Senior QC Analyst
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- Neuenburg
- Freiberuflich
- Vollzeit
- Conduct laboratory analyses and approvals following cGMPs and pharmacopoeia standards.
- Adhere to SOPs and safety protocols while performing QC activities.
- Document results accurately in logbooks and systems, ensuring compliance with Good Documentation Practices.
- Report non-conforming or invalid results promptly and initiate quality events as required.
- Ensure proper calibration and maintenance of laboratory equipment.
- Support training initiatives for analysts and act as a backup trainer for GMP education.
- Participate in risk analyses, equipment lifecycle management, and method harmonization projects.
- Collaborate with external partners and suppliers for technical issues and maintenance.
- Present expertise during inspections and audits.
- Contribute to corrective and preventive actions within the laboratory.
- Maintain a clean and organized workspace following 5S standards.
- Proficiency in laboratory methods and cGMP standards.
- Strong knowledge of data integrity principles.
- Comfortable using standard office tools and IT systems (e.g., Microsoft Office).
- Technical proficiency in French and English (minimum B2 level in English).
- Ability to work collaboratively, communicate effectively, and demonstrate exemplary behavior.
- Organized, patient-oriented, and aligned with values such as honesty, integrity, fairness, and perseverance.
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