Senior Scientist, Analytical Quality Control

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

Job summary

A global life sciences service provider is seeking a QC Scientist to support manufacturing and process chemistry activities. The role involves conducting QC testing, writing SOPs, and maintaining GMP compliance. Ideal candidates should have relevant QC experience, strong analytical skills, and the ability to work in teams. This position offers comprehensive benefits and fosters an inclusive culture.

Benefits

Health insurance

401(k)

Wellness programs

Qualifications

• Relevant experience in QC testing and method validation.
• Strong documentation and analytical skills required.
• Ability to work independently and in teams.

Responsibilities

• Sample raw materials and conduct QC testing.
• Document and report results of experiments.
• Participate in method transfer or validation activities.
• Write, revise, and evaluate SOPs.
• Maintain GMP compliance in the lab.

Skills

QC testing

Method validation

SOP development

GMP compliance

Strong documentation skills

Analytical skills

Job description

Position: QC Scientist, Quality Control & Analytical

Location: Coventry, RI (ON-SITE)

Salary: $80,000-$100,000

FLSA Status: Exempt

We are seeking a QC Scientist to join our QC team at Pharmaron's manufacturing site in Coventry, RI. 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.
• Participate in method transfer or validation activities, including executing protocols and preparing 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 team/matrix environments and independently.
• Report lab events or deviations and participate in investigations.
• Ensure high quality in QC and analytical work, and accurately document relevant information as per cGMPs.
• Provide training to team members on instruments and testing methods.
• Support and facilitate site audits as required.
• Perform other related duties as assigned.

Experience and Education:

• Relevant experience in QC testing, method validation, SOP development, and GMP compliance.
• Strong documentation and analytical skills.
• Ability to work independently and in teams.

Why Pharmaron?

Pharmaron is a leading service provider in the life sciences industry, with extensive capabilities in research, development, and manufacturing. Founded in 2004, with over 21,000 employees globally, we are committed to innovation and excellence.

Our Culture and Benefits:

• Inclusive, collaborative environment emphasizing teamwork and innovation.
• Comprehensive benefits package including health insurance, 401(k), and wellness programs.

Join Pharmaron and be part of a team driving advances in biopharmaceutical research. Apply online today!

We are an Equal Opportunity Employer, fostering an inclusive environment where all individuals can succeed.