QC Analyst Salary at Laurus Labs Ltd BETA

Sr. QC Analyst, Microbiology needed! Overview: The Senior Quality Control Analyst- Microbiology will support quality control testing operations. The quality control testing programs include in-process and final drug product microbial testing such as bioburden, endotoxins, mycoplasma, gram stain, environmental monitoring, and sterility techniques. This position works across different shifts. Depending on your assigned shift, you may be required to work overtime, weekends, and holidays to complete assigned work. Essential Functions and Responsibilities: Perform daily cGMP quality control laboratory microbiological testing activities. Perform environmental monitoring of the cleanroom areas as scheduled. Perform data analysis and result reporting of microbiology assays to support product lot release with adherence to turnaround times. Perform all activities for cGMP compliance. Support thorough cGMP investigations for out-of-specification test results. Support technical problem-solving. Su

Our client, a dynamic biopharmaceutical company with a global footprint in both R&D and manufacturing, is seeking a QC Analyst to join their growing team. Type: Direct Hire Rate: Up to $80K Location: Middlesex County, NJ Essential Duties & Responsibilities Perform analytical testing to support in-process, release, raw materials, and stability programs. Perform both bioassays and chemical analysis. Review, analyze, and report analytical data. Collaborate with internal teams for quality investigations/reporting. Qualifications: Bachelor’s degree in biology, chemistry, biochemistry, etc. and 2+ years of related QC experience. Previous experience in a cGMP laboratory with hands on expertise with techniques such as HPLC, cell-based assays, and Empower software. This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

Job Title: QC Analyst III, Radiopharmaceuticals Location: Brownsburg, Indiana, United States (No Sponsorship) Department: Quality Control Reports To: QC Manager / Supervisor Position Summary: My client is seeking an experienced and detail-oriented QC Analyst III to join their Quality Control team focused on radiopharmaceuticals. The ideal candidate will have in-depth knowledge of current Good Manufacturing Practices (cGMPs), Standard Operating Procedures (SOPs), and regulatory guidelines, with proven experience in managing stability studies and handling rare radioactive materials in a pharmaceutical or radiopharmaceutical manufacturing environment on site in Brownsburg, Indiana, United States. Key Responsibilities: Plan, organize, and manage stability studies in accordance with ICH and FDA guidelines. Review and analyze stability data, identify trends, and communicate findings effectively to internal stakeholders. Ensure all work complies with cGMPs, internal SOPs, and regulatory stand

Our client, a leading organization in the quality assurance sector, is seeking a Quality Control to join their team. As a Quality Control, you will be part of the Quality Assurance department supporting various teams. The ideal candidate will have strong attention to detail, excellent analytical skills, and a proactive mindset which will align successfully in the organization. Job Title: Quality Control Location: Marietta, GA Pay Range: What's the Job? Conduct thorough quality inspections and testing of products. Document and report findings to ensure compliance with quality standards. Collaborate with team members to identify areas for improvement. Assist in the development and implementation of quality control procedures. Participate in training sessions to enhance quality assurance skills. What's Needed? Strong attention to detail and a commitment to quality. Ability to analyze data and make informed decisions. Excellent communication skills, both written and verbal. Proficiency in

Job Description: We are seeking a 3rd shift QC Analyst In-Process Laboratory position supports the Quality Control In-Process and conducts biochemical, microbiological, and general chemical testing of in-process or final product samples submitted to the QC laboratories. The position requires analytical testing to be completed in compliance with all applicable procedures, standards and GMP regulations. This position requires high attention to detail, organizational leadership, interpersonal skills, a quality mindset, critical thinking, and technical writing skills. This position will be the shift leader and primarily work independently. Key Responsibilities: Perform analytical testing in compliance with applicable GMP regulations while maintaining a safe work environment in compliance with all applicable environmental, health, and safety regulations. Conduct biochemical, microbiological, and/or general chemical testing of raw material/utility, in-process, or final product samples submit

Glenmark Pharmaceuticals Inc., USA is a subsidiary of Glenmark Pharmaceuticals Ltd., a leading player in the discovery of new molecules – both New Chemical Entities (NCE's) and New Biological Entities (NBEs'), with eight molecules in various stages of clinical development. Glenmark Pharmaceuticals Inc., USA is a fast growing and robust US generics business, with plans to move into the innovative market as well. POSITION SUMMARY: This position is for a highly motivated member of the Quality Control (QC) Lab at the Monroe manufacturing facility, reporting to the QC Manager. Primary responsibilities for this position will be: perform QC analysis in compliance to cGMP in line with standards prescribed by USFDA. Maintain compliance to data integrity and cGMP in QC lab in line with standards prescribed by USFDA. Perform IOQ/Calibration for instruments in QC lab at Monroe with guidance of CQA. Execute and complete procedures and systems for RM, PM, FD and in process testing in QC lab. Provide

Quality Control Analyst – Radiopharmaceuticals Location: Indianapolis, IN | Full-Time | On-Site Ready to be part of something bigger than just another test run? Join a team where every sample, every method, and every result contributes directly to advancing cancer treatment. We’re a growing radiopharmaceutical company developing next-generation therapies, and we're looking for a hands-on, detail-obsessed QC Analyst to help build the foundation of quality from the ground up. What You'll Do: Perform GMP testing on final products, in-process materials, raw materials, and stability samples Work with advanced instrumentation including HPLC, GC, Ion Chromatography, and radionuclide assays Support method transfer, validation, and equipment qualification Conduct environmental monitoring and contribute to lab investigations and CAPAs Draft and review documentation: test records, CofAs, stability summaries, and technical reports Collaborate cross-functionally with QA, manufacturing, and regulato

Company Description PropertyRate is a rapidly growing, venture capital backed Valuation Services Provider to the real estate and mortgage services industry, located in Orange, CA. We are currently seeking a Quality Control Analyst to join our team. We are passionate about making the often-complex process of home ownership, financing and appraisal process easier for borrowers, lenders and the professionals who help homeowners close their mortgage loans. We offer associates a supportive, casual, and energetic environment with significant opportunity for personal and professional growth and advancement. We provide associates with a meaningful opportunity to impact the culture while gaining exposure and mentorship from senior team members. This role is ideal for a driven problem solver with a high attention to detail and a strong interest in developing their professional expertise and knowledge as both an individual contributor and supportive team member. Compensation and Benefits The Qual