Manager, Quality Assurance in California

ABOUT MURRAY COMPANY

At Murray Company, how we operate is defined by shared values that are 100 years in the making -Safety, Quality, Honesty, Hard Work and Pride of Ownership. These values have led to our company consistently being in the top 15% on ENRs Best Specialty Contractor’s list. Bring your enthusiasm and unique perspective to Murray Company where you will have the opportunity to grow with us professionally, personally, and financially. Join a team that cares about helping you thrive and succeed. You'll work alongside talented colleagues while establishing lifelong friendships and making a difference in our company and the specialty contracting community. As a part of Murray Company, you'll build long-term wealth by enjoying employee-ownership, great compensation, health & wellness benefits, and matched 401(k) retirement plan.

POSITION SUMMARY:

The Process Piping Quality Assurance Quality Control Manager will...

CSBio is a peptide contract manufacturing founded in 1993. Our initial products were a complete line of automated synthesizers for manufacturing and process development, with a focus on cGMP production. In 1994, we opened our custom peptide facility and began producing high quality compounds for research organizations and pharmaceutical companies worldwide. In 2004, we opened our peptide production facility in Menlo Park, CA and in 2014, we expanded our production capability through the addition of a new, state of the art building dedicated to cGMP peptide production. In 2017, we passed a FDA inspection and were recommended to be approved for commercial drug substance manufacturing. In 2023, we added additional cGMP clinical production capacity in Milpitas, CA.

CSBio is seeking an experienced Quality Assurance Associate Manager to provide oversight in Quality Systems, API operations and validation activities including facilities, equipment, utilities, systems, process,...

The Tsui Group is seeking a candidate with proven experience in working on complex, multi‐phase, multi‐million dollar design and construction projects to provide as-needed, lessons learned facilitation and support services. The candidate must be flexible and able to assist the Program Management Office in the daily tasks of managing the Lessons Learned Program. Assignments to include Lessons Learned workshop preparation, facilitation, and Lessons Learned Registers for database. The Lessons Learned database will provide potential risk areas to focus attention and resources. They key is to focus the discussion of the item on what occurred and the discussion of the area of improvement on how this item could have been mitigated. 

The candidate must also be able to demonstrate a professional demeanor, and have a clear understanding of project cost, schedule, documentation, and risk assessment principles, and able to multi‐task and work in a fast‐paced work environment. ...

JOB SUMMARY
The Plant Quality Manager plays a crucial role in overseeing and managing quality control processes in our modular manufacturing plant in Southern California. The Plant Quality Manager is responsible for implementing and maintaining quality management systems, ensuring compliance with ICC-NTA guidelines, and driving continuous improvement initiatives to enhance product quality and reliability.

• Salary Range: $120,000-$140,000 depending on experience.
• On-site @ 740 E. 111th Pl, Los Angeles, CA 90059

ABOUT MODEL/Z

Model/Z is a trailblazing enterprise focused on reinventing multifamily housing through the development of standardized, modular units. Our mission is to provide high-quality, low-cost, and net-zero-ready housing solutions that are both scalable and practical, aiming to significantly mitigate homelessness and enhance living conditions for underrepresented...

CSBio is a fast-paced peptide CMO founded in 1993. Our initial products were a complete line of automated synthesizers for manufacturing and process development, with a focus on cGMP production. In 1994, we opened our custom peptide facility and began producing high quality compounds for research organizations and pharmaceutical companies worldwide. In 2004, we opened our peptide production facility in Menlo Park, CA and in 2014, we expanded our production capability through the addition of a new, state of the art building dedicated to cGMP peptide production. In 2017, we passed a FDA inspection for commercial drug substance manufacturing. In 2019, we expanded into Milpitas, CA for non-clinical production and in 2022, completed our cGMP patient specific cancer vaccine peptide production facility.

We are seeking a qualified individual to join us as the Manager of Quality Assurance at our Menlo Park facility. This position reports to the Direct of Operations. Job...

We are seeking an experienced Senior Manager of CMC Quality Assurance to spearhead the quality assurance initiatives for our pioneering curative stem-cell therapies. This role involves establishing and refining the quality assurance processes for the development of HSPC based, HDR (homology directed repair) therapies.

What You Will Do:

• Lead cGMP quality assurance activities for all relevant manufacturing operations, including product disposition via batch record and certificate of analysis (COA) review, in collaboration with our Contract Manufacturing Organization (CMO).
• Develop, implement and manage a comprehensive electronic Quality Management System (eQMS) to support pre-clinical and clinical manufacturing and clinical operations, including development, review and approval of internal documentation, such as Standard Operating Procedures (SOPs) and methods.
• Support development and implementation of Clinical Affairs...