Cleaning Specialist Process Validation (Pharmaceuticals)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
TL;DR
Cleaning Specialist Process Validation (Pharmaceuticals): Executing cleaning validation activities for pharmaceutical manufacturing with an accent on washing machine validation and CIP station implementation. Focus on designing validation strategies, ensuring GMP compliance, and performing risk assessments.
Location: On-site in Belgium
Company
is an independent technology consulting firm providing guidance and solutions across Information Systems, Telecom, Life Sciences, and Engineering.
What you will do
- Support washing machine validation including protocol preparation, execution, and data analysis.
- Design and execute validation strategies for new CIP stations, including URS, protocols, and reports.
- Perform risk assessments and define acceptance criteria for cleaning processes.
- Ensure all validation activities comply with GMP, regulatory requirements, and internal procedures.
- Collaborate with Manufacturing, QA, Engineering, and MSAT teams to optimize cleaning processes.
- Provide technical support and training to operational teams on cleaning and validation topics.
Requirements
- 4–6 years of experience in pharmaceutical, biotech, or related regulated industries.
- Solid experience in cleaning validation, CIP/SIP, and equipment cleaning.
- Deep understanding of GMP and regulatory expectations.
- Proficiency in validation documentation, including risk assessments and CAPA.
- Fluent in French and English (spoken and written).
- Ability to work on-site in Belgium.
Culture & Benefits
- Rapid growth opportunities within a fast-expanding Belgian office.
- Chance to work on prestigious projects with renowned pharma and biotech clients.
- Agile and dynamic international environment promoting intrapreneurship and meritocracy.
- Inclusive workplace committed to diversity and equal opportunity.
Hiring process
- Brief virtual or phone call to align on motivations and role fit.
- Average of 3 interviews with line managers and team members.
- Possible technical assessment or case study depending on the position.
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