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89,000+ live jobsQuality Control Analyst
On-site in Salamanca·Full-time·Added today (last checked 6 Nov)
Our summary
- Contract
- Full-time
- Driving licence
- Required


Visa options
The ad doesn’t mention sponsorship
Not a refusal, but not a yes. Worth asking in your first message.
Skills
Nice to have
This job advert was originally written in Spanish.
Requirements
What we're looking for
- University degree or degree-level training in Laboratory science.
- Previous laboratory experience within the pharmaceutical industry.
- Knowledge of GMPs.
- Certification in sterile process gowning.
- Ability to work as part of a team.
- Strong written and verbal communication skills.
Nice to have
- Knowledge of SAP (valuable).
- English level B2 (valuable).
- Experience in microbiological control testing.
The role
Ensure the correct performance of microbiological control tasks in the laboratory, contributing to the release of intermediate product, final product, plant services, and stability studies, always under the established regulatory and quality requirements.
What you'll do
Job Description
At our company in Salamanca, we are looking to hire a Quality Control Analyst for the Laboratory Operations area, with a focus on Sterility and Microbiology activities. The position is located on-site and includes a working schedule from 7:00 to 15:00 or 14:00 to 22:00, Monday to Friday (and the occasional Saturday).
Selected individuals will be responsible for executing, reviewing, and documenting the necessary tests in accordance with established procedures, ensuring at all times compliance with quality standards and Good Manufacturing Practices (GMP).
Main responsibilities
- Perform microbiological control tests in the Sterility and Microbiology areas.
- Collaborate in the release of intermediate product, final product, plant services, and stability studies in accordance with official procedures.
- Carry out the monitoring and recording of laboratory equipment.
- Plan the consumption of materials and reagents, and place orders through SAP.
- Record results in authorized systems and forms within the required timeframes.
- Review tests performed by other analysts.
- Participate in preliminary investigations regarding incidents and collaborate in laboratory investigations when necessary.
- Manage the control of assay standards.
Requirements
- Proficiency in the Microsoft Office suite.
Valued skills
- Effective communication
- Quality control
- GMP compliance
- Document management
- Laboratory investigations and OOS
- GMP Laboratory
- Laboratory analytical techniques
- Materials and testing management
- Technical writing
- Handling of LIMS, SAP, and technical procedures
Compound Management, GMP Compliance, GMP Laboratory, Keen Observation, Laboratory Analytical Techniques, Laboratory Information Management System (LIMS), Laboratory Investigations, Laboratory Operations, OOS Investigations, Quality Standards, Recordkeeping, Standard Operating Procedure (SOP) Writing, Sterility Testing, Technical Procedures, Technical Writing
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
Travel Requirements
Flexible Work Arrangements: Not Applicable
Hazardous Material(s)
Job Posting End Date: 11/15/2026
About MSD
MSD (Merck Sharp & Dohme) is the Spanish affiliate of Merck & Co., Inc., a global research-driven pharmaceutical company headquartered in Rahway, New Jersey, USA. The company discovers, develops, and manufactures innovative medicines and vaccines across therapeutic areas including oncology, infectious diseases, and cardiovascular health. With operations in over 140 countries and a workforce of roughly 70,000 employees worldwide, MSD is one of the largest and most influential healthcare companies in the world.
In Spain, MSD operates from its offices in Madrid, serving as the commercial and medical hub for the Iberian region. The Spanish affiliate is known for a professional, science-driven culture that values collaboration and innovation, and it regularly hires international talent across functions such as clinical research, medical affairs, and commercial operations. For international professionals, MSD offers a global career framework, competitive compensation, and the opportunity to work on medicines that reach patients worldwide, making it an attractive employer for those seeking a stable, multinational environment in Spain.
- Industry
- Pharma
- Founded
- 1891
- Employees
- 50,000–100,000
- Headquarters
- Rahway, USA
- In Spain
- Madrid
Good to know if you are moving
- MSD operates globally under the name MSD (Merck Sharp & Dohme) outside the US and Canada, so the Spanish entity is MSD Spain.
- The Spanish affiliate is based in Madrid and is one of the company's key European hubs for medical, regulatory, and commercial activities.
- The company offers a global mobility framework, making it feasible for international hires to move to Spain and later rotate to other countries.
- English is the working language for many internal communications, easing the transition for non-Spanish speakers.
- MSD is known for strong investment in R&D, with annual R&D budgets exceeding $10 billion, offering exposure to cutting-edge science.
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