Sr. Scientist, QC

Pharmaron • Coventry, RI

5d • $100,000 - $140,000 • Onsite

About The Position

The Senior Scientist - QC will support technology transfer and GMP manufacturing activities through analytical method transfer, verification, validation and sample testing in compliance with all applicable guidelines. Will also solve moderate complexity analytical and quality control issues for assigned projects and/or initiatives.

Requirements

• MS with 8+ years of experience or BS with 10 years of experience in pharmaceutical industry.
• Evidence of experience in successful application of analytical skill sets to resolve scientific problems related to method optimization and/or implementation
• Experienced troubleshooter of technical problems
• 6 years of experience with core analytical instrumentation such as HPLC, GC, FTIR, Mass Spectrometry.
• Evidence of ability to effectively contribute to multi-disciplinary scientific teams
• Working knowledge of cGLP/cGMP and applicable FDA, EMA and ICH guidance
• Evidence of ability to effectively scientifically supervise staff
• Expert application of core laboratory techniques and instrumentation to impact API, intermediates and starting materials

Responsibilities

• Participate in method transfer activities, including writing protocols, executing experiments and writing reports.
• Supervise QC scientist daily work, provide technical and compliance related guidance.
• Review experimental data, notebooks, method, protocols / reports.
• Actively participate in investigations, problem solving, and troubleshooting. Write investigation reports.
• Coordinating QC testing, notebook and data review.
• Prepare and present data summaries (written and oral) as necessary. Present to cross functional teams and effectively communicate critical QC/analytical issues and solutions.
• Ability to work successfully in both a team/matrix environment as well as independently.
• Ensure high-quality QC work and accurately document all necessary and relevant information in a clear concise manner as per cGMPs.
• Participate, support and facilitate site audits as directed and required.
• SME for instrument training.
• Maintain good laboratory practices and GMP in compliance with safety and environmental requirements.
• Write, revise, develop, and evaluate SOPs.
• Perform other related assignments and duties, as required and assigned.

Benefits

• Comprehensive Medical, Dental & Vision Insurance with significant employer contributions
• 401(k) Retirement Plan with generous employer matching
• Generous Paid Time Off (PTO), Paid Sick Leave & Company Holidays to support work-life balance
• Employer-funded Health Savings Account (HSA) contributions (for eligible plans), plus Healthcare & Dependent Care Flexible Spending Accounts
• 100% Employer-paid Employee Life Insurance, AD&D, Short- and Long-Term Disability Insurance
• Employee Assistance Program (EAP), mental health resources, and wellness programs
• Family-friendly benefits, including fertility support and maternity resources
• Professional development and career growth opportunities within a leading global CRO/CDMO

What This Job Offers

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