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Capa Manager Jobs in Humacao, PR (NOW HIRING)

Deviations Owner

Juncos, PR · On-site

$80 - $100/hr

Experience with deviation tracking systems, CAPA management, and electronic quality management systems (eQMS). * Excellent analytical, organizational, and problem-solving skills. * Strong ...

Experience with deviation tracking systems, CAPA management, and electronic quality management systems (eQMS). * Excellent analytical, organizational, and problem-solving skills. * Strong ...

Process Technology Manager

Guayama, PR · On-site

$114K - $157K/yr

The Process Technology Manager will manage technical activities across multiple dosage forms with ... Troubleshooting and CAPA implementation / effectiveness for technical related issues. * Product ...

Senior Engineer

Juncos, PR · On-site

$85 - $110/hr

CAPA Management * SME Responsibilities The Personality Part: * Picture yourself in a lab... with all the equipment you need to put your multitasking, scientific, creative (to come up with all those ...

Compliance Engineer

Gurabo, PR · On-site

$70 - $90/hr

This role is responsible for supporting investigations, CAPA activities, change management coordination, GMP documentation review, compliance tracking, and quality system support activities ...

This role is responsible for supporting investigations, CAPA activities, change management coordination, GMP documentation review, compliance tracking, and quality system support activities ...

This role is responsible for supporting investigations, CAPA activities, change management coordination, GMP documentation review, compliance tracking, and quality system support activities ...

This role is responsible for supporting investigations, CAPA activities, change management coordination, GMP documentation review, compliance tracking, and quality system support activities ...

This role is responsible for supporting investigations, CAPA activities, change management coordination, GMP documentation review, compliance tracking, and quality system support activities ...

Compliance Engineer

Juncos, PR · On-site

$70 - $90/hr

This role is responsible for supporting investigations, CAPA activities, change management coordination, GMP documentation review, compliance tracking, and quality system support activities ...

This role is responsible for supporting investigations, CAPA activities, change management coordination, GMP documentation review, compliance tracking, and quality system support activities ...

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Capa Manager information

What does a CAPA manager do?

A CAPA (Corrective and Preventive Action) Manager is responsible for overseeing an organization's CAPA process to ensure compliance with quality and regulatory requirements. They investigate quality issues, identify root causes, and implement corrective and preventive measures to prevent recurrence. CAPA Managers work closely with cross-functional teams to improve processes, maintain regulatory compliance, and enhance overall product or service quality.

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

To thrive as a CAPA Manager (Corrective and Preventive Action Manager), you typically need a background in quality assurance, strong analytical and problem-solving abilities, and experience with regulatory compliance, often supported by a degree in a science or engineering field. Familiarity with quality management systems (QMS), risk management tools, root cause analysis methodologies (such as 5 Whys or Fishbone diagrams), and industry certifications like Six Sigma or ISO 9001 are highly valued. Outstanding candidates demonstrate excellent communication, leadership, and organizational skills to effectively drive cross-functional teams and ensure timely resolution of quality issues. These skills are crucial for identifying, addressing, and preventing compliance gaps or product issues, thereby maintaining high standards and avoiding costly regulatory penalties.

What are some common challenges a CAPA manager faces, and how are they typically addressed?

One common challenge CAPA Managers face is ensuring timely and thorough investigations into quality issues while coordinating input from multiple departments. Balancing the need for fast resolution with the rigor required for regulatory compliance can be demanding, especially in highly regulated industries like pharmaceuticals or medical devices. Successful CAPA Managers often address these challenges through clear process documentation, effective project management, and fostering strong collaboration among stakeholders. By leveraging root cause analysis tools and maintaining open communication, they help create a continuous improvement culture that benefits both the organization and its customers.

What are popular job titles related to Capa Manager jobs in Humacao, PR?

For Capa Manager jobs in Humacao, PR, the most frequently searched job titles are:

What cities near Humacao, PR are hiring for Capa Manager jobs?

Cities near Humacao, PR with the most Capa Manager job openings:

Infographic showing various Capa Manager job openings in Humacao, PR as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution.

Investigation Specialist (CAPA & Deviations)

Weil Group, Inc.

Juncos, PR • On-site

Full-time

Posted 3 days ago

New


Job description

Looking for an Investigation Specialist that manages deviation investigations for manufacturing, ensures compliance with GMP/FDA regulations, and oversees corrective actions.
The Investigation Specialist will be responsible for the following deliverables:
•Ensure that all QE's, NTR's, NOE's and CAPA's are completed / closed within the established timeframe, utilizing the right tools to prevent reoccurrence.
•Reviews and provides input to regulatory submissions applicable to area of responsibility.
•Leads QE's and CAPA's trend evaluation.
•Participates in the new product introduction process to determine requirements for documentation, materials, training and equipment modifications.
•Supports establishment of process monitoring parameters and control limits.
•Supports the assessment of deviations and process monitoring data
•Monitors and evaluates parameters in existing (on-going) processes to optimize process times/productivity, equipment performance, yields and quality.
•Provides technical assistance to identify, recommend and implement process and equipment modifications to improve process performance; to identify and assist in the implementation of cost reduction projects and assuring the manufacturing area is in cGMP's compliance.
•Write, evaluate and revise the required manufacturing documentation (i.e. SOP's, MBR's, etc.) and may assist in providing training on scientific or technical aspects of the processes.
•Assists with generation and execution of validation protocols and reports.
•Participate in regulatory inspection when necessary.
•Assists the area managers and supervisory personnel to solve any production technical problem (i.e. Process / equipment troubleshooting, yield, cycle time, quality and productivity).
•Provides alternatives and recommendations to improve and maximize processes and equipment.
•Participates in Environmental Regulatory and Compliance Permits and Process Safety Hazards evaluation.
•Promote and model the Client Core Behaviors, facilitating teamwork.
•Supports all site Initiatives and any other assignments based on business needs.
*Weil Group is proud to be an Equal Employment Opportunity Employer.*