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- Tasks: Ensure compliance and efficiency in the QC Micro department while supporting customer needs.
- Company: Join Norbrook Laboratories, a leader in pharmaceutical manufacturing.
- Benefits: Permanent position with opportunities for growth and development.
- Why this job: Make a real impact in a dynamic lab environment focused on quality and safety.
- Qualifications: Degree in science or 2 years lab experience; strong communication and organisational skills.
- Other info: Be part of a diverse team committed to excellence and continuous improvement.
The predicted salary is between 36000 - 60000 £ per year.
The successful candidate will ensure the QC Micro department operates in a safe, efficient and compliant manner and deliver to the needs of our customers.
Main Activities/Tasks:
- Compilation of Standard Operation Procedure, Method of Analysis, Equipment Qualification Test Protocols, Reports, Raw Material Specifications, and Finished Product Specifications in accordance with GMP.
- Review and approval of logbooks ensuring compliance to GMP.
- Trending and reporting of analytical data and generation of key KPI's.
- Preparing for and participation in regulatory and customer audits.
- Assist investigations into OOS & OOT results and determination of root cause.
- Reading and recording of test results.
- Approval of analytical data.
- Assist in the training of staff in new and existing techniques.
- Ensure that adequate stocks of all laboratory consumables are available.
- Raising, investigating and closing change controls, deviations and other key QMS parameters.
- Management of computerised systems within the department, from introduction, qualification and completion of ongoing review.
- Perform monthly backup and data archive for the computerised system.
- Completion of periodic reviews and oversight of standalone computer system requirements.
- Champion adherence to Health and Safety requirements and drive a culture of improvement within the laboratory.
- Identify and deliver projects that lead to improved compliance (Quality and EHS) and efficiency gains.
- Maintain a CAPEX forecast plan.
- Any other duties as deemed necessary by management.
Essential Criteria:
- Possess a degree in a science related discipline OR have a minimum of 2 years relevant experience in a laboratory.
- Possess good communication skills, written and oral as demonstrated on their application form and at interview.
- Demonstrate good organisational skills, be flexible, motivated, and willing to work shift patterns when necessary.
- Demonstrate the ability to work as part of a busy team as well as working on own initiative.
Desirable Criteria:
- Use of Quality Management Software like Trackwise for the creation and closure of deviation and change controls.
- Experience of computer system validation (csv) requirements throughout the whole system lifecycle.
- Practical knowledge of laboratory instrumentation and microbiology analytical methods.
- Experience in training other analysts.
Applicants should be able to provide proof that they have a right to work in the UK at the time of their application. We regret that applications received after the closing date and time will not be accepted. This role is based on a site that produces penicillin and as such, would not be suitable for those with a penicillin allergy. Norbook Laboratories Limited employs a workforce with members of all sections of the community and is committed to appointing people purely on the basis of merit. In accordance with our equal opportunities policy, we would particularly like to welcome applicants from the Protestant Community.
To Apply: Please forward your CV via the APPLY Now button below.
Compliance & Operational Support Analyst in Newry employer: Norbrook
Contact Detail:
Norbrook Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Compliance & Operational Support Analyst in Newry
✨Tip Number 1
Get to know the company inside out! Research their values, mission, and recent projects. This will help you tailor your conversations and show that you're genuinely interested in being part of their team.
✨Tip Number 2
Network like a pro! Reach out to current employees on LinkedIn or attend industry events. Building connections can give you insider info and might even lead to a referral, which is always a bonus!
✨Tip Number 3
Prepare for the interview by practising common questions and scenarios related to compliance and operational support. Use the STAR method (Situation, Task, Action, Result) to structure your answers and showcase your skills effectively.
✨Tip Number 4
Don’t forget to follow up after your interview! A quick thank-you email reiterating your interest in the role can leave a lasting impression and keep you top of mind for the hiring team.
We think you need these skills to ace Compliance & Operational Support Analyst in Newry
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Compliance & Operational Support Analyst role. Highlight your relevant experience and skills that match the job description, especially in areas like GMP compliance and laboratory practices.
Showcase Your Communication Skills: Since good communication is key for this role, ensure your written application reflects your ability to convey information clearly. Use concise language and structure your CV and cover letter well to demonstrate your organisational skills.
Highlight Relevant Experience: If you have experience with Quality Management Software or computer system validation, make it stand out! Mention specific projects or tasks where you’ve used these skills, as they’re highly desirable for this position.
Apply Through Our Website: We encourage you to apply through our website for a smoother process. Make sure to double-check your application before hitting send, and don’t forget to include proof of your right to work in the UK!
How to prepare for a job interview at Norbrook
✨Know Your GMP Inside Out
Make sure you brush up on Good Manufacturing Practices (GMP) before your interview. Familiarise yourself with the key principles and how they apply to the QC Micro department. Being able to discuss specific examples of how you've adhered to GMP in past roles will show that you're serious about compliance.
✨Showcase Your Analytical Skills
Prepare to discuss your experience with analytical data and how you've contributed to generating key KPIs. Think of specific instances where you've identified trends or resolved out-of-specification (OOS) results. This will demonstrate your ability to handle the responsibilities of the role effectively.
✨Be Ready for Team Dynamics
Since teamwork is crucial in this role, be prepared to talk about your experiences working in a busy team environment. Share examples of how you've collaborated with others, trained staff, or taken the initiative to improve processes. This will highlight your flexibility and motivation.
✨Understand the Role of Technology
Familiarise yourself with Quality Management Software like Trackwise and any computer system validation (CSV) requirements. If you have experience with these tools, be ready to discuss how you've used them to manage deviations and change controls. This knowledge will set you apart from other candidates.