QC Scientist II, Analytical Chemistry (3rd shift)

Pharmaron • Coventry, RI

1d • Onsite

About The Position

The QC Scientist II, Analytical Chemistry supports manufacturing and process chemistry activities through analytical method validation and transfer, sample testing, and ensuring that the QC laboratory complies with applicable guidelines. This is a third-shift role with working hours of 11:00 pm to 7:30 am.

Pharmaron is a global contract research organization supporting pharmaceutical and biotechnology companies across drug discovery, development, and manufacturing. The company describes a collaborative and inclusive culture centered on employees and clients.

Requirements

• BS or MS degree in chemistry or a related field.
• At least 2 years of pharmaceutical industry experience.
• Ability to perform routine QC work independently with minimal guidance.
• Proven skills in analytical method verification and validation of small molecules.
• Ability to manage multiple competing activities and deliver to timelines.
• Ability to work in a cross-functional environment.
• Experience with HPLC, GC, FTIR, UV, and wet chemistry.
• Working knowledge of cGMP and applicable FDA, EMA, and ICH guidance.
• Effective verbal and written communication skills.

Responsibilities

• Sample raw materials and conduct QC testing of raw materials, intermediates, API, in-process control (IPC), and cleaning verification samples according to established procedures.
• Document and report experimental results promptly in accordance with department practices and governing procedures.
• Participate in method transfer and validation activities, including executing protocols and preparing reports.
• Review experimental data, notebooks, and instrument qualification protocols and reports.
• Write, revise, develop, and evaluate SOPs.
• Maintain good laboratory practices and GMP in compliance with safety and environmental requirements.
• Work effectively both independently and in a team or matrix environment.
• Report laboratory events or deviations and participate in investigations.
• Ensure high quality in QC and analytical work and accurately document relevant information in a clear, concise manner in accordance with cGMPs.
• Train team members on instruments and testing methods.
• Participate in, support, and facilitate site audits as directed and required.
• Perform other related assignments and duties as required and assigned.

Benefits

• Medical, dental, and vision insurance with significant employer contributions.
• Employer-funded Health Reimbursement Account.
• Healthcare and 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.

What This Job Offers

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