Quality Assurance Specialist

g2 Recruitment; Alkmaar; On-site; EUR 55,000 - 85,000; Full time

Benefits offered by this job

Bonus

Travel allowance

Pension

27 days annual leave

12 ADV days

Relocation allowance

Job summary

G2 are partnering with a market leader near Alkmaar, North Holland, to hire a Senior QA Specialist on a permanent basis.

You will be working on QA and some QC, closely with the engineering and manufacturing teams to ensure GMP/GLP/CAPAs are followed, with a clear progression path.

Qualifications

• Masters degree in chemistry, biotech, pharmaceuticals, or similar.
• Background as QA Officer, Specialist, Qualified Person, or similar.
• Experience working on QA, documentation, GMP, CAPAs and GLP.
• Working history in scientific fields such as chemistry, pharma, biopharma, radiopharma, etc.
• Ability to work independently, coordinating multiple processes simultaneously.
• Fluent English essential, must be able to read in Dutch.

Responsibilities

• QA and some QC responsibilities, closely with engineering and manufacturing teams to ensure adherence to relevant standards.
• Focus on GMP, GLP and CAPAs.

Skills

Fluent English

Dutch reading

Education

Master's degree in chemistry/biotech/pharmaceuticals

Job description

G2 are partnering with a market leader based near to Alkmaar, North Holland, who are looking for a Senior QA Specialist to join their team on a permanent basis.

The client specialise in various sectors including pharmaceuticals, chemical and highly regulated process industries on full manufacturing processes, from research and NPI through to product manufacturing and validation phases.

You will be working on QA and some QC responsibilities, closely with the engineering and manufacturing teams, ensuring relevant standards are adhered to, with a specific focus on GMP, GLP and CAPAs. The client ideally want people who have experience in scientific fields, primarily pharmaceuticals.

Permanent Opportunity - QA Specialist - Alkmaar area, North Holland

Contract type: Permanent

Package: Bonus, travel allowance, pension, 27 days annual leave +12 ADV days, relocation allowance (if required)

• Masters degree in chemistry, biotech, pharmaceuticals, or similar
• Background as QA Officer, Specialist, Qualified Person, or similar
• Experience working on QA, documentation, GMP, CAPAs and GLP
• Working history in scientific fields such as chemistry, pharma, biopharma, radiopharma, etc.
• Ability to work independently, coordinating multiple processes simultaneously
• Fluent English essential, must be able to read in Dutch

The successful candidate has a direct route to becoming overall QA Manager for the department within the next 2-3 years, so the role comes with clear progression.