Skill
Corrective And Preventive Action (CAPA)
Manufacturing and Industrial
Corrective and Preventive Action (CAPA) is a systematic quality management process used to investigate and resolve nonconformities or defects, and to prevent their recurrence. It is widely used in regulated industries like pharmaceuticals, medical devices, and manufacturing, where quality assurance teams document root causes, implement fixes, and verify effectiveness. CAPA is a core requirement of quality systems standards such as ISO 9001 and FDA regulations.
Corrective And Preventive Action (CAPA) in the job market
Last checked September 14, 2026
- Open roles
- 23
- Employers
- 14
- Median pay
- —
- Disclose pay
- —
on Career App right now
hiring for it
not enough disclosed
of these roles
Open roles requiring Corrective And Preventive Action (CAPA) (23)
Quality Manager, Peptide API & Development
Hims and Hers
Full-time · Menlo Park, CA · $130,000 – $155,000
This role leads the establishment and scaling of quality systems for a newly built peptide API manufacturing site with early-phase development capabilities. The ideal candidate is a hands-on quality leader who thrives in startup environments, can build practical GMP-compliant systems from the ground up, and works closely with operations and technical teams to ensure inspection readready manufacturing and development operations.
Listed on Hims and Hers’s careers site · Apply there ↗
Sr Quality Engineer
Crane Co.
Piqua, OH
This role owns the quality management system and leads continuous improvement efforts in a manufacturing environment, including CAPA processes, root cause investigations, and supplier quality. It suits someone with 2–3 years of quality or manufacturing experience who wants to grow technical expertise in process control and quality systems.
Listed on Crane Co.’s careers site · Apply there ↗
Staff Quality Assurance-Supplier Quality Engineer
Beckman Coulter
Full-time · Chaska, MN · $140,000 – $160,000
This is a senior quality engineering role managing supplier transitions and cost-reduction design changes for medical diagnostic equipment at a life sciences company. It suits someone with 12+ years in quality engineering who wants to drive product improvements and supplier qualification in a regulated manufacturing environment.
Listed on Beckman Coulter’s careers site · Apply there ↗
Director, Risk Intelligence and Analytics
Biogen
Full-time · Cambridge, MA · $188,000 – $259,000
This director-level role leads a team building data systems and intelligence to monitor risks across Biogen's manufacturing and supply network, translating complex operational data into executive guidance for strategic decisions. The position suits experienced analytics leaders with deep pharmaceutical manufacturing knowledge who can combine technical rigor with clear stakeholder communication.
Listed on Biogen’s careers site · Apply there ↗
Director, Technical Operations (Small Molecule Drug Product)
Merck
Full-time · Elkton, VA · $173,200 – $272,600
A director-level technical operations role leading small molecule drug manufacturing at a biopharmaceutical facility, responsible for process excellence, technology transfer, regulatory compliance, and building high-performing teams. This position suits experienced manufacturing leaders who combine deep process expertise with the ability to drive organizational transformation across a regulated environment.
Listed on Merck’s careers site · Apply there ↗
Sr Quality Engineer
Medtronic
Humacao, Puerto Rico, United States of America
This role supports quality assurance in a regulated medical device manufacturing environment, managing investigations, compliance documentation, and continuous improvement across production processes. It suits engineers with healthcare manufacturing experience who are comfortable with FDA/ISO systems and can work cross-functionally to resolve quality issues.
Listed on Medtronic’s careers site · Apply there ↗
EHS&S Sr. Manager
Moderna
$130,800 – $209,400
This senior manager role oversees environmental health and safety operations at Moderna's Norwood manufacturing facility, leading complex EHS programs, investigations, and compliance initiatives across R&D and production environments. The position suits experienced EHS professionals with strong expertise in regulated biopharmaceutical operations who can drive culture change and manage high-risk work activities across cross-functional teams.
Listed on Moderna’s careers site · Apply there ↗
Manager, Supplier Quality
Bristol Myers Squibb
Full-time · Indianapolis, IN · $124,449 – $150,803
This role manages supplier quality and compliance for a biotech company developing radiopharmaceutical therapies, overseeing vendor qualifications, material lifecycle management, audits, and regulatory adherence across manufacturing operations. It suits someone with quality assurance experience in regulated environments who can lead cross-functional teams and navigate complex vendor relationships in a GMP-controlled setting.
Listed on Bristol Myers Squibb’s careers site · Apply there ↗
Sr. Quality Assurance Specialist
Gilead Sciences
La Verne, CA · $123,930 – $160,380
A senior quality assurance role at a pharmaceutical company focused on batch release, regulatory compliance, and product oversight for drugs and biologics across manufacturing and development stages. Suited for experienced QA professionals with pharma or biotech backgrounds seeking responsibility for finished product release decisions and quality system management.
Listed on Gilead Sciences’s careers site · Apply there ↗
Material Quality Engineer
Samsung Semiconductor
Full-time · Taylor, TX · $106,000 – $174,500
This role oversees the quality and supply chain of raw materials used in semiconductor fabrication, working with suppliers to solve problems and drive continuous improvement. It suits engineers with deep experience in photolithography processes and fab manufacturing who enjoy cross-functional collaboration and technical problem-solving.
Listed on Samsung Semiconductor’s careers site · Apply there ↗
Asked for alongside Corrective And Preventive Action (CAPA)
Measured from the 23 open roles that name Corrective And Preventive Action (CAPA) — not from a curated list.
- Root Cause Analysis11 roles47.8%
- Change Control5 roles21.7%
- Failure Mode and Effects Analysis (FMEA)5 roles21.7%
- Process Validation5 roles21.7%
- Good Manufacturing Practice (GMP)4 roles17.4%
- Data Analysis3 roles13.0%
- ISO 134853 roles13.0%
- Microsoft Excel3 roles13.0%
Roles that use Corrective And Preventive Action (CAPA)
Employers hiring for Corrective And Preventive Action (CAPA)
14 in total, most open roles first.
- HHHims and Hers4 roles
- Beckman Coulter3 roles
- Moderna3 roles
- Biogen2 roles
- RSRelativity Space2 roles
- ARAgility Robotics1 role
Related skills
Curated neighbors in the taxonomy, whether or not employers ask for them together.