Manager, QC Salary at Binsky BETA

Hiring for QC Analysts Level's I-III Essential Functions And Responsibilities Run routine experiments such as flow cytometry, cell culture, ELISA, qPCR, endotoxin, ect. Performs the accurate execution of all company and/or client test methods and procedures of cellular products to ensure the safety and/or efficacy of different cell populations Performs maintenance, monitoring, and troubleshooting of pertinent equipment Performs and assists in the training of other Quality Control technicians Maintains training records and coordinates records retention with Document Control and Training groups Tests, documents, and reports results for products or materials following company and/or client procedures following CGMP and/or GTP guidelines Performs state proficiency testing and/or client proficiency testing under direct supervision as applicable Participates in managing QC materials and supplies Performs and assists in equipment and method qualification/validation activities as needed Perfor

QC Analytical Associate III – Allendale, NJ Our vision is creating future cell therapy miracles together. We are a leading global contract development and manufacturing organization dedicated to the advancement of cell and gene therapy products. We believe in the transformative potential of cell and gene therapies, and we are shaping the future of medicine. We open doors in the regenerative medicine industry for those looking to transform medicine while continuously improving an innovative, growing company. The Quality Control Analytical Associate III serves as a support role to clinical and commercial production. The QC Analytical Associate III will assist with process check point, stability, and release analytical testing to ensure that quality standards are upheld for all products produced at the facility. Essential Functions and Responsibilities: Performs accurate execution of all company and/or client test methods and procedures of cellular products to ensure the safety and/or eff

QC Microbiology Manager – Allendale, NJ The Manager, QC Microbiology plans, organizes, schedules, and directs the department to effectively utilize employees and equipment to meet and exceed GMP requirements, established KPIs, and material utilization while adhering to quality control-microbiological and technical standards. The Manager provides direct on-site analysis of the day-to-day operation including adjustment of workflow, test performance, and quality compliance. Essential Functions and Responsibilities: Devising sound hiring strategies based on business needs (S&OP and LE). Maintaining adequate staffing by interviewing, hiring, training, and performing the competency assessment of personnel. Performing scheduling, planning, staffing, and monitoring of workflows based on business needs. Providing staff development through feedback aimed towards performance development and review. Performing corrective counseling, when necessary. Procuring appropriate supplies and equipment to m

PPG is a sister company of QISG under the parent Quanta Services, Inc. This posting is for a direct hire position of Phoenix Power Group and is solely for the purpose of Phoenix Power Group. Phoenix Power Group Inc. (PPG) is a leading Construction Services Company providing Engineering, Procurement and Construction (EPC) services specializing in the installation of utility and industrial process infrastructure including substations, power generation, industrial process facilities, and renewable fuel projects in North America. PPG is a subsidiary of Quanta Services Inc., the largest specialty contractor in North America, providing large single-source solutions and leading the industry in its ability to deliver a collective scope of services, expertise and manpower. PPG is an EPC contractor specializing in the installation of utility and industrial process infrastructure including substations, power generation, industrial process facilities, and renewable fuel projects. PPG utilizes a mo

Duties & Responsibilities Refine and maintain the company written QA/QC Plan. Conduct new hire training on the key aspects of the QA/QC plan, as well as periodic recurrent training for existing employees. Meet with every project team to ensure they have a project specific QA/QC plan in place at the beginning of the project. Provide assistance as needed. At a minimum the plan should include / require: Preconstruction meetings with each subcontractor Subcontractor QA/QC plans Mock ups of key components First day inspections of each trade's work Pre-planned phase inspections Waterproofing and roofing inspection/testing Deficiency tracking and notification Punch-list process Owner turnover procedures Warranty hand-off Periodically audit the program for each project to ensure compliance and effectiveness. Provide a written summary of the results of the audit to the General Superintendent. Facilitate a handoff meeting from operations to warranty, ensuring the punchlist is complete and accept

Our client is looking to fill the role of Quality Control Analyst. This position will be located on site in the Fairfield office 5 days a week. Salary: $55-65k Responsibilities: Responsible for daily balance and pH calibration Manage filing of COAs, purchasing documents, receipt records and other documents Log in all incoming samples Manage Chemical Inventory and Waste Management/Disposal Prepare Samples for Customers, Contract Lab testing, and Stability Manage QC Sample and Retain Inventories Sample and test incoming raw materials, in-process , and finished product and packaging materials Perform compendial monograph testing and company required testing Perform wet chemistry tests following procedures and methods as required Work with Contract Laboratories and Service Providers as required. Support Laboratory Investigations, all Investigations, CAPA, Change Controls, Validations, Stability Programs, APR, statistical analysis, environmental monitoring of air, water, and surfaces, as ne

About the job Associate manager, QC (pharma/biotech) Essential Duties and Responsibilities include, but are not limited to, the following: Coordinates with members of stakeholder groups to provide analytical support. Manages QC Analysts, distributes work load, and monitors progress. Oversees product testing. Reviews test reports. Ensures QC Analysts receive proper training. Attends meetings to keep informed of manufacturing priorities. Ensures that safety standards are maintained. Ensures compliance with applicable cGMP regulations and SOPs. Investigates atypical test results as necessary. Tracks monthly testing and compliance metrics Performs personnel management functions including time sheet submissions, scheduling of vacations, personnel development/feedback, and performance evaluations.Knowledge, Skills And Abilities Coordinate, organize and assign daily activities of operations Ability to motivate employees and build team morale Continuously drive to improve processes for improve

Essential Functions: Ensures that equipment cleaning, sanitizations and job start-ups are performed correctly and are properly recorded on forms Verify components brought into production area are correct as compared to the bill of materials and that bulk, laminate, tubes, bottles, etc. are accepted for use (approved and within expiration schedule) Audits documentation that verifies materials, fills, codes, pressures and markings (Run Instruction details) in order to be sure they meet specifications at different stages of the production run Verifies that case packing meets specifications or if directed by the QC Manager, revises specifications accordingly Helps to inform/remind machine operators/packers what is needed when running and packing jobs Recommends improvements to mechanics and production when necessary Audits work of process lead Records results of inspection, sampling and testing in a clear, complete and correct manner in approved format on appropriate paperwork Helps to mon