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Senior Associate QA Breda SIRE Life Sciences

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Gevraagd

  • 37 - 40 uur
  • MBO of hoger
  • Senior
  • Engels (taal)

Aanbod

  • Vast contract
  • Ploegen
 

Vacature in het kort

Breda
Join a leading global biotechnology company in a pivotal role as a Senior Associate QA. At the cutting-edge facility, you'll ensure compliance with GMP standards by providing on-the-floor quality assurance during pharmaceutical packaging and labeling operations. Engage in batch record reviews, deviation handling, and real-time QA guidance. Enjoy a dynamic work environment with a rotating shift schedule and be part of a team dedicated to transforming patient lives through science and innovation. See how you can contribute to our success by reading further.
 

Over het bedrijf

SIRE Life Sciences
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The Company
Our client is a leading global biotechnology company dedicated to transforming the lives of patients through science and innovation. With a strong presence in the Netherlands, their state-of-the-art facility in Breda is a critical hub for the assembly, packaging, and labeling of life-saving medicines distributed to over 100 countries.

Role Description
As a Senior Associate QA, you’ll provide quality assurance support on the production floor, ensuring compliance with GMP standards. Your key tasks include batch record reviews, deviation handling, and real-time QA guidance during packaging and labeling operations.

Responsibilities

  • Provide on-the-floor QA support during pharmaceutical packaging and labeling operations
  • Perform in-process product checks and GMP compliance monitoring
  • Review and approve batch record data entries before and after production
  • Act as a first point of contact for quality-related questions in production
  • Support investigations, deviations, and change control activities
  • Assist in writing and reviewing Standard Operating Procedures (SOPs) and Work Instructions
Requirement
  • MBO, HBO, or BSc degree in Life Sciences, Pharmaceutical Technology, Biotechnology, Chemistry, or related fields
  • A strong interest in working in GMP-compliant pharmaceutical environments
  • Excellent communication skills and a proactive, collaborative mindset
  • Comfortable working in a 3-shift structure
Shift Schedule (rotating weekly):
Early: 06:30 – 15:00
Late: 14:30 – 23:00
Night: 22:30 – 07:00

Other information  
Apply to our vacancy for more information. Looking forward to getting in touch!   

55568

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