About Our Client
Our client is a leading global biopharmaceutical manufacturer, with a state-of-the-art production facility in Leiden. Known for producing high-quality biologics across a wide range of therapeutic areas, the organization operates within a highly regulated GMP environment.
Role Overview
You’ll support daily operations, solve problems on the production floor, and help improve quality, efficiency, and processes. Remote or hybrid work is not possible.
Responsibilities:
- Help fix daily issues in production
- Look into problems and find ways to reduce them
- Write and update procedures (SOPs)
- Support process and equipment improvements
- Work with teams to ensure safety, quality, and service
- Test new ideas, tools, and equipment
- Prepare documentation and training materials
Requirements:
- Vocational or technical education (preferred)
- 2–4 years in manufacturing or a similar environment
- Experience in a regulated industry is a plus
- Knowledge of GMP, ISO standards, and medical regulations
- Understanding of product and process validation
- LEAN Six Sigma Green Belt (preferred)
Other Information
Are you interested and do want to apply for this role, please fill out your application via the apply button below
55350
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Since 2012, SIRE Life Sciences is the most innovative and engaged consultancy company for the life sciences industries.
SIRE Life Sciences is proud of its ability to adapt to changing trends while always maintaining the highest level of quality for both our clients and our candidates.
Our team of knowledgeable professionals provides customized staffing services to clients and candidates, including secondment, direct hire, temporary-to-hire, temporary staffing, brokering, Statement of Work and we approach each type with the same degree of professional assessment. Our refined and collaborative style is unmatched in the staffing industry. We’re able to see beyond the surface to create matches that result in successful careers for our candidates and valuable talent for our clients.
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