Work Schedule
Standard (Mon-Fri)

Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Strong Odors (chemical, lubricants, biological products etc.)

Job Description

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.

• Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis.
• Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing.
• Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines.
• Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications.

• Bachelor's degree (Life Sciences degree preferred) or equivalent and relevant formal academic / vocational qualification

• Previous experience that provides the knowledge, skills, and abilities to perform the job
• Previous work experience which is comparable to 0-2 years, or equivalent combination of education, training, and experience.
• In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

• Knowledge of routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines
• Knowledge of applicable regulatory authority, compendia and ICH guidelines
• Excellent manual dexterity skills
• Good written and oral communication skills
• Time management and project management skills
• Proven solving and troubleshooting abilities
• Ability to cross-train on sample preparation techniques with another laboratory group
• Ability to work in a collaborative work environment with a team
• Manual dexterity and can follow detailed written and verbal instruction
• Cooperate with coworkers within an organized team environment or work alone with supervision
• Manage time effectively to complete assignments in expected time frame

• 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 prioritizing and handling multiple projects or activities.