QC Lab Analyst I - Littleton, NH

PURPOSE AND SCOPEThe Quality Control Laboratory Analyst I is primarily responsible for daily performance of the testing of all raw materials, batches, and finished goods.

ESSENTIAL JOB FUNCTIONS Test and release applicable raw materials.

Test and release bulk batches.

Complete finished goods testing.

Complete stability testing.

Ability to preform analytical and microbial testing.

Preparing as needed and shipping samples for outside microbiological and analytical testing.

Prepare and execute in-house microbiological testing for environmental and production samples.

Prepare and execute analytical methods based on Approved Laboratory Methods.

Assist in ordering and maintaining stock of all laboratory equipment and chemical standards.

Assist QC Manger and QA/RA Manager in developing and maintaining laboratory GLP’s.Monitor work activities to ensure adherence to Standard Operating Procedures, QA Manuals and programs.

Assist with developing new testing validations and methods on Analytical Equipment Provide QC assistance and support to managers, supervisors, and manufacturing personnel.

Undergo training on SOP’s as listed on the accompanying Training Matrix.

Participate and interact in internal and external training programs.

Other duties as assigned ABOUT OUR COMPANY:

At Adventure Ready Brands we pride ourselves on exhibiting quality in all we do. We are built upon core values that cultivate a culture of growth focused on results, customer satisfaction, leadership, innovation and initiative, as well as communication and teamwork.

We offer Medical, Dental, and Vision insurance, FSA, HSA, Supplemental Life Insurance, Long Term Disability, 401k with matching program, paid maternity and parental leave, as well as company paid Short Term Disability, a company paid Life Insurance policy. At ARB, we provide weekends off, Paid Time Off after 90 days, paid holidays after 30 days, and a work environment with a hardworking, dedicated, and friendly staff!0–3 years laboratory experience or the equivalent combination of education (associates degree, or relevant life science courses and experience).Understanding

or Previous experience in a GMP and GLP environment.

Proficiency with Microsoft Office (Excel and Word)
Understanding and knowledge of pharmaceutical cGMP, FDA guidelines and industry standards.

Must be well organized.
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