Senior QA Associate - GMP & Batch Release (Pharma)

Jobster

Breda

On-site

EUR 65,000 - 90,000

Full time

4 hours ago
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Benefits offered by this job

Competitive salary
Travel reimbursement
30 holidays
Contract through Undutchables

Job summary

Jobster is seeking a Senior Associate QA to provide hands-on QA support in a GMP-regulated production site, ensuring compliance and reviewing batch documentation prior to release. You will play a key role in supporting production teams and QA processes.

Requirements include a life sciences bachelor’s (or equivalent), 3+ years in QA/manufacturing within pharma or medical devices, fluency in English, and GMP knowledge. The role involves shiftwork and a 1-year contract through Undutchables in Breda.

Qualifications

  • MBO or Bachelor's degree in Life Sciences, Pharmaceutical Sciences, or related field.
  • Minimum 3 years of QA or manufacturing experience within pharma or medical devices.
  • Experience with batch record review and investigations.
  • Fluent in English.
  • Solid understanding of GMP (GDP/GCP knowledge is a plus).
  • Ability to interpret and apply regulatory requirements in day-to-day operations.
  • Analytical mindset with problem-solving capabilities.
  • Strong communication skills and ability to engage with multiple stakeholders.
  • Detail-oriented with strong administrative and documentation skills.
  • Able to prioritize and perform under pressure in a fast-paced environment.
  • Proactive, solution-driven mindset.

Responsibilities

  • Provide daily QA support and guidance to production teams.
  • Act as the first point of contact for quality-related questions during packaging and labeling.
  • Review and approve batch records before and after production.
  • Perform finished checks during commercial production runs.
  • Compile and review batch documentation for Qualified Person (QP) disposition.
  • Conduct GMP compliance checks on the production floor.
  • Review, approve, and manage deviation records.
  • Initiate and own QA deviations where required.
  • Author and review SOPs and Work Instructions.
  • Support GMP training for QA and production staff.
  • Participate in investigations, projects, and continuous improvement initiatives.
  • Prepare weekly/monthly QA metrics and maintain performance boards.

Skills

Fluent English

Education

Bachelor's degree in Life Sciences, Pharmaceutical Sciences, or related field

Job description

Jobster is seeking a Senior Associate QA to provide hands-on QA support in a GMP-regulated production site, ensuring compliance and reviewing batch documentation prior to release. You will play a key role in supporting production teams and QA processes.

Requirements include a life sciences bachelor’s (or equivalent), 3+ years in QA/manufacturing within pharma or medical devices, fluency in English, and GMP knowledge. The role involves shiftwork and a 1-year contract through Undutchables in Breda.

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