QA Manager, RP, RPi - Pharmaceuticals
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- England,West Midlands,Coventry
- Full Time, Permanent
- Salary negotiable
Job Description:
Smart4 Sciences are supporting well-established pharmaceutical company to a recruit a QA Manager for their UK Head Office. This is a highly visible role with broad exposure across GMP, GDP, supplier quality and regulatory interfaces, offering genuine long-term development - including the opportunity to progress into RP/RPi responsibilities.
The role
Reporting into the Head of Quality, you will play a central role in maintaining and improving Quality Assurance systems across licensed medicines, medical devices and food supplements. The position has a strong focus on third-party manufacturing oversight, supplier management and GDP operations, making it ideal for a QA professional who enjoys working cross-functionally and taking ownership.
Key responsibilities include:
*Maintaining and improving Quality Management Systems, SOPs and work instructions
*Oversight of third-party contract manufacturers, including technical agreements, audits and supplier performance
*Management of deviations, change controls, complaints and quality investigations
*Supporting GDP warehouse and distribution activities, including batch and delivery documentation for QP/RP release
*Leading self-inspection programmes, CAPA management and audit reporting
*Supporting regulatory activities, including licence variations and artwork changes
*Contributing to management review, quality metrics and continuous improvement initiatives
*Supporting GMP/GDP training and inspection readiness
There is also scope to act as RP/RPi and Medical Device PRRC, subject to experience and training.
About you
You’ll be a confident and detail-driven QA professional with solid regulated industry experience and the ability to work autonomously in a fast-moving environment.
You will ideally have:
*A degree in a scientific or pharmaceutical discipline (or equivalent experience)
*Strong working knowledge of GMP and GDP
*Experience working with third-party manufacturers and suppliers
*Excellent organisational skills and attention to detail
*Confidence dealing with audits, investigations and regulatory stakeholders
*Strong IT skills (MS Word & Excel)
*A flexible, proactive mindset and strong problem-solving ability
Medical device experience and RP/RPi aspirations are highly desirable but not essential.
What’s on offer
*Hybrid working model
*Broad, end-to-end QA exposure
*Clear development pathway within Quality and Regulatory
*Supportive, inclusive company culture
*Competitive salary and benefits package
This is an excellent opportunity for a QA Manager or experienced Senior QA professional looking to step into a high-impact, career-defining role within a stable and growing organisation.
Please apply today or contact Gareth Gooley @Smart4 Sciences for more a confidential chat.
The role
Reporting into the Head of Quality, you will play a central role in maintaining and improving Quality Assurance systems across licensed medicines, medical devices and food supplements. The position has a strong focus on third-party manufacturing oversight, supplier management and GDP operations, making it ideal for a QA professional who enjoys working cross-functionally and taking ownership.
Key responsibilities include:
*Maintaining and improving Quality Management Systems, SOPs and work instructions
*Oversight of third-party contract manufacturers, including technical agreements, audits and supplier performance
*Management of deviations, change controls, complaints and quality investigations
*Supporting GDP warehouse and distribution activities, including batch and delivery documentation for QP/RP release
*Leading self-inspection programmes, CAPA management and audit reporting
*Supporting regulatory activities, including licence variations and artwork changes
*Contributing to management review, quality metrics and continuous improvement initiatives
*Supporting GMP/GDP training and inspection readiness
There is also scope to act as RP/RPi and Medical Device PRRC, subject to experience and training.
About you
You’ll be a confident and detail-driven QA professional with solid regulated industry experience and the ability to work autonomously in a fast-moving environment.
You will ideally have:
*A degree in a scientific or pharmaceutical discipline (or equivalent experience)
*Strong working knowledge of GMP and GDP
*Experience working with third-party manufacturers and suppliers
*Excellent organisational skills and attention to detail
*Confidence dealing with audits, investigations and regulatory stakeholders
*Strong IT skills (MS Word & Excel)
*A flexible, proactive mindset and strong problem-solving ability
Medical device experience and RP/RPi aspirations are highly desirable but not essential.
What’s on offer
*Hybrid working model
*Broad, end-to-end QA exposure
*Clear development pathway within Quality and Regulatory
*Supportive, inclusive company culture
*Competitive salary and benefits package
This is an excellent opportunity for a QA Manager or experienced Senior QA professional looking to step into a high-impact, career-defining role within a stable and growing organisation.
Please apply today or contact Gareth Gooley @Smart4 Sciences for more a confidential chat.
Job number 3393362
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