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  1. home
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  6. drug product specialist – consulting assignment at astrazeneca, södertälje
pharmacist
professional

drug product specialist – consulting assignment at astrazeneca, södertälje

nacka, stockholm
posted today
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job details

last day to apply 4

summary

  • nacka, stockholm
  • contingent
  • full-time

posted 6 august 2026

number of offers
2
reference number
JN -082026-619525

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randstad professional

randstad professional

we bring diverse and pre qualified professional talent and businesses together to connect the right people with the right roles. by building specialized teams, we help individuals flourish in their careers and businesses succeed.

job details

Are you passionate about working at the intersection of biological science and commercial manufacturing? On behalf of AstraZeneca, Randstad Life Sciences is currently seeking an ambitious and experienced Drug Product Specialist (also known as 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 state-of-the-art facility in Södertälje.

As a Drug Product Specialist, you will be responsible for the scientific and technical aspects of new product introductions, technology transfers, and commercial manufacturing support within drug product processes. The role encompasses both the implementation of new processes and support for existing commercial products, bringing your scientific expertise to areas such as formulation, aseptic filling, lyophilization, and visual inspection.

Key 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.

Who We Are Looking For

We are looking for someone with a strong scientific foundation who thrives in an environment where science meets manufacturing. You are comfortable taking ownership, driving technical and scientific topics forward, and translating complex data and process challenges into clear decisions and practical solutions. You are adaptable and proactive in identifying improvements to increase organizational effectiveness.

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 specific focus on drug products.
  • Technical Expertise: Hands-on experience in one or more relevant areas, including formulation, aseptic filling, lyophilization, and visual inspection.
  • Language: Excellent written and spoken communication skills in English.

Desirable 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.

Important Information & Candidate Process

  • Consulting Details: This role is a contract assignment through Randstad Life Sciences based at AstraZeneca in Södertälje.
  • Background Check: All candidates chosen for this assignment must successfully complete a standard background check as well as an alcohol and drug screening prior to employment.
  • Application: Applications must be submitted in English using the required ERMO CV format.

About AstraZeneca & Randstad Life Sciences

AstraZeneca is a global, science-led biopharmaceutical company that focuses on the discovery, development, and commercialization of prescription medicines. Operating in Södertälje, one of the world's largest medicines manufacturing sites, AstraZeneca turns ideas into life-changing medicines to improve patients' lives worldwide.

Randstad Life Sciences specializes in matching top-tier scientific and engineering talent with leading life science companies. As a consultant with Randstad, you gain access to exciting assignments, career development opportunities, and a supportive employer network.

How to Apply

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

...

Are you passionate about working at the intersection of biological science and commercial manufacturing? On behalf of AstraZeneca, Randstad Life Sciences is currently seeking an ambitious and experienced Drug Product Specialist (also known as 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 state-of-the-art facility in Södertälje.

As a Drug Product Specialist, you will be responsible for the scientific and technical aspects of new product introductions, technology transfers, and commercial manufacturing support within drug product processes. The role encompasses both the implementation of new processes and support for existing commercial products, bringing your scientific expertise to areas such as formulation, aseptic filling, lyophilization, and visual inspection.

Key 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.

Who We Are Looking For

We are looking for someone with a strong scientific foundation who thrives in an environment where science meets manufacturing. You are comfortable taking ownership, driving technical and scientific topics forward, and translating complex data and process challenges into clear decisions and practical solutions. You are adaptable and proactive in identifying improvements to increase organizational effectiveness.

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 specific focus on drug products.
  • Technical Expertise: Hands-on experience in one or more relevant areas, including formulation, aseptic filling, lyophilization, and visual inspection.
  • Language: Excellent written and spoken communication skills in English.

Desirable 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.

Important Information & Candidate Process

  • Consulting Details: This role is a contract assignment through Randstad Life Sciences based at AstraZeneca in Södertälje.
  • Background Check: All candidates chosen for this assignment must successfully complete a standard background check as well as an alcohol and drug screening prior to employment.
  • Application: Applications must be submitted in English using the required ERMO CV format.

About AstraZeneca & Randstad Life Sciences

AstraZeneca is a global, science-led biopharmaceutical company that focuses on the discovery, development, and commercialization of prescription medicines. Operating in Södertälje, one of the world's largest medicines manufacturing sites, AstraZeneca turns ideas into life-changing medicines to improve patients' lives worldwide.

Randstad Life Sciences specializes in matching top-tier scientific and engineering talent with leading life science companies. As a consultant with Randstad, you gain access to exciting assignments, career development opportunities, and a supportive employer network.

How to Apply

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

  • experience

    Senior
  • qualification

    • 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.


  • key 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.


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