QC Supervisor

Employer
Location
Leeds, England
Salary
Negotiable
Posted
Sep 15, 2016
Closes
Oct 13, 2016
Ref
374909
Contact
Alex Langrish
Result Type
Jobs
Position Type
Permanent
Hours
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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