MANAGER QUALITY (5023)
Nice Pak Products
The Manager, Quality Assurance is accountable for the performance and compliance of assigned quality systems and operational areas within a regulated contract manufacturing environment. This position provides final quality review and disposition decisions for raw materials, in-process materials, and finished goods, ensuring products meet established specifications, regulatory requirements, and customer expectations.
This role operates with a high degree of autonomy and decision-making authority, serving as a primary Quality leader for the site. The Manager, Quality Assurance is responsible for ensuring effective implementation of cGMP requirements (21 CFR Parts 210/211), maintaining inspection readiness, and supporting a proactive quality culture focused on risk mitigation and continuous improvement. The position serves as a primary Quality representative for contract manufacturing customers, owning quality communications, documentation, and audit readiness. Key Responsibilities Quality System Ownership & Decision Authority- Own and maintain assigned quality systems, including but not limited to deviations, investigations (OOS/OOT), CAPA, change control, batch record review, and product disposition
- Provide final quality review and release/disposition decisions for materials and finished products
- Exercise independent decision-making authority for routine and non-routine quality events, ensuring compliance with cGMP and customer requirements
- Escalate significant quality risks (e.g., recall risk, critical events) in accordance with established procedures
- Provide QA oversight of liquid fill manufacturing operations to ensure compliance with cGMPs, internal procedures, and customer-specific requirements
- Support real-time decision-making on the production floor related to deviations, non-conforming materials, and process issues
- Ensure effective execution of in-process controls and finished product inspection requirements
- Serve as the primary Quality representative for assigned contract manufacturing customers
- Lead customer quality discussions, governance meetings, and issue resolution calls independently
- Own all customer quality communications, including:
- Deviations and investigations
- Complaint responses
- Customer notifications and regulatory commitments
- Prepare and review customer-specific documentation, including:
- Questionnaires and technical requests
- Specifications and supporting quality data
- Audit responses and follow-up documentation
- Lead and/or support customer audits, ensuring transparency, professionalism, and inspection readiness
- Ensure compliance with applicable regulatory requirements, including FDA, EPA, DNR, ATF, and OSHA
- Maintain inspection readiness at all times; support and lead regulatory inspections and customer audits
- Ensure adherence to data integrity principles (ALCOA+) across all quality systems and documentation
- Ensure consistent and compliant application of site procedures and quality standards
- Lead and approve investigations, including OOS, OOT, deviations, and nonconformances
- Ensure robust root cause analysis and implementation of effective corrective and preventive actions
- Monitor and trend quality data to identify emerging risks and drive proactive improvements
- Apply risk-based decision making consistent with ICH Q9 principles
- Ensure validation programs comply with regulatory requirements and internal procedures
- Oversee quality impact assessments and approvals within the change control system
- Ensure appropriate evaluation of changes for regulatory, product quality, and customer impact
- Directly supervise and develop quality personnel, including both hourly and salaried employees
- Ensure effective training, qualification, and ongoing development of staff
- Provide performance management, coaching, and leadership to drive a high-performing quality organization
- Foster a culture of accountability, ownership, and continuous improvement
- Partner cross-functionally with Manufacturing, Supply Chain, Engineering, and R&D to resolve quality issues and improve performance
- Drive continuous improvement initiatives to enhance product quality, reduce variability, and improve efficiency
- Support site quality metrics and ensure alignment with business and customer expectations
- Bachelor's degree in Chemistry, Microbiology, Engineering, or related scientific discipline required
- Minimum 10 years of experience in a regulated industry (OTC drug, pharmaceutical, cosmetic, or similar)
- Minimum 5 years of progressive leadership experience in Quality Assurance or Quality Systems
- Demonstrated experience supporting FDA inspections and customer audits
- Experience in a contract manufacturing environment strongly preferred
- Strong knowledge of cGMP requirements (21 CFR Parts 210/211) and quality system expectations
- Demonstrated ability to make independent, risk-based quality decisions
- Strong investigation skills, including root cause analysis and CAPA effectiveness
- Excellent technical writing and documentation skills
- Strong communication skills with the ability to interface effectively with customers and all levels of the organization
- Ability to manage multiple priorities in a fast-paced manufacturing environment
- High level of accountability, ownership, and professional judgment
- Work is performed in a combination of office, laboratory-adjacent, and manufacturing environments
- Regular exposure to production areas with varying temperatures, noise levels, and proximity to operating equipment
- Required use of appropriate personal protective equipment (PPE)
- Regularly required to stand, walk, use hands, and communicate effectively
- Frequently required to move throughout manufacturing and warehouse areas
- Occasional lifting of materials up to 40-50 pounds; frequent handling of light samples (1-5 pounds)
- Requires visual acuity for detailed review of documentation and inspection activities, including ability to distinguish color and fine detail
- Bachelor's degree in Chemistry, Microbiology, Engineering, or related scientific discipline required
- Minimum 10 years of experience in a regulated industry (OTC drug, pharmaceutical, cosmetic, or similar)
- Minimum 5 years of progressive leadership experience in Quality Assurance or Quality Systems
- Demonstrated experience supporting FDA inspections and customer audits
- Experience in a contract manufacturing environment strongly preferred
- Strong knowledge of cGMP requirements (21 CFR Parts 210/211) and quality system expectations
- Demonstrated ability to make independent, risk-based quality decisions
- Strong investigation skills, including root cause analysis and CAPA effectiveness
- Excellent technical writing and documentation skills
- Strong communication skills with the ability to interface effectively with customers and all levels of the organization
- Ability to manage multiple priorities in a fast-paced manufacturing environment
- High level of accountability, ownership, and professional judgment
- Work is performed in a combination of office, laboratory-adjacent, and manufacturing environments
- Regular exposure to production areas with varying temperatures, noise levels, and proximity to operating equipment
- Required use of appropriate personal protective equipment (PPE)
- Regularly required to stand, walk, use hands, and communicate effectively
- Frequently required to move throughout manufacturing and warehouse areas
- Occasional lifting of materials up to 40-50 pounds; frequent handling of light samples (1-5 pounds)
- Requires visual acuity for detailed review of documentation and inspection activities, including ability to distinguish color and fine detail
Vacancy posted 3 days ago
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