QC Project Lead ASAT

Amsterdam Metropolitan Area, Netherlands

Type: n/a

Category: Administration

Requirements: English
Company: Gi Life Sciences
Region: Amsterdam Metropolitan Area ,

Job Title: QC Project Lead Analytical Science & Technology (GMP, Biopharma)

Location: Amsterdam, Netherlands

Work Model: On-site, Full-Time (40 hours/week, 32 hours negotiable)

Salary: Up to 72,500 per year

Contract Type: Direct, Permanent Employment

Join a global biotechnology and pharmaceutical company in Amsterdam as a QC Project Lead within the Analytical Science & Technology (ASAT) team.

This is a strategic Quality Control position with no hands-on laboratory work, at the intersection of project management, client communication, and regulatory documentation.

You will ensure analytical projects are executed to the highest standards of quality and compliance in a GMP environment.

Offer

• Competitive salary up to 72,500 per year
• Permanent employment with full benefits
• Flexible working hours (40 hours/week, with 32-hour option)
• High-impact work in support of life-saving medicines
• Clear career development pathways and continuous training
• A collaborative, quality-focused work environment in a GMP-regulated setting

Key Responsibilities

• Serve as the primary liaison between external clients and the QC department
• Represent Quality Control in cross-functional project teams
• Lead analytical method validation, qualification, and verification projects
• Manage multiple concurrent client-driven projects from start to finish
• Ensure all project milestones are delivered on time and in full compliance with GMP
• Write, review, and approve validation and qualification documentation
• Monitor project risks and proactively implement mitigation strategies

Your Qualifications and Experience Profile

• Education: University degree (BSc or MSc) in Biotechnology, Biochemistry, Analytical Chemistry, Microbiology, Medical Biology, or a related field. HBO/HLO graduates with significant experience are also encouraged to apply
• Experience: At least 3 years in a Quality Control role within the biotech or pharmaceutical industry
• Expertise: Proven, in-depth knowledge of analytical method validation, qualification, and verification in a GMP-regulated environment
• Knowledge: Solid understanding of GMP and pharmaceutical regulatory requirements
• Skills: Strong project management, multitasking, and communication abilities
• Language: Fluent in English, both spoken and written

Ready to lead vital analytical projects in a dynamic biotech environment?

Apply Now!

Click "Easy Apply" to submit your updated CV, and feel free to contact:

Mah Rukh Chohdri, Recruitment Consultant at Gi Life Sciences Netherlands

0643636656

mahrukh.chohdri@grafton.com

"Good Manufacturing Practice (GMP)", "Analytical Chemistry", "Analytical Method Validation", "Quality Control", "Method Development", "Validation (Drug Manufacture)", "cGMP", "FDA Regulations", "Chromatography", "High-Performance Liquid Chromatography (HPLC)", "Standard Operating Procedure (SOP)", "Biotechnology", "Regulatory Compliance", "Deviation Management", "Corrective and Preventive Actions (CAPA)", "Quality Assurance", "Process Validation", "Change Control", "Pharmaceuticals", "Biopharmaceuticals", "Analytical Methods Development", "Project Management", "Regulatory Submissions", "Laboratory Information Management System (LIMS)", "Computer System Validation", "SOP Authoring", "Life Sciences", "Equipment Qualification", "Client Relationship Management", "Documentation"

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