Qc. Salary at Planitroi Inc BETA

Our client is actively looking for a QC Stability Program Manager for their growing team. This is an on-site position in Cranbury NJ. You should apply if you have: B.S. with 6+ years of QC lab experience in an FDA regulated environment(Pharma preferred) Management and/or project management experience Experience leading/owning stability programs Experience overseeing analytical testing and validation processes

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 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

**Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . At Bristol Myers Squibb we are reimagining the future of cell t

Overview: At Corgan we are passionate about great design but the best thing we build is each other. Here, youll find camaraderie and collaboration as abundantly as curiosity and creativity. Corgan is a welcoming and supportive environment that provides significant career advantages. Youll find room to grow, freedom to explore and the safety to fail. Thank you for your interest in joining our curious, passionate, hardworking team. Corgan is actively recruiting a dynamic architectural QA/QC Manager to join the firm as part of our Data Centers team. Tackle these responsibilities alongside a team of creative, highly motivated individuals who are passionate about their work and ready to collaborate to achieve outstanding results. Our ideal team member is passionate and progressively seeking more responsibilities to expand their expertise. Responsibilities: Support the development, maintenance, and implementation of Quality Assurance standards to improve quality and timely delivery of projec

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

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

Our client is urgently looking for a QC Microbiology Supervisor. This is an on-site position in the greater Cranbury, NJ area supporting a sterile manufacturing facility and managing a team of 6-8 employees. You should apply if you have: B.S. in Science related discipline 5+ years of pharmaceutical experience. Strong leadership and communication skills. Management or supervisory experience is mandatory. Experience with aseptic sterile filling process, media fill validation activities, and development of testing methods is a heavy preference.