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- Tasks: Join our QA team to support quality assurance projects in a fast-paced sterile manufacturing environment.
- Company: We're a growing pharmaceutical company based in Surrey, focused on innovation and quality.
- Benefits: Enjoy a flexible work schedule with potential for long-term opportunities after the contract ends.
- Why this job: This role offers hands-on experience in a dynamic setting, perfect for those looking to grow their careers.
- Qualifications: 2+ years in a QA role within pharmaceutical manufacturing, especially in sterile environments.
- Other info: Immediate start available; great for those transitioning between jobs or contracts.
The predicted salary is between 36000 - 60000 £ per year.
Due to urgent need on a key sterile manufacturing facility based in Surrey, we are now looking to appoint interim support to support the QA team on site.
You will take on a broad range of duties in relation to the QMS and wider quality assurance projects, given the amount of positive growth taking place in the business. As the company grows in headcount, introduces new products and looks to upgrade current equipment and processes, you will need to be comfortable getting hands on in a range of tasks and conflicting priorities.
Looking for someone to join the site asap, this contract will last for 3-6 months and may have longer term prospects for the right individual.
You do not have to be a seasoned contractor to take on this position. As long as you have experience working within pharmaceutical manufacturing and ideally sterile/aseptic facilities, this could present an excellent opportunity for those in between jobs or currently in fixed term contracts coming to conclusion.
This role will be site based, Monday to Friday for 37.5hrs – some flexibility is required.
Please apply or contact Mark Bux-Ryan for more information.
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Experience within a specific QA role for at least 2+ years.
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Must have worked in the pharmaceutical industry
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Experience (or at minimum a solid understanding) of sterile manufacturing
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Confidence and experience with the application of GMP
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Flexible and adaptable in a fast-paced manufacturing setting
Manufacturing, pharmaceutical, quality, officer, QA, specialist, executive, capa, deviation, investigation, QMS, system, validation, SOP, protocols, project
Location Manchester, Lancashire, UK
QA Officer employer: Pharmiweb
Contact Detail:
Pharmiweb Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QA Officer
✨Tip Number 1
Make sure to familiarize yourself with the specific quality management systems (QMS) used in pharmaceutical manufacturing. Understanding these systems will not only help you during the interview but also demonstrate your commitment to the role.
✨Tip Number 2
Highlight any hands-on experience you have in sterile or aseptic environments. Be prepared to discuss specific projects or tasks where you successfully applied Good Manufacturing Practices (GMP) to showcase your practical knowledge.
✨Tip Number 3
Since this role requires flexibility, think of examples from your past work where you adapted to changing priorities or took on multiple tasks simultaneously. This will show that you can thrive in a fast-paced manufacturing setting.
✨Tip Number 4
Reach out to current or former employees in similar roles to gain insights about the company culture and expectations. This information can be invaluable during your discussions with Mark Bux-Ryan and can help you tailor your approach.
We think you need these skills to ace QA Officer
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in pharmaceutical manufacturing and any specific roles related to quality assurance. Emphasize your familiarity with sterile/aseptic facilities and GMP application.
Craft a Strong Cover Letter: In your cover letter, express your enthusiasm for the role and the company. Mention your relevant experience and how it aligns with the responsibilities outlined in the job description. Be sure to convey your adaptability in fast-paced environments.
Highlight Relevant Skills: When detailing your experience, focus on skills that are crucial for the QA Officer position, such as CAPA, deviation investigation, and QMS knowledge. Use specific examples to demonstrate your expertise.
Proofread Your Application: Before submitting your application, carefully proofread all documents to ensure there are no errors. A polished application reflects your attention to detail, which is essential in quality assurance roles.
How to prepare for a job interview at Pharmiweb
✨Show Your Understanding of QMS
Make sure to demonstrate your knowledge of Quality Management Systems (QMS) during the interview. Be prepared to discuss specific experiences where you contributed to or improved QMS processes in your previous roles.
✨Highlight Your Pharmaceutical Experience
Since the role requires experience in the pharmaceutical industry, be ready to share relevant examples from your past work. Discuss any specific projects or challenges you faced in sterile manufacturing environments.
✨Emphasize Flexibility and Adaptability
Given the fast-paced nature of the role, it's important to convey your ability to adapt to changing priorities. Share instances where you successfully managed multiple tasks or adjusted to new processes in a manufacturing setting.
✨Prepare for Technical Questions
Expect technical questions related to Good Manufacturing Practices (GMP) and sterile manufacturing. Brush up on key concepts and be ready to explain how you've applied these principles in your previous positions.
