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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:

+ Identifies and validates molecular targets that play a key role in a particular disease process.

+ Studies origin, relationship, development, anatomy, functions, and chemical processes of living organisms; this may include studies in the growth, structure, and development of bacteria and other microorganisms.

+ Conducts research to determine the effects of materials such as nutrients, drugs, serums, hormones, and other substances on tissues and vital processes of living organisms.

+ Analyzes materials to determine their toxic or nontoxic properties, binding and efficacy.

+ Isolates or purifies analyses, and identifies hormones, minerals, proteins, and/or cultures of microorganisms to determine their biological properties.

+ Examines chemical aspects of formation of antibodies and conducts research into chemistry of cells and cell division.

+ May identify and produce small quantities of new drugs, pharmaceutical compounds and/or nutrients.

Qualifications:

+ Bachelor’s degree in Science (Microbiology preferable)

+ 2-3 years experience with Sterilization Validation/ Microbiology is desirable

+ Team work skills

+ Must be bilingual (English and Spanish)

+ Available to work 1st and 2nd 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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