QC Scientist, Quality Control & Analytical

ZipRecruiter; Coventry; On-site; GBP 59,000 - 75,000; Full time

Job summary

A biopharmaceutical organization based in Coventry is seeking a QC Scientist to support analytical processes and manufacturing activities. The successful candidate will conduct quality control testing, maintain compliance with safety standards, and work collaboratively within the team. A relevant degree and QC testing experience are ideal. The position offers competitive salary and comprehensive benefits.

Benefits

Medical and dental insurance

401(k) plan with match

Employee Assistance Program

Qualifications

• Experience in QC testing of raw materials and intermediates is essential.
• Proficiency in documentation and compliance with cGMPs.
• Ability to provide training on testing methods.

Responsibilities

• Conduct QC testing of raw materials and maintain records.
• Review data and prepare reports for method validation.
• Train team members and participate in audits.

Skills

QC testing

Good laboratory practices

GMP compliance

Team collaboration

Education

Bachelor's degree in a relevant field

Tools

Analytical equipment

Job description

Overview

Position: QC Scientist, Quality Control & Analytical
Location: Coventry, RI (ON-SITE)
Salary: $80,000-$100,000
FLSA Status: Exempt

We are on the search for a 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. This role requires availability to work on either first or second shift, depending on business needs.

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.
• Ability to work successfully in both a team/matrix environment as well as independently.
• Report lab event or deviation 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 method.
• Participate, support and facilitate site audits as directed and required.
• Perform other related assignments and duties as required and assigned.

Experience and Education

• 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.
• Ability to work successfully in both a team/matrix environment as well as independently.
• Report lab event or deviation 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 method.
• Participate, support and facilitate site audits as directed and required.
• Perform other related assignments and duties as required and assigned.

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

• As part of our commitment to your well-being, we offer a comprehensive benefits package, including:
• 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 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 and 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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