QA Manager in Stockport

QA Manager in Stockport

Stockport Full-Time 36000 - 60000 £ / year (est.) No home office possible
SRG

At a Glance

  • Tasks: Lead a dynamic QA team ensuring compliance with GMP standards in pharmaceutical manufacturing.
  • Company: Join an award-winning CDMO focused on innovative pharmaceutical solutions.
  • Benefits: Highly attractive salary and opportunities for professional growth.
  • Why this job: Make a real impact in the pharmaceutical industry while leading quality assurance initiatives.
  • Qualifications: 5+ years in Quality Assurance within a GMP facility and proven leadership skills.
  • Other info: Exciting career development opportunities in a supportive and collaborative environment.

The predicted salary is between 36000 - 60000 £ per year.

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

Type: Permanent

Salary: Highly attractive

Location: Northwest, England

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:

  • Ensure full compliance with UK/EU GMP Regulatory Standards and company procedures.
  • Lead and manage the Quality Assurance Team at an IMP manufacturing site, focused on Phase I and Phase II clinical trial materials.
  • Maintain QA systems and processes, reviewing and supporting ongoing improvement activities.
  • Ensure effective management of documents through lifecycle, ensuring compliance with regulations and industry best practices. This includes creating, reviewing, and approving key documentation such as specifications, SOPs, protocols, and methods associated with all products and procedures.
  • Support batch documentation review and provide quality oversight for the certification and release of IMPs by the QP.
  • Investigating and approval of deviations, complaints and OOS to prevent future reoccurrences of nonconformance, providing support on SMART CAPA plans.
  • Supplier Management: Managing supplier approval and ongoing performance.
  • Evaluating site compliance and implementing improvements through the internal audit process, as an Internal Auditor and Report approver.
  • Supporting Client projects as a Quality Assurance representative and Customer liaison.
  • Support generation and cascade of quality training packages, including but not limited to GMP induction and annual refresher.
  • Assist with management of Regulatory inspections: inspection readiness, inspection and response.

Essential Requirements:

  • Minimum of 5 years' of recent experience in Quality Assurance within a Pharmaceutical (GMP) facility, preferably Investigational Medicinal Products (IMPs).
  • Proven Leadership/ Management experience.
  • Degree or equivalent in a relevant scientific discipline desired.
  • Experience in working with analytical laboratories and/or GMP production areas.

QA Manager in Stockport employer: SRG

Join a dynamic and award-winning contract development and manufacturing organisation in the Northwest of England, where your expertise as a Quality Assurance Manager will be valued and nurtured. With a strong commitment to compliance and continuous improvement, the company fosters a collaborative work culture that prioritises employee growth through training and development opportunities. Enjoy a highly attractive salary and the chance to make a meaningful impact in the pharmaceutical industry while working alongside passionate professionals dedicated to excellence.
SRG

Contact Detail:

SRG Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land QA Manager in Stockport

✨Tip Number 1

Network like a pro! Reach out to your connections in the pharmaceutical industry and let them know you're on the hunt for a QA Manager role. You never know who might have the inside scoop on an opening or can put in a good word for you.

✨Tip Number 2

Prepare for interviews by brushing up on your knowledge of UK/EU GMP Regulatory Standards. Be ready to discuss how you've ensured compliance in your previous roles, as this will show you're the right fit for the job.

✨Tip Number 3

Showcase your leadership skills! Think of examples where you've successfully managed a team or improved QA processes. This is key for a Quality Assurance Manager position, so make sure to highlight these experiences during interviews.

✨Tip Number 4

Don't forget to apply through our website! We’ve got loads of exciting opportunities waiting for you, and applying directly can give you a better chance of landing that dream job in quality assurance.

We think you need these skills to ace QA Manager in Stockport

GMP Regulatory Standards
Quality Assurance Management
Document Management
Deviation Investigation
CAPA Planning
Supplier Management
Internal Auditing
Client Liaison
Quality Training Development
Regulatory Inspection Management
Analytical Laboratory Experience
Leadership Skills
Scientific Background

Some tips for your application 🫡

Tailor Your CV: Make sure your CV is tailored to the QA Manager role. Highlight your experience in Quality Assurance, especially within pharmaceutical settings. We want to see how your skills align with the job description, so don’t hold back!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for our team. Share specific examples of your leadership and compliance experience that relate to the responsibilities listed in the job description.

Showcase Your Achievements: Don’t just list your duties; showcase your achievements! Whether it’s improving QA processes or leading successful audits, we want to know how you’ve made a difference in your previous roles.

Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It helps us keep track of your application and ensures you don’t miss out on any important updates from us!

How to prepare for a job interview at SRG

✨Know Your GMP Inside Out

Make sure you brush up on UK/EU GMP Regulatory Standards before the interview. Being able to discuss specific regulations and how they apply to Quality Assurance will show that you're not just familiar with the basics, but that you truly understand the nuances of the role.

✨Showcase Your Leadership Skills

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

✨Prepare for Scenario Questions

Expect questions about handling deviations, complaints, and OOS results. Think of specific instances where you've implemented SMART CAPA plans or improved processes. This will help you illustrate your problem-solving skills and your proactive approach to quality assurance.

✨Understand the Company’s Culture and Values

Research the company’s mission and values, especially their focus on providing expert intelligence and support. Be ready to discuss how your personal values align with theirs and how you can contribute to their success. This shows that you're not just looking for any job, but that you're genuinely interested in being part of their team.

QA Manager in Stockport
SRG
Location: Stockport

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