At a Glance
- Tasks: Review analytical data and coordinate QC laboratory testing in a pharmaceutical environment.
- Company: Join LM Manufacturing Limited, a leader in pharmaceutical quality control.
- Benefits: Enjoy competitive salary, generous leave, pension scheme, and professional development.
- Other info: Stable career growth opportunities in a supportive team environment.
- Why this job: Make a real impact in quality control and ensure compliance in a dynamic industry.
- Qualifications: 5-8 years in QC with strong analytical skills and GMP knowledge.
The predicted salary is between 40000 - 50000 £ per year.
LM Manufacturing Limited is seeking an experienced Senior QC Reviewer & Laboratory Planner to join our growing Quality Control team within a pharmaceutical manufacturing environment. This role is ideal for candidates with strong experience in analytical data review, laboratory coordination, GMP compliance, QC documentation review, and QC planning activities within regulated pharmaceutical laboratories.
The successful Senior QC Reviewer will support laboratory review activities, QC compliance, laboratory planning, GMP documentation review, and coordination of Quality Control testing schedules.
Key Responsibilities:- Review analytical data generated from QC testing activities
- Coordinate and support QC laboratory testing schedules and planning activities
- Review analytical data from HPLC, UV, FTIR, and Karl Fischer testing
- Ensure compliance with ALCOA++, data integrity, and GMP requirements
- Support laboratory investigations including OOS, OOT, deviations, and CAPAs
- Review laboratory documentation in line with quality and regulatory standards
- Support method validation and verification activities
- Ensure compliance with ICH guidelines and 21 CFR requirements
- Work collaboratively with QC, QA, Production, and other site departments
- Support continuous improvement initiatives within the QC function
- 5–8 years’ experience within Quality Control in a pharmaceutical or regulated laboratory environment
- Strong experience as a QC Reviewer, GMP Reviewer, or QC Compliance Reviewer
- Experience reviewing analytical data and laboratory documentation
- Hands-on knowledge of HPLC, UV, FTIR, and Karl Fischer analysis
- Good understanding of GMP, data integrity, and regulatory compliance
- Experience with Chromeleon or similar CDS software preferred
- Strong organisational skills and attention to detail
- Excellent communication and problem-solving skills
- Experience with OOS/OOT investigations and deviation management
- Exposure to method validation and method transfer activities
- Degree in Chemistry, Pharmacy, or related scientific discipline
- Competitive salary depending on experience
- 21 days annual leave plus bank holidays
- Additional annual leave based on service
- Pension scheme
- Paid sick leave after probation
- Time Off in Lieu (TOIL)
- Free parking
- GP on-demand service
- Stable long-term career opportunities and development support
Location: NN7, Weedon Bec, Northamptonshire
Job Type: Permanent | Full Time | Day Shift
Please note: Sponsorship is not available for this role.
Senior QC Reviewer & Laboratory Planner employer: L M MANUFACTURING LIMITED
At LM Manufacturing Limited, we pride ourselves on being an excellent employer, offering a supportive work culture that fosters collaboration and continuous improvement within our Quality Control team. Located in the picturesque Northamptonshire, we provide competitive salaries, generous annual leave, and a range of benefits including a pension scheme and professional development opportunities, making it an ideal place for experienced professionals seeking meaningful and rewarding careers in the pharmaceutical industry.
StudySmarter Expert Advice🤫
We think this is how you could land Senior QC Reviewer & Laboratory Planner
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those who work in QC or laboratory roles. A friendly chat can lead to insider info about job openings and even referrals.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of GMP compliance and analytical techniques like HPLC and FTIR. We recommend practising common interview questions related to QC and having examples ready that showcase your experience.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values and career goals. Check out our website for openings at LM Manufacturing Limited and tailor your approach to show why you’re the perfect fit for their team.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can keep you fresh in the interviewer’s mind. It shows your enthusiasm for the role and gives you another chance to highlight your skills and experience.
We think you need these skills to ace Senior QC Reviewer & Laboratory Planner
Some tips for your application 🫡
Tailor Your CV:Make sure your CV highlights your experience in QC and laboratory planning. Use keywords from the job description to show we’re on the same page about what you bring to the table.
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Share specific examples of your past work that align with our needs, especially around GMP compliance and analytical data review.
Showcase Your Skills:Don’t forget to mention your hands-on experience with HPLC, UV, FTIR, and Karl Fischer analysis. We want to see how your skills fit into our QC team!
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and get you in the loop for this exciting opportunity!
How to prepare for a job interview at L M MANUFACTURING LIMITED
✨Know Your Analytical Data
Make sure you brush up on your knowledge of analytical data review, especially with HPLC, UV, FTIR, and Karl Fischer testing. Be prepared to discuss specific examples from your past experience where you successfully reviewed or coordinated QC testing activities.
✨Understand GMP Compliance Inside Out
Since this role heavily focuses on GMP compliance, it’s crucial to have a solid understanding of ALCOA++ principles and data integrity. Familiarise yourself with relevant regulations and be ready to explain how you've ensured compliance in previous roles.
✨Showcase Your Problem-Solving Skills
Prepare to discuss any OOS, OOT investigations, or deviations you've managed. Highlight your problem-solving approach and how you contributed to CAPAs or continuous improvement initiatives within the QC function.
✨Communicate Effectively
Strong communication skills are key for this position. Practice articulating your thoughts clearly and concisely, especially when discussing complex topics like method validation or regulatory standards. Remember, it's not just about what you say, but how you say it!
