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Thermo Fisher Scientific · 3 days ago

Senior Scientist – Quality Control

Boston, MA

Full-time

Onsite

Mid, Senior Level

$95K/yr - $110K/yr

4+ years exp

Thermo Fisher Scientific is a leading global contract research organization dedicated to enabling customers to make the world healthier, safer, and cleaner. The Senior Scientist in Quality Control will be responsible for performing testing and ensuring compliance with established methodologies and safety standards, contributing to the advancement of drug development and quality assurance in laboratory settings.

BioinformaticsBiotechnologyCloud Data ServicesConsultingHealth CareLife ScienceManagement Information SystemsOffice SuppliesPrecision Medicine

No H1B

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 the assistance of manager when necessary

May participates in author and review of data, SOPs, analytical methods, protocols and reports

May participate in compliance related teams working towards the goal of continuous improvement

Report OOT/OOS results and other deviations to area management

Perform other laboratory duties as assigned

Qualification

CGMP conceptsChromatographyHPLCAnalytical methodsAttention to detailCommunication skills

Required

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

Bachelor's degree in lab sciences such as Chemistry, Biochemistry, Material Science, Immunology, Biology, Molecular Biology or similar

Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 4+ years')

OR Masters degree and previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years')

OR PhD

Understand cGMP concepts and general practices

Knowledge and experience in chromatography, dissolution, and Karl Fisher

Knowledge of various complex laboratory equipment including HPLC, GC, KF, dissolution, TOC, UV, IR, pH meter, and balance

Strong attention to detail

Demonstrate good communication skills both oral and written

Typically requires 4 years of experience in GMP pharmaceutical/biopharmaceutical industry

Benefits

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