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Validation Specialist at QRC Group, Inc

Cayey, , Puerto Rico -

Full Time

Start Date

Immediate

Expiry Date

08 Jun, 26

Salary

0.0

Posted On

10 Mar, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Validation, Biochemical Processes, Laboratory Equipment Validation, Manufacturing Equipment Validation, Validation Life Cycle, Method Transfer, Biotechnology Process Test Methods Validation, Equipment Validation, Protocols Execution, IQ/OQ/PQ, Documentation, Bilingual (Spanish/English)

Industry

Staffing and Recruiting

Description

Company Description QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields. Log on now to our website http://www.qrcgroup.com/ to learn more about our services and solutions! Job Description Validation Specialist to provide support in validation of biochemical processes. Must have experience and knowledge in validation of laboratory and manufacturing equipment and validation life cycle. To perform: Method Transfer in Biotechnology Process Test Methods Validation Equipment Validation (Laboratory and Manufacturing) Qualifications Bachelor of Sciences in Biotechnology or related field and 5 years of experience in the Biotechnology Industries or Medical Devices Knowledgeable in Biochemist Validation Process, Protocols execution, IQ/OQ/PQ, Documentation and validation activities Bilingual (Spanish/English)(Verbal/Written) Additional Information Benefits What We Offer Opportunities for learning, development, and professional growth. A collaborative and supportive work environment. The opportunity to work with industry-leading clients on impactful projects. Your information will be kept confidential according to EEO guidelines.

Responsibilities

The Validation Specialist will provide support in the validation of biochemical processes, which includes performing Method Transfer in Biotechnology Process Test Methods Validation and Equipment Validation for both laboratory and manufacturing equipment. This role requires executing validation protocols and managing associated documentation.