CSV & CQV

JC Automation; Gurabo (PR); On-site; USD 85,000 - 110,000; Full time

Job summary

JC Automation Corp. seeks experienced CSV/CQV professionals to support a high-priority automation program in a cGMP pharmaceutical environment.

You will author validation deliverables, lead change control activities, and support commissioning and equipment qualification. The role requires strong regulatory knowledge, rigorous documentation discipline, data integrity (ALCOA++), and the ability to work independently within a established quality system across facilities and utilities, with

Qualifications

• Bachelor's degree in Engineering, Life Sciences, or a related discipline.
• 2–4 years of CSV or CQV experience in pharma GMP environments.
• Experience with URS, Design Specs, IQ/OQ/PQ, and Traceability Matrix.
• Experience presenting change controls within a pharmaceutical quality system.
• Data Integrity knowledge and ALCOA++.
• Bilingual in English and Spanish (oral and written).

Responsibilities

• Participate in team meetings to align on timeline, tasks, and status.
• Execute CSV and CQV activities for computerized systems, facilities, and utilities.
• Support commissioning and qualification for GMP facilities and utilities.
• Develop and revise procedures to meet regulatory expectations.
• Lead change control activities and present to the Change Control Board.
• Assist external connectivity validation as needed.

Skills

English and Spanish bilingual

Documentation discipline

Regulatory compliance knowledge

CSV/CQV

Education

Bachelor's degree in Engineering or Life Sciences

Job description

JC Automation Corp. (JCA) was founded in 1997 with the mission of filling a gap between technology and regulatory requirements in the life science manufacturing industry. The company offers highly capable resources at an affordable cost to build solutions and execute projects in: Automation, Control Systems Integration, Information Technology, System Integration and Regulatory Compliance.

JCA is a HUBZone Certified Small Business Firm, NMSDC Certified Minority Business Enterprise, and Certified Critical Industry Supplier. It’s mission is to add value by delivering quality services & solutions on time all the time by transforming processes & technology into business advantages.

ABOUT THE ROLE

We are seeking experienced Computer System Validation (CSV) and Commissioning, Qualification & Validation (CQV) professionals to support a high-priority automation and computerized systems program within a cGMP pharmaceutical manufacturing environment. Resources will contribute to the full validation and qualification lifecycle for critical manufacturing systems.In this role, you will author and execute validation deliverables, lead change control activities, perform Data Integrity assessments, and support commissioning and equipment qualification. Strong regulatory knowledge, excellent documentation discipline, and the ability to work independently within an established quality system are essential.

RESPONSIBILITIES

• Team Participation:Actively participate in team meetings to provide input on project timeline considerations, activities, escalations, and status of assigned tasks.
• CSV & CQV Execution: Execute Computer System Validation and Commissioning & Qualification activities for computerized systems, equipment, facilities, and utilities, including commissioning support and qualification activities such as Validation Plans, Security Plans, Administration and Operational SOPs, Installation and Operational Verification, Test Summaries, Risk Assessments, Master Document Lists, Traceability Matrices, Disaster Recovery Plans, Business Continuity Plans, Performance Qualification, System Inventory Lists, Source Code Reviews, User Requirements, and Design Specifications.
• Facilities & Utilities Commissioning: Support commissioning and qualification activities for GMP facilities and utilities, including installation verification, functional testing, system turnover, punch list resolution, and applicable IQ/OQ/PQ documentation.
• Procedure Development: Develop and revise controlled procedures in alignment with current regulatory expectations and site quality systems.
• Data Integrity: Perform Data Integrity assessments and support remediation activities for computerized systems.
• Change Control: Lead change control meetings, generate change control documentation for computer system validation and equipment qualifications, and present changes to the Change Control Review Board.
• External Connectivity: Support external system connectivity installation and operational verification.

REQUIREMENTS & QUALIFICATIONS

Required

• Bachelor's degree in Engineering (Computer, Electrical, Mechanical, Chemical), Life Sciences, or a related technical discipline.
• Minimum 2–4 years of experience authoring and executing CSV or CQV deliverables in a pharmaceutical or biotech GMP environment.
• Demonstrated experience with full CSV lifecycle documentation — URS, Design Specs, IQ/OQ/PQ, Traceability Matrix, Risk Assessment, Summary Reports.
• Experience generating and presenting change controls in a formal pharmaceutical quality system.
• Working knowledge of Data Integrity principles and ALCOA++.
• Bilingual in English and Spanish (oral and written)