QC Scientist, Quality Control & Analytical

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

Job summary

A life sciences service provider is seeking a QC Scientist to support manufacturing in Coventry, RI. The ideal candidate will conduct QC testing of materials, document results, and ensure compliance with GMP standards. You will thrive in a collaborative environment and contribute to innovative solutions in biopharmaceutical research. A comprehensive benefits package and a commitment to employee welfare are offered.

Benefits

Medical, Dental & Vision Insurance

401(k) plan with generous employer match

Employee Assistance Program

Qualifications

• Strong understanding of laboratory practices and GMP compliance.
• Experience in conducting QC testing of raw materials and intermediates.
• Ability to write and revise SOPs.

Responsibilities

• Conduct QC testing of raw materials and intermediates.
• Document and report experimental results timely.
• Participate in method transfer and validation activities.
• Ensure high quality in QC work and maintain compliance.

Skills

QC testing

Analytical methods

Documentation skills

Teamwork

Problem-solving

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.

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.

Qualifications

• 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 diversity 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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