Qc Salary at Solo BETA

81024 TSR is a premier National U.S. Staffing company with over 50 years of staffing excellence. Our client, a leading pharmaceutical company is hiring an Assistant QC Scientist. Please ONLY local candidates to Warren NJ. Required Skills: 2+ years of hands-on experience with bioanalytical techniques such as ELISA, Potency, Cell based assays, etc. 1+ year experience working in regulated environment (e.g. cGMP, cGLP) Previous Assay Transfer, assay validation experience Previous CAR-T experience preferred Technical understanding and troubleshooting skills Experience/knowledge in deviation, CAPA, Change Control Work Location: Warren NJ Pay: $40-41/hour W2 Responsibilities: The QC Analyst is responsible for supporting Quality Control bioanalytical testing for release of clinical and commercial products Experience in assay transfer, technology transfer, validation from Analytical Developmental group to Quality Control group Ability to accurately and completely understand, follow, interpret a

Net2Source Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth of 300% in the last 3 years with over 5500+ employees globally, with over 30+ locations in the US and global operations in 32 countries. We believe in providing staffing solutions to address the current talent gap – Right Talent – Right Time – Right Place – Right Price and acting as a Career Coach to our consultants. Job Title: Assistant QC Scientist Location: Warren, NJ 07059 100% onsite Duration: 12 months contract Work Schedule: Mon - Fri, 8AM - 4:30PM EST Must Haves: 2+ years of hands-on experience with bioanalytical technique such as ELISA, Potency, Cell based assays, etc. 1+ Experience working in regulated environment (e.g. cGMP, cGLP) Previous Assay Transfer, assay validation experience Previous CAR-T experience preferred Technical understanding and troubleshooting skills Experience/knowledge in deviation, CAPA, Change Control Team player, fle

QC Administrative Assistant JOB RESPONSIBILITIES: The Quality Control Administrative Assistant position is responsible for performing administrative work within the Quality Control department. This position aids and supports the Quality Control Manager in ensuring the laboratory's compliance with cGMPs Responsibilities include but are not limited to the following: Follow company policies and procedures. Receiving samples submitted to the laboratory Monitoring inventory, ordering and receiving laboratory supplies and chemicals Maintaining material specifications in LIMS Preparation of Certificates of Analysis Maintain outside laboratory qualification program Coordinating the sending of samples for outside testing Inputting outside test results into LIMS Maintain laboratory calibration program Maintain laboratory records and retains Perform additional Quality Control support tasks as assigned REQUIREMENTS (Qualifications): Education/Experience: High school diploma/GED and 1 year of exper

Details: L.J. Gonzer Associates is looking for individuals to join our pool of qualified candidates for potential assignment as a QA/QC Manager. The Quality Control Manager is responsible for all aspects of Quality measurement, product inspection and in-process testing. The primary responsibility is to ensure that Quality Control personnel perform the required inspection accurately and as specified by the appropriate quality documentation. This position will allocate resources to efficiently maintain orders on schedule. The Quality Control Manager is responsible for the training, the discipline and morale of the Quality Control - Product Inspection and Release Testing of materials required to produce a finished product and the final product to confirm compliance to issued specifications. QC Inspectors are responsible for (but not limited to) Physical - Dimensions, Hardness, Drop test, tap test, net weight; Visual - Color (e.g. color matching), Appearance; Sensory - Odor, Texture Produc

Details: In this role, you will report directly to the Plant Manager. As the Quality Manager, you will develop and maintain an integrated quality system which conforms to ISO 9001:2015 standard. The Quality Manager will oversee all quality activities of the facility, develop training programs and activities to monitor and improve quality of products and customer satisfaction.. The ideal candidate will possess the ability to drive operational excellence in quality initiatives, processes, and practices; and use strong project and change management skills. The Quality Manager builds partnerships with all levels of team members. Strong leadership skills and business knowledge are keys to success in this position, along with the ability to thrive in an environment of both strategy and active hands-on execution. ESSENTIAL JOB DUTIES AND RESPONSIBILITIES: In addition to those listed in the Summary section above, the following are duties necessary to meet the minimum requirements of the positi

Supervisor, QC Microbiology – 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 Supervisor, QC Microbiology will organize, and direct staff to meet and exceed cGMP requirements, and establish KPI’s, while adhering to quality control-microbiological and technical standards. The QC Environmental Monitoring Supervisor will also provide oversight of day-to-day activities including adjustment of workflow, test performance, and quality compliance. Essential Functions and Responsibilities:Ensures compliance with regulatory agency requirements by enforcing a quality

Job Description Job Description We are seeking QC Inspector to join our team! Responsibilities: Perform Receiving, In-Process, and Final Inspection of precision dip brazed, machined and sheet metal components and assemblies. Generate First Article Inspection reports Calibrate and maintain precision measuring tools Generate non-conformance reports Review and measure parts in production for compliance with blueprint and Shop Traveler requirements Maintain accurate records and comply with AS9100 procedures Additional responsibilities as assigned by supervisor Qualifications: Minimum of 2 years mechanical inspection experience in a production environment Experience with measuring devices such as height gauges, calipers, micrometers, etc. Working knowledge of blueprints, tolerances, and Mil-Spec standards Must be able to work independently Experience creating AS9100 FAI reports Excellent written and verbal communication skills Hours are 7:00 am-3:30 pm Monday to Friday To be considered, ple

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