QC Supervisor

Leeds, England
Sep 15, 2016
Oct 13, 2016
Alex Langrish
Result Type
Position Type
Full Time

Key responsibilities and accountabilities:

* Supervises and Coordinates all QC activities related to incoming raw materials and finished products testing.
* Review and approve all analytical data generated within QC
* Direct team members towards achieving daily and long term business goals. Effectively monitor and manage progress and performance and provide timely feedback to the relevant teams and team members.
* Pro-actively lead operations and processes to ensure quality standards are met, e.g. GMP / GLP / H&S.
* Drive compliance to MHRA, FDA, Regulatory and Company requirements / standards.
* The job holder will have specific responsibilities detailed in the following Standard Operating Procedures (SOPs).
* Ensure effective and timely delivery of business metrics and reviews.
* Participate in problems-solving and continuous improvement initiatives across all functions within QC / Business including lean related thinking (5S principals, elimination of waste, streamlining operations with no impact on quality).
* Manage team performance and objectives to ensure that the QC department achieve objectives on Quality, Cost, Safety, Delivery and Business goals / aims.

Key Skills Required:

* BSc in Chemistry or a related discipline
* Ideal candidates should have significant hands on experience of analysis within a pharmaceutical environment under a cGMP quality system in a fast paced environment
* Capable using techniques such as HPLC, GC and FTIR ideally gained within an industrial or lab based environment
* Knowledge of stability testing, performing and managing stability studies is desirable.
* Supervisory experience in a laboratory environment would be highly desirable.

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