QC Engineer/Scientist I

Thermo Fisher Scientific • Frederick, MD

5d • $54,900 - $82,350 • Onsite

About The Position

The QC Engineer/Scientist I is a site-based role in Frederick, Maryland, on Thermo Fisher Scientific’s Quality Control team. The position supports the quality and reliability of products and the development of therapeutic products by performing quality control testing and analysis of raw materials, in-process samples, and finished products using analytical techniques. The role includes documenting and analyzing test results, participating in investigations, and contributing to continuous improvement initiatives. It offers opportunities for professional growth while working with colleagues committed to excellence and innovation.

The role is conducted in a laboratory setting and requires adherence to Good Manufacturing Practices (GMP) safety standards. Employees may work with hazardous or toxic materials and must use required personal protective equipment. The position follows a standard Monday–Friday schedule, although flexible scheduling may be required.

Requirements

• Bachelor’s degree in a scientific field; no prior experience is required.
• Strong knowledge of cGMP, GLP, and quality management systems.
• Proficiency in analytical techniques such as HPLC, ICP-MS, UV-Vis spectroscopy, and dissolution testing.
• Experience with microbiological testing methods and aseptic techniques.
• Ability to follow SOPs and maintain detailed documentation per GDP requirements.
• Strong computer skills, including LIMS, Microsoft Office, and analytical software.
• Excellent attention to detail and organizational skills.
• Strong analytical and problem-solving capabilities.
• Ability to work independently and collaboratively in a team environment.
• Clear written and verbal communication skills.
• Experience with laboratory equipment maintenance and calibration.
• Knowledge of relevant pharmacopeia standards and regulatory requirements.
• Ability to manage multiple priorities effectively.
• Physical ability to perform laboratory work, including PPE usage.
• Ability to lift 40 lbs. without assistance.
• Ability to adhere to GMP safety standards and work with hazardous or toxic materials.

Nice To Haves

• Experience in a quality control laboratory environment, preferably in the pharmaceutical or biotechnology industry.
• Preferred fields of study: Chemistry, Biochemistry, Biology, Molecular Biology, or a related scientific field.

Responsibilities

• Perform quality control testing and analysis of raw materials, in-process samples, and finished products using analytical techniques.
• Document and analyze test results.
• Participate in investigations.
• Contribute to continuous improvement initiatives.
• Maintain and calibrate laboratory equipment.
• Follow SOPs and maintain detailed documentation in accordance with GDP requirements.

Benefits

• 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 of paid time off and 10 paid holidays annually.
• Paid parental leave, including 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.
• Competitive 401(k) U.S. retirement savings plan.
• Employees’ Stock Purchase Plan offering eligible colleagues the opportunity to purchase company stock at a discount.
• May be eligible for a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level