MSD
Quality Assurance Specialist
How your CV stacks up
Upload your CV to see how well it fits this job role
?%
Job Description
Make a real impact on patient safety and product quality. Join our Global Development Quality (GDQ) team in London as a QA Specialist, where you’ll play a key role in GMP Quality Assurance activities supporting our GDQ IMP Licence. You’ll partner across functions, shape quality standards, and help ensure our products meet the highest regulatory and ethical benchmarks.
What you’ll do
- Lead and perform GMP audits to ensure compliance with SOPs, GMPs, and applicable regulations
- Review and approve production and analytical documentation for drug substance, drug product, and packaged finished goods, supporting QP certification
- Collaborate across functional teams to resolve comments and issues identified during audits and reviews
- Support product recalls and stock recoveries when required
- Identify compliance gaps and drive continuous improvement initiatives
- Create, update, and maintain assigned SOPs
- Perform and review complaints, deviation investigations, change controls, and CAPAs
- Contribute to onboarding and training of new starters and colleagues
- Follow standard procedures and consult with your manager to resolve exceptions
- Compile data for reports and presentations, interpret findings, and draw actionable conclusions
- Deliver work to high standards of compliance, efficiency, innovation, accuracy, and safety
- Stay current with cGMP requirements and evolving global regulations
- Represent GDQ on cross-functional teams and support additional activities as assigned
Reasons to use Rodeo
Start with a chat, not a search bar
Grad scheme, placement, apprenticeship? Not sure what you want yet — that's fine. Your agent talks it through with you and turns "I have no idea" into a shortlist.
It searches the market for you
Every day your agent scans the market matching roles against what actually matters to you, not just keywords on a CV.
Only hits
No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.
What you’ll bring
- Bachelor’s degree in a life science or related discipline
- Applied professional experience in pharmaceutical Quality roles
- Strong, collaborative communication skills and a self-motivated mindset
- Demonstrated understanding of GMP and solid technical knowledge
- Proven ability to lead and contribute as a team player; capable of prioritising and delivering across multiple projects and tasks
- Advanced problem-solving and sound decision-making skills
- Proficiency with Microsoft applications and readiness to learn and use GMP-related software
Why join us
- Be part of a mission-driven team ensuring products are safe, effective, and compliant
- Work in a collaborative environment with clear impact on regulatory success and patient outcomes
- Opportunities to grow your expertise across audits, quality systems, and cross-functional projects
Ready to elevate quality with us? If this sounds like your next step, we’d love to hear from you.
Closing date for applications: 05/06/2026
Required Skills:
Auditing, Complaints Investigation, Compliance Reporting, Data Analysis, GMP Compliance, Good Manufacturing Practices (GMP), Investigation Management, Process Improvements, Quality Assurance (QA), Quality Control Management, Quality Management, Regulatory Compliance, Regulatory Requirements
Get help with your application
Your very own career expert that helps elevate your application to the next level.
Preferred Skills:
Current Employees apply HERE
Current Contingent Workers apply HERE
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status: Regular
Relocation: No relocation
VISA Sponsorship: No
Travel Requirements: No Travel Required
Flexible Work Arrangements: Hybrid
Shift: Not Indicated
Valid Driving License: No
Hazardous Material(s): N/A
Job Posting End Date: 08/6/2026
A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
“It took my CV and asked me questions relevant to understanding what kind of jobs to suggest for me. Suggestions were almost perfect. Jobs were exactly what I’ve been looking for.”
Jessica, London
Skills
Location