Pharmaceutical Scientist, Consultancy Assignment at AstraZeneca
Randstad AB
Job Description
Full description from the employer, as published by JobTech.
Job description
Are you an experienced scientist or engineer in pharmaceutical or formulation science looking for your next challenge? On behalf of AstraZeneca in Södertälje, Randstad Life Sciences is seeking a Pharmaceutical Scientist (Senior Scientist / Associate Principal Scientist level) to join the Technical Operations, Science and Innovation (TOSI) team.
Please note: This position is a full-time consultancy assignment where you will be employed by Randstad Life Sciences and work on-site as a consultant at AstraZeneca.
About AstraZeneca
AstraZeneca is a major international healthcare business engaged in the research, development, manufacture, and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Co-workers are empowered to express diverse perspectives-and are made to feel valued, energized, and rewarded for their ideas and creativity.
The Role & Responsibilities
In this role, you will support changes and issues for commercial oral solid drug products. You will collaborate closely with site technical teams and TOSI colleagues to resolve issues, drive improvements, and assess technical changes. The role is office-based.
Key responsibilities include:
- Analyzing outputs such as finished product analytical results and process information across multiple manufacturing sites (both internal and external to AstraZeneca).
- Supporting the regulatory department with technical input to respond to health authority inquiries.
- Facilitating technical risk assessments.
Key Requirements
- Education: BSc or MSc in Pharmaceutics, Chemistry, Chemical Engineering, or a related discipline with relevant skills.
- Industry Experience: Proven background in the pharmaceutical industry, preferably working with tablet/capsule formulations within a technical or quality function.
- GMP Standards: Solid understanding and practical experience working within a Good Manufacturing Practice (GMP) environment.
- Language Skills: Excellent written and spoken English is essential (Swedish is a plus, but not mandatory).
Personal Profile
As a person, you should have the ability to operate independently, take ownership, and drive work to completion. You are well-organized, analytical, and flexible. Strong communication and cross-functional teamwork skills across different functions and skill levels are highly valued.
Additional Information & Requirements
- Employment Structure: Consultancy assignment through Randstad Life Sciences at AstraZeneca Gärtuna, Södertälje.
- Assignment Period: Starting ASAP until May 31, 2027.
- Screening Process: All selected candidates will undergo a standard background check as well as an alcohol and drug test.
How to Apply
Please submit your application and CV in English as soon as possible. Applications are reviewed on an ongoing basis.
Welcome with your application!
Responsibilities
- Analyzing outputs such as finished product analytical results and process information across multiple manufacturing sites (both internal and external to AstraZeneca).
- Supporting the regulatory department with technical input to respond to health authority inquiries.
- Facilitating technical risk assessments.
Qualifications
- Education: BSc or MSc in Pharmaceutics, Chemistry, Chemical Engineering, or a related discipline with relevant expertise.
- Industry Experience: Demonstrated background within the pharmaceutical industry, preferably working with tablet/capsule formulations in a technical or quality capacity.
- GMP Standards: Proven understanding and hands-on experience working within a Good Manufacturing Practice (GMP) environment.
- Language Skills: Excellent knowledge of written and spoken English is required. (Swedish skills are considered a plus, but are not mandatory).
About the company
Randstad
På Randstad vet vi att alla människor har en plats på arbetsmarknaden. Med verksamhet över hela landet och inom alla kompetensområden hjälper vi människor att hitta ett jobb som känns bra, och där de får möjlighet att växa, utvecklas och uppnå sin fulla potential. Med närmare 600 000 anställda i 38 länder är Randstad världsledande inom HR-tjänster, med målsättningen att bli världens främsta och mest uppskattade partner på arbetsmarknaden. Genom att kombinera vår passion för människor med kraften i dagens teknologi hjälper vi människor och företag att uppnå deras fulla potential. Vi kallar det Human Forward.Apply for this job
Job Overview
Company
Randstad AB
Location
Södertälje, Sweden
Job Type
Full-time
About This Listing
This job comes from JobTech and is shown as published there. Dev Global Jobs has not checked the employer. Apply only on the official page and never pay a fee to apply.
At a glance
| Location | Södertälje, Sweden |
|---|---|
| Job type | Full-time |
| Date posted | 22 Oct 2026 |
| Apply by | 27 Oct 2026 |
| Open jobs in this city | 204 in Södertälje |
| Source | JobTech; apply on randstad.se |
What this job asks for
- Education: Master's degree, Bachelor's degree
- Languages: English, Swedish (a plus)
Main tasks, in the employer's words:
- Analyzing outputs such as finished product analytical results and process information across multiple manufacturing sites (both internal and external to AstraZeneca).
- Supporting the regulatory department with technical input to respond to health authority inquiries.
- Facilitating technical risk assessments.
About Randstad AB
90+ open jobs on Dev Global Jobs.
Sweden: pay, work visa, cost of living, Europass-style CV, interview questions.
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