Documentation Specialist

Documentation Specialist (Quality Operations) in Hoofddorp, min. 2 jaar documentmanagement in gereguleerde omgeving, start 14-09-2026.

De eerdere warme-stoelbeoordeling heeft beperkte onderbouwing.

Bekijk en reageer bij SIRE Life Sciences B.V. (externe link)

Eisen

  • Ability to meet deadlines in a fast paced environment
  • Minimum 2 years of document management experience within a regulated environment
  • Strong organizational and prioritization skills
  • Excellent attention to detail and commitment to accuracy
  • Strong knowledge of GMP regulations and documentation practices
  • Advanced English communication skills
  • Effective stakeholder management and communication skills
  • Strong problem solving and investigation skills
  • HBO or WO level education
Volledige omschrijving

The Company: A leading organization in the life sciences and pharmaceutical manufacturing sector focused on producing high quality products in a highly regulated environment. The company operates under strict quality and compliance standards, ensuring patient safety and regulatory excellence through robust GMP practices.

Role description: As a Quality Operations Documentation Specialist I, you will play a key role in ensuring the accuracy, control, and compliance of GMP documentation used throughout manufacturing operations. The position focuses on the issuance, verification, and management of controlled documents, labels, and logbooks while supporting continuous improvement initiatives and maintaining regulatory compliance.

Responsibilities: Verify controlled issued batch documents and label packages, including final product labels, in accordance with cGMP requirements; Verify controlled issued logbooks for accuracy and completeness; Ensure timely consumption of GMP materials and consumables or communicate inventory requirements to responsible personnel; Maintain accuracy and completeness of QA issued documents; Identify and escalate compliance gaps within the controlled issuance process; Support process improvement initiatives related to document control and issuance; Investigate and support deviations related to controlled issuance activities; Develop and implement corrective action plans when required; Communicate document issuance requirements and guidelines to internal stakeholders; Cross train colleagues and customers on document issuance processes; Collaborate effectively with peers, stakeholders, and senior colleagues; Consider operational impacts when making decisions related to documentation processes; Perform additional duties as assigned.

Requirements: HBO or WO level education; Minimum 2 years of document management experience within a regulated environment; Advanced English communication skills; Strong knowledge of GMP regulations and documentation practices; Excellent attention to detail and commitment to accuracy; Strong organizational and prioritization skills; Ability to meet deadlines in a fast paced environment; Strong problem solving and investigation skills; Effective stakeholder management and communication skills.

Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me.

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