Release Operations Specialist

☞ Pfizer

View: 145

Update day: 12-11-2025

Location: Puurs Antwerp

Category: Quality Assurance / Quality Control

Industry: Pharmaceutical Manufacturing

Position: Associate

Job type: Full-time

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Job content

Job Description

This position is accountable for daily support of the Covid release operations colleagues. He/she is accountable for the creation, monitoring and improvement of processes related to their field of expertise. This position reports to the Lead RO Covid vx.

Principal accountabilities:
  • Accountable for daily support of the Covid release operations colleagues. Supports problem solving for release operations colleagues.
  • Accountable for the creation, monitoring and improvement of processes related to their field of expertise. Act as CI Specialist for different release operations teams.
Ensures operational excellence through:

Compliant, effective and efficient systems

Continuous improvement

Effective process teamwork and organization in general
  • Leading or participating in projects linked with or in support of release operations.
  • Follow up on actions defined in the CAPA management system to assure quality/compliance improvements of manufacturing processes of pharmaceutical and MDCP products.
  • Provide feedback and timely escalate issues to Management regarding the Process or Project (Management Review, QMS Steering, Inspection Readiness,….).
  • Can act as a process owner on defined Quality Processes from the Site Quality Management System (QMS) and manage some of the Quality Processes.
  • Can act as primary contact during inspections for topics related to processes within release operations.
  • Respect the PGS vision, mission, values in order to realize the PGS objectives related to quality, GMP, customer satisfaction, right first time.
Job profile
  • This function requires a master degree in the pharmaceutical and/or biological manufacturing or scientific field.
  • Following, although not limiting, educations are acceptable: Bio Engineer, (Industrial) Pharmacist, Master in Biology, Biochemistry, Biotechnology, Engineering, …
  • 2 or more years of relevant experience in pharmaceutical, combination product or medical device industry with specific experience in relevant guidelines, operations and/or Quality.
  • Good analytical and problem solving skills
  • Strong OpEx mindset
  • Team player
  • Excellent oral and written communication (Dutch & English)
Offer
  • Permanent contract with numerous fringe benefits
  • A culture of entrepreneurship and innovation
  • Largest production and packaging site in Europe within the Pfizer network
  • High investment rhythm
  • High-tech environment
De Pfizer site in Puurs is één van de grootste productie- en verpakkingssites van Pfizer wereldwijd, gespecialiseerd in aseptische productie en verpakking. Jaarlijks worden in Puurs meer dan 400 miljoen doses injecteerbare vaccins en medicijnen geproduceerd. Deze zijn ter plaatse verpakt in ampullen, flacons, plastic flessen, spuiten en patronen voor pennen.

De medicijnen die in Puurs worden gemaakt, zijn bestemd voor patiënten in meer dan 170 landen wereldwijd. 30% van de productie uit Puurs is bestemd voor ontwikkelingslanden, in samenwerking met UNICEF, WHO, GAVI en ngo’s.

Met het gebruik van twee windturbines, zonnepanelen en een warmtekrachtcentrale richten we ons op hernieuwbare energie.

Quality Assurance and Control

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Deadline: 27-12-2025

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