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Sterile/aseptic clean room is preferred. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio.
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The Operations Supervisor is an exempt level position working within Technical Operations team, responsible for directing the daily production of a personalized cell therapy to support both clinical and commercial requirements in a sterile cGMP environment.
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This individualwill be responsible for overseeing the production of a personalized cell therapy to support both clinical andcommercial requirements in a sterile cGMP environment. This individualwill be responsible for overseeing the production of a personalized cell therapy to support both clinical andcommercial requirements in a sterile cGMP environment.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Provide adjunct care for the patient, including ice packs, non-sterile dressings and therapeutic baths. Job Title: CNA/ T-CNA Contract. Immunization Report HebB MMR, Varicella TDAP (If available, share the report with us.
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Knowledge of GMP, FDA/ICH, sterile/aseptic processes. 3-5 years’ in pharmaceutical manufacturing involving change control, quality assurance. Support Document Control, Training Program, stay informed on regulations, cGMP trends, FDA/ICH Guidelines.
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Understands aseptic and sterile field management including but not limited to scrubbing, gowning, gloving, preparing the sterile field, and identifying breaks in sterility. Proficient computer skills that may include but are not limited to Microsoft Office and/or Google SuiteCertified Surgical Technologist (CST) unless exempt per NJ Surgical Technology Certification Law. AHA Basic Health Care Life Support HCP Certification.
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Perform sterile filtrations using peristaltic pumps and other equipment. Work in a cGMP area and/or clean room environment. Accurately complete documentation in batch records, logbooks, forms and other GMP documents; Verify and enter production parameters per SOP and Batch Records.
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Experience working in a sterile biological/pharmaceutical manufacturing environment is preferred. Janssen Pharmaceuticals, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for a Computerized Maintenance Management System Specialist.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Assists with infection control, general cleanliness and sterile conditions for the dental unit. Maintains and cleans the x-ray unit, film processor, autoclave, wet tank and dental unit in accordance to specifications.
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Evaluate technical and regulatory requirements against business needs in development and maintenance of corporate level policies, procedures and strategies impacting all Ethicon, Inc sterile, single-use and reusable products, facilities and contractors.
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Adheres to aseptic technique when opening sterile packages and preparing for the procedure. Establishes and maintains sterile field during surgical procedures in the operating room. Reports observed or suspected breaks in sterile technique and takes action according to policy.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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The QA Investigations Supervisor has the responsibilities for providing quality oversight over the production of a personalized cell therapy to support both clinical and commercial requirements in a sterile GMP environment.
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