Senior Data Reviewer - Cell & Gene Therapy (GMP)

Thermo Fisher Scientific•Middleton, WI

1d•Remote

About The Position

This is a fully remote role supporting our GMP Lab in Middleton, WI. We welcome applicants from all locations within the United States. 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. Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic experts. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations.

Requirements

Bachelor's degree or equivalent and relevant formal academic / vocational qualification
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years). 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.
Solid understanding and knowledge of general chemistry and separation science
Full understanding of laboratory requirements, PPD & client SOPs, ICH guidelines, USP requirements and FDA guidance
Ability to apply Microsoft Excel and Word to perform tasks
Proficiency on technical operating systems
Proven problem solving and troubleshooting abilities
Effective oral and written communication skills
Proven ability in technical writing skills
Time management and project management skills
Ability to work in a collaborative work environment with a team
Proven problem solving and troubleshooting abilities
Ability to train junior staff
Must be legally authorized to work in the United States without sponsorship.
Must be able to pass a comprehensive background check, which includes a drug screening.

Nice To Haves

Prior GMP experience preferred

Responsibilities

Performs complex laboratory analysis of pharmaceutical products and proficiently uses analytical instrumentation, calculates and analyzes data and records data in adherence with PPD SOP's and the industry.
Routinely acts as the project leader on multiple projects, interacts with clients, reviews and evaluates data, writes reports and protocols.
Responsible for the scientific conduct of the project and communication of regulatory issues with senior level team members.
Independently performs method validations, method transfers and analytical testing of pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or delivery systems.
Understands and conforms to methods and protocols applicable to assigned tasks.
Designs and drives experiments with minimal supervision.
Prepares study protocols, project status reports, final study reports and other project-related technical documents.
Communicates data and technical issues to the client and responds to client needs and questions.
Mentors, trains and coordinates laboratory activities of other team members and assists in troubleshooting instrument and analytical problems.
Assists with quality systems and new equipment.
Assists in designing method validation or method transfer protocols and establish project timelines.
Reviews, interprets, and analyzes data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP).
Performs self and peer review of the data for accuracy and compliance with reporting requirements prior to submission to QA and issuance to customers.