QA Validation Supervisor - #1746991
TieTalent
Date: 1 day ago
City: Leeds
Contract type: Full time
Work schedule: Full day
About
Job Title: QA Validation Supervisor
Salary: Highly competitive basic salary, bonuses & benefits!
Location: West Yorkshire (Hybrid role)
SRG is exclusively working with a global pharmaceutical company who require a QA Validation Supervisor to join their well-established Quality Assurance Validation team, supervising a team of 4 responsible for QA Validation activities, as required.
The successfully QA Validation Lead will ensure validation studies and activities are planned and executed in line with company SOPs and GMP Requirements and Regulations, supporting validation manager with management of the validation team.
Responsibilities
Writing, executing and reviewing validation protocols in accordance with procedural requirements and current regulatory standards. Writing and reviewing validation reports ensuring outcome of protocol objectives are documented. Ensuring Validation Incident reports are raised, investigated with resolutions in place and closed in a timely manner. Act as a deputy to line manager and supervise as required. Lead and author risk assessment, FMEA and other root cause analysis techniques to provide appropriate information on product and processes. Ability to identify suitable mitigations and actions. Ensures validation is in accordance with the SVMP and Regulations. Maintains a good knowledge of updates to regulations and ensures standard procedures are updated in accordance with changes to the regulations. Leads the execution of validation activities. Ensures all validation deliverables are met within agreed project timescales. Leading key QA validation projects. Monitors and reports delivery of key Quality Organisation Metrics in relation to Validation activities . Providing guidance with process improvement projects and Tech Transfer of new products ensuring the process and cleaning validation is performed in line with procedural and regulatory requirements. Develop and implement systems that will improve validation activities and work efficiencies.
Requirements
Extensive recent experience in a leadership role within a GMP Quality Assurance Validation environment, preferably Cleaning Validation activities. Line Management Experience within a quality assurance/validation team in a GMP environment. Proved track record of leading pharmaceutical validation projects across cross functional teams.
SRG are the UK number 1 recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors.
As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.
If you have a scientific background and this position is not relevant / suitable for you please feel free to get in touch or visit (url removed) to view our other vacancies.
Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy
Nice-to-have skills
Job Title: QA Validation Supervisor
Salary: Highly competitive basic salary, bonuses & benefits!
Location: West Yorkshire (Hybrid role)
SRG is exclusively working with a global pharmaceutical company who require a QA Validation Supervisor to join their well-established Quality Assurance Validation team, supervising a team of 4 responsible for QA Validation activities, as required.
The successfully QA Validation Lead will ensure validation studies and activities are planned and executed in line with company SOPs and GMP Requirements and Regulations, supporting validation manager with management of the validation team.
Responsibilities
Writing, executing and reviewing validation protocols in accordance with procedural requirements and current regulatory standards. Writing and reviewing validation reports ensuring outcome of protocol objectives are documented. Ensuring Validation Incident reports are raised, investigated with resolutions in place and closed in a timely manner. Act as a deputy to line manager and supervise as required. Lead and author risk assessment, FMEA and other root cause analysis techniques to provide appropriate information on product and processes. Ability to identify suitable mitigations and actions. Ensures validation is in accordance with the SVMP and Regulations. Maintains a good knowledge of updates to regulations and ensures standard procedures are updated in accordance with changes to the regulations. Leads the execution of validation activities. Ensures all validation deliverables are met within agreed project timescales. Leading key QA validation projects. Monitors and reports delivery of key Quality Organisation Metrics in relation to Validation activities . Providing guidance with process improvement projects and Tech Transfer of new products ensuring the process and cleaning validation is performed in line with procedural and regulatory requirements. Develop and implement systems that will improve validation activities and work efficiencies.
Requirements
Extensive recent experience in a leadership role within a GMP Quality Assurance Validation environment, preferably Cleaning Validation activities. Line Management Experience within a quality assurance/validation team in a GMP environment. Proved track record of leading pharmaceutical validation projects across cross functional teams.
SRG are the UK number 1 recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors.
As scientists ourselves, our specialist sector knowledge and our passion are second to none. It's this combination that makes us different. We're committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.
If you have a scientific background and this position is not relevant / suitable for you please feel free to get in touch or visit (url removed) to view our other vacancies.
Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy
Nice-to-have skills
- Root Cause Analysis
- Leeds, England
- QA
- English
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