QC Lead

Proclinical Group; Basel; Vor Ort; CHF 110.000 - 150.000; Vollzeit

Zusammenfassung

Proclinical Group is seeking a QC Lead in Basel to ensure quality standards are met by authoring and reviewing quality records, and by driving process improvements. A proactive profile with strong analytical chemistry expertise and GMP knowledge is required.

The role emphasizes collaboration across QA and QC, CAPA-driven root-cause analyses, and ongoing quality-related tasks to uphold site operations with precision.

Qualifikationen

• Bachelor's degree in Pharmaceutical Sciences, Biochemistry, Chemistry, or related field.
• Master's degree preferred in a related discipline.
• Business-fluent English; basic German skills are a plus.
• Must have the right to work in Basel, Switzerland (EU passport acceptable).

Aufgaben

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

Kenntnisse

Analytical chemistry

GMP topics

Quality records authoring

Leadership

Agility

Collaboration

Business acumen

Customer focus

Results orientation

Ausbildung

Bachelor's degree in Pharmaceutical Sciences, Biochemistry, Chemistry, or related field

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.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.proclinical.com/privacy-policy.