Senior QC Scientist - Onsite in Boston

ThermoFisher Scientific; Boston (MA); On-site; USD 95,000 - 100,000; Full time

Benefits offered by this job

Health insurance

401(k) plan

Paid time off

Tuition reimbursement

Employee stock purchase plan

Job summary

Thermo Fisher Scientific is seeking a Sr. Scientist – Quality Control in Boston, MA for a full-time on-site role. The position requires strong cGMP knowledge, extensive laboratory methods experience, and the ability to lead in-process and release testing.

Responsibilities include method validations, data review, and maintaining compliant records, with a focus on accuracy and continuous improvement within a GMP environment. Competitive benefits and relocation not provided.

Qualifications

• Bachelor degree in lab sciences such as Chemistry, Biochemistry, Material Science, Immunology, Biology, Molecular Biology or similar.
• Sr. Scientist: 4+ years of experience comparable to the role.
• Master's degree plus experience comparable to 2+ years, or PhD.
• Equivalency may be considered based on education and experience.

Responsibilities

• Perform in-process, release, and stability testing and/or review independently following established methodology, procedures and SOPs.
• Maintain accurate testing records and adhere to cGMP/GDP expectations.
• May participate in executing method validations and/or method transfers.
• Assist in troubleshooting of analytical methods with manager support.
• Participate in authoring and reviewing data, SOPs, methods, protocols and reports.
• Participate in compliance-related teams for continuous improvement.
• Report OOT/OOS results and other deviations to area management.
• Perform other laboratory duties as assigned.

Skills

cGMP concepts

Laboratory techniques

Communication skills

Education

Bachelor in science

Sr. Scientist 4+ years

Masters degree

PhD

Tools

HPLC

GC

KF

Dissolution

TOC

UV

IR

pH meter

Balance

Job description

Thermo Fisher Scientific is seeking a Sr. Scientist – Quality Control in Boston, MA for a full-time on-site role. The position requires strong cGMP knowledge, extensive laboratory methods experience, and the ability to lead in-process and release testing.

Responsibilities include method validations, data review, and maintaining compliant records, with a focus on accuracy and continuous improvement within a GMP environment. Competitive benefits and relocation not provided.