Work Schedule
Other

Environmental Conditions
Office

Job Description

GC Scientist, Pharma

At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.

• Perform a variety of complex sample preparations on GC
• Analysis procedures to quantitatively measure pharmaceutical compounds in a variety of formulations for stability testing and other studies for analytical testing support
• Review and compilation of results
• Performing work assignments accurately, timely and in a safe manner
• Training on routine operation, maintenance and theory of analytical instrumentation, SOPs, and regulatory procedures and guidelines.
• Works with multiple functional groups to meet business needs.
• Sets up and maintains analytical instrumentation.
• Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory procedures and guidelines.
• Ensures QA findings are addressed appropriately.
• Communicates project status to project leader.
• Performs work assignments accurately, and in a timely and safe manner.
• Reviews, interprets, and analyses data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP).

• Educated to a bachelor's degree level in a relevant area, ie chemistry, pharmaceutical analysis, or similar
• 3+ years' relevant industry experience within a GMP laboratory with GC experience as a necessity

• Proven ability to interpret data by performing trend analysis
• Proven technical writing skills
• Proven problem solving skills
• Detailed knowledge of method validation; method development would be an advantage.
• The ability to plan, schedule and carry out work for successful project completion
• A positive attitude and ability to work well with others
• The ability to write protocols and reports with minimum supervision
• Excellent attention to detail
• Be able to communicate effectively and follow detailed written and verbal instruction

• Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.
• Able to work upright and stationary and/or standing for typical working hours.
• Able to lift and move objects up to 25 pounds.
• Able to work in non-traditional work environments.
• Able to use and learn standard office equipment and technology with proficiency.
• May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments.
• Able to perform successfully under pressure while prioritising and handling multiple projects or activities.