Process Validation Specialist

3 days left

Location
Wiltshire
Salary
£33000 per annum
Posted
02 Aug 2017
Closes
23 Aug 2017
Ref
J4167
Contact
Georgia St John-Smith
Contract Type
Contract
Hours
Full Time
We are currently looking for a Process Validation Specialist to join a leading Life Sciences company based in the Wiltshire area.

As the Process Validation Specialist you will be responsible for writing, updating and executing Process Validation plans and protocols in a GMP environment.

KEY DUTIES AND RESPONSIBILITIES:

Your duties as the Process Validation Specialist will be varied however the key duties and responsibilities are as follows:

1. Perform process validation activities to ensure cGMP requirements are met by writing and executing Process Validation protocols. This should include protocol compilation, execution, report generation and approval.

2. Develop process validation plans, protocols and reports by analysing, monitoring and generating statistical data and control charts as a part of Continued Process Verification (CPV).

3. Investigation of processing deviations, route cause analysis and implement appropriate CAPAs.

4. Contribute to the Quality Improvement Program by initiating and approving technical change controls, batch and validation documentation in order to generate Process Validation, Periodic Validation and Continuous Validation reports.

ROLE REQUIREMENTS:

To be successful in your application to this exciting opportunity as the Process Validation Engineer we are looking to identify the following on your profile and past history:

1. Relevant degree in a Life Sciences or Chemistry Discipline.

2. Proven industry experience in validation within a Pharmaceutical or Biopharmaceutical manufacturing environment.

3. A working knowledge and practical experience with Process Validation to GMP standards and or/ GLP Quality System experience of the generation analysis, management & control of GxP documentation, data and records.

As the successful candidate you will have a thorough understanding of MHRA and FDA regulatory requirements for process validation.

Key Words: Validation / Biopharmaceutical / Pharmaceutical / Cleaning Validation / GMP /GLP / GxP / Process Validation / Sterile / Process Development / Continuous Validation / Technical Change Control / Documentation / Technical Development

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for our talent development. We welcome applications for any applicant who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment processionals and scientists. We look forward to helping you with your next career moves.

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