Manager, Quality Control (USA) Salary at Stonhard Ltd BETA

Quality Control Manager The Quality Control Manager is responsible for overseeing and managing the quality control processes related to primary packaging materials and finished products. This role ensures that packaging materials meet quality standards, regulatory requirements, and company specifications. Responsibilities: Develop, implement, and maintain quality control procedures and standards for primary packaging materials Conduct regular inspections and testing of packaging materials to ensure compliance with specifications and regulatory requirements Identify and address any quality issues, including investigating root causes and implementing corrective actions Maintain accurate and detailed records of quality control inspections, test results, and compliance reports Prepare and present quality reports and metrics to management, highlighting key issues, trends, and improvements Ensure all documentation is up-to-date and in compliance with company policies and regulatory standards

Ideal candidates will have extensive experience in FDA, AATB and other applicable regulations and standards. LHH Recruitment Solutions has Quality Control Manager opening for our client in the Conshohocken, PA area. This direct hire role allows you to collaborate with numerous departments to facilitate quality control and process improvement as well as strategic sourcing. This on-site position requires a bachelor’s degree in Biological Science or similar, and 5+ years in a medical device manufacturing Quality Control Manager role. Ideal candidates will have extensive experience in FDA, AATB and other applicable regulations and standards. Salary range: $80,000 to $90,000 RESPONSIBILITIES: Oversee the planning, directing, and/or coordinating quality programs, quality control, within laboratory and production efforts in a manufacturing environment. Maintain a constant working knowledge of FDA 21 CFR 1271, FDA 21 CFR 820, AATB, other regulations and industry standards Create, revise and im

Type: full time/direct hire Salary: $130k - $140k Location: Pennington, NJ (100% onsite) Position Overview Quality Control Raw Material Manager will ensure that the raw materials and consumables used in production meet the required quality standards. Key Responsibilities Oversight: Oversee or execute the inspection, sampling and testing of incoming raw materials and consumables. Manage technology transfer of raw materials and consumables test methods. Compliance: Design and implement Raw Materials Qualification program in compliance with FDA and EMA regulations. Ability to conduct risk assessments and implement risk mitigation strategies for raw materials. Manage laboratory activities: Oversee or execute testing as needed on incoming raw materials and consumables, review the associated data, maintain accurate records of all inspections, test, vendor notifications and supplier evaluations. Problem Solving: Resolve technical problems in the lab. Lead investigation for out of specificatio

POSITION SUMMARY: To efficiently manage the day-to-day operation of the shift manufacturing function while producing top quality and safe beverage products following company policies and procedures. REPRESENTATIVE RESPONSIBILITIES: The following responsibilities are general duties that a particular employee in this position may or may not be required to perform. The actual duties required of this position will vary. Directs a work force of between 15 and 20 hourly employees, including line machine operators, lab technicians and mechanics. Works closely with other shift production supervisors for exchange of information and to assure continuity of production activities across shifts. Partner with Maintenance Supervisor to coordinate repairs and preventive maintenance of production equipment; Quality Control Manager to coordinate quality control activities and corrective actions; Warehouse Supervisors to coordinate availability of materials stored in warehouse; Logistics Supervisor and o

Job Description Job Description Job Summary: Manage, direct, and guide all laboratory operations and oversee the activities of QC Technicians. Responsibilities: · Provide supervision and direction to quality Control staff consisting of QC technicians and QC laboratory Technicians. · Performs the role of SQF practitioner for the facility, responsible for the development, implementation, oversight and continuous improvement of the SQF 2000 program. Responsible for the Food Safety and Food Quality functions of the SQF Program, overseeing both programs and ensuring dissemination of regulatory requirements and compliance with raw material and finished product specifications. · Monitor products and process performance with respect to compliance to established government, customer and company standards. · Maintain the main production laboratory equipment, chemicals, reagents and supplies that are required to perform production and laboratory quality Control functions. · Provide the company th

Job Description Job Description Doyon Government Group (DGG) provides Design-Build and General Construction Services on demolition, new construction, renovations, repairs, and civil projects at government-owned facilities and military installations. DGG hires Construction QC Managers nationwide for U.S. Army Corps of Engineers (USACE) and Naval Facilities Engineering Command (NAVFAC) construction projects. The Construction Quality Control Manager (QCM) holds the primary responsibility of directly reporting to the Project Manager and Corporate Management regarding the verification of adherence to all quality standards across our projects. Operating at the project level, the Quality Control Manager plans, coordinates, and supervises the implementation of construction quality control and quality assurance programs. Additionally, this position is tasked with creating, reviewing, and amending Project Quality Plans to keep current and ensure compliance with the contract, established standard

Shift: Monday to Friday from 11:00pm to 7:30am Overview The Manager, Quality Control (QC) Microbiology, is responsible for oversight of day-to-day microbial QC operations at Cell Therapy Center (iCTC). The role will be responsible for working in a GMP- regulated environment and have good understanding of QC microbiology test methods and environmental monitoring. This role must be able to apply phase appropriate cGMPs and regulatory requirements in the product development life cycle, including but not limited to: lot release and stability testing, method qualification and validation, method technology transfers, and writing/review of QC procedures. Essential Functions and Responsibilities Manage several analysts at the iCTC in the day-to-day cGMP QC testing of drug products for lot release and stability; Manage microbial testing at contract laboratories Manage the technical transfer, qualification, and validation of microbiology test methods for in- process materials, lot release, and/o

Why Endo? We want the best and brightest people at Endo to help us achieve our mission to develop and deliver life-enhancing products through focused execution. Our nearly 3,000 global team members understand the important role we play in delivering healthcare and are dedicated to supporting each other as we work to bring the best treatments forward. Our shared values of Integrity & Quality, Innovation, Drive, Collaboration and Empathy guide our team and enable us to deliver upon our vision of helping everyone we serve live their best life. At Endo, we are building a diverse, equitable and inclusive workplace, and we are looking for talented individuals to join our team. Job Description Summary The QC Analyst II - Microbiology will perform microbiological testing, release of in-process, intermediates and finished products, and testing for validation purposes. This role is responsible for authoring new SOPs and/or revising of existing documentation. Additionally, this role is responsibl