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Pharmaceutical QA Manager

Kenton Black Ltd

Lower Hopton

On-site

GBP 60,000 - 90,000

Full time

6 days ago
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Job summary

An established industry player is seeking a QA Manager to join their dynamic team in West Yorkshire. This role offers the chance to lead a talented team of quality assurance professionals while ensuring compliance with European and US cGMP regulations. You will play a crucial role in managing quality metrics, participating in audits, and driving quality systems on site. If you are passionate about quality management and thrive in a fast-paced environment, this is the perfect opportunity to make a significant impact in a global pharmaceutical company. Join a forward-thinking organization that values innovation and excellence in quality assurance.

Qualifications

  • Experience in a Pharmaceutical GMP environment is essential.
  • Strong leadership and management capabilities are required.

Responsibilities

  • Manage a team of 7, focusing on recruitment and performance management.
  • Lead regulatory audits and ensure compliance with cGMP guidelines.

Skills

Leadership Skills
Interpersonal Skills
Organizational Skills
Decision-Making Skills
Communication Skills

Education

BSc or equivalent in a Scientific subject

Job description

QA Manager
West Yorkshire – commutable from Huddersfield, Mirfield, Halifax, Bradford, Dewsbury and Leeds
Up to £90,000 with a substantial benefits package

My client, a global pharmaceutical company, has a rare opportunity for a QA Manager to join their team in West Yorkshire!

As part of the Site Leadership team, you will manage a team of 7 and be present on site 5 days a week.

Responsibilities of the QA Manager will be:
  1. Recruitment, training, and performance management of team members
  2. Collation and reporting of quality metrics at site and business level
  3. Interpreting European and US cGMP guidelines and regulations and applying to ways of working and integrating into the QMS at site
  4. Champions key quality systems on site: Change Control, Validation and Cleaning Validation
  5. Participate in and lead regulatory and customer audits – MHRA and FDA
  6. Provide expertise and support on Quality and cGMP aspects to other departments
  7. Ensures that all incidents, OOS and OOT results are investigated, root caused and appropriate CAPAs are put in place.

This is a fantastic opportunity for a dynamic, experienced and change-focused candidate who will possess a broad knowledge of the business, effective communication, interpersonal, organisation & decision-making skills with the ability to lead, manage and motivate teams within a pressurised environment.

The ideal candidate for the QA Manager will have:
  1. A BSc or equivalent in a Scientific subject
  2. Experience working in a Pharmaceutical GMP environment
  3. Excellent leadership and management skills.

If you are an experienced QA Manager or QA Head looking for your next challenge then please apply now!

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