Quality Advisor
Oxy
Overview Oxy produces, markets and transports oil and natural gas to maximize value and provide resources fundamental to life. The company leverages its global leadership in carbon management to advance lower-carbon technologies and products. Headquartered in Houston, Oxy primarily operates in the United States, the Middle East and North Africa. To learn more, visit Oxy. Oxy strives to attract and retain talented employees by investing in their professional development and providing rewarding opportunities for personal growth. Our goal is to meet the highest employer standards by ensuring the health and safety of our employees, protecting the environment and positively impacting our communities where we do business. The Quality Advisor is a consulting, mentoring, and guidance role for the Quality team, serving as front-end to completion liaison to Project Management, leading and training inspection auditing personnel, and managing third party inspection resources and quality project related processes for project document review. This position will be based in The Woodlands, TX office. #J-18808-Ljbffr
- ...Position Overview The Quality Auditor understands auditing principles, practices, and techniques to evaluate the adequacy and effectiveness of the Quality Management System (QMS) on assigned projects. The Quality Auditor is responsible for independently planning, scheduling...SuggestedFull timeContract workFor contractorsWork at officeRelocationWeekend work
$65k - $80k
...relevant to the release of plasmid DNA (e.g., HPLC, PCR, ELISA, Agarose Gel Electrophoresis), regulatory requirements (cGMP), and quality standards. Working closely with development scientists, manufacturing personnel, and quality assurance teams to facilitate seamless...SuggestedFull timeWork at office- Cellipont Bioservices is seeking a QC Analyst I, Environmental Monitoring to support environmental sampling, testing and reporting in a GMP manufacturing setting for cell therapy products. You will perform EMPQ, growth promotion, sterility, endotoxin and mycoplasma testing...Suggested
- ...analyzing, and reporting results, and microbiological testing to support manufacturing. Works in a fast‑paced environment supporting the quality control department of a CMDO for manufacturing of cell therapy drug substance, sterile finished drug product, and fill/finish. The...SuggestedWork at officeFlexible hours
- ...Developing and manufacturing your cell therapies from benchtop to bedside" Summary The Senior QA Specialist is a key member of the Quality Operations function. Within the Quality Operation function these individual responsibilities would include, batch release...SuggestedImmediate startFlexible hoursShift work
- ...Job Description Job Description Quality Control Technician Schedule Shift: 6:00am to 6:00 pm What We Offer: Top-tier Medical, Dental, and Vision Benefits Profit Sharing Bonus Programs Life and Supplement Life Company Matched 401K Retirement Plan...For contractorsLocal areaShift work
- ...quo and take Cellipont and its clients to the next level. The QC Lead Analyst works in a fast-paced environment supporting the quality control department of a CDMO for manufacturing cell therapies. The QC Lead Analyst will be responsible for routine testing, assay...Flexible hours
- ...analyzing, and reporting results, and microbiological testing to support manufacturing. Works in a fast-paced environment supporting the quality control department of a CMDO for manufacturing of cell therapy drug substance, sterile finished drug product, and fill/finish....Work at officeFlexible hours
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