What are the responsibilities and job description for the Quality Control Chemist position at Lyne Laboratories?
Lyne Laboratories is looking for a Full-Time on-site Quality Control Chemist to contribute to the Quality Control daily operations. Lyne Laboratories, with more than 35 years of experience, is a privately held, well-established company with a successful history of manufacturing liquid, semi-solid and powder formulations of both prescription and OTC products.
The ideal candidate must be a highly professional team player, with a strong attention to detail and excellent organizational skills.
Quality Control – Chemist 1
Duties and Responsibilities (include, but are not limited to):
- Perform all required physical, chemical, and microbiological testing activities. Support Quality Control, Manufacturing, Research and Development and Quality Assurance, with respect to raw materials, in-process materials, finished product, stability studies and some special projects. May also be required to assist/support method and process validation, method qualifications and verifications when required.
- Perform, as required, in the absence of appropriate personnel, the responsibilities of sampling and physical testing of raw material and packaging components, as needed.
- Assist, with the help of other Lyne personnel, various QC functions including validation, stability studies, and calibration program.
- Comply with all safety requirements, order chemicals and laboratory supplies on time, perform laboratory waster pickup and drop-offs on weekly basis, and take part in other laboratory chores as instructed by Laboratory Supervisor or Director.
- Assist, as delegated, in the writing Standard Operating Procedures (SOP’s) for instrument/equipment operations and testing methods.
- Maintain in a precise, up-to-date order, all laboratory calibration, repair and usage logs, notebooks, charts, and other record-keeping devises
- Maintain QC laboratory in a clean, orderly, and organized manner
- Perform other duties as assigned by Lab Supervisor, Director and/or VP of Quality Control .
Experience/Knowledge/Requirements:
- Bachelor’s Degree in Chemistry
- 2 years of experience (could include internships), within the pharmaceutical, environmental, health care or chemical arena having performed analytical chemistry, method development and validation, stability, and chemical testing
- Knowledge and experience in cGMPs, GLP, USP/NF testing and laboratory instrumentation (e.g., HPLC, GC, IR, UV/VIS, TOC, AA) for the analysist of drug dosage forms may be required.
Job Type: Full-time
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Flexible spending account
- Health insurance
- Life insurance
- Paid time off
- Tuition reimbursement
- Vision insurance
Schedule:
- 8 hour shift
- Monday to Friday
Work Location: In person
Salary : $60,000