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- Tasks: Ensure quality standards in a dynamic lab environment, performing checks and audits.
- Company: Join Intertek, a global leader in quality assurance across various industries.
- Benefits: Enjoy career development opportunities and work in a diverse, motivated team.
- Why this job: Make a real impact on product safety and quality while growing your skills.
- Qualifications: Degree in BioChemistry or Chemistry preferred; strong communication and analytical skills required.
- Other info: Entry-level position with full-time hours in a supportive and inclusive workplace.
The predicted salary is between 28800 - 43200 £ per year.
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Talent Acquisition Business Partner at Intertek
ABOUT YOU
As the Quality Officer, you will have excellent communications skills and the ability to converse succinctly with key stakeholders, providing them with accurate information and progress reports on a consistent basis.
Required skills and experience:
- Clear written and verbal communications skills with the ability to clearly convey processes, results and key messages and able to build rapport, quickly and effectively
- Excellent interpersonal skills with the ability to network and build strong relationships to collaborate with key stakeholders
- The ability to effectively time manage workloads and work on multiple projects as required
- Ideally degree qualified in BioChemistry or Chemistry (or related scientific discipline)
- A sound working knowledge of GMP and other analytical related quality standards is preferable
- Proven industry experience of performing detailed experimental checks within the above regulatory framework
- Industry experience in analytical science (chromatographic methods e.g. HPLC, GC, LC etc. and/ or other pharmaceutical characterisation techniques)
ABOUT THE OPPORTUNITY
This opportunity will take place in an environment that has an extensive range of analytical instrumentation and that provides analytical services to customers in the pharmaceutical, biopharmaceutical, personal care and speciality chemical sectors in a GMP regulated laboratory. This role will review deviations, OOS and change control records, perform internal audits and review of equipment qualifications as well as perform checks GMP data as necessary in accordance with experimental checking procedures.
Key activities:
- Perform GMP and related quality system checks necessary to ensure that appropriate standards and effective working systems are employed to meet our company and customer requirements
- Assist the Quality Assurance Team Leader in the overall implementation of the Quality function
- Check analytical technical data, associated records, facility and operational systems, to monitor and assure management of the appropriate standard procedures being followed as required by relevant regulatory requirements
- Provide general support to all Quality Team activities relating to GMP, and other similar Quality Systems established to ensure that the appropriate standards and effective working systems and relationships are maintained and where necessary improved
- and completely reflect the raw data and meet current Good Clinical Practice standards and regulations
- Identify and contribute to areas for improvement within the quality management systems to ensure compliant and efficient systems
- Carry out internal audits and support in the hosting of client and regulatory audits
- Review and approval of Equipment Qualifications
- Review and Approval of QMS records such as Deviations, OOS Investigations and Change Controls.
WHAT WE OFFER
Join Intertek and become part of our global network of inspiring and entrepreneurial colleagues. We are a global family that values diversity and we thrive working together with precision, pace, and passion. We are working to make the world Ever Better, ensuring the quality, safety and sustainability of products and services used by millions of people around the world.
- Development and career opportunities around the Globe
- Working in a highly motivated team and dynamic working environment
We are an Equal Opportunity Employer who do not discriminate against applicants. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex or national origin.
Intertek operates a preferred supplier arrangement, and we do not accept unsolicited approaches from agencies.
Seniority level
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Seniority level
Entry level
Employment type
-
Employment type
Full-time
Job function
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Job function
Quality Assurance
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Industries
Pharmaceutical Manufacturing
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Quality Assurance Officer employer: Intertek
Contact Detail:
Intertek Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Assurance Officer
✨Tip Number 1
Familiarise yourself with GMP and other quality standards relevant to the pharmaceutical industry. Understanding these regulations will not only help you in interviews but also demonstrate your commitment to quality assurance.
✨Tip Number 2
Network with professionals in the quality assurance field, especially those working in GMP regulated environments. Engaging with them can provide insights into the role and may even lead to referrals.
✨Tip Number 3
Prepare to discuss specific analytical techniques like HPLC or GC during your conversations. Being able to articulate your experience with these methods will show your technical competence and relevance to the role.
✨Tip Number 4
Demonstrate your communication skills by practicing how to convey complex information clearly and succinctly. This is crucial for the Quality Assurance Officer role, as you'll need to interact with various stakeholders effectively.
We think you need these skills to ace Quality Assurance Officer
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in quality assurance and analytical science. Emphasise your skills in GMP, chromatographic methods, and any specific projects that demonstrate your ability to manage multiple tasks effectively.
Craft a Strong Cover Letter: In your cover letter, clearly articulate your communication skills and how they relate to the role. Provide examples of how you've built relationships with stakeholders and contributed to quality management systems in previous positions.
Highlight Relevant Qualifications: If you have a degree in Biochemistry, Chemistry, or a related field, make sure to mention it prominently. Also, include any certifications or training related to GMP and quality assurance that could set you apart from other candidates.
Showcase Problem-Solving Skills: Use specific examples in your application to demonstrate your ability to identify areas for improvement within quality management systems. Discuss any internal audits you've conducted or participated in, and how you contributed to compliance and efficiency.
How to prepare for a job interview at Intertek
✨Showcase Your Communication Skills
As a Quality Assurance Officer, clear communication is key. Prepare to demonstrate your ability to convey complex information succinctly and effectively during the interview. Think of examples where you've successfully communicated with stakeholders or resolved misunderstandings.
✨Highlight Your Technical Knowledge
Make sure to brush up on GMP and analytical techniques relevant to the role, such as HPLC and GC. Be ready to discuss your experience with these methods and how they apply to quality assurance processes. This will show that you have the technical expertise needed for the job.
✨Demonstrate Your Interpersonal Skills
Building rapport with colleagues and stakeholders is crucial in this role. Prepare examples of how you've successfully collaborated with others in previous positions. This could include teamwork on projects or resolving conflicts, showcasing your ability to foster strong working relationships.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving abilities in quality assurance scenarios. Think about past experiences where you identified areas for improvement or handled deviations. Practising your responses to these types of questions can help you articulate your thought process clearly.
