JT678 - CHEMIST

Jayuya, Puerto Rico

Temporary

Medical Devices

Mid Level

QUALITY CONSULTING GROUP, es una compañía líder en la industria farmacéutica, biotecnológica, de dispositivos médicos y fabricación. Con una experiencia combinada de más 25 años proveemos servicios de alta calidad a nuestros clientes. Reclutamos recursos para todo tipo de industrias y buscamos recursos talentosos, altamente motivados que quieran unirse a nuestro equipo.

Responsibilities:

Provides technical support to the chemistry laboratory personnel. Performs and/ or review/ approve chemistry laboratory tests to avoid delay in the release of the product, assuring a quality and safety work.
Review and/or approval of laboratory documentation.
Approves and reviews documents, assures that the Department complies with internal and external regulations and standards.
Should be aware of potential problems that could occur during the testing process and should watch for problems that could create inaccurate results.
Performs any work to avoid the delay in the release of the product.
Analyzes purchase raw materials against established procedures assuring compliance with all regulations and specifications.
Must follow the current Good Manufacturing Practices (cGMP’s), current Good Documentation Practices (cGDP’s) and current Good Laboratory Practices (cGLP).
Audits chemical test procedures, retests, additional testing’s and SOP's in the laboratory.
Requests and order all materials required in the laboratory on timely basis to assure an efficient performance (make request of accessories, equipment, reagents, etc.; including the issuance of purchase orders).
Initiates and implement changes or new chemical procedures including data gathering.
Capable to develops, modifies and analyzes protocols and procedures as required.
Prepares general material and solutions needed for laboratory tests, as required.
Should be able to work with many projects and handle multiple tasks at the same time.
Willing to work extra hours, at any shift when its required, on Holidays and during special periods (eg. shutdowns, internal and external audits, special projects).

Qualitfications:

Bachelor Degree in Chemist
Two (2) years of experience in a Pharmaceutical Industry (preferable)
Strong knowledge in HPLC, Atomic Absorption, FT-IR, Karl Fisher, UV/VIS, TOC Analyzer, Polarimeter.
Strongly oriented to GMP’s, GLP’s, OSHA, US Pharmacopeia, EP, Good troubleshooting resolution techniques.
Strong knowledge in LIMS etc.
Bilingual
Availability for 2nd and 3erd shift

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.

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