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Protocol Manager Jobs in Puerto Rico (NOW HIRING)

JC Automation Corp

PR · On-site

$74K - $101K/yr

Execute equipment validation protocols, manage line trials, and support seamless product transfers, ensuring all activities are documented and compliant with regulatory standards. * Equipment ...

AbbVie

PR · On-site

Responsible for the audit, pre-approval and post-approval of all process validations protocols ... Member of the Quality Risk Management and participate in development of FMEAs and Risk Control ...

Mace

Design Manager

Carolina, PR

You will manage the implementation of design management systems, processes and protocols to meet statutory, legal, and contractual requirements. You will support the long term development of strategy ...

Biosimilar Sciences PR LLC

PR · On-site

Validation Manager About Ocyonbio: OcyonBio is a biotechnology CDMO based in Aguadilla, Puerto Rico ... Approve IQ/OQ/PQ protocols, reports, and traceability matrices Team & Resource Leadership * Lead ...

Palmas Hospitality Management LLC

PR · On-site

... protocols. • Working knowledge of property management systems (PMS), radios, and operational communication tools; ability to learn new systems quickly. • Must possess strong computer proficiency ...

Palmas Hospitality Management LLC

PR · On-site

... protocols. • Working knowledge of property management systems (PMS), radios, and operational communication tools; ability to learn new systems quickly. • Must possess strong computer proficiency ...

WESTCARE INC

Case Manager (51106)

Caguas, PR · On-site

$13/hr

Oversees clients' medication management using agency protocols. Monitors that prescriptions and other medications are filled or purchased using established protocols. Ensures that prescriptions are ...

WESTCARE INC

Case Manager (51106)

Caguas, PR · On-site

$13/hr

Oversees clients' medication management using agency protocols. Monitors that prescriptions and other medications are filled or purchased using established protocols. Ensures that prescriptions are ...

Ser Familia, Inc - PR

Case Manager

Guaynabo, PR

$18/hr

Be able to help a client in a crisis situation as outline in the agency's protocol. * Listen to ... Manger Supervisor. * Maintain effective usage of time, high levels of organization and detail

MMR Consulting

PR · On-site

IQ/OQ/PQ protocols * Validation documentation * Deviations and CAPAs * Change controls ... Manage third-party CQV consultants, contractors, and vendors. * Provide risk assessments and ...

MMR Consulting

PR · On-site

IQ/OQ/PQ protocols * Validation documentation * Deviations and CAPAs * Change controls ... Manage third-party CQV consultants, contractors, and vendors. * Provide risk assessments and ...

MMR Consulting

PR · On-site

IQ/OQ/PQ protocols * Validation documentation * Deviations and CAPAs * Change controls ... Manage third-party CQV consultants, contractors, and vendors. * Provide risk assessments and ...

FITS LLC

Project Manager

Manati, PR · On-site

For Project Management services in Capital Projects. WHAT MAKES YOU A FIT: The Technical Part ... Utilize technical writing skills for the creation and revision of protocols and reports. * Oversee ...

FITS LLC

Project Manager

Barceloneta, PR · On-site

Develop, review, and approve C&Q documentation including risk assessments, protocols (IQ/OQ/PQ ... managed and resolved. * Support regulatory inspections, audits, and internal quality reviews ...

Housing Works

Case Manager - Puerto Rico

Fajardo, PR · On-site

$16 - $18/hr

Case Manager & Outreach Worker at Intercambios Puerto Rico, Inc. with main offices in Fajardo and ... Carry out the processes in compliance with the rules, procedures, and protocols of the organization.

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Protocol Manager information

What are the key skills and qualifications needed to thrive as a Protocol Manager, and why are they important?

To thrive as a Protocol Manager, you need strong organizational, project management, and interpersonal skills, typically supported by a bachelor's degree in business, international relations, or a related field. Familiarity with protocol guidelines, event management software, and office productivity tools is often required, along with certifications in event planning or protocol management. Exceptional attention to detail, cross-cultural communication, and discretion help individuals stand out in this role. These skills ensure seamless coordination of high-profile events, proper diplomatic interactions, and the maintenance of an organization's professional reputation.

What is the difference between Protocol Manager vs Clinical Research Coordinator?

AspectProtocol ManagerClinical Research Coordinator
Required CredentialsBachelor's degree, experience in clinical protocolsBachelor's degree, often certification in clinical research
Work EnvironmentOffice-based, overseeing multiple protocolsClinical settings, directly interacting with patients and sites
Employer & IndustryPharmaceutical companies, research institutionsHospitals, research centers, clinics
Common Search/ComparisonProtocol Manager vs Clinical Research Coordinator

The Protocol Manager primarily oversees the development and management of clinical protocols, ensuring compliance and coordination across projects. In contrast, the Clinical Research Coordinator handles the day-to-day operations at clinical sites, working directly with patients and data collection. Both roles are essential in clinical research but differ in scope, responsibilities, and work environment.

What are some common challenges Protocol Managers face when coordinating high-profile events or visits?

Protocol Managers often encounter challenges such as managing last-minute changes, accommodating diverse cultural expectations, and ensuring seamless communication among multiple stakeholders. They must pay close attention to detail to prevent protocol breaches and maintain confidentiality. Additionally, balancing the needs of VIP guests with organizational policies requires strong problem-solving skills and adaptability.

What are Protocol Managers?

Protocol Managers are professionals responsible for overseeing and coordinating the procedures and formalities that govern official events, diplomatic functions, or research studies. They ensure that established protocols, such as etiquette, rules, and guidelines, are followed to facilitate smooth operations and maintain professionalism. In research or clinical settings, Protocol Managers also manage study protocols, regulatory compliance, and documentation. Their role is crucial for minimizing misunderstandings, ensuring legal or diplomatic correctness, and guaranteeing that all stakeholders are aligned with procedures.
What job categories do people searching Protocol Manager jobs in Puerto Rico look for? The top searched job categories for Protocol Manager jobs in Puerto Rico are:
What cities in Puerto Rico are hiring for Protocol Manager jobs? Cities in Puerto Rico with the most Protocol Manager job openings:
Protocol Manager jobs near you

Sr Parenteral Inspection Technology Engineer

JC Automation Corp

PR • On-site

$74K - $101K/yr

Full-time

Posted 21 days ago

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

We are seeking a Senior Inspection Technology Engineer to lead inspection engineering activities for sterile and biologics parenteral products. This role combines deep technical expertise in automated inspection systems with hands-on project leadership — from technology development and implementation to validation, line trials, and operational support.

The ideal candidate brings strong problem-solving capabilities, experience in pharmaceutical sterile manufacturing, and the cross-functional collaboration skills needed to align inspection efforts with manufacturing, quality, and validation teams.


RESPONSIBILITIES

  • Inspection Technology Development: Lead the development, deployment, and lifecycle management of new parenteral inspection technologies and automated inspection systems for sterile and biologics products.
  • Process Improvement & Project Leadership: Identify and lead process improvement initiatives related to inspection systems. Manage inspection-related capital or operational projects to maximize efficiency, quality, and compliance.
  • Validation & Line Trials: Execute equipment validation protocols, manage line trials, and support seamless product transfers, ensuring all activities are documented and compliant with regulatory standards.
  • Equipment Troubleshooting: Apply advanced technical problem-solving capabilities to troubleshoot complex inspection equipment and resolve operational bottlenecks in a timely manner.
  • Cross-Functional Collaboration: Partner closely with manufacturing, engineering, quality, and validation teams to ensure inspection systems meet site priorities and stringent regulatory requirements.
  • Regulatory Compliance: Ensure all inspection engineering activities are aligned with cGMP regulations, FDA guidelines, and internal site procedures throughout the product lifecycle.


REQUIREMENTS & QUALIFICATIONS

Required

  • Bachelor's degree in Engineering (Mechanical, Electrical, Biomedical, or Automation), Computer Science, or a related technical discipline.
  • Strong foundation in inspection engineering activities specifically for sterile and biologics parenteral products.
  • Proven track record in the development, deployment, and lifecycle management of automated inspection technologies.
  • Extensive hands-on experience executing equipment validation protocols, managing line trials, and supporting product transfers.
  • Advanced troubleshooting capabilities for complex inspection equipment and control systems.
  • Demonstrated ability to lead process improvements and manage inspection-related projects end-to-end.
  • Experience in pharmaceutical sterile manufacturing environments with knowledge of cGMP and FDA requirements.


Preferred

  • Experience with automated vision inspection systems or machine learning-based inspection technologies.
  • Familiarity with lyophilized parenteral products and associated inspection challenges.
  • PMP or equivalent project management certification.
  • Experience supporting regulatory audits or inspections related to parenteral inspection systems.


SKILLS

Technical Skills

  • Inspection engineering for sterile and biologics parenteral products
  • Automated inspection system development, implementation, and lifecycle management
  • Equipment validation protocols (IQ/OQ/PQ) and line trial execution
  • Advanced troubleshooting of inspection equipment and control systems
  • Process improvement methodologies in regulated manufacturing environments
  • cGMP compliance, FDA guidelines, and regulatory documentation
  • Microsoft Office 365


Soft Skills

  • Strong cross-functional collaboration with manufacturing, quality, and validation teams
  • Technical leadership and subject matter expertise
  • Structured problem-solving and root cause analysis
  • Project management and execution in high-complexity environments
  • Clear technical communication with multidisciplinary stakeholders
  • Adaptability and availability to support other shifts as business needs require