QA Manager

QA Manager

Full-Time 48000 - 84000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead a team ensuring top-notch quality in pharmaceutical manufacturing.
  • Company: Join an award-winning CDMO known for its expertise and innovation.
  • Benefits: Enjoy competitive pay, career growth opportunities, and a dynamic work environment.
  • Why this job: Be part of a mission-driven team making a real impact in healthcare.
  • Qualifications: Degree in life sciences and extensive QA leadership experience required.
  • Other info: Opportunity to work with regulatory bodies and enhance your professional skills.

The predicted salary is between 48000 - 84000 £ per year.

Are you an experienced Quality Assurance Leader looking for a challenge with a really exciting CDMO focused on Pharmaceutical Manufacturing?

SRG is currently working exclusively with a highly successful, award winning, contract development and manufacturing organisation focused on providing expert intelligence and support to their partners, driven by their capabilities. As a result of expansion, we are looking for a Quality Assurance Manager to join their quality team.

Typical responsibilities/accountabilities:

  • Lead a team of pharmaceutical Quality Assurance professionals working to the highest quality and compliance standards.
  • Work with Qualified Person to enable the efficient evaluation and release of IMP to clinical studies on our clients' behalf.
  • Take the lead on regulatory inspections and client audits and take accountability (with the Site Leadership Team) for the approval and maintenance of the site MHRA MIA (IMP) licence.
  • To lead Management Reviews of Quality performance.
  • To provide support and leadership on a range of activities including but not limited to: non-conformance management, including CAPA, events, root cause analysis, continuous improvement, key supplier issues, complaint investigations etc.
  • To ensure compliance with regulatory filings and regulatory agency reporting, and the implementation of compliance site initiatives and procedures.
  • To oversee compliance during the design, construction, start-up, validation, and retirement of equipment, process, utilities, facilities, computer systems, etc.
  • To be responsible for Quality Metrics development and monitoring compliance, internal/external audits etc.

Essential Requirements:

  • Degree of equivalent in a life science.
  • Extensive recent experience of QA leadership in a Pharma/CMO company.
  • Excellent knowledge of global regulations, and experience of dealing with MHRA.
  • Good communication skills internally and in a client facing role.

QA Manager employer: SRG

Joining our team as a Quality Assurance Manager in Northwest England means becoming part of an award-winning CDMO that prioritises excellence and innovation in pharmaceutical manufacturing. We foster a collaborative work culture that values professional growth, offering ample opportunities for career advancement and skill development, while also providing a supportive environment where your contributions directly impact our success. With a focus on compliance and quality, you will lead a dedicated team and engage in meaningful work that shapes the future of healthcare.
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Contact Detail:

SRG Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land QA Manager

✨Tip Number 1

Network with professionals in the pharmaceutical industry, especially those who have experience in Quality Assurance. Attend industry conferences or webinars to connect with potential colleagues and learn about the latest trends and challenges in QA management.

✨Tip Number 2

Familiarise yourself with the specific regulations and compliance standards relevant to the role, particularly those set by the MHRA. This knowledge will not only boost your confidence but also demonstrate your commitment to quality assurance during interviews.

✨Tip Number 3

Prepare to discuss your leadership style and experiences in managing QA teams. Think of specific examples where you successfully led a team through audits or regulatory inspections, as this will showcase your capability to handle the responsibilities of the role.

✨Tip Number 4

Research the company’s recent achievements and projects in the pharmaceutical sector. Being knowledgeable about their work will allow you to tailor your conversation during interviews and show that you are genuinely interested in contributing to their success.

We think you need these skills to ace QA Manager

Quality Assurance Leadership
Pharmaceutical Manufacturing Knowledge
Regulatory Compliance Expertise
MHRA Regulations Familiarity
Non-Conformance Management
CAPA Implementation
Root Cause Analysis
Continuous Improvement Methodologies
Audit Management
Quality Metrics Development
Team Leadership
Client Relationship Management
Excellent Communication Skills
Problem-Solving Skills
Project Management

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in Quality Assurance, particularly in pharmaceutical manufacturing. Emphasise your leadership roles and any specific achievements related to compliance and regulatory inspections.

Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for quality assurance and your understanding of the pharmaceutical industry. Mention your familiarity with MHRA regulations and how your skills align with the responsibilities outlined in the job description.

Highlight Relevant Experience: In your application, focus on your extensive QA leadership experience. Provide examples of how you've successfully managed non-conformance issues, led audits, or improved quality metrics in previous roles.

Proofread Your Application: Before submitting, carefully proofread your application for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in a QA role.

How to prepare for a job interview at SRG

✨Showcase Your Leadership Experience

As a QA Manager, you'll be leading a team, so it's crucial to highlight your leadership skills. Prepare examples of how you've successfully managed teams in the past, particularly in high-pressure environments like pharmaceutical manufacturing.

✨Demonstrate Regulatory Knowledge

Familiarise yourself with global regulations and specifically MHRA guidelines. Be ready to discuss your experience with regulatory inspections and audits, as this will be a key part of the role.

✨Prepare for Scenario-Based Questions

Expect questions that assess your problem-solving abilities, especially regarding non-conformance management and CAPA processes. Think of specific situations where you identified issues and implemented effective solutions.

✨Communicate Clearly and Confidently

Good communication is essential in this role, both internally and with clients. Practice articulating your thoughts clearly and confidently, ensuring you can convey complex information in an understandable way.

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