GMP Officer; QC; Quality & Compliance

A global life sciences organisation is seeking an experienced GMP Officer (QC) to support quality and compliance activities within the QC function. This role requires strong expertise in analytical chemistry
, GMP topics, and the authorship and review of quality-related records, with a particular focus on deviations, change requests, investigations, root-cause analysis, and CAPAs.

In this role, you will provide guidance and review of quality-related records and facilitate collaboration between QA and QC to ensure records are completed on time and in line with internal standards. You will also support additional quality-related tasks as required and contribute to a culture of process improvement, problem solving, and effective cross-functional collaboration.

• BSc degree required
• Preferred fields:
  Pharmaceutical, Biochemistry, Chemistry, or similar
• Minimum 5 years of experience in analytical chemistry
• Minimum 5 years of experience with GMP topics, including areas such as OOX and data integrity
• Minimum 5 years of experience authoring quality-relevant records, including deviations and change requests
• Experience authoring change requests and investigations, including root-cause analysis and definition of CAPAs
• Experience providing guidance and reviewing quality-related records
• Ability to facilitate effectively between QA and QC to ensure timely completion of records and adherence to internal standards
• Strong understanding of GMP and quality-related processes
• Ability to maintain quality standards while delivering results within required timelines
• Strong collaboration and communication skills across teams and functions

• Start Date:
  
  ASAP
• Contract Type: 1 year - Extensions possible
• Team: QC
• Scope: GMP, quality records, investigations, and QA/QC collaboration