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Director Computer System Validation Csv Jobs in Bayamon, PR

Veg Group

Specialist QA (5:00 pm - 5:30 am)

Juncos, PR · On-site

$80 - $100/hr

Experience in computer systems validation (CSV) or computer systems quality assurance, including consulting level technical proficiency. * Experience with validation of GxP applications, including ...

Frey Consulting Group

QA Specialist- ProQN669

Juncos, PR · On-site

$60 - $80/hr

Experience with computer systems validation (CSV) or computer systems quality assurance (CSA/CSQA), particularly within regulated environments. * Experience supporting medical device environments and ...

Pinnaql

Specialist QA (5:00 pm - 5:30 am)

Juncos, PR · On-site

Experience in computer systems validation (CSV) or computer systems quality assurance, including consulting level technical proficiency. Experience with validation of GxP applications, including ...

PACIV

IT / CSV Specialist

San Juan, PR · On-site

... systems, infrastructure, and validation activities within a pharmaceutical manufacturing ... Bachelor's degree in IT, Computer Science, Engineering, or a related field preferred.

Pinnaql

C&Q Specialist

Juncos, PR · On-site

Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services ... Projects may support one or more of the following areas: manufacturing systems, process equipment ...

Pinnaql

C&Q Specialist

Gurabo, PR · On-site

Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services ... Projects may support one or more of the following areas: manufacturing systems, process equipment ...

Weil Group, Inc

Manufacturing Engineer II

Villalba, PR

$70K - $91K/yr

Computer and software validation CSV SOP Development Change control of Medical Devices MES system ... May act as a mentor to colleagues or may direct the work of other lower level professionals. The ...

Weil Group, Inc.

Manufacturing Engineer II

Villalba, PR · On-site +1

$70K - $91K/yr

Computer and software validation CSV SOP Development Change control of Medical Devices MES system ... May act as a mentor to colleagues or may direct the work of other lower level professionals. The ...

Mentor Technical Group

Sr. C&Q Specialist

Juncos, PR · On-site

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)

Weil Group, Inc.

Manufacturing Engineer II

Villalba, PR · On-site +1

$70K - $91K/yr

May act as a mentor to colleagues or may direct the work of other lower level professionals. The ... Computer and software validation CSV SOP Development Change control of Medical Devices MES system ...

Weil Group, Inc

Manufacturing Engineer II

Villalba, PR

$70K - $91K/yr

May act as a mentor to colleagues or may direct the work of other lower level professionals. The ... Computer and software validation CSV SOP Development Change control of Medical Devices MES system ...

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How much do director computer system validation csv jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for director computer system validation csv in Bayamon, PR is $46.66, according to ZipRecruiter salary data. Most workers in this role earn between $35.10 and $58.03 per hour, depending on experience, location, and employer.

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Director Computer System Validation Csv jobs near you

Sr. CSV & (C&Q) Specialist

Mentor Technical Group

Manati, PR • On-site

Full-time

Re-posted 27 days ago

Job description

Overview:
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 lab 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 other regulatory requirements.
  • More than 5 years of experience in Equipment and Computer System Validation within pharmaceutical facilities.
  • Experience with digital validation solutions (e.g., ALM or equivalent).
  • Excellent skills in writing validation, commissioning, and technical documentation in English.
  • Proficient in MS Office applications (Word, Excel, PowerPoint, etc.).
  • Bilingual: fluent 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.

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