Find & Apply For Quality Control Systems Manager Jobs in Wall Township, New Jersey

Quality Control Manager Location:

Wall, NJ Salary Range:

$90,000-$100,000

Requirement:

Bilingual Position Overview We are seeking an experienced Quality Control Manager to oversee and manage Quality Control (QC) operations within a regulated manufacturing environment. The Quality Control Manager will ensure that raw materials, in-process materials, finished products, and laboratory activities meet established quality standards, specifications, regulatory requirements, and customer expectations. This individual will lead the QC team and oversee laboratory testing, documentation, material and product release, investigations, and continuous improvement initiatives. The Quality Control Manager will work closely with Quality Assurance, Manufacturing, R&D, Warehouse, and Supply Chain to maintain a strong culture of quality and compliance. Candidates must be bilingual. Key Responsibilities Quality Control Management Manage day-to-day QC activities, including laboratory testing, sampling, inspection, and product evaluation. Lead, coach, train, and develop QC personnel. Establish department priorities, schedules, and workload assignments to support production timelines. Ensure raw materials, packaging components, in-process materials, and finished products are tested according to approved specifications and procedures. Review and approve laboratory results, test data, and QC documentation for accuracy and compliance. Ensure timely communication of testing results to Quality Assurance and other departments. Monitor testing turnaround times and identify opportunities to improve laboratory efficiency. Laboratory & Testing Oversee laboratory testing using established methods, specifications, and procedures. Ensure appropriate sampling and testing of incoming raw materials and finished products. Manage analytical testing performed internally and through third-party laboratories. Review Certificates of Analysis (COAs) and analytical reports. Ensure laboratory equipment is properly maintained, calibrated, and qualified. Maintain appropriate laboratory controls, records, and documentation. Ensure testing methods remain current and compliant with applicable requirements. Investigations & Nonconformance Lead and support investigations involving Out-of-Specification (OOS), Out-of-Trend (OOT), deviations, nonconformances, complaints, and laboratory errors . Partner with Quality Assurance to conduct root-cause analysis and implement Corrective and Preventive Actions (CAPA) . Ensure investigations are thorough, timely, scientifically sound, and properly documented. Identify recurring quality issues and recommend corrective actions and process improvements. cGMP & Regulatory Compliance Ensure QC activities comply with applicable FDA requirements, cGMP regulations, company policies, SOPs, and quality standards . Maintain compliance with requirements applicable to dietary supplement and nutraceutical manufacturing . Support internal, customer, regulatory, and third-party audits and inspections. Provide QC documentation and technical information during audits. Maintain accurate, complete, and traceable laboratory records. Promote strong data integrity and Good Documentation Practices (GDP) throughout the department. Cross-Functional Collaboration Partner with Quality Assurance to support product release and overall quality systems. Work with Manufacturing to resolve production-related quality issues. Collaborate with R&D on product specifications, testing requirements, and analytical methods. Partner with Purchasing and Supply Chain on raw-material and supplier quality concerns. Communicate quality trends, risks, and concerns to senior management. Provide technical guidance regarding testing, specifications, and quality requirements. Continuous Improvement Identify opportunities to improve QC processes, laboratory efficiency, testing procedures, and documentation. Establish and monitor KPIs and quality metrics . Participate in quality and process-optimization initiatives. Develop and update QC SOPs, specifications, forms, and work instructions. Support implementation of new laboratory equipment, technologies, and testing methodologies. Leadership Responsibilities Directly supervise and develop QC employees. Conduct training, coaching, and performance evaluations. Ensure employees are properly trained on SOPs, laboratory procedures, cGMP requirements, safety practices, and documentation standards . Establish clear expectations and accountability. Promote teamwork, professionalism, and a quality-focused culture. Qualifications Required Bilingual proficiency required. Bachelor's degree in Chemistry, Biology, Food Science, Pharmaceutical Science, Quality, or a related scientific discipline . 5+ years of Quality Control, Quality Assurance, laboratory operations, or related experience within a regulated manufacturing environment. 2+ years of supervisory or management experience. Experience within a cGMP-regulated manufacturing environment . Strong knowledge of laboratory testing, specifications, sampling, and quality documentation. Experience with OOS investigations, deviations, CAPA, and root-cause analysis . Strong understanding of cGMP and GDP requirements . Strong analytical, organizational, problem-solving, and communication skills. Ability to manage multiple priorities in a fast-paced manufacturing environment. Preferred Experience within nutraceutical, dietary supplement, food, pharmaceutical, or similar regulated manufacturing environments . FDA-regulated manufacturing experience. Raw-material and finished-product testing experience. Experience managing third-party laboratory testing. Familiarity with LIMS, ERP, and/or eQMS systems . Experience supporting customer, regulatory, and third-party audits.

HACCP, PCQI, ASQ

, or related quality certifications. Knowledge & Skills Strong knowledge of cGMP requirements and quality systems. Understanding of dietary supplement/nutraceutical manufacturing. Strong understanding of laboratory testing and analytical principles. Ability to interpret specifications, laboratory results, COAs, and technical documentation. Strong investigation and root-cause analysis capabilities. Excellent written and verbal communication skills. Strong leadership and team-management skills. Data-driven decision-making abilities. Strong organizational and time-management skills. Proficiency with Microsoft Office, particularly Excel and Word. Key Performance Indicators Performance may be measured through: QC testing turnaround time and timely product/material release. OOS/OOT investigation completion. Laboratory error rate and testing accuracy. Data integrity and audit findings. CAPA effectiveness. Equipment calibration and maintenance compliance. SOP and training compliance. QC department productivity and efficiency. Customer and internal quality complaints. Physical Requirements Ability to work in manufacturing and laboratory environments. Ability to stand, walk, and move throughout the facility as required. Ability to occasionally lift or move materials and laboratory supplies. Ability to wear required personal protective equipment (PPE). Ability to work around active manufacturing operations. MOHR Talent is an equal-opportunity employer and complies with all applicable federal, state, and local nondiscrimination laws. We provide equal employment opportunities regardless of race, color, religion, sex, national origin, age, disability, marital status, sexual orientation, gender identity, genetic information, military/veteran status, or any other protected status. If you believe you have been discriminated against or have concerns about our compliance, please contact our Human Resources department at hr@themohrgrp.com