QC Lead

Proclinical Staffing; Basel; Vor Ort; CHF 120.000 - 180.000; Vollzeit

Zusammenfassung

Proclinical Staffing is seeking a QC Lead in Basel, Switzerland to ensure quality standards by authoring and reviewing quality records, guiding QA/QC collaboration, and driving process improvements. Strong analytical chemistry background and GMP knowledge are essential, with fluency in English and German a plus.

This role requires the right to work in Switzerland or an EU passport. The ideal candidate has a degree in Pharmaceutical Sciences or related field, and an emphasis on CAPA and deviation

Qualifikationen

• Bachelor's degree in Pharmaceutical Sciences, Biochemistry, Chemistry, or related field; Master’s degree preferred.
• Strong background in analytical chemistry and GMP topics, including OOX data integrity.
• Experience authoring quality-relevant records such as deviations and change requests.
• Business-fluent English; German skills are a plus.

Aufgaben

• Author change requests, investigations, and deviations, including root-cause analyses and CAPAs.
• Provide guidance and review quality-related records to ensure timely completion and adherence to internal standards.
• Act as a liaison between QA and QC teams to facilitate efficient workflows.
• Support additional quality-related tasks as needed.

Kenntnisse

Analytical chemistry

GMP knowledge

OOX data integrity

Quality records

Leadership

Agility

Business acumen

Collaboration

Customer focus

Ausbildung

Bachelor's degree in Pharmaceutical Sciences

Master's degree preferred

Jobbeschreibung

Join a high‑performing CMO where your quality expertise keeps site operations running with precision, efficiency, and flawless coordination.

Proclinical is seeking a QC Lead to play a key part in ensuring quality standards are met by authoring and reviewing quality-related records, facilitating collaboration between QA and QC teams, and driving process improvements. This position requires a proactive individual with strong analytical chemistry expertise and a solid understanding of GMP principles.

Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.

Responsibilities:

• Author change requests, investigations, and deviations, including conducting root-cause analyses and defining CAPAs.
• Provide guidance and review quality-related records to ensure timely completion and adherence to internal standards.
• Act as a liaison between QA and QC teams to facilitate efficient workflows.
• Support additional quality-related tasks as needed.

Key Skills and Requirements:

• Strong background in analytical chemistry and GMP topics, including OOX data integrity.
• Proven experience in authoring quality-relevant records such as deviations and change requests.
• Bachelor's degree in Pharmaceutical Sciences, Biochemistry, Chemistry, or a related field (Master's degree preferred).
• Business-fluent English; basic German skills are a plus.
• Demonstrated competencies in agility, business acumen, collaboration, customer focus, results orientation, and leadership.