Demo

Quality Control Associate

Infotree Global Solutions
West Greenwich, RI Contractor
POSTED ON 4/23/2025 CLOSED ON 4/25/2025

What are the responsibilities and job description for the Quality Control Associate position at Infotree Global Solutions?

The Associate Quality Control (QC) position will provide general support to Quality Control laboratories at Rhode Island. The role will be based out of Rhode Island and will work under the guidance of the hiring manager. It is an administrative 100% onsite shift, Monday through Friday 8:00AM – 5:00PM. Occasional need to start 7:00 AM.


Ideal Candidate: B.S. and 1-3 YOE.


The Quality Control team provides analytical expertise in testing of drug substance and raw materials to meet client specifications and ensure a constant supply of raw materials for client products.


Quality Control is searching is for an analyst to support routine testing of Raw Materials in the Wet Chemistry laboratory.


This person will be responsible for working in the Quality analytical laboratory, using GMPs and GDPs to execute analytical testing.


The ideal candidate enjoys tackling challenges and excels at time management with attention to detail.


Top 3 Must Have Skill Sets:

• Strong Analytical Skills – Ideal candidate will have experience 1-3 years performing analytical testing

• Attention to Detail – Ideal candidate will be thorough and deliver polished work product.

• Can Do Attitude – Ideal Candidate will have a positive attitude and be willing to

participate in lean initiatives on site.


Preferred Qualifications

• 1-3 years of experience in GMP analytical laboratory

• Experience with bench chemistry

• Experience with Compendial testing

• Self-motivated, strong organizational skills and ability to manage multiple tasks at one

time with minimal supervision

• Strong communication skills (both written and oral), facilitation and presentation skills

• Understanding and application of principles, concepts, theories and standards of GMP

QC analytical laboratories.

• Understanding of biopharmaceuticals process and related unit operations

• Strong analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy

• Independent, self-motivated, organized, able to multi-task in time-sensitive

environments

• Demonstrated experience

Assembly and Quality Control Associate
Spherion -
Sterling, CT
Associate Quality Control
Actalent -
West Greenwich, RI
Analytical Quality Control Associate
US Tech Solutions -
West Greenwich, RI

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