Pharmaron
QC Scientist / Snr QC Scientist , Quality Control & Analytical
Pharmaron, Coventry, Rhode Island, us, 02816
QC Scientist / Sr. Scientist, Quality Control & Analytical
We are seeking a 3rd shift QC Scientist to join our QC team at Pharmaron’s manufacturing site in Coventry, RI. The role supports manufacturing and process chemistry activities through analytical method verification, optimization, and sample testing in compliance with all applicable guidelines. Position:
QC Scientist/Sr. Scientist (3rd shift, 11:00 p.m. – 7:00 a.m.) Location:
Coventry, RI (ON‑SITE) FLSA Status:
Exempt Primary Responsibilities
Sample raw materials and conduct QC testing of raw materials, intermediates, API, IPC, and cleaning verification samples following established procedures. Document and report results of all experiments in a timely manner consistent with department practices and governing procedures. Participate in method transfer or validation activities, including executing the protocols and preparing the reports. Review experimental data, notebooks, and instrument qualification protocols/reports. Write, revise, develop, and evaluate SOPs. Maintain good laboratory practices and GMP in compliance with safety and environmental requirements. Work successfully in both a team/matrix environment and independently. Report lab events or deviations and participate in the investigation. Ensure high quality in QC and analytical work and accurately document all necessary and relevant information in a clear, concise manner as per cGMP. Provide training to other team members on instruments and testing methods. Participate, support, and facilitate site audits as directed and required. Perform other related assignments and duties as required. Experience and Education
BS in Chemistry with 3+ years of experience or MSc in Chemistry with 1+ year of experience. Experience with HPLC, GC, FTIR, and KF instrumentation. Ability to perform routine QC work independently or with minimal guidance. Excellent verbal and written communication skills. Effective in managing multiple competing activities and delivering to timelines. Experience in cross‑functional environments. Working knowledge of cGLP/cGMP and applicable FDA, EMA, and ICH guidance (preferred). Benefits
Medical, Dental & Vision Insurance 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. Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, we are committed to research, development, and manufacturing services across the entire drug development process. We employ over 21,000 people worldwide. Equal Employment Opportunity:
Pharmaron is an equal employment opportunity and affirmative action employer. We value diversity and inclusion and invite all qualified candidates to apply.
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We are seeking a 3rd shift QC Scientist to join our QC team at Pharmaron’s manufacturing site in Coventry, RI. The role supports manufacturing and process chemistry activities through analytical method verification, optimization, and sample testing in compliance with all applicable guidelines. Position:
QC Scientist/Sr. Scientist (3rd shift, 11:00 p.m. – 7:00 a.m.) Location:
Coventry, RI (ON‑SITE) FLSA Status:
Exempt Primary Responsibilities
Sample raw materials and conduct QC testing of raw materials, intermediates, API, IPC, and cleaning verification samples following established procedures. Document and report results of all experiments in a timely manner consistent with department practices and governing procedures. Participate in method transfer or validation activities, including executing the protocols and preparing the reports. Review experimental data, notebooks, and instrument qualification protocols/reports. Write, revise, develop, and evaluate SOPs. Maintain good laboratory practices and GMP in compliance with safety and environmental requirements. Work successfully in both a team/matrix environment and independently. Report lab events or deviations and participate in the investigation. Ensure high quality in QC and analytical work and accurately document all necessary and relevant information in a clear, concise manner as per cGMP. Provide training to other team members on instruments and testing methods. Participate, support, and facilitate site audits as directed and required. Perform other related assignments and duties as required. Experience and Education
BS in Chemistry with 3+ years of experience or MSc in Chemistry with 1+ year of experience. Experience with HPLC, GC, FTIR, and KF instrumentation. Ability to perform routine QC work independently or with minimal guidance. Excellent verbal and written communication skills. Effective in managing multiple competing activities and delivering to timelines. Experience in cross‑functional environments. Working knowledge of cGLP/cGMP and applicable FDA, EMA, and ICH guidance (preferred). Benefits
Medical, Dental & Vision Insurance 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. Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, we are committed to research, development, and manufacturing services across the entire drug development process. We employ over 21,000 people worldwide. Equal Employment Opportunity:
Pharmaron is an equal employment opportunity and affirmative action employer. We value diversity and inclusion and invite all qualified candidates to apply.
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