Facilities & Utilities Engineer
Hace 5 días
Juncos, Puerto Rico
EQVAL Group, Inc
Trabajo remoto
Jornada completa
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*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:
- 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.*
* ). 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:
- 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.*