- J&J Family of Companies (Santa Clara, CA)
- …working in the medical devices industry is preferred + Practical knowledge of cGMP requirements + Working knowledge of MS word, excel and other database systems. ... Knowledge of Solid Works or other draw programs preferred + Ability to work in a fast-paced environment while managing multiple priorities + Must have strong written and verbal skills, and be able to effectively communicate with all levels of the organization… more
- J&J Family of Companies (Santa Clara, CA)
- …working in the medical device industry is preferred + Practical knowledge of cGMP requirements + Working knowledge of MS word, excel and other database systems. ... Knowledge of Solid Works or other draw programs preferred + Ability to work in a fast-paced environment while managing multiple priorities + Must have strong written and verbal skills, and be able to effectively communicate with all levels of the organization… more
- Grifols Shared Services North America, Inc (San Diego, CA)
- …manufacturing operations with minimum downtime and cost effectiveness. + Comply with all cGMP , OSHA, and Environmental & Safety policies and procedures. + Promote a ... culture of ownership of equipment and one's area of responsibility. + Maintain a rapport with Human Resources to ensure compliance with applicable internal policies and practices as well as promotions, recruitment activities, performance management, etc. +… more
- Catalent Pharma Solutions (San Diego, CA)
- …Process Engineering, Project Management personnel and clients to co-managing cGMP runs. Participating in group meetings, inter- and intra-department meetings, ... conference calls and interactions with clients with minimal assistance from the department head + Generation and review of manufacturing batch records, manage Catalent San Diego Master Batch Record modules + Responsible to be on-site for manufacturing… more
- Amgen (Thousand Oaks, CA)
- …development and to improve sustainability and process efficiency + Support cGMP manufacturing and technology transfer to our internal manufacturing facilities and ... external contract manufacturers + Ensure process performance through process understanding, modeling and characterization + Contribute to drug substance development teams by providing experimental results, technical updates, documentation, data interpretation,… more
- Interstate Blood Bank (Vista, CA)
- …activities are performed accurately, efficiently, and in compliance with cGMP , GLP, and applicable regulatory requirements. **Primary Responsibilities:** + Supervise ... the day-to-day operations of the specified testing department (routine testing or NAT/Pooling) + Ensure strict adherence to standard operation procedures, regulatory requirements, and company policies + Perform department review of source data prior to release… more
- Actalent (Santa Ana, CA)
- …FDA quality experience, Bachelors at least 1 year. Pharmaceutical experience preferred FDA/ cGMP Experience - 1 year Experience with Microsoft office suite Master ... control experience is preferred. Pay and Benefits The pay range for this position is $25.00 - $37.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may… more
- Takeda Pharmaceuticals (Thousand Oaks, CA)
- …approaches and execution of system validation activities in accordance with cGMP and applicable regulations, procedures, and industry guidance. + Advanced ... understanding of data and statistical analysis of validation test results. + Basic understanding of data and statistical analysis of validation test results. + Knowledge of cGMPs or equivalent regulations, validation associated regulations, guidelines, and… more
- Mallinckrodt Pharmaceuticals (Sacramento, CA)
- …equivalent military experience + 4+ years of experience in medical device cGMP service, manufacturing, or a comparable combination of service and support experience ... + Proven ability to work independently and lead staff toward meeting deadlines + Strong problem-solving abilities with a focus on process improvement + Must work Pacific Standard Time (PST) zone Preferred Qualifications + Product management experience,… more
- General Atomics (Poway, CA)
- Diazyme, an affiliate of General Atomics, is a cGMP and ISO 13485 certified medical device manufacturer. Diazyme uses its proprietary enzyme technologies to develop ... diagnostic reagents which can be used on most automated chemistry analyzers in user-friendly formats. Their products include test kits for diagnosis of cardiovascular disease, liver disease, cancer markers, renal disease, diabetes, and electrolytes. Under… more