PHYSICAL, MENTAL & ENVIRONMENTAL DEMANDS: To comply with the Rehabilitation Act of 1973 the essential physical, mental and environmental requirements for this job are listed below. San Francisco, CA30+ days ago The position requires maintaining a consistent on-site presence, coordinating with project teams, reviewing and certifying submittals, inspecting work for conformance, and leading documentation and reporting efforts. Mentorship Program designed for employees to formalize a working relationship between seasoned professionals and young professionals to develop specific areas of knowledge to grow their careers within the family of companies. Redwood City, CA11 days ago p style="background-color:rgb( 255 , 255 , 255 );margin:5pt 0pt">Role Summary: - Serve as a Subject Matter Expert (SME) in Quality Control within the Pharmaceutical Development & Manufacturing, Analytical Development & QC department, supporting clinical and commercial programs.
Qualifications: - BS or MS in Chemistry, Pharmaceutical Sciences, or a related discipline, with 6+ years of relevant industry experience in analytical development/QC.
San Francisco, California30+ days ago p>Please visit our careers page at www.calistabrice.com and select Brice Builders LLC under the company tab. The position requires maintaining a consistent on-site presence, coordinating with project teams, reviewing and certifying submittals, inspecting work for conformance, and leading documentation and reporting efforts. San Francisco, CA1 day ago li>Completion of the thirty (30) hour OSHA Construction safety class or as an equivalent, thirty (30) hours of formal construction safety and health training covering the subjects of the OSHA thirty (30) hour course (See EM three 385-1-1 Appendix A, paragraph 4.b) applicable to the work to be performed (Section 00 22, Table 1 – Specialized Work) and given by qualified instructors. - CQC: A Bachelor's Degree in engineering or Sciences with a minimum of three (3) years experience (within the last ten (10) years), as a Construction CQC in Construction for the installation of work described in Section 00 22 10, Table 1- Specialist Work for Completed systems .
Work closely with manufacturing and product development teams and participate in pro-active functions that impact production, increase efficiency, solve problems, generate cost savings, improve quality and provide new product support. Strong understanding of chemistry, environmental monitoring, microbiological (e.g., pyrogen, bioburden), sterilization and/or real-time stability testingMust know quality laboratory operations and government regulations pertaining to pharmaceutical and medical device manufacturing labs. San Francisco, CA22 days ago Applicants must currently be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time. For hires based in the United States, Vir Biotechnology, participates in E-Verify. |