Sr. C&Q Specialist Facilities & Utilities at Mentor Technical Group

Barrio Pueblo, Puerto Rico, United States -

Full Time

Start Date

Immediate

Expiry Date

25 Sep, 26

Salary

0.0

Posted On

27 Jun, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Commissioning and Qualification, cGMP, Equipment Validation, Computer System Validation, Technical Writing, Root Cause Investigation, Change Control, Digital Validation Solutions, HVAC Systems, Sterile Packaging Operations, Microsoft Office, Bilingual English/Spanish

Industry

Pharmaceutical Manufacturing

Description

Mentor Technical Group (MTG) provides specialized technical support and solutions for FDA-regulated industries. MTG is recognized for its expertise in life sciences engineering, ensuring compliance with pharmaceutical, biotechnology, and medical device safety and efficacy standards. Resources considered for this RFP will support pharmaceutical manufacturing operations and must meet the following minimum qualifications. Responsibilities Support Commissioning and Qualification (C&Q) activities for plants and equipment. Develop, review, and maintain commissioning and qualification procedures and documentation. Write, review, and approve C&Q protocols and reports for various systems, including HVAC, utilities, production equipment, and laboratory equipment. Execute commissioning and qualification activities and coordinate with internal teams and external consultants to ensure timely delivery. Manage change controls and deviations related to plants and equipment. Support maintenance and calibration functions to improve compliance and quality. Provide expertise in troubleshooting and root cause investigations. Facilitate the transfer of technical knowledge across units and sites. Qualifications / Requirements / Knowledge / Skills Proven background in pharmaceutical product manufacturing, specifically in sterile packaging operations. Demonstrated experience in Commissioning and Qualification (C&Q) activities. Strong knowledge of current Good Manufacturing Practices (cGMP) and applicable regulatory requirements. More than five years of experience in Equipment and Computer System Validation within pharmaceutical facilities. Experience with digital validation solutions (e.g., ALM or equivalent systems). Excellent skills in writing validation, commissioning, and technical documentation in English. Proficient in Microsoft Office applications (Word, Excel, PowerPoint, etc.). Bilingual proficiency in English and Spanish. Mentor Technical Group es un empleador que ofrece igualdad de oportunidades y todos los solicitantes calificados recibirán consideración para el empleo sin importar raza, color, religión, sexo, orientación sexual, identidad de género, información genética, origen nacional, estado de veterano protegido, estado de discapacidad o cualquier otro grupo protegido por ley. Mentor Technical Group 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.

Responsibilities

Support Commissioning and Qualification (C&Q) activities for pharmaceutical plants, equipment, and utilities. Develop and execute protocols, manage change controls, and provide expertise in troubleshooting and root cause investigations.