

För den här tjänsten behöver du vara legitimerad receptarie eller apotekare, med ett tydligt intresse för människor, hälsa och läkemedel.

• Du är en erfaren farmaceut eller nyexaminerad.

• Du har ett varmt och professionellt bemötande där du ser varje kund.

• Du samarbetar gärna och bidrar positivt till teamet.

• Vi tror att du trivs i ett sammanhang där struktur och resultat går hand i hand.

• Friskvårdsbidrag: 5000 kr per år.

• Personalrabatt: Förmånliga priser på många av våra produkter.

• Flexibla helgdagar: Möjlighet att byta arbetsfria helgdagar mot andra dagar på året.

• Förmånsportal (Benifex): Erbjudanden inom bland annat kollektivtrafik, leasingbil, gym och hälsobehandlingar.

• Trygga försäkringar: Förstärkt föräldrapenning, tjänstepension (ITP) och kompletterande försäkringar.

Apoteket grundades 1971 och ägs av svenska staten, vilket innebär att vi arbetar både ansvarsfullt och långsiktigt. Vårt viktiga samhällsuppdrag handlar om att förbättra människors hälsa, läkemedelsanvändning och bidra till ökad patientsäkerhet. Med omkring 400 apotek och 3000 medarbetare över hela landet har vi nära samarbete med hälso- och sjukvården – alltid med omtanke om både människor och miljö.

Vårt mål är tydligt: Ett liv i hälsa, för alla.

Hör av dig om rollen fångar ditt intresse! Vi berättar gärna mer om tjänsten och vår verksamhet – så du får en tydligare bild och kan avgöra om det känns helt rätt. Vänta bara inte för länge, urval och intervju sker löpande och tjänsten kan tillsättas innan sista ansökningsdatum.

Skicka ditt CV tillsammans med svar på våra urvalsfrågor. Du behöver inte skriva ett personligt brev – frågorna är utformade för att hjälpa oss förstå mer om dina erfarenheter och kompetenser för matchning mot tjänst.

Vi använder tester för objektivt urval som en del av vår rekryteringsprocess. Provanställning tillämpas.

Job description

About the Role

Are you passionate about working at the intersection of biological science and commercial manufacturing? On behalf of AstraZeneca, Randstad Life Sciences is looking for an ambitious and experienced Drug Product Specialist (Process Scientist) to join the Manufacturing Science & Technology (MS&T) team in Södertälje.

This is a full-time consulting assignment where you will be employed by Randstad Life Sciences and work on-site at AstraZeneca's facility in Södertälje.

You will be responsible for the scientific and technical aspects of new product introductions, technology transfers, and commercial manufacturing support within drug product processes (e.g., formulation, aseptic filling, lyophilization, and visual inspection).

Key Responsibilities

• Technology Transfer: Lead scientific aspects in new product introductions and technology transfers for drug product processes.
• Process Robustness: Ensure commercial process robustness through risk assessments, technical studies, data analysis, and scientific recommendations.
• Validation & Maintenance: Lead process performance qualification (PPQ) and contribute to product maintenance.
• Operational Support: Provide product-specific technical support to ongoing commercial operations.
• Cross-Functional Collaboration: Partner with Operations, Engineering, QA, QC, Supply Chain, and global teams.
• Compliance: Contribute to GMP documentation and regulatory submissions.

Requirements

Essential Requirements

• Education: MSc or higher in biotechnology, chemical engineering, pharmacy, or another relevant life science/engineering discipline.
• Experience: 3+ years of experience in biologics, pharmaceutical development, technology transfer, or commercial manufacturing, with a focus on drug products.
• Technical Expertise: Hands-on experience in one or more areas: formulation, aseptic filling, lyophilization, or visual inspection.
• Language: Excellent written and spoken communication skills in English.

Desirable Qualifications

• PhD or advanced specialization in a relevant field.
• Previous experience at AstraZeneca.
• Experience working in global and cross-functional teams.
• Knowledge of single-use systems, isolator technology, or finished pack manufacturing.
• Experience with project management, digital transformation, or AI applications in manufacturing.

Soft Skills & Profile

• Organized, analytical, adaptable, and detail-oriented.
• Strong teamwork abilities combined with the confidence to work independently.
• Proactive mindset—takes initiative to drive progress rather than waiting for instructions.

Important Information

• Consulting Details: Full-time contract assignment through Randstad Life Sciences based on-site at AstraZeneca in Södertälje.
• Background Check: Selected candidates must successfully complete a standard background check and drug/alcohol screening prior to employment.

How to Apply

Please submit your application and CV in English as soon as possible. Applications are evaluated continuously!

Responsibilities

• Technology Transfer & Product Introduction: Lead scientific aspects in new product introductions and technology transfers for drug product processes.
• Process Robustness & Quality: Ensure commercial process robustness through process understanding, risk assessments, technical studies, data analysis, and sound scientific recommendations.
• Validation & Maintenance: Lead process validation / process performance qualification and contribute to product maintenance.
• Operational Support: Provide product-specific scientific and technical support to ongoing commercial operations.
• Continuous Improvement: Contribute to the development of ways of working, digital templates, and risk-based approaches to enable consistency and efficiency across MS&T activities.
• Cross-Functional Collaboration: Work closely with Operations, Engineering, QA, QC, Supply Chain, global teams, development functions, and external partners.
• Compliance: Contribute to GMP documentation and regulatory submissions.

Qualifications

• PhD or advanced specialization in a relevant field.
• Previous experience working at AstraZeneca.
• Proven experience working in global and cross-functional teams.
• Knowledge of single-use systems, isolator technology, or finished pack manufacturing.
• Previous project management experience.
• Understanding of digital transformation and AI applications in manufacturing, process monitoring, or technical support activities.

Soft Skills & Personal Profile

• Highly organized, analytical, adaptable, and detail-oriented.
• Strong teamwork capabilities combined with the confidence to work independently.
• Demonstrates initiative, takes a proactive approach to challenges, and actively drives progress rather than waiting for instructions or resisting change.

About the company

Randstad

Job description

About the Role

Are you passionate about working at the intersection of biological science and commercial manufacturing? On behalf of AstraZeneca, Randstad Life Sciences is looking for an ambitious and experienced Drug Product Specialist (Process Scientist) to join the Manufacturing Science & Technology (MS&T) team in Södertälje.

This is a full-time consulting assignment where you will be employed by Randstad Life Sciences and work on-site at AstraZeneca's facility in Södertälje.

You will be responsible for the scientific and technical aspects of new product introductions, technology transfers, and commercial manufacturing support within drug product processes (e.g., formulation, aseptic filling, lyophilization, and visual inspection).

Key Responsibilities

• Technology Transfer: Lead scientific aspects in new product introductions and technology transfers for drug product processes.
• Process Robustness: Ensure commercial process robustness through risk assessments, technical studies, data analysis, and scientific recommendations.
• Validation & Maintenance: Lead process performance qualification (PPQ) and contribute to product maintenance.
• Operational Support: Provide product-specific technical support to ongoing commercial operations.
• Cross-Functional Collaboration: Partner with Operations, Engineering, QA, QC, Supply Chain, and global teams.
• Compliance: Contribute to GMP documentation and regulatory submissions.

Requirements

Essential Requirements

• Education: MSc or higher in biotechnology, chemical engineering, pharmacy, or another relevant life science/engineering discipline.
• Experience: 3+ years of experience in biologics, pharmaceutical development, technology transfer, or commercial manufacturing, with a focus on drug products.
• Technical Expertise: Hands-on experience in one or more areas: formulation, aseptic filling, lyophilization, or visual inspection.
• Language: Excellent written and spoken communication skills in English.

Desirable Qualifications

• PhD or advanced specialization in a relevant field.
• Previous experience at AstraZeneca.
• Experience working in global and cross-functional teams.
• Knowledge of single-use systems, isolator technology, or finished pack manufacturing.
• Experience with project management, digital transformation, or AI applications in manufacturing.

Soft Skills & Profile

• Organized, analytical, adaptable, and detail-oriented.
• Strong teamwork abilities combined with the confidence to work independently.
• Proactive mindset—takes initiative to drive progress rather than waiting for instructions.

Important Information

• Consulting Details: Full-time contract assignment through Randstad Life Sciences based on-site at AstraZeneca in Södertälje.
• Background Check: Selected candidates must successfully complete a standard background check and drug/alcohol screening prior to employment.

How to Apply

Please submit your application and CV in English as soon as possible. Applications are evaluated continuously!

Responsibilities

• Technology Transfer & Product Introduction: Lead scientific aspects in new product introductions and technology transfers for drug product processes.
• Process Robustness & Quality: Ensure commercial process robustness through process understanding, risk assessments, technical studies, data analysis, and sound scientific recommendations.
• Validation & Maintenance: Lead process validation / process performance qualification and contribute to product maintenance.
• Operational Support: Provide product-specific scientific and technical support to ongoing commercial operations.
• Continuous Improvement: Contribute to the development of ways of working, digital templates, and risk-based approaches to enable consistency and efficiency across MS&T activities.
• Cross-Functional Collaboration: Work closely with Operations, Engineering, QA, QC, Supply Chain, global teams, development functions, and external partners.
• Compliance: Contribute to GMP documentation and regulatory submissions.

Qualifications

• PhD or advanced specialization in a relevant field.
• Previous experience working at AstraZeneca.
• Proven experience working in global and cross-functional teams.
• Knowledge of single-use systems, isolator technology, or finished pack manufacturing.
• Previous project management experience.
• Understanding of digital transformation and AI applications in manufacturing, process monitoring, or technical support activities.

Soft Skills & Personal Profile

• Highly organized, analytical, adaptable, and detail-oriented.
• Strong teamwork capabilities combined with the confidence to work independently.
• Demonstrates initiative, takes a proactive approach to challenges, and actively drives progress rather than waiting for instructions or resisting change.

About the company

Randstad

Job description

About the Role

Are you passionate about working at the intersection of biological science and commercial manufacturing? On behalf of AstraZeneca, Randstad Life Sciences is looking for an ambitious and experienced Drug Product Specialist (Process Scientist) to join the Manufacturing Science & Technology (MS&T) team in Södertälje.

This is a full-time consulting assignment where you will be employed by Randstad Life Sciences and work on-site at AstraZeneca's facility in Södertälje.

You will be responsible for the scientific and technical aspects of new product introductions, technology transfers, and commercial manufacturing support within drug product processes (e.g., formulation, aseptic filling, lyophilization, and visual inspection).

Key Responsibilities

• Technology Transfer: Lead scientific aspects in new product introductions and technology transfers for drug product processes.
• Process Robustness: Ensure commercial process robustness through risk assessments, technical studies, data analysis, and scientific recommendations.
• Validation & Maintenance: Lead process performance qualification (PPQ) and contribute to product maintenance.
• Operational Support: Provide product-specific technical support to ongoing commercial operations.
• Cross-Functional Collaboration: Partner with Operations, Engineering, QA, QC, Supply Chain, and global teams.
• Compliance: Contribute to GMP documentation and regulatory submissions.

Requirements

Essential Requirements

• Education: MSc or higher in biotechnology, chemical engineering, pharmacy, or another relevant life science/engineering discipline.
• Experience: 3+ years of experience in biologics, pharmaceutical development, technology transfer, or commercial manufacturing, with a focus on drug products.
• Technical Expertise: Hands-on experience in one or more areas: formulation, aseptic filling, lyophilization, or visual inspection.
• Language: Excellent written and spoken communication skills in English.

Desirable Qualifications

• PhD or advanced specialization in a relevant field.
• Previous experience at AstraZeneca.
• Experience working in global and cross-functional teams.
• Knowledge of single-use systems, isolator technology, or finished pack manufacturing.
• Experience with project management, digital transformation, or AI applications in manufacturing.

Soft Skills & Profile

• Organized, analytical, adaptable, and detail-oriented.
• Strong teamwork abilities combined with the confidence to work independently.
• Proactive mindset—takes initiative to drive progress rather than waiting for instructions.

Important Information

• Consulting Details: Full-time contract assignment through Randstad Life Sciences based on-site at AstraZeneca in Södertälje.
• Background Check: Selected candidates must successfully complete a standard background check and drug/alcohol screening prior to employment.

How to Apply

Please submit your application and CV in English as soon as possible. Applications are evaluated continuously!

Responsibilities

• Technology Transfer & Product Introduction: Lead scientific aspects in new product introductions and technology transfers for drug product processes.
• Process Robustness & Quality: Ensure commercial process robustness through process understanding, risk assessments, technical studies, data analysis, and sound scientific recommendations.
• Validation & Maintenance: Lead process validation / process performance qualification and contribute to product maintenance.
• Operational Support: Provide product-specific scientific and technical support to ongoing commercial operations.
• Continuous Improvement: Contribute to the development of ways of working, digital templates, and risk-based approaches to enable consistency and efficiency across MS&T activities.
• Cross-Functional Collaboration: Work closely with Operations, Engineering, QA, QC, Supply Chain, global teams, development functions, and external partners.
• Compliance: Contribute to GMP documentation and regulatory submissions.

Qualifications

• PhD or advanced specialization in a relevant field.
• Previous experience working at AstraZeneca.
• Proven experience working in global and cross-functional teams.
• Knowledge of single-use systems, isolator technology, or finished pack manufacturing.
• Previous project management experience.
• Understanding of digital transformation and AI applications in manufacturing, process monitoring, or technical support activities.

Soft Skills & Personal Profile

• Highly organized, analytical, adaptable, and detail-oriented.
• Strong teamwork capabilities combined with the confidence to work independently.
• Demonstrates initiative, takes a proactive approach to challenges, and actively drives progress rather than waiting for instructions or resisting change.

About the company

Randstad

Job description

About the Role

Are you passionate about working at the intersection of biological science and commercial manufacturing? On behalf of AstraZeneca, Randstad Life Sciences is looking for an ambitious and experienced Drug Product Specialist (Process Scientist) to join the Manufacturing Science & Technology (MS&T) team in Södertälje.

This is a full-time consulting assignment where you will be employed by Randstad Life Sciences and work on-site at AstraZeneca's facility in Södertälje.

You will be responsible for the scientific and technical aspects of new product introductions, technology transfers, and commercial manufacturing support within drug product processes (e.g., formulation, aseptic filling, lyophilization, and visual inspection).

Key Responsibilities

• Technology Transfer: Lead scientific aspects in new product introductions and technology transfers for drug product processes.
• Process Robustness: Ensure commercial process robustness through risk assessments, technical studies, data analysis, and scientific recommendations.
• Validation & Maintenance: Lead process performance qualification (PPQ) and contribute to product maintenance.
• Operational Support: Provide product-specific technical support to ongoing commercial operations.
• Cross-Functional Collaboration: Partner with Operations, Engineering, QA, QC, Supply Chain, and global teams.
• Compliance: Contribute to GMP documentation and regulatory submissions.

Requirements

Essential Requirements

• Education: MSc or higher in biotechnology, chemical engineering, pharmacy, or another relevant life science/engineering discipline.
• Experience: 3+ years of experience in biologics, pharmaceutical development, technology transfer, or commercial manufacturing, with a focus on drug products.
• Technical Expertise: Hands-on experience in one or more areas: formulation, aseptic filling, lyophilization, or visual inspection.
• Language: Excellent written and spoken communication skills in English.

Desirable Qualifications

• PhD or advanced specialization in a relevant field.
• Previous experience at AstraZeneca.
• Experience working in global and cross-functional teams.
• Knowledge of single-use systems, isolator technology, or finished pack manufacturing.
• Experience with project management, digital transformation, or AI applications in manufacturing.

Soft Skills & Profile

• Organized, analytical, adaptable, and detail-oriented.
• Strong teamwork abilities combined with the confidence to work independently.
• Proactive mindset—takes initiative to drive progress rather than waiting for instructions.

Important Information

• Consulting Details: Full-time contract assignment through Randstad Life Sciences based on-site at AstraZeneca in Södertälje.
• Background Check: Selected candidates must successfully complete a standard background check and drug/alcohol screening prior to employment.

How to Apply

Please submit your application and CV in English as soon as possible. Applications are evaluated continuously!

Responsibilities

• Technology Transfer & Product Introduction: Lead scientific aspects in new product introductions and technology transfers for drug product processes.
• Process Robustness & Quality: Ensure commercial process robustness through process understanding, risk assessments, technical studies, data analysis, and sound scientific recommendations.
• Validation & Maintenance: Lead process validation / process performance qualification and contribute to product maintenance.
• Operational Support: Provide product-specific scientific and technical support to ongoing commercial operations.
• Continuous Improvement: Contribute to the development of ways of working, digital templates, and risk-based approaches to enable consistency and efficiency across MS&T activities.
• Cross-Functional Collaboration: Work closely with Operations, Engineering, QA, QC, Supply Chain, global teams, development functions, and external partners.
• Compliance: Contribute to GMP documentation and regulatory submissions.

Qualifications

• PhD or advanced specialization in a relevant field.
• Previous experience working at AstraZeneca.
• Proven experience working in global and cross-functional teams.
• Knowledge of single-use systems, isolator technology, or finished pack manufacturing.
• Previous project management experience.
• Understanding of digital transformation and AI applications in manufacturing, process monitoring, or technical support activities.

Soft Skills & Personal Profile

• Highly organized, analytical, adaptable, and detail-oriented.
• Strong teamwork capabilities combined with the confidence to work independently.
• Demonstrates initiative, takes a proactive approach to challenges, and actively drives progress rather than waiting for instructions or resisting change.

About the company

Randstad

Job description

About the Role

Are you passionate about working at the intersection of biological science and commercial manufacturing? On behalf of AstraZeneca, Randstad Life Sciences is looking for an ambitious and experienced Drug Product Specialist (Process Scientist) to join the Manufacturing Science & Technology (MS&T) team in Södertälje.

This is a full-time consulting assignment where you will be employed by Randstad Life Sciences and work on-site at AstraZeneca's facility in Södertälje.

You will be responsible for the scientific and technical aspects of new product introductions, technology transfers, and commercial manufacturing support within drug product processes (e.g., formulation, aseptic filling, lyophilization, and visual inspection).

Key Responsibilities

• Technology Transfer: Lead scientific aspects in new product introductions and technology transfers for drug product processes.
• Process Robustness: Ensure commercial process robustness through risk assessments, technical studies, data analysis, and scientific recommendations.
• Validation & Maintenance: Lead process performance qualification (PPQ) and contribute to product maintenance.
• Operational Support: Provide product-specific technical support to ongoing commercial operations.
• Cross-Functional Collaboration: Partner with Operations, Engineering, QA, QC, Supply Chain, and global teams.
• Compliance: Contribute to GMP documentation and regulatory submissions.

Requirements

Essential Requirements

• Education: MSc or higher in biotechnology, chemical engineering, pharmacy, or another relevant life science/engineering discipline.
• Experience: 3+ years of experience in biologics, pharmaceutical development, technology transfer, or commercial manufacturing, with a focus on drug products.
• Technical Expertise: Hands-on experience in one or more areas: formulation, aseptic filling, lyophilization, or visual inspection.
• Language: Excellent written and spoken communication skills in English.

Desirable Qualifications

• PhD or advanced specialization in a relevant field.
• Previous experience at AstraZeneca.
• Experience working in global and cross-functional teams.
• Knowledge of single-use systems, isolator technology, or finished pack manufacturing.
• Experience with project management, digital transformation, or AI applications in manufacturing.

Soft Skills & Profile

• Organized, analytical, adaptable, and detail-oriented.
• Strong teamwork abilities combined with the confidence to work independently.
• Proactive mindset—takes initiative to drive progress rather than waiting for instructions.

Important Information

• Consulting Details: Full-time contract assignment through Randstad Life Sciences based on-site at AstraZeneca in Södertälje.
• Background Check: Selected candidates must successfully complete a standard background check and drug/alcohol screening prior to employment.

How to Apply

Please submit your application and CV in English as soon as possible. Applications are evaluated continuously!

Responsibilities

• Technology Transfer & Product Introduction: Lead scientific aspects in new product introductions and technology transfers for drug product processes.
• Process Robustness & Quality: Ensure commercial process robustness through process understanding, risk assessments, technical studies, data analysis, and sound scientific recommendations.
• Validation & Maintenance: Lead process validation / process performance qualification and contribute to product maintenance.
• Operational Support: Provide product-specific scientific and technical support to ongoing commercial operations.
• Continuous Improvement: Contribute to the development of ways of working, digital templates, and risk-based approaches to enable consistency and efficiency across MS&T activities.
• Cross-Functional Collaboration: Work closely with Operations, Engineering, QA, QC, Supply Chain, global teams, development functions, and external partners.
• Compliance: Contribute to GMP documentation and regulatory submissions.

Qualifications

• PhD or advanced specialization in a relevant field.
• Previous experience working at AstraZeneca.
• Proven experience working in global and cross-functional teams.
• Knowledge of single-use systems, isolator technology, or finished pack manufacturing.
• Previous project management experience.
• Understanding of digital transformation and AI applications in manufacturing, process monitoring, or technical support activities.

Soft Skills & Personal Profile

• Highly organized, analytical, adaptable, and detail-oriented.
• Strong teamwork capabilities combined with the confidence to work independently.
• Demonstrates initiative, takes a proactive approach to challenges, and actively drives progress rather than waiting for instructions or resisting change.

About the company

Randstad

Job description

About the Role

Are you passionate about working at the intersection of biological science and commercial manufacturing? On behalf of AstraZeneca, Randstad Life Sciences is looking for an ambitious and experienced Drug Product Specialist (Process Scientist) to join the Manufacturing Science & Technology (MS&T) team in Södertälje.

This is a full-time consulting assignment where you will be employed by Randstad Life Sciences and work on-site at AstraZeneca's facility in Södertälje.

You will be responsible for the scientific and technical aspects of new product introductions, technology transfers, and commercial manufacturing support within drug product processes (e.g., formulation, aseptic filling, lyophilization, and visual inspection).

Key Responsibilities

• Technology Transfer: Lead scientific aspects in new product introductions and technology transfers for drug product processes.
• Process Robustness: Ensure commercial process robustness through risk assessments, technical studies, data analysis, and scientific recommendations.
• Validation & Maintenance: Lead process performance qualification (PPQ) and contribute to product maintenance.
• Operational Support: Provide product-specific technical support to ongoing commercial operations.
• Cross-Functional Collaboration: Partner with Operations, Engineering, QA, QC, Supply Chain, and global teams.
• Compliance: Contribute to GMP documentation and regulatory submissions.

Requirements

Essential Requirements

• Education: MSc or higher in biotechnology, chemical engineering, pharmacy, or another relevant life science/engineering discipline.
• Experience: 3+ years of experience in biologics, pharmaceutical development, technology transfer, or commercial manufacturing, with a focus on drug products.
• Technical Expertise: Hands-on experience in one or more areas: formulation, aseptic filling, lyophilization, or visual inspection.
• Language: Excellent written and spoken communication skills in English.

Desirable Qualifications

• PhD or advanced specialization in a relevant field.
• Previous experience at AstraZeneca.
• Experience working in global and cross-functional teams.
• Knowledge of single-use systems, isolator technology, or finished pack manufacturing.
• Experience with project management, digital transformation, or AI applications in manufacturing.

Soft Skills & Profile

• Organized, analytical, adaptable, and detail-oriented.
• Strong teamwork abilities combined with the confidence to work independently.
• Proactive mindset—takes initiative to drive progress rather than waiting for instructions.

Important Information

• Consulting Details: Full-time contract assignment through Randstad Life Sciences based on-site at AstraZeneca in Södertälje.
• Background Check: Selected candidates must successfully complete a standard background check and drug/alcohol screening prior to employment.

How to Apply

Please submit your application and CV in English as soon as possible. Applications are evaluated continuously!

Responsibilities

• Technology Transfer & Product Introduction: Lead scientific aspects in new product introductions and technology transfers for drug product processes.
• Process Robustness & Quality: Ensure commercial process robustness through process understanding, risk assessments, technical studies, data analysis, and sound scientific recommendations.
• Validation & Maintenance: Lead process validation / process performance qualification and contribute to product maintenance.
• Operational Support: Provide product-specific scientific and technical support to ongoing commercial operations.
• Continuous Improvement: Contribute to the development of ways of working, digital templates, and risk-based approaches to enable consistency and efficiency across MS&T activities.
• Cross-Functional Collaboration: Work closely with Operations, Engineering, QA, QC, Supply Chain, global teams, development functions, and external partners.
• Compliance: Contribute to GMP documentation and regulatory submissions.

Qualifications

• PhD or advanced specialization in a relevant field.
• Previous experience working at AstraZeneca.
• Proven experience working in global and cross-functional teams.
• Knowledge of single-use systems, isolator technology, or finished pack manufacturing.
• Previous project management experience.
• Understanding of digital transformation and AI applications in manufacturing, process monitoring, or technical support activities.

Soft Skills & Personal Profile

• Highly organized, analytical, adaptable, and detail-oriented.
• Strong teamwork capabilities combined with the confidence to work independently.
• Demonstrates initiative, takes a proactive approach to challenges, and actively drives progress rather than waiting for instructions or resisting change.

About the company

Randstad

Job description

About the Role

Are you passionate about working at the intersection of biological science and commercial manufacturing? On behalf of AstraZeneca, Randstad Life Sciences is looking for an ambitious and experienced Drug Product Specialist (Process Scientist) to join the Manufacturing Science & Technology (MS&T) team in Södertälje.

This is a full-time consulting assignment where you will be employed by Randstad Life Sciences and work on-site at AstraZeneca's facility in Södertälje.

You will be responsible for the scientific and technical aspects of new product introductions, technology transfers, and commercial manufacturing support within drug product processes (e.g., formulation, aseptic filling, lyophilization, and visual inspection).

Key Responsibilities

• Technology Transfer: Lead scientific aspects in new product introductions and technology transfers for drug product processes.
• Process Robustness: Ensure commercial process robustness through risk assessments, technical studies, data analysis, and scientific recommendations.
• Validation & Maintenance: Lead process performance qualification (PPQ) and contribute to product maintenance.
• Operational Support: Provide product-specific technical support to ongoing commercial operations.
• Cross-Functional Collaboration: Partner with Operations, Engineering, QA, QC, Supply Chain, and global teams.
• Compliance: Contribute to GMP documentation and regulatory submissions.

Requirements

Essential Requirements

• Education: MSc or higher in biotechnology, chemical engineering, pharmacy, or another relevant life science/engineering discipline.
• Experience: 3+ years of experience in biologics, pharmaceutical development, technology transfer, or commercial manufacturing, with a focus on drug products.
• Technical Expertise: Hands-on experience in one or more areas: formulation, aseptic filling, lyophilization, or visual inspection.
• Language: Excellent written and spoken communication skills in English.

Desirable Qualifications

• PhD or advanced specialization in a relevant field.
• Previous experience at AstraZeneca.
• Experience working in global and cross-functional teams.
• Knowledge of single-use systems, isolator technology, or finished pack manufacturing.
• Experience with project management, digital transformation, or AI applications in manufacturing.

Soft Skills & Profile

• Organized, analytical, adaptable, and detail-oriented.
• Strong teamwork abilities combined with the confidence to work independently.
• Proactive mindset—takes initiative to drive progress rather than waiting for instructions.

Important Information

• Consulting Details: Full-time contract assignment through Randstad Life Sciences based on-site at AstraZeneca in Södertälje.
• Background Check: Selected candidates must successfully complete a standard background check and drug/alcohol screening prior to employment.

How to Apply

Please submit your application and CV in English as soon as possible. Applications are evaluated continuously!

Responsibilities

• Technology Transfer & Product Introduction: Lead scientific aspects in new product introductions and technology transfers for drug product processes.
• Process Robustness & Quality: Ensure commercial process robustness through process understanding, risk assessments, technical studies, data analysis, and sound scientific recommendations.
• Validation & Maintenance: Lead process validation / process performance qualification and contribute to product maintenance.
• Operational Support: Provide product-specific scientific and technical support to ongoing commercial operations.
• Continuous Improvement: Contribute to the development of ways of working, digital templates, and risk-based approaches to enable consistency and efficiency across MS&T activities.
• Cross-Functional Collaboration: Work closely with Operations, Engineering, QA, QC, Supply Chain, global teams, development functions, and external partners.
• Compliance: Contribute to GMP documentation and regulatory submissions.

Qualifications

• PhD or advanced specialization in a relevant field.
• Previous experience working at AstraZeneca.
• Proven experience working in global and cross-functional teams.
• Knowledge of single-use systems, isolator technology, or finished pack manufacturing.
• Previous project management experience.
• Understanding of digital transformation and AI applications in manufacturing, process monitoring, or technical support activities.

Soft Skills & Personal Profile

• Highly organized, analytical, adaptable, and detail-oriented.
• Strong teamwork capabilities combined with the confidence to work independently.
• Demonstrates initiative, takes a proactive approach to challenges, and actively drives progress rather than waiting for instructions or resisting change.

About the company

Randstad

Job description

About the Role

Are you passionate about working at the intersection of biological science and commercial manufacturing? On behalf of AstraZeneca, Randstad Life Sciences is looking for an ambitious and experienced Drug Product Specialist (Process Scientist) to join the Manufacturing Science & Technology (MS&T) team in Södertälje.

This is a full-time consulting assignment where you will be employed by Randstad Life Sciences and work on-site at AstraZeneca's facility in Södertälje.

You will be responsible for the scientific and technical aspects of new product introductions, technology transfers, and commercial manufacturing support within drug product processes (e.g., formulation, aseptic filling, lyophilization, and visual inspection).

Key Responsibilities

• Technology Transfer: Lead scientific aspects in new product introductions and technology transfers for drug product processes.
• Process Robustness: Ensure commercial process robustness through risk assessments, technical studies, data analysis, and scientific recommendations.
• Validation & Maintenance: Lead process performance qualification (PPQ) and contribute to product maintenance.
• Operational Support: Provide product-specific technical support to ongoing commercial operations.
• Cross-Functional Collaboration: Partner with Operations, Engineering, QA, QC, Supply Chain, and global teams.
• Compliance: Contribute to GMP documentation and regulatory submissions.

Requirements

Essential Requirements

• Education: MSc or higher in biotechnology, chemical engineering, pharmacy, or another relevant life science/engineering discipline.
• Experience: 3+ years of experience in biologics, pharmaceutical development, technology transfer, or commercial manufacturing, with a focus on drug products.
• Technical Expertise: Hands-on experience in one or more areas: formulation, aseptic filling, lyophilization, or visual inspection.
• Language: Excellent written and spoken communication skills in English.

Desirable Qualifications

• PhD or advanced specialization in a relevant field.
• Previous experience at AstraZeneca.
• Experience working in global and cross-functional teams.
• Knowledge of single-use systems, isolator technology, or finished pack manufacturing.
• Experience with project management, digital transformation, or AI applications in manufacturing.

Soft Skills & Profile

• Organized, analytical, adaptable, and detail-oriented.
• Strong teamwork abilities combined with the confidence to work independently.
• Proactive mindset—takes initiative to drive progress rather than waiting for instructions.

Important Information

• Consulting Details: Full-time contract assignment through Randstad Life Sciences based on-site at AstraZeneca in Södertälje.
• Background Check: Selected candidates must successfully complete a standard background check and drug/alcohol screening prior to employment.

How to Apply

Please submit your application and CV in English as soon as possible. Applications are evaluated continuously!

Responsibilities

• Technology Transfer & Product Introduction: Lead scientific aspects in new product introductions and technology transfers for drug product processes.
• Process Robustness & Quality: Ensure commercial process robustness through process understanding, risk assessments, technical studies, data analysis, and sound scientific recommendations.
• Validation & Maintenance: Lead process validation / process performance qualification and contribute to product maintenance.
• Operational Support: Provide product-specific scientific and technical support to ongoing commercial operations.
• Continuous Improvement: Contribute to the development of ways of working, digital templates, and risk-based approaches to enable consistency and efficiency across MS&T activities.
• Cross-Functional Collaboration: Work closely with Operations, Engineering, QA, QC, Supply Chain, global teams, development functions, and external partners.
• Compliance: Contribute to GMP documentation and regulatory submissions.

Qualifications

• PhD or advanced specialization in a relevant field.
• Previous experience working at AstraZeneca.
• Proven experience working in global and cross-functional teams.
• Knowledge of single-use systems, isolator technology, or finished pack manufacturing.
• Previous project management experience.
• Understanding of digital transformation and AI applications in manufacturing, process monitoring, or technical support activities.

Soft Skills & Personal Profile

• Highly organized, analytical, adaptable, and detail-oriented.
• Strong teamwork capabilities combined with the confidence to work independently.
• Demonstrates initiative, takes a proactive approach to challenges, and actively drives progress rather than waiting for instructions or resisting change.

About the company

Randstad

Job description

About the Role

Are you passionate about working at the intersection of biological science and commercial manufacturing? On behalf of AstraZeneca, Randstad Life Sciences is looking for an ambitious and experienced Drug Product Specialist (Process Scientist) to join the Manufacturing Science & Technology (MS&T) team in Södertälje.

This is a full-time consulting assignment where you will be employed by Randstad Life Sciences and work on-site at AstraZeneca's facility in Södertälje.

You will be responsible for the scientific and technical aspects of new product introductions, technology transfers, and commercial manufacturing support within drug product processes (e.g., formulation, aseptic filling, lyophilization, and visual inspection).

Key Responsibilities

• Technology Transfer: Lead scientific aspects in new product introductions and technology transfers for drug product processes.
• Process Robustness: Ensure commercial process robustness through risk assessments, technical studies, data analysis, and scientific recommendations.
• Validation & Maintenance: Lead process performance qualification (PPQ) and contribute to product maintenance.
• Operational Support: Provide product-specific technical support to ongoing commercial operations.
• Cross-Functional Collaboration: Partner with Operations, Engineering, QA, QC, Supply Chain, and global teams.
• Compliance: Contribute to GMP documentation and regulatory submissions.

Requirements

Essential Requirements

• Education: MSc or higher in biotechnology, chemical engineering, pharmacy, or another relevant life science/engineering discipline.
• Experience: 3+ years of experience in biologics, pharmaceutical development, technology transfer, or commercial manufacturing, with a focus on drug products.
• Technical Expertise: Hands-on experience in one or more areas: formulation, aseptic filling, lyophilization, or visual inspection.
• Language: Excellent written and spoken communication skills in English.

Desirable Qualifications

• PhD or advanced specialization in a relevant field.
• Previous experience at AstraZeneca.
• Experience working in global and cross-functional teams.
• Knowledge of single-use systems, isolator technology, or finished pack manufacturing.
• Experience with project management, digital transformation, or AI applications in manufacturing.

Soft Skills & Profile

• Organized, analytical, adaptable, and detail-oriented.
• Strong teamwork abilities combined with the confidence to work independently.
• Proactive mindset—takes initiative to drive progress rather than waiting for instructions.

Important Information

• Consulting Details: Full-time contract assignment through Randstad Life Sciences based on-site at AstraZeneca in Södertälje.
• Background Check: Selected candidates must successfully complete a standard background check and drug/alcohol screening prior to employment.

How to Apply

Please submit your application and CV in English as soon as possible. Applications are evaluated continuously!

Responsibilities

• Technology Transfer & Product Introduction: Lead scientific aspects in new product introductions and technology transfers for drug product processes.
• Process Robustness & Quality: Ensure commercial process robustness through process understanding, risk assessments, technical studies, data analysis, and sound scientific recommendations.
• Validation & Maintenance: Lead process validation / process performance qualification and contribute to product maintenance.
• Operational Support: Provide product-specific scientific and technical support to ongoing commercial operations.
• Continuous Improvement: Contribute to the development of ways of working, digital templates, and risk-based approaches to enable consistency and efficiency across MS&T activities.
• Cross-Functional Collaboration: Work closely with Operations, Engineering, QA, QC, Supply Chain, global teams, development functions, and external partners.
• Compliance: Contribute to GMP documentation and regulatory submissions.

Qualifications

• PhD or advanced specialization in a relevant field.
• Previous experience working at AstraZeneca.
• Proven experience working in global and cross-functional teams.
• Knowledge of single-use systems, isolator technology, or finished pack manufacturing.
• Previous project management experience.
• Understanding of digital transformation and AI applications in manufacturing, process monitoring, or technical support activities.

Soft Skills & Personal Profile

• Highly organized, analytical, adaptable, and detail-oriented.
• Strong teamwork capabilities combined with the confidence to work independently.
• Demonstrates initiative, takes a proactive approach to challenges, and actively drives progress rather than waiting for instructions or resisting change.

About the company

Randstad