Qc Salary at Amerlux Llc BETA

Job Description Job Description Position Summary: This position will report to quality management (QA/QC Manager). The QC Data Reviewer will be responsible for review of various data and documentations generated by Quality control department as per cGMP and company procedures. The QC Data Reviewer will meet departmental, company, and Quality goals by accomplishing the following responsibilities: Essential functions and Responsibilities: Quality review of QC lab generated data and documentation for accuracy, completeness, and compliance in timely manner. Audit trails review of analytical instrumentation to ensure data integrity. Raw data note book review for documented information such as calculation verification, standard/sample preparation, reagent preparation, instrument calibration, reagent expires, logbook entries, control charts, etc. Facilitates laboratory data or documentation corrections with analysts to ensure accuracy. Must have a working knowledge of the analytical instrumen

QC Microbiology Analyst II – 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. This position will report to the Supervisor of QC Microbiology. The Quality Control Microbiology Analyst II serves as a support role to clinical and/or commercial production. The QC Microbiology Analyst will perform environmental monitoring activities including, but not limited to, non-viable particulate testing, active air viable, passive air viable, surface viable, and personnel monitoring. Essential Functions and Responsibilities: Environmental monitoring in controlled environments

QC Microbiology Analyst II – 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. This position will report into the Manager of QC Microbiology. The Quality Control Microbiology Analyst serves as a support role to clinical and commercial production at the Allendale, NJ facility. The QC Microbiology Analyst will perform environmental monitoring activities including, but not limited to, non-viable particulate testing, active air viable, passive air viable, surface viable, and personnel monitoring. Essential Functions and ResponsibilitiesEnvironmental monitoring in controlled environments: Non-viable particulate monitoring Active viable air monitoring Personnel monitoring Surface sampling Passive air monitoring Equipm

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 Below is the summary of the role responsibilities. This is not an exhaustive list of all responsibilities, duties, skills, efforts, requirements or working conditions associated with

QC Analyst 2 Job Title: Quality Control Laboratory Analyst 2 – Radiopharmaceuticals About Us Evergreen Theragnostics, Inc. is a radiopharmaceutical company beginning operations in Springfield, NJ. The state-of-the-art facility will provide contract development and manufacturing services for radiopharmaceutical companies, including therapeutics and centrally distributed diagnostics. The company expects rapid growth in the next few years. Evergreen is a small team, where all team members support each other in a variety of activities. Job Description: We are seeking a highly motivated and detail-oriented Quality Control Laboratory Analyst 2 to join our team. This individual will play a key role in ensuring the highest standards of quality and compliance in our radiopharmaceutical release processes. The ideal candidate will have a background in pharmaceutical or life sciences, and hands-on experience with analytical techniques such as GC (Gas Chromatography), TLC (Thin Layer Chromatography

QC Analyst 3 Job Title: Quality Control Laboratory Analyst 3 – Radiopharmaceuticals About Us Evergreen Theragnostics, Inc. is a radiopharmaceutical company beginning operations in Springfield, NJ. The state-of-the-art facility will provide contract development and manufacturing services for radiopharmaceutical companies, including therapeutics and centrally distributed diagnostics. Evergreen is a small team, where all team members support each other in a variety of activities. Job Description: We are looking for an experienced and proactive Quality Control Laboratory Analyst 3 to join our team. In this role, the candidate will participate in critical quality control processes for our radiopharmaceutical products, ensuring all operations comply with stringent industry standards and regulatory guidelines. The ideal candidate will have significant experience in pharmaceutical or radiopharmaceutical environments, a strong background in analytical techniques, and the ability to troubleshoot

Job Title: Associate IJob Description Perform testing to help develop methods for flow cytometry and analysis. Perform cell culture and cell counting to analyze for quality control. Help perform analysis for flow methods and complexity testing. Provide input to improve workflow and laboratory activity. Provide input and proficiency in relevant testing. Provide training and some oversight to new employees on the team. Perform 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. Perform maintenance, monitoring, and troubleshooting of pertinent equipment, including routine start-ups and shutdowns. Test, document, and report results for products or materials following company and/or client procedures under CGMP and/or GTP guidelines. Perform client proficiency testing under direct supervision as applicable. Organize the lab and put supplies away in a neat and organized manner

Job Type Full-time Description Position Summary The QC Analyst III will be responsible for analytical testing and data verification/review supporting both late-stage clinical and commercial small molecule and biosimilar products in cGMP-compliant laboratories. A strong background in protein chemistry will be essential to perform and troubleshoot techniques such as HPLC, SDS-PAGE, cell-based bioassays, capillary electrophoresis, SDS-PAGE, ELISA, and standard compendial assays. A demonstrated ability to collaborate across multiple departments to drive timely resolution of projects, laboratory investigations, and process improvements is required. Essential Duties & Responsibilities •Analytical testing to support product in-process, release, and stability programs. •Perform the data verification/Review process as assigned. •Participate in Method Validation activity. •Preparation of the Protocols/Reports as assigned. •Strong knowledge of cGMP, Quality Systems, and ICH / regulatory guidance.