Quality Control Raw Materials Associate

Quality Control Raw Materials Associate

Contract Duration 6+ months

Pay rate up to $0.69/hr - $38.54/hr

The Role:

Reporting to the Associate Director of Quality Control, our client is seeking a Quality Control Raw Materials Associate II based at their Norwood, MA site.

The individual in this role will perform QC Raw Material activities in support of GMP Manufacturing and further support special projects as assigned.

This position will be 1st shift working Monday through Friday.

Here's What You'll Do:

Requesting, sampling, and peer review of raw materials.

Sample coordination including cross-functional collaboration with internal and external labs.

Train and perform testing for methods including HPLC, Bioanalyzer, osmolality, pH, conductivity, TruScan RM spectroscopy, appearance, and dimensional verification.

Inspect raw material retain samples.

LIMS (LabVantage) sample logging and result entry.

Raw material and consumable component inspection and release.

Clean room gowning and aseptic techniques.

Managing/stocking QC lab supplies and routine lab cleaning.

Complete and maintain cGMP documentation for work performed.

Participate in supporting quality systems records such as deviations, change controls, CAPAs and investigations

Establish and maintain a safe laboratory working environment.

Foster a positive and inclusive work culture that promotes collaboration, innovation, and continuous improvement.

Follow all relevant GxP regulations, guidelines, and company policies to ensure compliance with regulatory and internal requirements.

Execute tasks precisely as defined in internal guiding documents including but not limited to standard operating procedures (SOPs) and work instructions

Follow Good Documentation Practices and Data Integrity requirements to ensure data, documentation, and records are completed and maintained for use by the business and available to support audits or inspections.

Complete training in the assigned required learning plan according to the defined timing and the prescribed requalification cadence

Here's What You'll Bring to the Table:

Education: Bachelor's degree in a relevant scientific discipline.

Experience:

1-2 Years with BS or 4+ experience in GMP QC laboratory setting.

Demonstrated aptitude or ability to learn in order to gain a strong understanding of GxP regulations.

Benefits:

Medical, Vision, and Dental Insurance Plans

401k Retirement Fund

About The Company:

Our client operates as a developer of messenger RNA therapeutics. The company develops and discovers drugs that produce proteins or antibodies inside patient cells. Its pipeline includes various drug modalities such as prophylactic vaccines, therapeutic vaccines, intratumoral immuno-oncology, localized therapeutics, and liver intracellular. Through its mRNA therapeutics platform, they develops and produce human proteins, antibodies, and Client proteins, which help in preventing, treating, and curing diseases. It also develops therapeutics in the areas of infectious disease, rare liver disease, immuno-oncology, and cardiovascular disease.

mRNA is now a turning point in the history of science, medicine, technology, and even humankind itself. With this breakthrough discovery, many of the world's biggest and most challenging medical problems are no longer a question of "how?" but merely a question of "when?"

Come with us as we pursue the uncharted reaches of possibility and make your mark on the future of medicine.

(phone number removed)