QC Senior Scientist II

Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 locations in the US, UK and China, we support drug discovery through to manufacturing with fully integrated, high-quality services.

Position: QC Senior Scientist II

Salary Range: $110k - $130k

Location: Coventry, RI

Pharmaron is seeking a QC Senior Scientist II to play a critical role in supporting API manufacturing and technology transfer programs within a GMP-regulated environment. The QC Senior Scientist II will serve as a technical leader within QC, working cross-functionally with Analytical Development, Manufacturing, and Quality to ensure the successful execution of complex programs.

• Participate in method transfer activities, including writing protocols, executing experiments and writing reports.
• Provide technical leadership and mentorship to QC team members.
• Review and approve analytical data, protocols, and reports to ensure scientific rigor and compliance.
• Drive root cause investigations and deviation resolutions, identifying practical and scalable solutions.
• Serve as a subject matter expert (SME) for analytical instrumentation and QC processes.
• Collaborate cross-functionally with Process Chemistry, Analytical Development, and QA.
• Support regulatory inspections and audits, ensuring inspection readiness.
• Contribute to continuous improvement initiatives to enhance efficiency and compliance.
• Prepare and present data summaries (written and oral) as necessary, and effectively communicate critical QC/analytical issues and solutions to cross functional teams.
• Lead on the implementation and adoption of key internal business practices and applicable external regulations (e.g. GxP), and adhere to all policies governing their business activities.
• Perform other related assignments and duties, as required and assigned.

• D. in Chemistry (or related field) with 5+ years of experience, OR MS with 8+ years, OR BS with 10+ years in pharmaceutical/CDMO environments.
• Strong hands‑on expertise with HPLC, GC, FTIR, and Mass Spectrometry.
• Proven experience in method transfer, validation, and GMP testing.
• Deep understanding of cGMP, FDA, EMA, and ICH guidelines.
• Demonstrated ability to troubleshoot complex analytical challenges.
• Experience mentoring or leading junior scientists is highly preferred.
• Strong communication skills and ability to work in fast‑paced manufacturing environments.

• Insurance including Medical, Dental & Vision with significant employer contributions.
• Employer‑funded Health Reimbursement Account.
• Healthcare & Dependent Care Flexible Spending Accounts.
• 100% Employer‑paid Employee Life and AD&D Insurance, Short‑ and Long‑Term Disability Insurance.
• 401(k) plan with generous employer match.
• Access to an Employee Assistance Program.

As an Equal Employment Opportunity and affirmative action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed.