Quality Control Scientist (3rd shift)

Pharmaron • Coventry, RI

9d • $80,000 - $90,000 • Onsite

About The Position

The Quality Control Scientist will support quality control testing for API manufacturing and development activities at Pharmaron's Coventry, RI facility. This role performs analytical testing of raw materials, intermediates, and active pharmaceutical ingredients using a variety of analytical techniques in a cGMP-regulated laboratory environment. This role offers an excellent opportunity to build expertise in GMP pharmaceutical manufacturing while working with advanced analytical instrumentation in a fast-paced CDMO environment.

Requirements

• BS or MS degree in Chemistry or related scientific discipline
• 2+ years of pharmaceutical or biotechnology industry experience in a GMP laboratory environment
• Hands-on experience with chromatography and analytical instrumentation including: HPLC GC FTIR UV spectroscopy wet chemistry techniques
• Working knowledge of cGMP and applicable FDA, EMA, and ICH regulatory guidelines
• Strong attention to detail and ability to maintain accurate laboratory documentation
• Ability to work both independently and within cross-functional scientific teams
• Strong written and verbal communication skills
• Ability to manage multiple priorities in a fast-paced laboratory environment

Nice To Haves

• Experience performing QC testing of APIs, intermediates, or raw materials preferred

Responsibilities

• Perform QC testing of raw materials, intermediates, APIs, IPC samples, and cleaning verification samples following established procedures.
• Document and report analytical results in compliance with cGMP and laboratory procedures.
• Participate in analytical method transfer and validation activities, including executing protocols and preparing reports.
• Review analytical data, laboratory notebooks, and instrument qualification documentation.
• Investigate laboratory deviations and support root cause analysis and corrective actions.
• Maintain laboratory equipment and support instrument qualification and maintenance activities.
• Prepare and revise standard operating procedures (SOPs) and technical documentation.
• Provide training to laboratory personnel on analytical instrumentation and testing methods.
• Support internal and external regulatory and client audits.
• Collaborate with cross-functional teams including Manufacturing, Process Chemistry, and Quality Assurance.
• Perform other related assignments and duties as required and assigned.

Benefits

• 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
• 401k plan with generous employer match
• Access to an Employee Assistance Program

What This Job Offers

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