Job Description
Prostaff Workforce Solutions is currently seeking a highly motivated and experienced
Manager, Quality Assurance to join our client’s team in the nutraceutical industry in
New Brunswick, NJ 08901 . If you believe you are qualified, we would be excited to connect and discuss this opportunity in more detail.
Full time OnSite
Direct Hire Responsibilities The Manager, Quality Assurance (QA) is responsible for overseeing quality activities regarding the safety, consistency, and quality of our products, This includes developing, implementing and maintaining quality programs, policies and procedures to improve product quality and ensure products are produced in compliance with product standards, good manufacturing practices and in accordance with government regulations
• In addition, this role will be required to interact with both internal and external customers, as well as quality and regulatory agencies and manage a staff of both quality assurance and quality control technicians
• The individual in this position must establish and maintain relationships with direct reports in addition to other departments in the organization to effectively cultivate a culture of continuous improvement in which quality, safety, and productivity goals are measured and met
• Responsible for all aspects of company Quality Assurance and Regulatory Affairs in compliance with local, state, and federal food safety standards at our dietary supplement manufacturing facility
• Develops, implements, monitors, and continuously improves programs to ensure compliance with industry standards for food and dietary supplements (cGMP, GLP, CFR 100, CFR 111, HACCP, FSMA, SQF, etc.)
• Leads internal, external customer & other regulatory agency audits & escalates any quality control and food safety issues and presents plausible solutions
• Works with R&D and Manufacturing departments in the development, scale-up, and testing of new products, processes, and equipment
• Produce release documentation for each lot of finished product
Develop statistically significant sampling plans for incoming raw ingredients and in-process quality checks to insure safety and quality
• Oversee and develop the corporate Facility Audit Program to help assure compliance to internal/external requirements, including customer requirements and strategic initiatives
• Conduct training and re-certification as appropriate for quality and other manufacturing personnel
• Recruit, train, develop, and lead staff to accomplish personal and organizational goals, adhere to policies/procedures and establish/maintain a ‘culture of quality’
• Ensures timely resolution to customer inquiries (audit findings and complaints)
• Generate, review or approve Quality Assurance related documentation required for customer relationship/product development (such as: development, supply and quality agreement), verification of compliance, or for filings with regulatory bodies
• Reviews data, analyzes results and recommends changes based upon findings and performs follow up to verify effectiveness
• Oversee Document Control and lead Change Control (formulas, raw materials, and packaging materials) systems
• Responsible for Raw Materials Supplier Qualification activities including the supplier audit program
• Organize and ensure the completion of all product investigations, Non-Conformances, OOS’s, and CAPAs, including documenting and reporting adverse and serious adverse events
• Prepare periodic reports, quality scorecards and analyses to executive management
• Direct and oversee the work of quality assurance and quality control technicians, including training, mentoring, and ensuring professional development
• Experience with quality assurance software that allows integration of product development, quality control (testing specs), quality assurance, project management, purchasing, as external vendors
• Develop and maintain a product testing lab for all composition and microbial testing of all raw ingredients and finished products
• Responsible for regulatory compliance of NFP’s, SFP’s and other product label claims
• Maintain all current facility certifications along with scoping and adding additional certifications
• Perform other duties as assigned depending upon business needs
Qualifications • Bachelor’s degree in a relevant field such as chemistry, biology, or pharmaceutical sciences
• Minimum of five years’ experience working in a Quality function at a food or dietary supplement manufacturing facility
• FDA Audit experience required
• 5+ years in QA/QC and Compliance
• HACCP certification or the ability to write a HACCP plan
• Ability to adapt to frequent changes, unexpected events and still yield an effective outcome
• Ability to use MS Word, Excel, Outlook, ERP, quality management software
• Strong interpersonal skills, detail oriented and able to coordinate/manage multiple tasks simultaneously
• Solid understanding of manufacturing processes, process development, and troubleshooting
• Maintains high level of confidentiality
• Ability to work within a team environment, as well as independently, with minimal supervision
• Excellent organizational and interpersonal skills
• Ability to perform effectively and efficiently in a fast-paced environment
• Effectively influences actions and opinions of others
• Accepts feedback from others, ability to engender enthusiasm, motivate peers and subordinates and team building
• Manages competing demands, makes timely and sound decisions, even under conditions of risk
Our client offers a competitive compensation package as well as an excellent benefits package for eligible candidates.
Please visit us at to explore all opportunities.
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Job Tags
Full time, Local area,