Scientist II – QC Analytical Chemistry

Pharmaron • Coventry, RI

1d

About The Position

The Scientist II – QC Analytical Chemistry will support analytical development activities for API process development and manufacturing programs at Pharmaron's Coventry, RI site. This role focuses on analytical method development, validation, transfer, and troubleshooting to support chemical process development and GMP manufacturing.
The successful candidate will collaborate closely with process chemistry, manufacturing, and quality teams to generate high-quality analytical data that supports development, scale-up, and production of active pharmaceutical ingredients.

Requirements

• Ph.D. in Chemistry or related field with no industry experience
• MS with 3+ years of experience or BS with 5 years of experience in pharmaceutical industry.
• Hands-on experience with analytical instrumentation such as: HPLC / UPLC GC LC-MS FTIR UV spectroscopy
• Familiarity with cGLP / cGMP laboratory environments.
• Strong analytical thinking, communication, and data interpretation skills.
• Ability to manage multiple priorities in a fast-paced development environment.

Nice To Haves

• Experience supporting small molecule or API development programs preferred.
• Demonstrated ability to troubleshoot analytical methods and technical challenges.
• Working knowledge of FDA, EMA, and ICH regulatory guidelines preferred.
• Ability to effectively contribute to multidisciplinary scientific teams.

Responsibilities

• Perform analytical method development, validation, and transfer supporting API process development and manufacturing programs.
• Conduct analytical testing using techniques such as HPLC/UPLC, GC, LC-MS, FTIR, and UV instrumentation.
• Support API process development and scale-up activities through analytical characterization of intermediates, starting materials, and drug substances.
• Design and execute experiments to solve analytical and process-related challenges.
• Interpret analytical data and present findings during project meetings and cross-functional discussions.
• Troubleshoot analytical methods and instrumentation to ensure reliable and accurate results.
• Maintain and support qualification of analytical laboratory equipment and instrumentation.
• Contribute to analytical investigations and root cause analysis for technical issues.
• Maintain accurate laboratory documentation including laboratory notebooks and technical records.
• Prepare technical reports and summaries to support project deliverables.
• Collaborate with multidisciplinary teams including Process Chemistry, Manufacturing, and Quality.
• Author and review analytical SOPs, protocols, and technical documentation.
• Maintain compliance with cGMP, safety, and environmental requirements.

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
• Education Level: Ph.D. or professional degree