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C&Q Specialist

Mentor Technical Group

Juncos, PRJobSeen 1mo agoSeen in employer's feed 2 days ago

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At a glance

Compensation
No compensation found
Location
Juncos, PR
Work Authorization
Not specified

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Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

Mentor Technical Group provides technical support and solutions for FDA‑regulated life‑science industries, serving clients across the United States, Puerto Rico, and international markets. The C&Q Specialist will develop, execute, and document commissioning and qualification activities, manage change controls, support maintenance, and facilitate knowledge transfer across sites.

Skills & qualifications

RequiredNice to have

Skills

Regulatory RequirementsGMP ManufacturingQuality StandardsAnalyticalProblem SolvingCommunicationTeam CollaborationEnglish

Qualifications

Bachelor's in Chemical Engineering or Pharmaceutical Technology or Related Scientific Field2+ Years GMP Manufacturing Experience

Full job description

Mentor Technical Group (MTG) provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. As a world leader in life science engineering and technical solutions, MTG has the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, Puerto Rico, and Boston, United States, we serve life sciences clients in six global markets: United States, Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South America.

Responsibilities:

  • Collaborate with C&Q Engineers to develop and maintain commissioning and qualification procedures and documents.

  • Write, review, and approve C&Q protocols and reports for various systems (e.g., HVAC, utilities, production equipment, lab equipment).

  • Execute commissioning and qualification activities for plants and equipment.

  • Coordinate with external consultants and internal resources to ensure timely document generation and execution.

  • 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/Education/Skills:

  • Bachelor's or Master's degree in Chemical Engineering, Pharmaceutical Technology, or a related scientific field.

  • At least 2 years of experience in GMP manufacturing relevant to the area of expertise.

  • Proficiency in English; additional language skills are a plus.

  • Strong understanding of regulatory requirements and quality standards.

  • Excellent analytical, problem-solving, and communication skills.

  • Ability to work collaboratively in a team environment.

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.

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