At a Glance
- Tasks: Ensure quality and compliance in pharmaceutical products while supporting continuous improvement.
- Company: Reputable pharmaceutical manufacturer committed to quality and safety.
- Benefits: Full-time role with career development, training, and a collaborative environment.
- Other info: Join a supportive team and grow your career in the STEM sector.
- Why this job: Make a real impact on healthcare product safety and quality.
- Qualifications: Degree in a scientific discipline or equivalent experience; knowledge of GMP regulations.
The predicted salary is between 30000 - 40000 £ per year.
We're working exclusively with a Pharmaceutical Manufacturer in the Lancashire region who are offering an exciting opportunity for a Quality Assurance Officer to join them. They are committed to delivering the highest standards of quality and safety. This full-time, on-site role offers the chance to play a vital part in maintaining compliance with strict industry regulations while supporting continuous improvement initiatives. You will work closely with cross-functional teams to uphold the integrity of pharmaceutical and biocide products, ensuring regulatory adherence and product excellence. In this vital position, you will be responsible for implementing and maintaining quality management systems, conducting audits, and supporting regulatory inspections. Your expertise and attention to detail will directly influence the company's reputation for quality and safety, contributing to its ongoing success and growth.
Key Duties and Responsibilities
- Ensure ongoing compliance with GMP, ISO9001, and 14001 standards by supporting the implementation, review, and auditing of quality systems.
- Assist in generating and reviewing SOPs and other quality documentation to ensure accuracy, clarity, and regulatory compliance.
- Maintain and improve document control processes, including archiving and tracking quality records and metrics.
- Support internal and external audits, including preparing documentation and participating in audit activities to demonstrate compliance.
- Support management during regulatory inspections and contribute to quality improvement projects across the site.
Role Requirements
- A Degree or higher level in a scientific discipline (e.g., Pharmaceutical Chemistry / Quality Assurance / Quality Management) or equivalent job experience.
- Proven understanding of GMP regulations, quality systems, and audit experience with knowledge of the MHRA Orange Guide.
- A dedicated team player with excellent attention to detail, problem-solving skills, and the ability to communicate clearly across departments.
What's in it for you?
This role offers a fantastic opportunity to develop your career within a reputable pharmaceutical company that values quality and integrity. You will be supported in your professional growth through training and exposure to various aspects of quality assurance, with the stability of a full-time, permanent position. Contributing directly to the safety of healthcare products, you'll have a meaningful impact within a collaborative and compliant environment.
Quality Assurance Officer in England employer: Hyper Recruitment Solutions LTD
Join a leading global medtech company in the Netherlands, where your clinical expertise will be highly valued and your contributions will have a meaningful impact on healthcare. With a dynamic work culture that fosters professional development and offers comprehensive training, this role provides an excellent opportunity to transition into the commercial sector while working with cutting-edge technology. Enjoy the unique advantage of leveraging your ICU experience in a customer-facing position, all within a supportive environment that prioritises employee growth and success.
Contact Details:
Hyper Recruitment Solutions LTD Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Quality Assurance Officer in England
✨Tip Number 1
Network like a pro! Reach out to professionals in the pharmaceutical industry on LinkedIn or at local events. We can’t stress enough how valuable personal connections can be in landing that Quality Assurance Officer role.
✨Tip Number 2
Prepare for interviews by brushing up on GMP regulations and quality systems. We recommend practising common interview questions related to quality assurance, so you can showcase your expertise and attention to detail.
✨Tip Number 3
Don’t forget to follow up after interviews! A quick thank-you email can leave a lasting impression. We believe it shows your enthusiasm for the role and keeps you fresh in their minds.
✨Tip Number 4
Apply through our website for the best chance of getting noticed! We make it easy for you to showcase your skills and experience directly to employers looking for top talent in quality assurance.
We think you need these skills to ace Quality Assurance Officer in England
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Quality Assurance Officer role. Highlight your experience with GMP, ISO standards, and any relevant audits you've conducted. We want to see how your skills align with what we're looking for!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about quality assurance in the pharmaceutical industry. Share specific examples of how you've contributed to compliance and quality improvement in past roles.
Showcase Your Attention to Detail:In quality assurance, attention to detail is key. When filling out your application, double-check for any typos or errors. We appreciate candidates who take the time to ensure their application reflects their meticulous nature.
Apply Through Our Website:We encourage you to apply directly through our website. This way, we can easily track your application and ensure it gets the attention it deserves. Plus, it’s the best way to stay updated on your application status!
How to prepare for a job interview at Hyper Recruitment Solutions LTD
✨Know Your Regulations
Make sure you brush up on GMP, ISO9001, and 14001 standards before the interview. Being able to discuss these regulations confidently will show that you understand the core of the role and are ready to uphold the company's commitment to quality and safety.
✨Showcase Your Attention to Detail
Prepare examples from your past experiences where your attention to detail made a difference. Whether it was during audits or while generating SOPs, having specific instances ready will demonstrate your capability in maintaining high standards.
✨Communicate Clearly
Since this role involves working with cross-functional teams, practice articulating your thoughts clearly. You might be asked how you would handle communication between departments, so think about how you can convey complex information simply and effectively.
✨Prepare for Audits and Inspections
Familiarise yourself with the audit process and regulatory inspections. Be ready to discuss how you would prepare documentation and participate in these activities. Showing that you have a proactive approach to compliance will set you apart from other candidates.
