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Business Manager, Key Account Management at BioTalent part of the IN Group
We are supporting a global pharmaceutical company who are seeking a Senior QC Analyst, where you will play a key role in analytical testing, method validation, and maintaining GMP compliance in a dynamic laboratory setting.
This is an excellent opportunity for a detail-oriented professional with strong expertise in HPLC, GC, and other analytical techniques to contribute to the success of product introduction activities.
Why Join Us?
* Work in a state-of-the-art QC laboratory within an innovative pharmaceutical company
* Lead validation and analytical excellence in a dynamic environment
* Be part of a collaborative and supportive team with strong career growth potential
* Competitive salary, benefits, and career development opportunities
Responsibilities:
* Perform analytical testing of raw materials, in-process samples, and finished products using HPLC, GC, UV/VIS, IR, dissolution, pH, TOC, titration, and more
* Review and approve analytical data while ensuring compliance with cGMP documentation requirements
* Write and review GMP documentation, including test methods, SOPs, validation protocols/reports, and investigation reports
* Lead and support method transfer and validation activities for QC
* Manage QC equipment selection, purchase, commissioning, calibration, and maintenance
* Handle deviations, OOS investigations, and change controls using the relevant software tools
* Act as a mentor and subject matter expert, providing training and technical support to QC team members
* Support internal and external audits to maintain GMP compliance of the QC laboratory
* Ensure all EHS (Environment, Health & Safety) protocols are met within the QC laboratory
Requirements:
* Federal Certificate of Capacity as a Laboratory Technician or equivalent
* 4-5 years of experience in a GMP environment within pharmaceutical QC
* Strong knowledge of HPLC, GC, UV/VIS, IR, dissolution, and CDS
* Experience with Ph. Eur. and USP analytical methods
* Proficiency in method validation and method transfer
* Experience with LIMS, lab software, and common office tools
* Strong communication, writing, teamwork, and mentoring skills
* Very good proficiency in English and French
Seniority level
Associate
Employment type
Full-time
Job function
Quality Assurance, Science, and Research
Industries
Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing
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