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- Process Engineer in Pharmaceuticals – Deviations & Change Control (Stockholm)
Process Engineer in Pharmaceuticals – Deviations & Change Control (Stockholm)
Randstad ABStockholms län, Stockholm
Previous experience is desired
26 days left
to apply for the job
Job Description
Are you an experienced Process Engineer with deep expertise in deviation investigations and Change Control? We are currently seeking a driven consultant for an exciting assignment with our client in the pharmaceutical industry. As a Process Engineer, you will play a key role for our client in Stockholm. You will step into a dynamic environment where you act as the bridge between production and quality. The role requires you to be confident in making decisions and have a natural ability to drive complex investigations forward. Since the role is operationally close and tightly linked to physical production, on-site work at the client's facility 5 days a week is required. The assignment starts immediately and requires presence throughout July and August, with summer vacation in June.
Being a consultant at Randstad:
Randstad Life Sciences is specialized in the field of natural sciences and is part of Randstad, which, with operations in 38 countries, is a world leader in recruitment and consultancy. Through this global network, combined with strong local roots, we can offer a wide range of varied and developmental assignments and services for you as a specialist in life sciences. Our mission is to help you reach your full potential with your career in focus.
Responsibilities
- Quality Work: Responsible for driving deviation investigations and managing Change Control (CC) in accordance with GMP and internal SOPs.
- Process Optimization: Act as expert support for the process and ensure efficiency and high quality in the workflows.
- Risk Assessments: Conduct technical risk assessments and ensure that processes comply with established requirements.
- Cross-functional Collaboration: Collaborate closely with production, quality assurance (QA), and development to solve production-related issues on-site.
- Documentation: Creation and updating of technical documentation and validation protocols as needed.
Qualifications
- Education: Master of Science in Engineering (Civilingenjör) in Chemistry, Biotechnology, or another relevant technical/natural science direction.
- Experience: Minimum 2–5 years of documented experience as a Process Engineer within Life Science, with a specific focus on deviations and Change Control.
- Presence: Ability and willingness to work on-site at the facility 5 days a week.
- Regulations: Very good familiarity and practical experience of working under strict GMP.
- Languages: Fluent skills in Swedish and English, both spoken and written.
- Personal Attributes: You are disciplined, meticulous, and risk-aware with a natural ability to collaborate with different professional categories directly in the production environment.
About the Company
Randstad
At Randstad, we know that everyone has a place in the labor market. With operations across the country and in all competence areas, we help people find a job that feels right, where they have the opportunity to grow, develop, and reach their full potential.
With nearly 600,000 employees in 38 countries, Randstad is a world leader in HR services, with the ambition to become the world's leading and most appreciated partner in the labor market. By combining our passion for people with the power of today's technology, we help people and companies reach their full potential. We call it Human Forward.
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