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Capa Manager Jobs in Raleigh, NC (NOW HIRING)

Stark Pharma Solutions Inc

CAPA Specialist

Durham, NC · On-site

I am working on CAPA Specialist position right now. Please send me your updated resume if you have ... Lead and manage CAPAs, Non-Conformances, Complaints, and Audit activities through closure. * Drive ...

Indivior

Sr. Specialist, Compliance QA

Raleigh, NC

$88K - $108K/yr

Function as a change controller and CAPA manager for site records. * Facilitate the compilation of data and author the Annual Product Review reports. * Author Quality Agreements * Create the self ...

Indivior PLC

Sr. Specialist, Compliance QA

Raleigh, NC · On-site

$88K - $108K/yr

Function as a change controller and CAPA manager for site records. * Facilitate the compilation of data and author the Annual Product Review reports. * Author Quality Agreements * Create the self ...

Deloitte

System Test and Validation Lead

Raleigh, NC · On-site +1

This role supports system validation strategy, audit readiness, CAPA management, and risk-based compliance activities across regulated technology environments. This role helps clients address ...

Deloitte

System Test and Validation Lead

Raleigh, NC · On-site +1

This role supports system validation strategy, audit readiness, CAPA management, and risk-based compliance activities across regulated technology environments. This role helps clients address ...

Deloitte

System Test and Validation Lead

Raleigh, NC · On-site +1

This role supports system validation strategy, audit readiness, CAPA management, and risk-based compliance activities across regulated technology environments. This role helps clients address ...

GSK

Senior Device Quality Engineer

Zebulon, NC · On-site

$75K - $101K/yr

Demonstrated hands-on experience conducting investigations, performing root cause analysis, and managing Corrective and Preventive Action (CAPA) processes. * Working knowledge of Quality Management ...

GlaxoSmithKline

Senior Device Quality Engineer

Zebulon, NC

$75K - $101K/yr

Demonstrated hands-on experience conducting investigations, performing root cause analysis, and managing Corrective and Preventive Action (CAPA) processes. * Working knowledge of Quality Management ...

MSD

Business Excellence Lead (Director)

Durham, NC

Adaptability, Adaptability, Benchmarking, Business Acumen, Business Process Re-Engineering (BPR), CAPA Management, Clinical Systems Implementation, Cross-Functional Teamwork, Data Analysis Tools ...

Actalent

Global Quality Manager

Cary, NC

Global Quality Manager The Global Quality Manager leads product quality, supplier quality, and ... Drive root cause investigations and implement corrective and preventive actions (CAPA) to eliminate ...

PowerSecure, Inc.

Production Manager

Durham, NC · On-site

Manages multiple work centers and manufacturing disciplines, monitoring performance and reinforcing ... Apply corrective and preventive action (CAPA) best practices to address quality, delivery, and ...

PowerSecure

Production Manager

Durham, NC · On-site

Manages multiple work centers and manufacturing disciplines, monitoring performance and reinforcing ... Apply corrective and preventive action (CAPA) best practices to address quality, delivery, and ...

PowerSecure

Production Manager

Durham, NC · On-site

Manages multiple work centers and manufacturing disciplines, monitoring performance and reinforcing ... Apply corrective and preventive action (CAPA) best practices to address quality, delivery, and ...

Sobi

Quality Operation Manager (GMP)

Morrisville, NC · On-site

CAPA * Change control * Risk management * Audit management * Complaint handling (if applicable) * Distribute and coordinate training of GXP procedures * Support for External Quality Operation, if ...

Sobi

Quality Operation Manager (GMP)

Morrisville, NC · On-site

CAPA * Change control * Risk management * Audit management * Complaint handling (if applicable) * Distribute and coordinate training of GXP procedures * Support for External Quality Operation, if ...

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All JobsCapa JobsCapa Manager JobsCapa Manager Jobs in Raleigh, NC

Capa Manager information

What is the role of a Capa specialist?

A CAPA (Corrective and Preventive Action) specialist is responsible for investigating quality issues, implementing corrective actions, and preventing recurrence of problems within a quality management system. They analyze data, ensure compliance with regulations, and often use tools like root cause analysis to improve product and process quality.

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 is a capa coordinator?

A CAPA (Corrective and Preventive Action) coordinator is responsible for managing and overseeing the CAPA process within a quality management system. They investigate quality issues, implement corrective actions, and ensure compliance with regulatory standards, often using tools like root cause analysis and tracking software. This role requires strong organizational skills and knowledge of quality regulations such as ISO or FDA requirements.

What is the highest paying manager position?

The highest paying manager positions are typically executive roles such as Chief Executive Officer (CEO), Chief Operating Officer (COO), and Chief Financial Officer (CFO), which often have salaries exceeding several hundred thousand dollars annually. In some industries, specialized managerial roles like Vice President or Director of certain departments can also command high compensation, especially with bonuses and stock options included.

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 the key skills and qualifications needed to thrive in the Capa Manager position, and why are they important?

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 does a capa manager do?

A CAPA (Corrective and Preventive Action) manager oversees the implementation of processes to identify, investigate, and resolve quality issues within an organization. They analyze root causes, develop action plans, and ensure compliance with regulatory standards, often using quality management systems and tools like CAPA software. The role requires strong problem-solving skills and knowledge of industry regulations such as ISO or FDA standards.
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Capa Manager jobs near you
Infographic showing various Capa Manager job openings in Raleigh, NC as of July 2026, with employment types broken down into 88% Full Time, 4% Part Time, 1% Temporary, 5% Contract, 1% Nights, and 1% Summer. Highlights an 94% Physical, 3% Hybrid, and 3% Remote job distribution.

CAPA Specialist

Stark Pharma Solutions Inc

Durham, NC • On-site

Contractor

Posted 12 days ago

Job description

Hi,

My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on CAPA Specialist position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job description is as follows

Position: CAPA Specialist

Location: Durham, NC
Duration: Long-Term Contract

Job Overview

We are seeking an experienced CAPA Specialist to support quality system remediation activities within a medical device manufacturing environment. The ideal candidate will have strong expertise in CAPA, Non-Conformances, Audits, Complaints, and Risk Management, with the ability to independently drive quality initiatives and ensure regulatory compliance.

Key Responsibilities

  • Lead and manage CAPAs, Non-Conformances, Complaints, and Audit activities through closure.
  • Drive quality system remediation projects and implement sustainable process improvements.
  • Develop, revise, and improve Risk Management procedures in compliance with FDA and ISO 13485 requirements.
  • Review and remediate existing quality records using risk-based decision-making.
  • Plan, conduct, and document internal and external audits.
  • Perform root cause investigations and verify CAPA effectiveness.
  • Collaborate with cross-functional teams to identify quality system gaps and implement corrective actions.
  • Ensure timely completion of quality activities while maintaining compliance with regulatory standards.

Required Qualifications

  • Bachelor's degree in Engineering, Life Sciences, or a related field.
  • Experience in the Medical Device industry is required.
  • Strong knowledge of CAPA, Non-Conformances, Complaints, Audits, and Risk Management.
  • Experience supporting or leading Quality System remediation projects.
  • Hands-on experience rewriting procedures and remediating quality records.
  • Working knowledge of FDA 21 CFR Part 820/Part 820 QMSR and ISO 13485.
  • Excellent problem-solving, documentation, and communication skills.
  • Ability to work independently in a fast-paced, regulated environment.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.  

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/

Thank you,

Karthik Mutyala

Recruiting Manager

Stark Pharma Solutions Inc

Email: karthik@starkpharma.com

15 Corporate Place S, Suite 350,

Piscataway, New Jersey 08854

www.starkpharma.com