Join a dynamic small company focused on providing analytical services in a GMP environment, where you will lead the Quality team. Manage and enhance the Quality Management System, and oversee non-conformities, CAPAs, audits, and SOPs. Collaborate internally and connect with external partners for quality matters. Enjoy a long-term, full-time role with a competitive salary and potential for hybrid working hours. This role offers a direct contract with the client. Read on to discover why this job might be perfect for you.

Over het bedrijf

Oxford Global Resources

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We are looking for a QA-Manager for a small company that does laboratory analysis under GMP-guidelines. You implement and own the Quality Management System, and lead the quality team. Read on below and apply if this suits you!

Job Description

You work for a relatively small company that recently obtained a GMP-license. With the laboratory team, you provide analytical services for pharmaceutical companies; there is no manufacturing team. There is a QMS in place now but this, of course, requires constant maintenance and updates. Your role has broad responsibilities, you supervise the small team, do final approval of CoAs, manage non-conformances, CAPAs, perform audits, and approve SOPs. Since you represent the entire Quality team, you will also give internal input on practical matters. Next to the internal communication, you are in contact with external parties for quality agreements, supplier qualification, and quality matters at clients. We are looking for someone with strong QA experience and some experience as a supervisor. You do not need to be a seasoned manager to qualify for this role but you should have experience beyond an Officer role.

Responsibilities

Implement, maintain, and improve the QMS
Supervise two Quality Officers
Train colleagues regarding GMP-guidelines
Approve Certificates of Analysis
Manage non-conformities and CAPAs
Manage internal audits and supplier audits
Client contact for quality agreements and quality matters

Profile

University-level education in a relevant field (Chemistry, Pharmaceutical Science, Life Science)
At least 3 years of QA-experience in a GMP-environment
Experience as a coordinator, supervisor, team lead, or manager
Professional English is a hard requirement, Dutch is a plus
You are allowed to work in The Netherlands indefinitely; our client cannot sponsor a visa

Benefits and practical information

Long-term position. Contract directly with our client
Full-time position in office hours (32-40 hours)
Office-based position, hybrid is an option in consultation
Salary range: €5000-€6500,- gross monthly, depending on experience
Location: Amsterdam
Vacaturenummer: 26661

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