Manager, QC Salary at Nexuspharma BETA

Senior Quality Control Analyst needed! Overview: Seeking a Senior Analyst, Quality Control (QC) Raw Materials, who will be responsible for the sampling, release testing, data review, and vendor qualification, for all raw material lots received for use in the manufacturing of product. These activities include chemical and biological raw materials, component inspection, and final packaging. A good understanding of QC test methods and raw materials release requirements per USP and EP compendia, is desired. Experience working in a GMP-regulated environment is essential. The position will report to the Raw Materials - QC Manager, 3rd Floor Laboratory. Essential Functions and Responsibilities: Support the planning and establishment of the initial setup of internal raw material testing laboratory. Perform day-to-day activities for raw material release testing, including but not limited to USP<71> Sterility, USP <61> Growth Promotion, USP <63> / EP 2.6.7 Mycoplasma, USP<85> Bacterial Endotoxin

We offer HEALTH & DENTAL BENEFITS DAY 1 OF HIRE! Blommer understands that our employees are our biggest assets. With this in mind we offer a generous benefits package, tuition reimbursement, and 10 pounds of free chocolate for your birthday! Blommer has been providing delicious, high quality chocolate and cocoa products to customers since 1939. Built as a family business, we are continuing to grow and are looking for motivated and reliable associates to help in our mission of Bringing Chocolate to Life! Job Purpose: The Food Safety & HACCP Coordinator is responsible for monitoring, maintaining, and improving food safety and quality systems in efforts to meet or exceed regulatory and customer expectations with regard to food safety and quality. This role is responsible for food safety activities within the operations. Essential Duties and Responsibilities: Food Safety Responsible for food safety functions including maintenance of food safety system, food safety forms, maintaining databa

A renowned biopharmaceutical organization is looking to hire a strong microbiology leader that'll be responsible for leading key activities within the microbiology team and provide oversight of the QC Microbiology team including managing the training of junior microbiology staff and the qualification and validation of new assays to name a few. If you're interested in utilizing your leadership skills and microbiology expertise to lead an exciting team, please apply in and read the below for more information: Responsible for planning and prioritizing resource allocation for the quality control microbiology laboratory to meet testing requirements for product release, raw materials, utilities, and in-process samples. Oversee the QC Microbiology testing area including bioburden and endotoxin, and other microbiology testing areas. Manage the transfer of assays from the development group, qualify and validate new assays, and implement assays for quality control purposes to support manufacturi

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 Quality Control 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, establi

Judge Direct Placement is seeking a Quality Control Manager in Willingboro, NJ area! Candidates must have experience in metals manufacturing environment. Responsibilities: Read blueprints and specifications. Monitor operations to ensure that they meet production standards. Recommend adjustments to the assembly or production process. Inspect, test, or measure materials. Measure products with calipers, gauges, or micrometers. Operate electronic inspection equipment and software.

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

The Quality Analyst Sr. works with different servicing departments and internal team to ensure the business meets guidelines and perform in accordance to procedures.. The Analyst may evaluate transaction folders, correspondence between team members, consumers, clients, and third parties to ensure that the business objectives are met. This role maintains deep knowledge of the business processes, changes to existing regulations and new procedures and requirements being implemented. The position collaborates with the line of business; management team to implement successful action plans that improve overall quality metrics and ensure quality performance leading to excellent customer service. Responsibilities: Monitors changes to operational procedures from relevant Business Units and Departments Performs ongoing, structured, and rigorous testing of key procedures and controls within all business units Identifies opportunities for cost and risk reduction, efficiency gains, and enhanced lev

Work Schedule First Shift (Days) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards Job Description Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission - to enable our clients to make the world healthier, safer, and cleaner. Within our Analytical Services team, we have a functional service provider solution, which is an outstanding partnership that allows our customers to use the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits. The Associate scientist will perform a variety of routine to complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices. Follow