Analytical Chemistry QC Laboratory Manager job in Salisbury, Wiltshire

Apply for Analytical Chemistry QC Laboratory Manager job in Salisbury, Wiltshire, Wiltshire, United Kingdom. Medical/Pharmaceutical/Scientific jobs in Salisbury, Wiltshire.

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Job Title: Analytical Chemistry QC Laboratory Manager
Job Type: Contract
Location: Salisbury, Wiltshire
Company: CV-Library
Category: Medical/Pharmaceutical/Scientific

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Job Description:
CV-Library jobs

GxP Recruitment invites applications on behalf of our biopharmaceutical client based in Wiltshire where an excellent opportunity exists for a Waters Analytical QC Laboratory Manager/ Stability Unit Manager to join their team on a permanent basis.

Job Purpose:

To lead and manage a specialist GMP analytical chemistry/biochemistry laboratory to provide compliant testing of licensed pharmaceutical products. Lead a team performing WFI and purified water testing to the EP and USP to support manufacturing operations. The role is responsible for running the stability program in a compliant manner. The role is also responsible for supporting in-process analysis during manufacturing operations.

Key duties include:

* Manage the stability program including organising batches to be placed on stability, writing stability protocols and reports. Any adverse trends must be identified and investigated.

* To operate the QC Analytical Services Laboratory

* To manage and lead the QC Analytical Services Laboratory and to meet manufacturing deadlines.

* Responsible for staff recruitment, appraisals and management to ‘Policies and Procedures’ documents. Planning of staff work schedules, resource management and costing work programmes.

* Utilising technical skills to validate specialised chemical and biochemical tests procedures to internationally recognised regulatory guidelines. Conduct problem solving investigations to resolve issues affecting Pharmaceutical manufacture.

* Train staff within the QC Analytical Services Department in laboratory techniques and Quality Management Systems to GMP requirements. Assist staff within QC Analytical Services Department with their ongoing development to aid their career and personal progression.

* Work with project teams and represent QC on these to contribute to the success of these business centres by delivering the required Analytical knowledge and services.

* Play a lead role with both internal and external customers. Present the department and its operation to Regulatory Inspectors representing their respective national bodies.

* Expenditure to financial limits.

* Sign off authority for Pharmaceutical batch release tests

* Review and approval of SOPs, Protocols and Risk Assessments.

The ideal candidate profile:

* HND/degree qualified in Chemistry or similar

* Extensive experience working to GMP

* Validation of analytical methods and stability studies

* Experience hosting regulatory audist

* Significant lab management experience

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