QC Lead
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What you'll do
- 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.
What they're looking for
- 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.
- Business-fluent English.
- Must have the right to work in this location or hold an EU passport.
Nice to have
- Master's degree.
- Basic German skills.
Summarised by NextRaise from the employer’s description, which follows in full below.
Full description from employer
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.
If you are having difficulty in applying or if you have any questions, please contact Olivier Worch at o.worch@proclinical.com.
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
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Company
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