QC Chemistry Associate I

PCI Pharma Services•San Diego, CA

3d•Onsite

About The Position

Entry level position, individual contributor responsible for conducting routine analysis of raw materials, proteins, peptides and small molecules under general supervision for in-process, release and stability testing. May focus on a specialized area and provide routine analysis and testing according to standard operating procedures in any of the following areas: raw materials, in-process, and finished formulations.

Requirements

High School Diploma required.
Minimum of zero to two years of relevant work experience
Ability to perform testing in a highly accurate and reproducible manner
Follow GMP guidelines and detailed direction in a laboratory environment
Familiarity with cGMP, manufacturing, instrument operations, troubleshooting and data entry
Strong communication and teamwork
Needs regular supervision to deliver goals and objectives

Nice To Haves

Bachelor’s degree in Life Sciences discipline or equivalent preferred.

Responsibilities

Perform routine analysis and testing in a GMP environment (including compendial assays, AQL inspections, and USP identification test methods, ensuring compliance with industry standards.
May participate in qualification/verification of assays
Perform Assay and documentation review.
Writes and reviews product specifications as required.
Collects and disposes of lab waste according to established procedures.
Contribute to lab readiness including lab cleaning, glass washing, and inventory management
Maintain personal training records.
Attend all required training.
Regular and reliable attendance on a full-time basis [or in accordance with posted schedule].
Responsible for exhibiting professional behavior with both internal and external business associates that reflects positively on the company and is consistent with the company’s policies and practices.
Embodies PCI Pharma’s cultural values and aligns daily actions with department goals and company culture.