GMP Officer (QC) - Quality & Compliance

Panda International; Basel; Vor Ort; CHF 110.000 - 160.000; Vollzeit

Zusammenfassung

Panda International is seeking an experienced GMP Officer (QC) to support quality and compliance activities within the QC function. The role emphasizes analytical chemistry, deviations, change requests, investigations and CAPAs, with focus on maintaining data integrity and OOX.

You will collaborate across QA and QC to ensure timely, standards-aligned records, and contribute to ongoing process improvements and cross-functional problem solving.

Qualifikationen

• BSc degree in pharmaceutical, biochemistry, chemistry, or related field.
• Minimum 5 years in analytical chemistry.
• Minimum 5 years experience with GMP topics including OOX and data integrity.
• Experience authoring quality-relevant records (deviations, change requests).
• Experience authoring investigations with root-cause analysis and CAPAs.
• Ability to facilitate between QA and QC to ensure timely records and adherence to standards.
• Strong GMP and quality-process understanding.
• Ability to maintain quality standards while delivering within timelines.

Aufgaben

• Provide guidance and review of quality-related records and facilitate QA/QC collaboration.
• Support additional quality-related tasks and contribute to process improvement and problem solving.

Kenntnisse

Analytical chemistry

GMP knowledge

Quality-records authoring

Root-cause analysis

CAPA definition

Cross-functional collaboration

Ausbildung

BSc degree

Jobbeschreibung

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.

Preferred Requirements

• 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

Practicalities

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