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Responsibilities:
* Serve as the first point of escalation for technical, compliance, and personnel problem resolution.
* Lead, plan, and coordinate routine team activities to meet business needs.
* Perform QC Chemistry analysis of incoming goods, in-process samples, intermediates, and finished product samples to Good Manufacturing Practice (GMP) standards.
* Conduct GMP analysis of stability samples.
* Complete, update, and review technical documentation, including analytical write-ups, standard operating procedures, and GMP forms.
* Verify and calibrate lab equipment.
* Maintain up-to-date training in line with GMP expectations.
* Manage QC chemical, reference standard, and consumable stock levels.
* Perform or coordinate QC batch release procedures and deliver lab throughput in line with the business plan.
* Manage and coordinate stability studies in compliance with business procedures and ICH guidelines.
* Maintain a thorough understanding of international regulatory requirements and act as a Subject Matter Expert during audits and inspections.
* Collaborate and coordinate initiatives with other QC Supervisors and Managers for improved compliance, efficiency, and working conditions.
* Identify and drive Practical Process Improvement (PPI) initiatives.
* Undertake ad-hoc activities as required by the business.
* Support and encourage a "Quality Culture" throughout QC.
* Deputize for the QC Manager in their absence.
Requirements:
* Degree in Chemistry or a strongly related scientific subject area, or equivalent experience.
* At least five years of relevant industrial experience.
* Extensive experience in instrumental and traditional analytical techniques.
* Supervisory experience is desirable.
* Effective communication skills at all internal and external levels.
* Proficient time management and project management skills.
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