Quality Assurance Associate
Key Skills
Job Description
The Company Our client is one of the leads from the Biotechnology industry who try to improve patients’ lives, by distributing their medicines to hospital and pharmacies in 100 different countries in the world, to over 10 million patients, in Europe, Turkey, Middle East and Africa Regions. Job Description As a Quality Assurance Associate, you will be responsible for the sampling, inspection, review, and release of incoming materials and packaging components in a GMP-regulated pharmaceutical environment. You will ensure quality and compliance requirements are met while working closely with internal teams and suppliers to resolve quality-related issues. Responsibilities Conduct sampling, inspection, review, and approval of incoming materials, including printed and non-printed packaging components Ensure all incoming materials meet procedural and quality requirements for release Collect data and communicate with internal teams or suppliers to resolve issues or deviations Perform additional sampling and damage inspections on received components as needed Provide quality oversight during the receipt and inspection of components to maintain compliance and standards Requirements MBO, Bachelor’s, or Master’s degree in Life Sciences or a related field, or equivalent experience (minimum three years in Quality Assurance or Control) Familiarity with GMP and GDP principles and their practical application Proficiency in English, both written and verbal Experience working with digital systems such as ERP (SAP) is preferred Strong attention to detail, good communication skills, and ability to work collaboratively within a team Other Information Apply to our vacancy for more information. We look forward to hearing from you!
Core Responsibilities
Responsible for the sampling, inspection, and release of incoming materials and packaging components in a GMP-regulated environment. Collaborates with internal teams and suppliers to resolve quality deviations and ensure compliance standards.
Requirements
Requires a degree in Life Sciences or related field with at least three years of experience in Quality Assurance or Control. Proficiency in English and familiarity with GMP/GDP principles and ERP systems like SAP are required.
About SIRE® Life Sciences 🧬
Industry: Biotechnology Research
Company size: 201-500 employees
SIRE® Life Sciences is the market-leading partner for Life Sciences consultancy, project management, and secondment services in the Netherlands. We specialize in connecting expert consultants and project managers with leading biotech, pharmaceutical, medical device, clinical research, and food technology organizations. Our services include: - Life Sciences recruitment & executive search - Interim management & secondment - SOW-based project outsourcing & delivery - RPO (Recruitment Process Outsourcing) - MSP workforce management & vendor-neutral solutions - GMP, GCP, GLP compliance staffing - Clinical research & regulatory affairs resourcing With 100,000+ professionals in our network and 25+ years of experience, SIRE® Life Sciences delivers measurable results for regulated organizations across the Netherlands and Europe. We work with pharma, biotech, medical device, CDMO, CRO, and food technology companies at every stage of the product lifecycle. What sets us apart: - Deep domain expertise in Life Sciences & regulated industries - Full compliance with GxP, ISO, WAADI, and Dutch labour law - Flexible engagement models: permanent, interim, project (SOW), and managed services - Proven delivery track record across Pharma, Biotech, MedTech & Food Science Based in Leiden Bio Science Park, Netherlands. www.sire-search.com