QC Chemist - 2nd Shift

Sheffield Pharmaceuticals, LLC; New London (CT); On-site; USD 52,000 - 68,000; Full time

Job summary

Sheffield Pharmaceuticals, the home of the original Sheffield Toothpaste, seeks a Quality Control Analyst to support QC analyses of raw materials, in-process samples, and finished products in our New London, CT facility. Under supervision, you will perform routine tests, inspect components, and help maintain accurate batch records.

The role emphasizes compliance with SOPs and regulatory requirements (FDA, cGMP, EPA, OSHA) and collaboration across departments to ensure product quality and safety.

Qualifications

• Bachelor's degree in chemistry or related field required.
• Minimum of one year experience in analytical or quality control laboratory preferred.
• Strong documentation and compliance with SOPs, EPA, OSHA, FDA, and cGMPs.

Responsibilities

• Perform QC analyses on raw materials, in-process and finished products.
• Conduct routine testing and inspection of parts and weights.
• Maintain QC documentation and batch records (PBRs).
• Assist in experiments and pilot batches for new products.
• Ensure safety and regulatory compliance across the lab.

Skills

Quality control

Analytical testing

Laboratory instrumentation

Documentation

Education

Bachelor's degree in chemistry or related field

Tools

Instrument calibration

Job description

At Sheffield Pharmaceuticals, the home of the original Sheffield Toothpaste, we offer exclusive, quality, branded products to promote wellness and relief to our customers. Our wellness and first aid products include a variety of creams and ointments, nasal products, and toothpaste all made in the USA since 1850.

Education / Experience

• EDUCATION/EXPERIENCE:** Bachelors degree in chemistry or related field. Minimum of one-year experience in analytical or quality control laboratory preferred.

Duties

• Under direction from the Laboratory Supervisor, performs quality control analysis on raw materials, in-process samples, finished/filled products, process validation/evaluation, and stability testing.
• Routine, repetitive checking and testing of production product, including visual and sample inspections of parts used, weights, and measures.
• Inspects production equipment for various Q.C. aspects.
• Maintains proper documentation for Filling department quality control.
• Assists in experiments relative to the discovery and development of new products.
• Makes pilot batches of experimental products.
• Creates processing batch sheets and batch records (PBR's), and checks artwork, crimp codes, log sheets, and shipping requirements.
• Prepare artwork ingredient list.
• General electronic and hard copy file, records, documents and database maintenance.
• Maintain cleanliness and appearance of department, and assist in the disposal of hazardous (laboratory) waste.
• Assist in laboratory instrument qualification and/or calibration.
• Act as subject matter expert for laboratory instrumentation or analytical techniques.
• Maintain proper liaison with all departments to contribute to the team philosophy.
• Responsible for following all safety regulations and complying with S.O.P.'s, DEP, EPA, OSHA, FDA, and cGMP's while performing duties.

Sheffield Pharmaceuticals is an Equal Employment Opportunity employer. We provide equal opportunity to employees and applicants for employment without regard to race, creed, color, religion, sex, age, national origin, physical or mental disability, sexual orientation, marital or familial status, genetic information, protected veteran status, or other basis protected by law.