GMP Officer (QC - 7099)

CTC Resourcing Solutions; Basel; Vor Ort; CHF 110.000 - 140.000; Vollzeit

Zusammenfassung

CTC is recruiting a GMP Officer (QC) in Basel, Switzerland to strengthen the QC analytical labs supporting biopharma manufacturing. The role leads deviation investigations, CAPA, and QA collaboration to meet timelines.

Requires 5+ years in analytical chemistry or GMP labs and a BSc in a related field; MSc/PhD preferred. On-site five days weekly with data integrity emphasis.

Qualifikationen

• Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related field.
• Minimum 5 years in analytical chemistry, bioanalytics or GMP lab.
• Experience authoring quality records, managing deviations and CAPA.

Aufgaben

• Drive compliance and operational excellence within QC analytical labs.
• Lead deviation investigations and RCA; author CAPA plans.
• Write and manage Quality Change Requests and documentation for timelines.
• Act as a bridge between QC analytical teams and QA stakeholders.
• Partner with lab technicians; gather data across physico-chemical and bioanalytical workflows.
• Support sample management and instrument qualification protocols.
• Mentor staff on data integrity standards and drive continuous QC improvements.

Kenntnisse

Root-cause analysis

CAPA

Data integrity

GMP knowledge

Quality systems

Ausbildung

Bachelor's degree (BSc)

MSc or PhD preferred

Tools

Instrument qualification

Jobbeschreibung

CTC is a specialized search and recruitment partner for the Life Sciences industry, serving clients and candidates since 1997. We enable careers by connecting talented professionals with meaningful opportunities, and we support our clients in engaging, retaining, and developing the right talent when needed.

Our client, a global market leader in the production and process support of active pharmaceutical ingredients, both in the chemical and biotechnology sectors, is looking for a:

GMP Officer (QC)

on a 12-month contract, with possibilities of extension. This role is based in Basel, Switzerland, and requires work-onsite 5 days per week.

Main responsibilities:

• Drive compliance and operational excellence within our Quality Control analytical laboratories supporting biopharmaceutical manufacturing.
• Lead end-to-end deviation investigations, root-cause analysis (RCA) and author comprehensive Corrective and Preventive Action (CAPA) plans.
• Write, review and manage Quality Change Requests and associated quality-relevant documentation to meet tight submission timelines.
• Act as a key compliance bridge between Quality Control (QC) analytical teams and central Quality Assurance (QA) stakeholders.
• Partner directly with lab technicians, conducting interviews and gathering analytical data across physico-chemical and bioanalytical workflows.
• Support compliance activities related to sample management processes and analytical instrument qualification protocols.
• Foster continuous process improvement within the QC track systems and mentor lab staff on data integrity standards.

Qualifications and Experience:

• Relevant working/residency permit or Swiss/EU-Citizenship required.
• Educational background with a Bachelor's degree (BSc required; MSc or PhD preferred) in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related discipline.
• Minimum 5 years of practical experience within analytical chemistry, bioanalytics or a GMP laboratory environment.
• Proven expertise in authoring quality-relevant records, managing deviations, OOX investigations and CAPA implementation.
• Strong practical knowledge of GMP principles, analytical methods, data integrity, instrument qualification and sample management.
• Demonstrated hands-on experience performing structured root-cause analysis techniques in a laboratory setting.
• Professional business fluency in English (written and spoken) is required; basic German language skills are an advantage.