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Open nowPosted 29 days ago

HAL Allergy Technical Writer

EURES job mobility portal28,938 open roles

Where
Agglomeratie Leiden en Bollenstreek, Netherlands
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Your applicationOpen nowHAL Allergy Technical WriterEURES job mobility portal · Agglomeratie Leiden en Bollenstreek, Netherlands

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  2. 3.4%3 days
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  4. 14.2%14 days
  5. 34.1%30 days
This job: posted 29 days ago

The posting

Technical Writer General information Technical Writer At HAL Allergy Group, we are committed to improving lives through high-quality allergy diagnostics and immunotherapy products. To support our growing manufacturing organization, we are looking for a detail-oriented and proactive Technical Writer who will play a key role in creating and maintaining GMP production documentation. As a Technical Writer, you will be responsible for the creation, maintenance, and continuous improvement of GMP documentation that supports our manufacturing operations. You will work closely with Production, Quality, and Technology Transfer teams to ensure documentation remains accurate, compliant, user-friendly, and aligned with current manufacturing practices. Your work will directly contribute to the reliable and compliant production of pharmaceutical products in a dynamic GMP environment. Your tasks - Create, revise and maintain Master Batch Records, SOPs, Work instructions and other GMP documentation required to support manufacturing operations. - Update effective/active Batch Records, e.g. as part of Change Controls or CAPAs. - Support the standardization and harmonization of GMP documentation across manufacturing operations by implementing and maintaining document templates for the operations in GMP. Ensure accurate set-up, maintenance and when necessary, re-design of templates and other documents. - Partner closely with Production, Quality, and subject matter experts to ensure GMP documentation accurately reflects current manufacturing processes and regulatory requirements. - Participate in lessons learned sessions, operational reviews, and continuous improvement initiatives, translating identified improvements into updated batch records, SOPs, work instructions, and other controlled documents. - Plan and monitor the document delivery process from draft to approval for batch records and other documents within the Production department. - ...

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