Business Services & Consulting • Waunakee, WI 53597
Job Title: Quality Systems Specialist – CAPAs and DeviationsJob Description
The Quality Systems Specialist supports cGMP quality system activities within a biopharmaceutical manufacturing environment, with a primary focus on managing corrective and preventive actions (CAPAs) and deviations. This role executes and maintains key quality processes, including GMP training programs, validation and qualification document review, investigations, change controls, and CAPAs. The specialist collaborates cross‑functionally to ensure adherence to quality system procedures, supports continuous improvement initiatives, and helps maintain regulatory compliance and product quality through effective governance of quality systems.
Responsibilities
Oversee the CAPA system on a daily basis, including tracking actions, monitoring progress, and driving timely closure of CAPAs.
Initiate, review, and manage deviations, ensuring accurate documentation, appropriate impact assessment, and effective follow‑up actions.
Request and manage CAPA and deviation extensions when necessary, ensuring clear justification and compliance with internal procedures.
Execute and maintain cGMP quality system processes, including GMP training programs, validation and qualification document review, and change controls.
Review quality documentation such as validation and qualification records, change control records, and batch records to ensure accuracy, completeness, and compliance.
Support and participate in internal audits, contributing to audit preparation, execution, and follow‑up activities.
Support external audit readiness by maintaining compliant quality systems, documentation, and training records.
Manage and maintain training documentation, ensuring that training records are accurate, up to date, and aligned with GMP requirements.
Contribute to the preparation of Annual Product Reviews (APRs) and support change control governance activities to maintain regulatory compliance.
Collaborate cross‑functionally with manufacturing, quality control, and other departments to resolve quality issues and drive continuous improvement.
Support continuous improvement initiatives within the quality management system, identifying opportunities to enhance processes and compliance.
Ensure quality system activities comply with FDA regulations, cGMP requirements, and internal quality policies and procedures.
Perform document control activities as needed, ensuring controlled documents are properly reviewed, approved, and maintained within the quality management system.
Essential Skills
Bachelor's degree or above in a scientific discipline.
At least 2 years of Quality Assurance or Quality Systems experience in the biopharmaceutical or pharmaceutical industry.
At least 2 years of experience working with CAPAs and deviations in a regulated environment.
Demonstrated experience with cGMP quality systems, including investigations, deviations, CAPAs, and change controls.
Working knowledge of FDA regulations and compliance expectations for biopharmaceutical or pharmaceutical manufacturing.
Experience with quality management systems and quality system procedures in a GMP environment.
Ability to review and interpret quality documentation, including validation and qualification documents, training records, and batch records.
Strong attention to detail and accuracy in documentation and record keeping.
Ability to collaborate effectively with cross‑functional teams and communicate clearly in a regulated environment.
Additional Skills & Qualifications
Experience with internal audits and familiarity with internal and external audit processes.
Exposure to or experience with quality auditing and audit preparation activities.
Experience with document control processes and systems within a quality management framework.
Experience reviewing batch records and related GMP documentation.
Familiarity with Annual Product Review (APR) preparation and change control governance.
Demonstrated ability to support continuous improvement initiatives within quality systems.
Strong organizational skills and the ability to manage multiple CAPAs, deviations, and quality system tasks simultaneously.
Work Environment
This role is based in a biopharmaceutical manufacturing environment that operates under cGMP and FDA regulatory requirements.The position is part of a quality systems team that includes Quality Management System Specialists and Document Control Technicians, with plans for team growth.The team sits together in a shared office space within a primary building, fostering collaboration and communication.The role follows a first‑shift schedule, Monday through Friday, with a flexible start time between 7:00 a.m. and 9:00 a.m., working an eight‑hour day.
The work involves regular interaction with manufacturing, quality control, and other functional groups, as well as extensive use of electronic quality systems and documentation tools.
Job Type & Location
This is a Permanent position based out of Waunakee, WI.
Pay and Benefits
The pay range for this position is $52000.00 - $80000.00/yr.
Competitive compensation; excellent benefits package - including Medical, Dental and Vision on Day 1; Life and AD&D Insurance, and Short and Long-term Disability; Health and Flexible Saving Account options; Employee Assistance Program, generous vacation; paid Holidays; 401k
Workplace Type
This is a fully onsite position in Waunakee,WI.
Application Deadline
This position is anticipated to close on Jul 8, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions.We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market.With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.
Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.
Job Title: Quality Systems Specialist – CAPAs and DeviationsJob Description
The Quality Systems Specialist supports cGMP quality system activities within a biopharmaceutical manufacturing environment, with a primary focus on managing corrective and preventive actions (CAPAs) and deviations. This role executes and maintains key quality processes, including GMP training programs, validation and qualification document review, investigations, change controls, and CAPAs. The specialist collaborates cross‑functionally to ensure adherence to quality system procedures, supports continuous improvement initiatives, and helps maintain regulatory compliance and product quality through effective governance of quality systems.
Responsibilities
Oversee the CAPA system on a daily basis, including tracking actions, monitoring progress, and driving timely closure of CAPAs.
Initiate, review, and manage deviations, ensuring accurate documentation, appropriate impact assessment, and effective follow‑up actions.
Request and manage CAPA and deviation extensions when necessary, ensuring clear justification and compliance with internal procedures.
Execute and maintain cGMP quality system processes, including GMP training programs, validation and qualification document review, and change controls.
Review quality documentation such as validation and qualification records, change control records, and batch records to ensure accuracy, completeness, and compliance.
Support and participate in internal audits, contributing to audit preparation, execution, and follow‑up activities.
Support external audit readiness by maintaining compliant quality systems, documentation, and training records.
Manage and maintain training documentation, ensuring that training records are accurate, up to date, and aligned with GMP requirements.
Contribute to the preparation of Annual Product Reviews (APRs) and support change control governance activities to maintain regulatory compliance.
Collaborate cross‑functionally with manufacturing, quality control, and other departments to resolve quality issues and drive continuous improvement.
Support continuous improvement initiatives within the quality management system, identifying opportunities to enhance processes and compliance.
Ensure quality system activities comply with FDA regulations, cGMP requirements, and internal quality policies and procedures.
Perform document control activities as needed, ensuring controlled documents are properly reviewed, approved, and maintained within the quality management system.
Essential Skills
Bachelor's degree or above in a scientific discipline.
At least 2 years of Quality Assurance or Quality Systems experience in the biopharmaceutical or pharmaceutical industry.
At least 2 years of experience working with CAPAs and deviations in a regulated environment.
Demonstrated experience with cGMP quality systems, including investigations, deviations, CAPAs, and change controls.
Working knowledge of FDA regulations and compliance expectations for biopharmaceutical or pharmaceutical manufacturing.
Experience with quality management systems and quality system procedures in a GMP environment.
Ability to review and interpret quality documentation, including validation and qualification documents, training records, and batch records.
Strong attention to detail and accuracy in documentation and record keeping.
Ability to collaborate effectively with cross‑functional teams and communicate clearly in a regulated environment.
Additional Skills & Qualifications
Experience with internal audits and familiarity with internal and external audit processes.
Exposure to or experience with quality auditing and audit preparation activities.
Experience with document control processes and systems within a quality management framework.
Experience reviewing batch records and related GMP documentation.
Familiarity with Annual Product Review (APR) preparation and change control governance.
Demonstrated ability to support continuous improvement initiatives within quality systems.
Strong organizational skills and the ability to manage multiple CAPAs, deviations, and quality system tasks simultaneously.
Work Environment
This role is based in a biopharmaceutical manufacturing environment that operates under cGMP and FDA regulatory requirements.The position is part of a quality systems team that includes Quality Management System Specialists and Document Control Technicians, with plans for team growth.The team sits together in a shared office space within a primary building, fostering collaboration and communication.The role follows a first‑shift schedule, Monday through Friday, with a flexible start time between 7:00 a.m. and 9:00 a.m., working an eight‑hour day.
The work involves regular interaction with manufacturing, quality control, and other functional groups, as well as extensive use of electronic quality systems and documentation tools.
Job Type & Location
This is a Permanent position based out of Waunakee, WI.
Pay and Benefits
The pay range for this position is $52000.00 - $80000.00/yr.
Competitive compensation; excellent benefits package - including Medical, Dental and Vision on Day 1; Life and AD&D Insurance, and Short and Long-term Disability; Health and Flexible Saving Account options; Employee Assistance Program, generous vacation; paid Holidays; 401k
Workplace Type
This is a fully onsite position in Waunakee,WI.
Application Deadline
This position is anticipated to close on Jul 8, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions.We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market.With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.
Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.
