Manufacturing Process operator
SIRE® Life Sciences
Manufacturing Process operator
Samenvatting
Wat krijg je?
Wat ga je doen?
- Carry out manual production tasks
- Perform packaging activities following guidelines
- Conduct in-process quality checks
- Maintain accurate GMP batch records
- Report and resolve production deviations
Wat verwachten wij?
- Ervaring in een soortgelijke productie- of productieomgeving
- Ervaring met handmatige productie volgens SOP richtlijnen
- Ervaring met batchrecords volgens GMP vereisten
- Uitvoeren van in-proces kwaliteitscontroles tijdens productie
Volledige vacaturetekst
Join a leading pharmaceutical organization in Breda as a Manufacturing Process Operator. You will execute manual production and packaging tasks within a high-quality, controlled environment. By conducting essential quality checks and supporting process improvements alongside the QA team, you ensure excellence in every batch. Dive into a precision-driven role where your contribution directly impacts global health standards. Ready to advance your manufacturing career? Discover your next step here.
Company Overview
Our client is a leading organization specializing in the production of high-quality pharmaceutical products. Operating within a highly regulated environment, they focus on delivering excellence in manufacturing and packaging through strict adherence to GMP standards and quality protocols.
Job Description
We are seeking a dedicated Manufacturing Process operator to join the team in Breda. This role involves executing manual production and packaging activities within a controlled environment, ensuring consistent, accurate, and compliant operations in line with GMP standards.
Responsibilities
-Carry out manual production tasks according to Standard Operating Procedures (SOPs)
-Perform packaging activities following established guidelines
-Conduct in-process quality checks to ensure product standards
-Maintain accurate and timely documentation, including batch records and logs, in compliance with GMP
requirements
-Identify, report, and support resolution of deviations or quality issues, participating in problem-solving -meetings with QA and Production teams
-Set up and close down production lines as required
-Perform routine cleaning activities on a daily, weekly, and monthly basis
-Ensure the workspace remains safe, compliant, and organized
-Execute repetitive manual tasks with precision and reliability
-Collaborate effectively with team members to maintain smooth production flow
Requirements
-Minimum experience in a similar production or manufacturing role
-Fluent in English
-Comfortable working in a highly structured environment with strict adherence to procedures
-Willing to commute to Breda
-Open to working in a 2-shift OR 3 shifts system
-Able to perform repetitive manual tasks with concentration and accuracy
Other Information
If you are interested and want to apply, please submit your application via the apply button below and contact me.
58862
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