Overview. This position is responsible to perform all type of analytical testing that is required for release of raw and packaging materials, final product and stability samples as well as all IPC testing. Additional responsibilities can be the support of stability studies, handling of deviations and change controls. As a QC team member, the person filling this position supports all activities to continuously maintain the GMP status of the QC Lab...
Job summary. Under general supervision of the VP of Quality Control. the Position Summary. The Quality Control Analyst holds a multi-faceted position within the company that works directly with production departments while reporting audit results to Senior Management. Thus, allowing the company an opportunity to examine and adjust policies and procedures, measure performance and ensure the standards and compliance requirements of government agenc...
JOB SUMMARY. The Quality Control Analyst is responsible for claims auditing and identifying examiner and system errors. This position also handles the auditing of claims special projects including risk pool, shared risk, Health Plan. ESSENTIAL DUTIES AND RESPONSIBILITIES. Include the following. Others may be assigned. Understands, interprets. . and applies coding and reimbursement guideline. provider and Health Plan contracts for professional cla...
Job Details. Quality Control Analyst must be a New Jersey resident. Job Description. Collaborate with management to establish Quality Assurance/Quality Control parameters for projects within a portfolio of Energy Efficiency Programs. Utilize Excel-based exception reports to identify missing project notation/documentation, inputs outside expected ranges, or duplicate submissions. Conduct comprehensive Quality Control reviews on a sample of project...
Role: GMP Test Technician. Location: Burlington NA. Type: W2 Contract. Job Description. Requirements. High school diploma or equivalent. associate degree in a relevant field preferred. Proven experience as a GMP Test Technician or similar role in a regulated manufacturing environment. In-depth knowledge of GMP regulations and quality assurance processes. Proficient in operating testing equipment and troubleshooting technical issues. Strong attent...
About the Department. Site New Hampshire, located in West Lebanon, is where Novo Nordisk’s life-saving treatments are brought to life. Our manufacturing facility produces a global supply of our hemophilia and growth hormone product lines, as well as our next generation of cutting-edge medications. What we offer you. Leading pay and annual performance bonus for all positions. 36 Paid days off including vacation, sick days & company holidays. Healt...
ACCOUNTABILITY. Responsible for reviewing, coordinating, and commenting on MEP drawings and specifications, and architectural, structural, civil, and other consultant documents for coordination of MEP systems design. RESPONSIBILITIES. . Review drawings and specifications in a timely manner. . Ensure documents are accurate, constructible, and biddable. . Ensure project documents meet all building and energy code requirements. . Ensure project docu...
Job Summary. Glenmark is actively seeking a Quality Control Analyst to join the growing team in Monroe, NC. The QC Chemistry Analyst position supports the Quality Control group to maintain process optimization and manufacturing activities. 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 st...
Job Details. Job Location. Vitality Works Inc - Albuquerque, NM. Salary Range. Undisclosed. Description. Come. Grow. with Us. Vitality Works mission is to create efficacious and therapeutic herbal, vitamin and nutraceutical supplements to help people get and stay well. While the FDA defines minimum quality, we strive for the highest level of quality. Vitality Works also operates in an environmentally sustainable way, recycling, composting, reduci...
Job Details. Hi. Please find the below Job Description. If interested, please share your updated resume along with below details. Job Title. QC Analyst. Location. Harrisburg, PA (Hybrid). Duration. Long Term. Responsibilities. Resource will be required to be on-site approximately 4 days a month. . We are looking for an individual proficient in CRM D365, ERP SAP with Back Office testing experience and the skills/ expertise outlined here. Descripti...
Description. Scope of Function. Work within the Analytical Chemistry area to provide analytical support, test results and qualification of analytical methods and stability studies for clients in pre clinical and clinical development. Work with process development and manufacturing groups by providing QC support to assess the purity, potency, strength and stability of in process and final vialed product. Specific Duties. Understand and perform a ...
Job Description. The QC Analyst is responsible for supporting Quality Control analytical testing of Incoming Raw Materials. This includes in house testing and sending out samples to contract testing labs. Some of the testing methods performed in house are HPLC/UPLC, Conductivity, OSMO, Titration, Melting Point and various other techniques. Perform testing of incoming Raw Materials. Utilize scientific principles to assist in analytical testing met...
