Pharmaron
QC Scientist / Snr QC Scientist , Quality Control & Analytical
Pharmaron, Coventry, Rhode Island, us, 02816
QC Scientist / Snr QC Scientist, Quality Control & Analytical
Position: QC Scientist/Sr. Scientist (3rd shift, working hours: 11 pm-7 am), Quality Control & Analytical
Location: Coventry, RI (ON-SITE)
FLSA Status: Exempt
We are searching for a 3rd‑shift QC Scientist to join our QC team at Pharmaron’s manufacturing site in Coventry, RI. In this position, the Scientist will support manufacturing and process chemistry activities through analytical method verification, optimization, and sample testing in compliance with all applicable guidelines.
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, as applicable.
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 cGMPs.
Provide training to other team members on instrument and testing methods.
Participate, support, and facilitate site audits as directed and required.
Perform other related assignments and duties as required and assigned.
Experience and Education
BS in Chemistry with 3+ years of experience or MSc in Chemistry with 1+ year of experience.
Experience using 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.
Ability to work in a cross‑functional environment.
Working knowledge of cGLP/cGMP and applicable FDA, EMA, and ICH guidance preferred.
Why Pharmaron? Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process. With over 21,000 employees and operations in the U.S., U.K., and China, Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.
Collaborative Culture You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. Our core cultural values are "Employees Number One" and "Clients Centered," setting Pharmaron apart from other organizations.
Benefits
Comprehensive benefits package, including 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.
Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!
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. Join us in our mission to make a difference in the world of life sciences.
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Location: Coventry, RI (ON-SITE)
FLSA Status: Exempt
We are searching for a 3rd‑shift QC Scientist to join our QC team at Pharmaron’s manufacturing site in Coventry, RI. In this position, the Scientist will support manufacturing and process chemistry activities through analytical method verification, optimization, and sample testing in compliance with all applicable guidelines.
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, as applicable.
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 cGMPs.
Provide training to other team members on instrument and testing methods.
Participate, support, and facilitate site audits as directed and required.
Perform other related assignments and duties as required and assigned.
Experience and Education
BS in Chemistry with 3+ years of experience or MSc in Chemistry with 1+ year of experience.
Experience using 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.
Ability to work in a cross‑functional environment.
Working knowledge of cGLP/cGMP and applicable FDA, EMA, and ICH guidance preferred.
Why Pharmaron? Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process. With over 21,000 employees and operations in the U.S., U.K., and China, Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.
Collaborative Culture You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. Our core cultural values are "Employees Number One" and "Clients Centered," setting Pharmaron apart from other organizations.
Benefits
Comprehensive benefits package, including 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.
Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!
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. Join us in our mission to make a difference in the world of life sciences.
#J-18808-Ljbffr