Employment Type: Full-Time
specializes in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a Manufacturing Specialist
to work for a leading Orange County area contract manufacturing company. Responsibilities: Collaborate with internal and external customers to prioritize GMP document review schedule Coordinate scheduling of formulation in-process sample testing with cross-functional organizations to ensure timely receipt of results for formulation release Facilitate submission of reviewed formulation BPRs with Quality Assurance and coordinate release of formulations for production use Facilitate and coordinate submission of reviewed operation BPRs with Quality Assurance to ensure lot disposition and release timelines are maintained Perform real-time review of in-progress formulation and operation BPRs within the GMP production suites Must be able to fully gown into ISO 8 (Class 100K) and ISO 7 (Class 10K) GMP production suites to perform real-time review of BPRs Qualifications : A Bachelor's degree in life sciences or engineering is required. Biopharmaceutical experience is required – may possess 3 to 5 years technical experience in industry or in graduate level studies. Experience working for a contract manufacturing organization in the life sciences field is preferred. Proficient in personal computer skills, including e-mail, record keeping, routine database activity, word processing, spreadsheets, and graphics. Ability to prioritize multiple tasks and projects simultaneously. Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively before groups of customers or employees of organization. The successful incumbent is meticulous and detail oriented.
Please send resumes email@example.com visit our website atwww.biophaseinc.comfor additional job opportunities!!!