Quality Assurance Head Position Purpose The purpose of the QA Associate position is to accurately review the chronological... manufacturing environment supporting Quality Control Laboratory and Manufacturing operations Basic knowledge and industry...
of Amgen's plan to be a carbon-neutral company by 2027. Sr Associate Facilities Maintenance What you will do Let... department Data verification of GMP information for pest control compliance Delegate for Facilities Sr Manager during period...
and downstream processing. Strong working knowledge of cGMP, Quality Systems (problem, deviations, change management, etc.), Safety... to integrate new technologies and cell-line platforms. The Associate Director, Process Operations Lead will be a member of the...
combination products cGMP, Quality System Regulation, FDA Human Factors guidance, ISO 14971, 11608 and 11040, EN 62366, Council...Job Description Associate Principal Scientist – Device Technical and Engineering Lead (Associate Director Equivalent...
Manufacturer(s) (CM) to support manufacturing supply, quality, and continuous process improvement of parenteral products... that are supplied to Lilly sites and the market. The Operations Associate is accountable to the Joint Process Team Leader. Key...
across all departments, such as Quality Assurance/ Control, Chemical Development, Program Management, Regulatory, Analytical Development... (in days) to receive an alert: Associate Director - Drug Product Manufacturing & Development Facility: Manufacturing...
across all departments, such as Quality Assurance/ Control, Chemical Development, Program Management, Regulatory, Analytical Development... with large pharmaceutical company quality, resources, and stability, uniting the best of both worlds to develop new medicines...
to maintain high standards of product quality and cGMP compliance. Title: QA Associate Location: South San Francisco...Yoh Life Sciences is hiring for Quality Assurance Associate in South San Francisco. You will support day-to-day quality...
, Manufacturing, Quality Control, Quality Assurance, Facilities, EHS, Warehouse/Supply Chain, and IT to gather technical content... like you, you’ve come to the right place. Kymanox is seeking an (Contract) Associate Technical Writer with a strong background in FDA-regulated...
Job Category: Engineering Job Description: Associate Director, Automation Engineering in Albuquerque, NM Build... reimbursement 401K program with matching contributions Learning platform And more! The Associate Director of Automation...
, investigate, and resolve deviations; support change control and CAPA processes in electronic quality systems. Author traceability... like you, you’ve come to the right place. The (Contract) Associate CQV Engineer will have direct experience in Commissioning, Qualification...
working outside of Cipla's U.S. Subsidiaries or Affiliates. Job Title: QA Associate II AQA FLSA Classification...) Reports To: Quality Assurance Manager Purpose: This position requires a strong analytical chemistry/lab background...
working outside of Cipla's U.S. Subsidiaries or Affiliates. Job Title: QA Associate (IT) Location: Hauppauge, NY (Onsite...: The QA Associate (IT) is responsible for review of batch production records, ensuring that all documentation complies...
to join our manufacturing team as a Manufacturing Associate I. As a Manufacturing Associate I, you will produce research grade components... work environment by following current good manufacturing practices (cGMP), and standard operating procedures. Keeps...
, including handling of excipients and residual API. 17. Collaborate with Analytical Development and Quality Control teams... of AI, not as a buzzword, but as a pragmatic tool to optimize manufacturing, strengthen quality systems, and ensure inspection readiness...
review, disposition, deviation management, and change control. Conduct and/or participate in quality audits of external... manufacturing sites to assess compliance with cGMP, regulatory expectations, and Eli Lilly's quality standards. Review and approve...
Associate will participate in the development of robust analytical techniques designed for seamless transition to a quality...Job Description: Analytical Development Associate Position Overview: Wheeler Bio is seeking a motivated analytical...
and adapting new manufacturing procedures and analytical methodology. · Cooperate with Quality Control (QC) and Quality Assurance... (QA) groups to ensure the quality of product and cGMP compliance. · Assist in internal inspections and audits to ensure...
such as material control or quality. Other highlights: 1st Shift position Monday- Friday 6:30am - 3:00pm, 2nd Shift 3:15 to 11:45... Associate I is responsible for assembling small to medium size components into quality finished products, per ISO...
understanding of cGMP, quality, and regulatory requirements for drug substance manufacturing Ability to effectively interface... future of biopharma. What You'll Do Sr. Manager/Associate Director, Drug Substance Development and Manufacturing...