Work Schedule
Rotational shift nights/weekendsEnvironmental Conditions
Laboratory SettingJob Description
As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
Location/Division Specific Information:
This position is based in our Quality Control laboratory, supporting pharmaceutical manufacturing operations in compliance with GMP standards and regulatory requirements.
How Will You Make an Impact?:
In this role, you will ensure the quality and safety of pharmaceutical products by performing critical analytical testing, managing laboratory documentation, and supporting validation activities that directly impact product quality and patient safety.
A Day in the Life:
Plan and execute analytical transfer/validation activities, sampling, and batch analysis while coordinating with cross- functional teams to meet quality standards and laboratory efficiency requirements
Perform quality control testing for assigned analyses, verify results against specifications, and manage Out of Specification (OOS) investigations to identify root causes and implement corrective actions
Maintain laboratory instruments through proper calibration and management, prepare and manage analytical documentation from receipt to archiving, and issue analytical reports in compliance with GMP and company procedures
Support technical training for laboratory personnel on new analytical methods and techniques, update procedures and documentation as needed, and ensure compliance with safety regulations including PPE usage and monthly KPI reporting
Request quotes from external laboratories for analytical activities on incoming projects and collaborate with Quality Assurance, Production, Warehouse, and other internal departments
REQUIREMENTS:
Education: (EMEA)
High School Diploma in Chemistry or Degree in Chemistry/Pharmaceutical Chemistry required.
Experience:
Required:Minimum of 2 years of work experience in analytical laboratory or pharmaceutical technical laboratory
Preferred:Degree in Chemistry and Pharmaceutical Technologies/Biotechnology; Knowledge of international standards, procedures, and certifications
Knowledge, Skills, Abilities:
Proficiency in Microsoft Office Suite and knowledge of company procedures, GMP, and statistical methods
Strong organizational and planning skills with the ability to manage multiple priorities and maintain accurate documentation in compliance with quality standards
Active listening and communication skills with flexibility and the ability to collaborate effectively in team environments
English language proficiency
Physical Requirements / Work Environment:
This position requires working in a laboratory environment with adherence to safety protocols, use of personal protective equipment (PPE), and compliance with GMP regulations. May involve handling chemical substances and operating laboratory instrumentation. This role requires shift work on a continuous 6x4 rotation (6 working days followed by 4 rest days), including night shifts, 7 days a week. Flexibility and adaptability to rotating shift schedules are essential.
What We Offer:
Compensation
Excellent Benefits