Qc Salary at Page Industries BETA

Join a Fast-Growing Medical Device Company – Pioneering Regenerative Healing A leading innovator in regenerative technologies is seeking a QC/Quality Inspector for a 100% onsite, 6-month contract-to-hire role in Oakland, NJ. This is a unique opportunity to contribute to the development of life-changing medical devices in a dynamic, FDA-regulated environment. Key Responsibilities: Perform quality inspections on incoming materials, in-process components, and finished products Ensure compliance with FDA and internal quality standards Accurately document inspection results (GDP compliance) Collaborate with manufacturing and engineering to resolve quality issues What You Bring: 1–2 years of QC experience in an FDA-regulated medical device setting Strong attention to detail and documentation skills

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.

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 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

Join our Natural Organics Inc / Natures Plus Family! For more than 50 years, Natural Organics Inc. headquartered in Melville, NY has been the gold standard in natural vitamins and supplements. Marketing our products under the Natures Plus brand, we are committed to producing the finest, most effective formulations available. Our employees embody the true spirit of our Natures Plus brand. We have one goal... Bringing you high-quality products with the guaranteed potency you deserve! QC Administrative Assistant 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 Mai

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