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il y a 4 semaines
As an MSAT Technical Writer you take ownership of cGMP documentation and ensure all process documents remain accurate, compliant and aligned with operational needs. You work closely with MSAT and manufacturing teams to maintain high-quality documentation that supports smooth and compliant production activities.What is offeredReady to grow your career and make real impact? Join MindCaptureWe offer competitive salaries, a full benefits package (meal vouchers, eco vouchers, DKV health insurance, group insurance, net expense allowance and a company car) — plus the opportunity to shape your future through personalized training and development.At MindCapture, you choose what you love, build on your strengths, and make a difference where it matters most.You will work as a MindCapture consultant for an international market leader in the healthcare industry.Job descriptionTechnical writing: You maintain and update master batch records and other process documentation to ensure they reflect current procedures and comply with cGMP requirements.Single point of contact: You act as the SPOC for both paper and electronic batch records. You align with the MES/document owners on required updates and follow-up on implementation across teams.Compliance support: This role is administrative in nature but requires scientific insight. You apply your process understanding to support documentation accuracy and compliance within a GMP environment.RequirementsBachelor’s degree in Biotechnology, Chemistry or another relevant fieldMin 2 y of experience in batch record review or other process related administrative roleFirst relevant experience is a plus but not requiredFluent in English and able to collaborate across functionsKnowledge of DutchExperience with MES is a plusUnderstanding of GMP manufacturing processes is a plus
