Thermo Fisher Scientific

Thermo Fisher Scientific

Posted via Workday

Associate Scientist - Immunochemistry Research and Development Biomarkers 

Apply by Oct 29, 2026

Posted Oct 23, 2026

Role at a glance

Job function
Engineering & R&D Biotechnology & Pharmaceutical R&D
Salary
Not yet verified Check the description for pay details; an amount or pay period has not been verified.
Location
Richmond, Virginia, United States
Work arrangement
On-site
Employment
Full-time
Experience
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 1+ 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.
Education
Bachelor's degree or equivalent and relevant formal academic / vocational qualification
Visa support
Must be legally authorized to work in the United States without sponsorship.

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Role Summary

AI-generated

This Associate Scientist role in the PPD Laboratory Services team performs sample preparation and analysis to quantitatively measure pharmaceutical and biopharmaceutical compounds in formulations and biological matrices. The role follows validated or experimental analytical procedures with periodic direct supervision and is fully onsite in Richmond, VA.

What You'll Do

  • Perform routine to complex sample preparation and analysis procedures for stability and analytical testing
  • Problem solve with assistance on extraction and/or instrumentation problems
  • Train on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory procedures
  • Manage QC/QA responsibilities without supervisor or QA input
  • Communicate project status to the project leader
  • Review, interpret, and analyze data for compliance with protocols, SOPs, GMP or GLP, and perform self and peer review before QA submission

Generated from the employer's posting. Verify important details before applying.

View full posting

Qualifications

Bachelor's degree or equivalent with comparable experience of 1+ years, plus knowledge of regulatory guidelines, GMP/GLP, and analytical and communication skills.

Required

  • 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 1+ years)
  • Knowledge of applicable regulatory authority, compendia and ICH guidelines
  • Ability to understand and independently apply GMPs and/or GLPs to everyday work with regard to documentation and instrument use
  • Ability to utilize Microsoft Excel and Word to perform tasks
  • Ability to independently optimize analytical methods
  • Good written and oral communication skills
  • Time management and project management skills

Original job description

Content provided by the employer

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

This is a fully onsite role based at our 2244 Dabney Road location in Richmond, VA.  We welcome applicants from all locations within the US. Please 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 without sponsorship. 


Must be able to pass a comprehensive background check, which includes a drug screening. 


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.


Discover Impactful Work:

Performs a variety of routine to complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices. Follows validated or experimental analytical procedures with periodic direct supervision. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications.


A Day in the Life:

  • Performs a variety of routine to 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.  Problem solves with assistance pertaining to extraction and/or instrumentation problems.
  • Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory procedures and guidelines.
  • Manages QC/QA responsibilities without supervisor or QA input.
  • Communicates project status to project leader.
  • Performs work assignments accurately, and in a timely and safe manner.
  • 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.

Keys to Success:

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 1+ 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.


Knowledge, Skills and Abilities:

  • Knowledge of applicable regulatory authority, compendia and ICH guidelines Ability to understand and independently apply GMPs and /or GLPs to everyday work with regard to documentation and instrument use
  • Ability to utilize Microsoft Excel and Word to perform tasks
  • Ability to independently optimize analytical methods
  • Good written and oral communication skills
  • Time management and project management skills
  • Problem solving and troubleshooting abilities
  • Ability to work in a collaborative work environment with a team

Working Conditions and Environment: 

Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive.  Below is listed the working environment/requirements for this role:

  • 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.  



 

Compensation and Benefits

The hourly pay range estimated for this position based in Virginia is $24.00–$25.00.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

  • A choice of national medical and dental plans, and a national vision plan, including health incentive programs

  • Employee assistance and family support programs, including commuter benefits and tuition reimbursement

  • At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy

  • Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan

  • Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

Thermo Fisher Scientific

About the company

Thermo Fisher Scientific

Large Enterprise

Thermo Fisher Scientific is a global leader in serving science, providing a wide range of analytical instruments, reagents, and software solutions for healthcare, pharmaceuticals, and life sciences research. With a commitment to innovation and quality, the company enables customers to make significant advancements in scientific discovery and healthcare diagnostics. Thermo Fisher operates in more than 50 countries and employs over 80,000 people, fostering a collaborative environment aimed at enhancing global health and safety. Through its broad portfolio of brands and technologies, the company plays a vital role in accelerating life-changing research and improving patient outcomes worldwide.