At a Glance
- Tasks: Join a friendly team ensuring quality and compliance in a fast-paced lab environment.
- Company: A contract testing lab supporting healthcare, focused on quality and compliance.
- Benefits: Full-time role with statutory sick pay and pension contributions after probation.
- Why this job: Exciting opportunity to work with industry standards and make a real impact.
- Qualifications: Attention to detail, QA experience, and knowledge of ISO 17025 or GMP required.
- Other info: Private transport needed; some overtime may be required.
The predicted salary is between 30000 - 42000 £ per year.
Job Title: QA Officer
Location: Near Buxton (Fully Onsite)
My client is a contract testing laboratory supporting the healthcare and related industries. We are looking for a highly motivated and detail-orientedQA Officerto join a small and friendly team based in Tideswell, UK. This is an exciting opportunity to work in a fast-paced environment, ensuring the quality and compliance of laboratory work in line with ISO 17025 and GMP standards.
Key Responsibilities:
- Ensure compliance with company policies and procedures, including Health and Safety, ISO 17025, and GMP.
- Review, write, and amend documentation such as SOPs.
- Manage controlled documentation and maintain its circulation and availability.
- Audit GMP data, including reviewing raw data prior to releasing GMP CoA or CoP.
- Coordinate quality issues, investigations, and CAPA.
- Assist with OOS, NC, NTF, CMP, RA, and CAPA investigations.
- Participate in the change control process to ensure changes maintain GMP compliance.
- Track, trend, and gather data for meetings as per procedures.
- Conduct staff training on quality matters when required.
- Liaise with customers or regulatory representatives.
- Host and manage external audits by customers or regulatory bodies.
- Respond to external audit report findings and plan corrective actions.
- Release and obtain necessary documentation in a controlled manner.
- Plan and conduct internal audits.
- Maintain the archives.
The Ideal Candidate:
- Strong attention to detail and commitment to compliance with industry standards.
- Experience in a QA role within a laboratory or regulated environment.
- Knowledge of ISO 17025 or GMP, and controlled documentation.
- Strong communication skills and the ability to liaise with internal and external stakeholders.
- Ability to work independently and manage multiple priorities.
Other Information:
- Please note – private transport is essential to access the site unless you live in the immediate area
- Full-time role, 37.5 hours per week (some overtime may be required).
- Statutory Sick Pay.
- Auto-enrolment into a pension scheme with a 6% employer contribution after probation.
If you\’re interested in the above role then please click apply or get in touch to discuss further.
Consult will endeavour to contact candidates within 14 days of application. However, if you do not hear back after 2 weeks then please assume on this occasion, unfortunately, you have not been successful.
IndScientific123
QA Officer in Buxton, Derbyshire employer: Consult Search and Selection
Contact Detail:
Consult Search and Selection Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QA Officer in Buxton, Derbyshire
✨Tip Number 1
Familiarize yourself with ISO 17025 and GMP standards. Understanding these regulations will not only help you in the interview but also demonstrate your commitment to quality assurance.
✨Tip Number 2
Highlight any previous experience you have in a QA role, especially in a laboratory or regulated environment. Be ready to discuss specific examples of how you've ensured compliance and managed documentation.
✨Tip Number 3
Prepare to showcase your strong communication skills. Think of instances where you've successfully liaised with internal teams or external stakeholders, as this is crucial for the role.
✨Tip Number 4
Since private transport is essential, make sure to mention your transportation arrangements during the application process. This shows that you're proactive and ready to commit to the role.
We think you need these skills to ace QA Officer in Buxton, Derbyshire
Some tips for your application 🫡
Understand the Role: Take the time to thoroughly read the job description for the QA Officer position. Make sure you understand the key responsibilities and the skills required, especially regarding ISO 17025 and GMP standards.
Tailor Your CV: Customize your CV to highlight relevant experience in quality assurance roles, particularly in laboratory or regulated environments. Emphasize your attention to detail and any specific knowledge of ISO 17025 or GMP.
Craft a Strong Cover Letter: Write a cover letter that showcases your motivation for applying and how your background aligns with the company's needs. Mention your ability to manage multiple priorities and communicate effectively with stakeholders.
Proofread Your Application: Before submitting your application, carefully proofread all documents for spelling and grammatical errors. A polished application reflects your attention to detail, which is crucial for a QA role.
How to prepare for a job interview at Consult Search and Selection
✨Know Your Standards
Familiarize yourself with ISO 17025 and GMP standards. Be prepared to discuss how you have applied these standards in your previous roles, as this will demonstrate your understanding of compliance and quality assurance.
✨Showcase Your Attention to Detail
Prepare examples that highlight your strong attention to detail. Discuss specific instances where your meticulousness led to successful outcomes in quality assurance or compliance tasks.
✨Communicate Effectively
Practice articulating your thoughts clearly and confidently. Since the role involves liaising with various stakeholders, showcasing your communication skills during the interview is crucial.
✨Be Ready for Scenario Questions
Expect scenario-based questions related to quality issues, investigations, and audits. Prepare to explain how you would handle specific situations, demonstrating your problem-solving skills and knowledge of QA processes.