Associate Research Scientist Molecular Genomics Microarray

Work Schedule

Environmental Conditions

Job Description

This is a fully onsite role basedatourlaboratory at 2244 Dabney Road Richmond VA. We welcome applicants from all locations within the note that relocation assistance is not provided for this position and any relocation costs will be the responsibility of the candidate.

Must be legally authorized to work in the United States withoutsponsorship.

Must be able to pass a comprehensive background check whichincludes a drug screening.

At Thermo Fisher Scientific youll 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.

Discover Impactful Work:

Independently performs a variety of complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices. Responsible for review and compilation of results and data comparison against SOP acceptance criteria methodology protocol and product specifications. Coordinates laboratory activities of other team members in conjunction with the lab management. Performs study design and protocol authoring. Leads data evaluation and study close-out. Provides technical guidance and mentorship to junior scientists. Trains on routine operation maintenance and theory of complex analytical instrumentation SOPs and regulatory procedures and guidelines.

A Day in the Life:

• Operate and maintain the SwiftArrayStudio instrument for routine hybridization and scanning.
• Perform RNA isolation labeling and QC using standard molecular biology tools.
• Develop SOPs conduct IQ/OQ/PQ and ensure assay reproducibility.
• Collaborate with vendors for training troubleshooting and performance qualification.
• Review and verify data quality before delivery to clients or data systems.
• Coordinate with automation and informatics teams for process efficiency.
• Trains on routine operation maintenance and theory of complex analytical instrumentation SOPs and regulatory procedures and guidelines.
• Independently performs and gives guidance on a variety of complex 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.
• Completes all laboratory documentation in clear and accurate language and according to SOP and GLPs.
• Leads troubleshooting for various equipment & instruments
• Reviews and compiles results from assignments and makes initial determination on acceptability per SOP acceptance criteria. Reviews overall study results.
• Navigates the OOS/OOT/Atypical investigation process. Leads more complex investigations and Root Cause Analysis and leads CAPAs.
• Independently manages QC responsibilities. Communicates project status to project leader and helps to address gaps and solutions to overcoming roadblocks in project team workflow. May act as project leader.
• Coordinates laboratory activities of other team members in conjunction with lab management.
• Performs study design & protocol authoring. Leads data evaluation and study close-out.
• Independently completes QA facing tasks. Authors and leads more complex quality records (eg. quality records which may require more in-depth investigation to identify true root causes quality records requiring cross departmental input and/or collation of data etc.)
• Mentors other staff members in applicable areas as needed.

Keys to Success:

BS and six years of experience OR

MS and four years of experienceOR

PhD and two years of 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 Skills and Abilities:

• Knowledge of relevant scientific principles applicable to role
• Ability to independently perform root cause analysis for quality records
• Proficiency on technical operating systems
• Proven problem solving and troubleshooting abilities
• Proven ability in technical writing skills
• Time management and project management skills
• Good written and oral communication skills
• Ability to work in a collaborative work environment with a team
• Ability to train junior staff
• Ability to mentor others on technical operating systems
• Full understanding of laboratory requirements SOPs ICH guidelines USP requirements and regulatory guidance

Working Conditions and Environment:

• Work is performed in a laboratory and/or a clinical environment with exposure to electrical office equipment.
• Occasional drives to site locations occasional domestic travel.
• Exposure to biological fluids with potential exposure to infectious organisms.
• Rare exposure to skin and lung irritants radiation toxic materials and hazardous waste.
• Personal protective equipment required such as protective eyewear garments and gloves.
• Exposure to fluctuating and/or extreme temperatures on rare occasions.