QC Technician

Pharmaron•Coventry, RI

21h•Onsite

About The Position

We are on the search for a 2nd or 3rd shift QC Technician to join our QC team at Pharmaron's manufacturing site in Coventry, RI. In this position, the Technician will support manufacturing and process chemistry activities through sampling, analytical sample testing and lab support in compliance with all applicable guidelines. 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 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.

Requirements

High School degree with 3+ years of pharmaceutical industry related experience.
Ability to perform routine QC work with guidance.
Excellent communication skills, both verbal and written.
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.

Responsibilities

Perform raw material sampling and manage retain sample inventory, tracking, movement, and disposal.
Maintain Chemical Inventory database, order and organize chemicals and consumables.
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.
Review experimental data, notebooks and other documents.
Write, revise, develop, and evaluate SOPs and other documents.
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.
Provide training to other team members on instrument and testing method as required.
Participate, support and facilitate site audits as directed and required.
Perform other related assignments and duties as required and assigned.