ZipRecruiter

Log In

1

Sterile Processing Manager Jobs in Puerto Rico (NOW HIRING)

JC Automation Corp

PR · On-site

SDD: Sterile Drug Delivery (or Spray Dry Dispersion) -- sterile processing skids, isolators ... Strong vendor management, contract administration, and FAT/SAT discipline. * Field-execution ...

Biosimilar Sciences PR LLC

PR · On-site

Job Overview The Sterility Assurance Lead is accountable for ensuring that aseptic processing ... Technical & Professional Competencies · Ability to apply Quality Risk Management (ICH Q9 ...

FITS LLC

Manager, Quality Assurance Scientist

Manati, PR · On-site

Supports actively the investigation processes in manufacturing areas (Sterile and Non Sterile) and ... Manages audit observation, investigations, change control, and CAPAs records in the applicable QMS ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Manage projects involving automation systems, process control systems, utilities, facility infrastructure upgrades, and sterile manufacturing support systems. * Facilitate project meetings and ...

LEGAL PROJECT MANAGEMENT PARTNERS LLC

PR · On-site

Manage projects involving automation systems, process control systems, utilities, facility infrastructure upgrades, and sterile manufacturing support systems. * Facilitate project meetings and ...

Biosimilar Sciences PR LLC

PR · On-site

Validation Manager About Ocyonbio: OcyonBio is a biotechnology CDMO based in Aguadilla, Puerto Rico ... Aseptic processing and sterilization validation * Equipment commissioning and lifecycle validation

MMR Consulting

PR · On-site

... sterile manufacturing, fill-finish, API, or biologics environments and will serve as a key liaison ... Process equipment * Clean utilities * HVAC systems * Automation and control systems * Manufacturing ...

MMR Consulting

PR · On-site

... sterile manufacturing, fill-finish, API, or biologics environments and will serve as a key liaison ... Process equipment * Clean utilities * HVAC systems * Automation and control systems * Manufacturing ...

MMR Consulting

PR · On-site

... sterile manufacturing, fill-finish, API, or biologics environments and will serve as a key liaison ... Process equipment * Clean utilities * HVAC systems * Automation and control systems * Manufacturing ...

next page

Showing results 1-20

All JobsSterile Processing JobsSterile Processing Manager JobsSterile Processing Manager Jobs in Puerto Rico

Sterile Processing Manager information

What is a sterile processing manager?

A sterile processing manager is in charge of the sterilization of surgical instruments and equipment, so they typically work in a hospital or outpatient clinic. Job duties include keeping operating rooms stocked, cleaning medical equipment, verifying that supplies have proper packing, and maintaining documentation. A sterile processing manager may also manage inventory of cleaning supplies and teach new employees how to disinfect surgical instruments and equipment according to medical standards.

What does a sterile processing manager do?

A Sterile Processing Manager oversees the sterilization and disinfection of medical instruments and equipment in healthcare facilities. They manage the sterile processing department, ensure compliance with safety and infection control standards, and supervise staff responsible for cleaning, assembling, and distributing medical devices. Their responsibilities also include inventory management, staff training, and staying updated with regulatory requirements to maintain a safe environment for patients and staff.

What are the key skills and qualifications needed to thrive as a sterile processing manager?

To thrive as a Sterile Processing Manager, you need expertise in sterilization techniques, infection control, inventory management, and typically a certification such as CRCST (Certified Registered Central Service Technician) or CSPDT (Certified Sterile Processing and Distribution Technician). Familiarity with sterilization equipment, tracking systems like instrument management software, and regulatory standards such as AAMI and OSHA guidelines is critical. Leadership, problem-solving, and strong communication skills help manage teams and ensure compliance with safety protocols. These skills are vital for maintaining patient safety, regulatory compliance, and efficient operations in healthcare environments.

What are some common challenges faced by sterile processing managers, and how can they be effectively addressed?

Sterile Processing Managers often encounter challenges such as maintaining strict regulatory compliance, ensuring staff competency, and adapting to evolving technology in instrument sterilization. Addressing these challenges involves ongoing staff education, implementing robust quality assurance protocols, and fostering open communication with surgical teams to anticipate needs and resolve issues promptly. Staying proactive with professional development and establishing strong relationships with vendors and other departments also helps ensure efficiency and a consistently safe environment for both patients and staff.

What is the difference between Sterile Processing Manager vs Sterile Processing Technician?

AspectSterile Processing ManagerSterile Processing Technician
CertificationsCBSPD or IAHCSMM certification often requiredTypically requires certification like CBSPD or IAHCSMM
Work EnvironmentSupervises sterile processing departments in hospitals or clinicsPerforms sterilization and processing tasks in sterile processing departments
ResponsibilitiesOversees staff, manages compliance, and ensures sterilization standardsOperates sterilization equipment, cleans, and prepares instruments

The Sterile Processing Manager oversees the entire sterile processing department, focusing on management, compliance, and staff supervision. In contrast, the Sterile Processing Technician handles the hands-on sterilization tasks. Both roles require similar certifications and work in the same environment, but their responsibilities differ significantly.

More about Sterile Processing Manager jobs

What are the most commonly searched types of Sterile Processing jobs in Puerto Rico?

The most popular types of Sterile Processing jobs in Puerto Rico are:

What are popular job titles related to Sterile Processing Manager jobs in Puerto Rico?

For Sterile Processing Manager jobs in Puerto Rico, the most frequently searched job titles are:

What job categories do people searching Sterile Processing Manager jobs in Puerto Rico look for?

The top searched job categories for Sterile Processing Manager jobs in Puerto Rico are:

What cities in Puerto Rico are hiring for Sterile Processing Manager jobs?

Cities in Puerto Rico with the most Sterile Processing Manager job openings:

Sterile Processing Manager jobs near you
Infographic showing various Sterile Processing Manager job openings in Puerto Rico as of August 2026, with employment types broken down into 87% Full Time, 12% Part Time, and 1% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution.

Equipment Manager

PR • On-site

JC Automation Corp
51 - 200 employees
Learn more about JC Automation Corpexternal

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

About Company:

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

The PM / WPO Equipment Manager is a combined project-management and work-package-owner role responsible for delivery of major equipment packages from vendor design through factory acceptance, site delivery, field installation, and turnover to C&Q. The role carries both PM-side accountabilities (scope, budget, schedule, vendor performance, design integration, FAT/SAT) and WPO-side accountabilities at the work-face (daily field execution, contractor / installer leadership, HSE, productivity, and system-by-system turnover). Each variant focuses on a specific equipment family but carries the same core accountabilities. This is an Owner representation role that supports in ensuring design, construction execution and quality are adhered to and set up for successful system turnover.

RESPONSIBILITIES


  • Support designer, contractor and procurement with equipment package end-to-end: scope, budget, schedule, vendor performance.
  • Support the Owner Furnished Equipment Owners for successful design, delivery, storage and installation.
  • Support DVLs in vendor design reviews, hold-point inspections, and FAT planning/execution.
  • Coordinate equipment design integration with the Design Interface Manager and BIM Coordinator.
  • Validate Design and CMs logistics: shipping, receiving, rigging, set-in-place, and protection during construction.
  • Support equipment installation with the assigned PM, WPO Leads, and Lead Construction Manager.
  • Lead SAT planning and execution coordination with C&Q and the System Turnover Lead.
  • Manage vendor change orders, claims, warranty terms, and spare-parts strategy.
  • Ensure compliance with GMP design expectations, materials of construction, and 3-A / ASME BPE where applicable.
  • Support and oversee field execution of the equipment installation work package; lead the vendor's and installer's site teams in delivery.
  • Drive HSE engagement at the work-face: pre-task plans, JHAs, SSoW review, field safety walks, BeyondZero/LIFE program reinforcement.
  • Coordinate with contractor and other vendors on daily and weekly look-ahead planning, set-in-place sequencing, and crew productivity for equipment installs.
  • Partner with Construction Quality Leads to enforce inspection and test plans, hold points, and quality gates on the equipment package.
  • Manage RFIs, field changes, and design clarifications through the Design Verification Leads.
  • Track and report progress (earned value, install quantities, productivity ratios) per the Project Controls cadence.

Discipline-Specific Variant Notes

  • ASRS: Automated Storage and Retrieval System for materials/finished goods — modular construction integration, vendor and installer management (Swisslog, or equivalent), controls/SCADA tie-in, set-in-place and field commissioning.
  • SDD: Sterile Drug Delivery (or Spray Dry Dispersion) — sterile processing skids, isolators, filling/packaging lines; stringent GMP and aseptic-design controls in both vendor design and field install.
  • OSD: Oral Solid Dosage — granulators, blenders, tablet presses, coaters, packaging, and associated containment systems.
  • Equipment (general / vendor packages): Non-discipline-specific major equipment and vendor packages — process and utility skids, lab/warehouse equipment, and other equipment-vendor packages supporting not covered by the ASRS, SDD, or OSD variants.

REQUIREMENTS & QUALIFICATIONS

Required

  • Bachelor's degree in Mechanical, Chemical, or Industrial Engineering.
  • 12+ years of pharma/biotech capital project experience; 5+ years managing major equipment packages from FAT through SAT.
  • Discipline-specific experience: ASRS — material handling and automation; SDD — sterile/aseptic equipment; OSD — solid dosage manufacturing equipment; Equipment — broad equipment / vendor-package portfolio.
  • Strong vendor management, contract administration, and FAT/SAT discipline.
  • Field-execution credibility: prior superintendent or WPO experience on equipment set-in-place / installation campaigns; OSHA 30 minimum.
  • Working knowledge of GMP, ASME BPE (where applicable), 3-A standards, and validation expectations.
  • English required.

Preferred

  • Spanish preferred.

SKILLS

Technical Skills

  • Vendor management, contract administration, and change order / claims / warranty management.
  • FAT/SAT planning and execution, hold-point inspections, and design review coordination.
  • GMP, ASME BPE, and 3-A compliance for equipment design and materials of construction.
  • Field execution of equipment installation: rigging, set-in-place, logistics, and productivity tracking.
  • Inspection and test plan enforcement, quality gates, and RFI / field change management.
  • Progress tracking and reporting (earned value, install quantities, productivity ratios).

Soft Skills

  • Leadership of vendor and installer site teams.
  • Cross-functional coordination with Design Interface Manager, BIM Coordinator, C&Q, and System Turnover Lead.
  • HSE engagement and safety culture reinforcement at the work-face.
  • Effective communication in English (Spanish preferred).