- Abbott (Alameda, CA)
- …implementing and following procedures. + Experience in Good Manufacturing Practice ( GMP ). + Experience working autonomously and with minimal supervision. + Computer ... proficiency, with expert knowledge of software packages, including Word and Excel.. Apply Now (https://www.jobs.abbott/us/en) **Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:**… more
- AbbVie (Pleasanton, CA)
- …all tasks according to medical device development life cycles, manufacturing processes & GMP ; & + working in a cross-functional team, in a multisite corporation, ... preparing & delivering reports &/or presentations to scientific & business audiences, including executive team, both orally & in writing. Work experience may be gained concurrently. Additional Information Salary Range: $108,393.48 - 122,000.00 per year. Apply… more
- ENFRA (Glendale, CA)
- …coordinates the management of the Contract delivery type Guaranteed Maximum Price ( GMP ), Lump Sum, or Concession Agreement. + Knows and understands the requirements ... of the Contract, including bonds, insurance, notifications, schedules, reporting, costs and energy savings requirements. + Oversee the set-up of the Project Job Management System (Procore) for all Change Management and Document Control procedures following… more
- BeOne Medicines (San Mateo, CA)
- …requirements. Knowledge/experience with regulatory requirements for rest of world regions and GMP regulation is a plus. + Demonstrated leadership as a people ... manager. + Experience in authoring complex technical documents, CTD M2 and M3 sections, and life cycle management. + Educational background in scientific disciplines and expertise in at least one area in pharmaceutical development (chemical process,… more
- Charles River Laboratories (Northridge, CA)
- …from phases 1 to 3, and commercialization with high-quality RUO and GMP -compliant starting material and apheresis collections. In January 2020, HemaCare was acquired ... by Charles River Laboratories, an early-stage contract research organization (CRO). Combined with Charles River's integrated, early-stage portfolio of discovery, safety assessment, and manufacturing support services, the acquisition creates a unique,… more
- Schwan's Company (City Of Industry, CA)
- …company regulations, policies and procedures (including Good Manufacturing Practices ( GMP 's) and safety regulations) The employing subsidiaries of Schwan's Company ... are Equal Employment Opportunity Employers. All qualified applicants will receive consideration for employment without regard to disability, age, race, color, religion, gender, vet status, national origin, or other protected classes. #LI-HK1 more
- Herbalife (Torrance, CA)
- …analytical method development, validation and technical leadership in a GMP -regulated lab (nutracetical or pharmacetical industry preferred). \#LI-GB1 At Herbalife, ... we value doing what's right. We are proud to be an equal opportunity employer, making decisions without regard to race, color, religion, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability, or any other… more
- Curia (Camarillo, CA)
- …compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices ( GMP ), and leading initiatives to enhance laboratory efficiency and effectiveness. ... Essential Duties and Responsibilities: + Complete tasks as required (in a timely manner), compliant with cGMP, regulatory and corporate requirements and conform to Health, Safety & Environmental responsibilities. + Mentor chemists and analysts + Write, review,… more
- Imperative Care (Campbell, CA)
- …meet governmental regulations such as FDA QSR, ISO 13485, the MDD, GMP , GDP procedures and requirements. + Knowledge of operations techniques including Just-In-Time ... (JIT) manufacturing, benchmarking, and other quality and continuous improvement tools (Lean). + Demonstrated technical skill in risk management and remediation processes. + Ability to create detail project plans effectively. + Familiar with Design Control… more
- Envista Holdings Corporation (Pomona, CA)
- …current process and process changes. + Maintains a working knowledge of FDA GMP , ISO 13485 standards and other applicable standards. + Documents data obtained during ... all quality assurance activities, consistent with company policies and procedures. + Prepares reports to communicate involvement and results of quality assurance and quality engineering activities. + Reviews all purchased products or components and provides… more