QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.
Responsibilities:
- Perform Quality Control analyses according to client procedures which include Specifications, Test Methods, Standard Operating Procedures (SOP's), Pharmacopoeia (USP, EP & JP) requirements and current Regulatory guidelines in a timely manner in order to support production processes, following instructions according to supervisor or designee request.
- Perform analysis in accordance with client Specifications, Test methods, SOP's,USP, EP and JP Procedures; comply with current regulations requirements (e.g.cGMP,cGLP, cGDP,etc); follow all Safety rules applicable to lab analyst work duties.
- Prepare and submit accurate and timely analysis reports for all laboratory work.
- Prepare and standarize solutions.
- Practice Proper laboratory housekeeping procedures as per specified by the established procedures and GLP's.
- Conduct the analytical testing, and release of raw materials and packaging components as required.
- Conduct all assigned tasks on a safe way and in compliance with the following: Test methods and SOP requirements, SDS handling and precautions, Federal and state legislated requirements (OSHA,EPA,FDA,EP, etc), Company requirements (safety rules and policies). Analyze complaint and Stability samples in a timely and accurate manner; report any quality issue to the lab Manager or designee.
- Assure analytical results are neat and accurate.
Qualifications
- Bachelor Degree in Chemistry
- One (1) year of experience
- Ability to read and understand English & Spanish
- Basic cGMP knowledge
- Computer literate (Word, Excel, Power Point)
- Ability to operate laboratory testing equipment.
- Able to interpret and convert units of measure such as temperature, pressure, flow, area, mass, distance, volume or other.
- Availability for 2nd shift and weekends
Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity,, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.
Job Types: Full-time, Contract, Temporary
Schedule:
- 8 hour shift
- Evening shift
- Weekends as needed
Education:
Experience:
- Regulated industry: 1 year (Preferred)
- Laboratory: 1 year (Preferred)
Work Location: In person