Quality Analyst / Pharma Controlled Substance-DEA Compliance (Hybrid Work) Duration: 4 months ... CAPA with stakeholders, creating and documenting audit records in system. Ensure all audit ...
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Quality Analyst / Pharma Controlled Substance-DEA Compliance (Hybrid Work) Duration: 4 months ... CAPA with stakeholders, creating and documenting audit records in system. Ensure all audit ...
Position Summary The Quality System Specialist - CAPA is responsible for supporting and maintaining ... Root Cause Analysis & Effectiveness * Support cross-functional teams in performing structured root ...
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Position Summary The Quality System Specialist - CAPA is responsible for supporting and maintaining ... Root Cause Analysis & Effectiveness * Support cross-functional teams in performing structured root ...
CAPA Manager
Salt Lake City, UT · On-site
Lead and develop quality analysts, quality engineers, or CAPA coordinators as applicable; provide coaching on quality systems, investigations, regulatory expectations, and talent development.
CAPA Manager
Salt Lake City, UT · On-site
Lead and develop quality analysts, quality engineers, or CAPA coordinators as applicable; provide coaching on quality systems, investigations, regulatory expectations, and talent development.
: Develop and maintain quality system processes, including metrics reporting and tracking Manage CAPA ... cause analyses through cross functional team involvement Leading Good Documentation Practice ...
: Develop and maintain quality system processes, including metrics reporting and tracking Manage CAPA ... cause analyses through cross functional team involvement Leading Good Documentation Practice ...
Position Summary The Quality System Specialist - CAPA is responsible for supporting and maintaining ... Root Cause Analysis & Effectiveness * Support cross-functional teams in performing structured root ...
Position Summary The Quality System Specialist - CAPA is responsible for supporting and maintaining ... Root Cause Analysis & Effectiveness * Support cross-functional teams in performing structured root ...
Quality Assurance CAPA Specialist Department: Quality Assurance Employment Type: Full Time Location ... This role requires structured root cause analysis, project management, and very strong ...
Quality Assurance CAPA Specialist Department: Quality Assurance Employment Type: Full Time Location ... This role requires structured root cause analysis, project management, and very strong ...
Quality Assurance CAPA Specialist Department: Quality Assurance Employment Type: Full Time Location ... This role requires structured root cause analysis, project management, and very strong ...
Quality Assurance CAPA Specialist Department: Quality Assurance Employment Type: Full Time Location ... This role requires structured root cause analysis, project management, and very strong ...
The Quality Assurance (QA) CAPA Specialist is responsible and accountable for the execution ... This role requires structured root cause analysis, project management, and very strong ...
The Quality Assurance (QA) CAPA Specialist is responsible and accountable for the execution ... This role requires structured root cause analysis, project management, and very strong ...
The Quality Assurance (QA) CAPA Specialist is responsible and accountable for the execution ... This role requires structured root cause analysis, project management, and very strong ...
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The Quality Assurance (QA) CAPA Specialist is responsible and accountable for the execution ... This role requires structured root cause analysis, project management, and very strong ...
Medical Device Quality Engineer
Madison, WI · On-site
$40 - $45/hr
... Analyst/Engineer is responsible for ensuring compliance and maintaining strong Quality Systems for the Madison facility. This role oversees CAPA, Change Management, investigations, deviations ...
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Medical Device Quality Engineer
Madison, WI · On-site
$40 - $45/hr
... Analyst/Engineer is responsible for ensuring compliance and maintaining strong Quality Systems for the Madison facility. This role oversees CAPA, Change Management, investigations, deviations ...
Quality Engineer - Complaints and CAPA
Itasca, IL · On-site
$100K - $115K/yr
Escalate complaint and CAPA-related findings requiring quality-system, process, product, supplier ... Analyze complaint investigation, service, repair, and failure-mode data to identify adverse trends ...
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Quality Engineer - Complaints and CAPA
Itasca, IL · On-site
$100K - $115K/yr
Escalate complaint and CAPA-related findings requiring quality-system, process, product, supplier ... Analyze complaint investigation, service, repair, and failure-mode data to identify adverse trends ...
CAPA Engineer
$65K - $84K/yr
The CAPA Engineer is responsible for leading and facilitating the Corrective and Preventive Action ... Data analysis and trending * Quality System Regulations * Statistical tools and quality improvement ...
CAPA Engineer
$65K - $84K/yr
The CAPA Engineer is responsible for leading and facilitating the Corrective and Preventive Action ... Data analysis and trending * Quality System Regulations * Statistical tools and quality improvement ...
Senior Quality Assurance Analyst (Medical devices) Location: Madison, WI Duration: 6+ months ... Manage CAPA initiation, review, surveillance, and reporting * Facilitate the site Quality ...
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Senior Quality Assurance Analyst (Medical devices) Location: Madison, WI Duration: 6+ months ... Manage CAPA initiation, review, surveillance, and reporting * Facilitate the site Quality ...
CAPA Engineer
El Paso, TX · On-site
$65K - $84K/yr
The CAPA Engineer is responsible for leading and facilitating the Corrective and Preventive Action ... Data analysis and trending * Quality System Regulations * Statistical tools and quality improvement ...
CAPA Engineer
El Paso, TX · On-site
$65K - $84K/yr
The CAPA Engineer is responsible for leading and facilitating the Corrective and Preventive Action ... Data analysis and trending * Quality System Regulations * Statistical tools and quality improvement ...
Quality Control / Quality Analyst Technician
Eldorado, TX · On-site
$50K - $60K/yr
... analysis, CAPA activities, mock recalls, and traceability exercises. • Collaborate with Operations, Maintenance, and FSQ teams to troubleshoot and resolve food safety and product quality issues.
New
Quality Control / Quality Analyst Technician
Eldorado, TX · On-site
$50K - $60K/yr
... analysis, CAPA activities, mock recalls, and traceability exercises. • Collaborate with Operations, Maintenance, and FSQ teams to troubleshoot and resolve food safety and product quality issues.
New
CAPA Engineer
El Paso, TX · On-site
$65K - $84K/yr
The CAPA Engineer is responsible for leading and facilitating the Corrective and Preventive Action ... Data analysis and trending * Quality System Regulations * Statistical tools and quality improvement ...
CAPA Engineer
El Paso, TX · On-site
$65K - $84K/yr
The CAPA Engineer is responsible for leading and facilitating the Corrective and Preventive Action ... Data analysis and trending * Quality System Regulations * Statistical tools and quality improvement ...
QA Engineer II - CAPA & Quality Systems Lead
Merrimack, NH · On-site
$90K/yr
CAPA * As a CAPA Coordinator, lead CAPA Request and CAPA teams throughout the CAPA process for ... Perform analysis on a new or revised standard and execute deliverables to support continuous ...
New
QA Engineer II - CAPA & Quality Systems Lead
Merrimack, NH · On-site
$90K/yr
CAPA * As a CAPA Coordinator, lead CAPA Request and CAPA teams throughout the CAPA process for ... Perform analysis on a new or revised standard and execute deliverables to support continuous ...
New
Principal Quality System Engineer - CAPA
Maple Grove, MN · On-site
$102K - $194K/yr
Provide guidance to CAPA owners and cross-functional teams on root cause analysis and solution ... Act as a Quality System resource for external audit readiness, including field action support ...
Principal Quality System Engineer - CAPA
Maple Grove, MN · On-site
$102K - $194K/yr
Provide guidance to CAPA owners and cross-functional teams on root cause analysis and solution ... Act as a Quality System resource for external audit readiness, including field action support ...
Provide guidance to CAPA owners and cross-functional teams on root cause analysis and solution ... Act as a Quality System resource for external audit readiness, including field action support ...
Provide guidance to CAPA owners and cross-functional teams on root cause analysis and solution ... Act as a Quality System resource for external audit readiness, including field action support ...
Provide guidance to CAPA owners and cross-functional teams on root cause analysis and solution ... Act as a Quality System resource for external audit readiness, including field action support ...
Provide guidance to CAPA owners and cross-functional teams on root cause analysis and solution ... Act as a Quality System resource for external audit readiness, including field action support ...
Quality Analyst Capa information
See salary details
$17.07 - $20.15
4% of jobs
$20.15 - $23.23
16% of jobs
$24.42 is the 25th percentile. Wages below this are outliers.
$23.23 - $26.31
12% of jobs
The median wage is $29.14 / hr.
$26.31 - $29.39
19% of jobs
$29.39 - $32.47
13% of jobs
$35.20 is the 75th percentile. Wages above this are outliers.
$32.47 - $35.56
12% of jobs
$35.56 - $38.64
6% of jobs
$38.64 - $41.72
6% of jobs
$41.72 - $44.80
5% of jobs
$44.80 - $47.88
3% of jobs
$47.88 - $50.96
2% of jobs
$17
$32
$50
How much do quality analyst capa jobs pay per hour?
As of Sep 11, 2026, the average hourly pay for quality analyst capa in the United States is $32.41, according to ZipRecruiter salary data. Most workers in this role earn between $24.28 and $37.02 per hour, depending on experience, location, and employer.
What cities are hiring for Quality Analyst Capa jobs?
Cities with the most Quality Analyst Capa job openings:
What states have the most Quality Analyst Capa jobs?
States with the most job openings for Quality Analyst Capa jobs include:
What are popular job titles related to Quality Analyst Capa jobs?
For Quality Analyst Capa jobs, the most frequently searched job titles are:
Quality Analyst / Pharma Controlled Substance-DEA Compliance (Hybrid Work)
Titusville, NJ • On-site
Pioneer Data
Contractor
Posted 8 days ago
Job description
Position Details:
Our client, a world-leading Pharmaceutical Company in Titusville, NJ or Horsham, PA is currently looking for a Quality Analyst to join their expanding team.
Job Title: Quality Analyst / Pharma Controlled Substance–DEA Compliance (Hybrid Work)
Duration: 4 months contract, extendable up to 24 Months
Location: Titusville, NJ or Horsham, PA
Duration: 4 months contract, extendable up to 24 Months
Location: Titusville, NJ or Horsham, PA
HYBRID, 3 days onsite, can be onsite in Titusville, NJ or Horsham, PA
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
NOTES FROM MANAGER:
Role will be HYBRID, 3 days onsite, can be onsite in Titusville, NJ or Horsham, PA
Bachelors degree is required
Must have at least 2-5 years of relevant exp
Must have Regulations knowledge
DEA Regulations knowledge as well
Exp with COMET system, or some type of Quality Mgmt System (QMS)
Must have prior Compliance exp
Role will be HYBRID, 3 days onsite, can be onsite in Titusville, NJ or Horsham, PA
Bachelors degree is required
Must have at least 2-5 years of relevant exp
Must have Regulations knowledge
DEA Regulations knowledge as well
Exp with COMET system, or some type of Quality Mgmt System (QMS)
Must have prior Compliance exp
Top 3 Skills:
Data analytics exp
Computer skills
Background in Quality or Compliance
Data analytics exp
Computer skills
Background in Quality or Compliance
Job Description:
Quality Analyst
The overall purpose of this position is to support quality activities for Commerical Quality including controlled substance requirements, quality complaints, change control, documentation, internal audit/ supplier audits. Adheres to environmental policy, procedures, and supports department environmental objectives.
The overall purpose of this position is to support quality activities for Commerical Quality including controlled substance requirements, quality complaints, change control, documentation, internal audit/ supplier audits. Adheres to environmental policy, procedures, and supports department environmental objectives.
Essential duties and responsibilities:
Process Know Your Customer applications to purchase a specific product (50%)
Conduct routine data analysis for Suspicious Order Monitoring. (10%)
Process day-to-day product quality complaint (PQC) in quality system including evaluating PQC, assigning investigation, conducting investigation, writing investigation summary. Proactively manage PQCs workflow with stakeholders to ensure all investigations are completed in a timely manner. (10%)
Process day-to-day quality events and change control records in COMET system (10%)
Coordinate documents and procedures in truVault system and any other document management system.(10%)
Coordinate internal and/or supplier audits including setting up logistic / preparation for the audits, drafting audit plan, supporting audit execution, coordinating audit response and CAPA with stakeholders, creating and documenting audit records in system. Ensure all audit commitments are delivered on time (10%)
Process Know Your Customer applications to purchase a specific product (50%)
Conduct routine data analysis for Suspicious Order Monitoring. (10%)
Process day-to-day product quality complaint (PQC) in quality system including evaluating PQC, assigning investigation, conducting investigation, writing investigation summary. Proactively manage PQCs workflow with stakeholders to ensure all investigations are completed in a timely manner. (10%)
Process day-to-day quality events and change control records in COMET system (10%)
Coordinate documents and procedures in truVault system and any other document management system.(10%)
Coordinate internal and/or supplier audits including setting up logistic / preparation for the audits, drafting audit plan, supporting audit execution, coordinating audit response and CAPA with stakeholders, creating and documenting audit records in system. Ensure all audit commitments are delivered on time (10%)
Required: BA/BS – Technical / Life Science
Desirable: MA/MS/MBA – Business / Technical /Life Science
Support Quality and Compliance Initiatives from Enterprise Quality and/or Global Business Quality
Desirable: MA/MS/MBA – Business / Technical /Life Science
Support Quality and Compliance Initiatives from Enterprise Quality and/or Global Business Quality
Essential knowledge and skills
Knowledge
2-5 years’ experience in the Pharmaceutical or related industry;
Up-to-date knowledge of relevant pharmaceutical legislation and GMP / GDP;
Up-to-date knowledge of DEA regulations
Experience working in the quality organization.
Knowledge
2-5 years’ experience in the Pharmaceutical or related industry;
Up-to-date knowledge of relevant pharmaceutical legislation and GMP / GDP;
Up-to-date knowledge of DEA regulations
Experience working in the quality organization.
Skills
Highly experienced in COMET system, generating query and report, and data analysis with excel spreadsheet
Results-driven leader who commits to stretch goals and delivers results.
Ability to build and nurture strong, positive relationships with business partners in IT, Manufacturing, Regulatory Affairs, Commercial and Quality functional groups.
Demonstrated understanding of regulatory requirements that impact Market Quality specifically, and client's more broadly. Experience in dealing with regulatory inspections and inspectional requirements
Highly experienced in COMET system, generating query and report, and data analysis with excel spreadsheet
Results-driven leader who commits to stretch goals and delivers results.
Ability to build and nurture strong, positive relationships with business partners in IT, Manufacturing, Regulatory Affairs, Commercial and Quality functional groups.
Demonstrated understanding of regulatory requirements that impact Market Quality specifically, and client's more broadly. Experience in dealing with regulatory inspections and inspectional requirements
Core competencies required for this role:
Credo Values
Innovation
Masters Complexity
Customer/ Marketplace Focus
Independent Partnering
Credo Values
Innovation
Masters Complexity
Customer/ Marketplace Focus
Independent Partnering