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Facilities Program Manager
Job Location:
Job Location:
Juncos - Puerto Rico
Monthly Salary:
Not provided by the employer
Monthly Salary:
Posted:
14 October 2026 (23 days ago)
Posted:
Application Deadline:
11 January 2027
Application Deadline:
Vacancies:
1 Vacancy
Vacancies:
Job Summary
EQVAL Group Inc. is a company that provides services to the manufacturing industry (Medical Devices Pharmaceuticals Biotechnologies others). We work with an extraordinary group of professionals (employees and contractors) to accomplish the requirements established by our customers in order to perform and provide a highly effective service.
The Facilities Program Manager will be responsible for support of all facility engineering related infrastructure projects. The role will support a broad array of projects at a clean medical device manufacturing facility including Compressed Air System (CAS) Dryers and Air Handling Units (HVAC).
Responsibilities:
Qualifications:
Benefits:
*This is a full-time position based in Puerto Rico. Remote work permitted for documentation development. On-site presence required during qualification testing activities.
We offer competitive compensation benefits and opportunities for career growth. If you are a motivated individual with passion we would love to hear from you. Apply now!!
EQVAL Group is an EEO. We comply with all federal local and state laws regarding non-discrimination.
The Facilities Program Manager will be responsible for support of all facility engineering related infrastructure projects. The role will support a broad array of projects at a clean medical device manufacturing facility including Compressed Air System (CAS) Dryers and Air Handling Units (HVAC).
Responsibilities:
- Develop review and execute qualification and validation protocols for Compressed Air Systems (CAS) Dryers and Air Handling Units (AHUs/HVAC).
- Support commissioning and qualification activities including IQ OQ and PQ.
- Review existing validation documentation and leverage established strategies and approved documentation as the basis for qualifying additional systems.
- Ensure validation activities comply with applicable regulatory requirements quality standards and internal procedures.
- Prepare and maintain accurate qualification documentation reports and supporting records.
- Coordinate on-site testing activities with engineering quality and manufacturing teams.
- Support qualification activities during scheduled manufacturing shutdowns.
- Manage assigned deliverables to meet established project milestones and deadlines.
- Travel may be required.
Qualifications:
- Proven experience in pharmaceutical or medical device manufacturing environments.
- Hands-on experience developing and executing validation and qualification protocols for CAS Dryers AHUs/HVAC.
- Experience working with critical utilities supporting controlled manufacturing environments and cleanrooms.
- Ability to independently execute qualification activities and prepare the associated documentation.
- Strong technical writing organizational and project coordination skills.
- Ability to work under tight project timelines and meet established deadlines.
- Flexibility to travel between sites as needed.
- Bilingual (English & Spanish) both spoken and written.
Benefits:
- Professional Growth (Courses and Certifications by EQVAL Academy)
- Referral Program
*This is a full-time position based in Puerto Rico. Remote work permitted for documentation development. On-site presence required during qualification testing activities.
We offer competitive compensation benefits and opportunities for career growth. If you are a motivated individual with passion we would love to hear from you. Apply now!!
EQVAL Group is an EEO. We comply with all federal local and state laws regarding non-discrimination.
