QC Lead

Proclinical Consulting; Basel; Vor Ort; CHF 110.000 - 160.000; Vollzeit

Zusammenfassung

Proclinical is seeking a QC Lead to ensure site quality standards in Basel, authoring and reviewing quality records, and driving process improvements in a GMP environment. The role requires strong analytical chemistry expertise and collaboration across QA and QC teams.

Candidates must have the right to work in Switzerland or an EU passport, with business-fluent English and a background in GMP and QA/QC practices. Leadership and proactive problem-solving are essential.

Qualifikationen

• Strong background in analytical chemistry and GMP topics.
• Experience authoring deviations, change requests and CAPAs.
• Fluent in business English; German a plus.

Aufgaben

• Author change requests, investigations, deviations and CAPAs.
• Review quality-related records to ensure timely completion.
• Liaise between QA and QC to enable efficient workflows.
• Support additional quality tasks as needed.

Kenntnisse

Analytical chemistry

GMP topics

OOX data integrity

Authoring quality records

Deviations and change requests

QA-QC liaison

Agility

Leadership

Ausbildung

Bachelor's degree in Pharmaceutical Sciences / Biochemistry / Chemistry

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.