- Merck & Co. (Rahway, NJ)
- …and Biopharmaceutics team is responsible for the research and development of sterile & parenteral drug products for biologics including monoclonal antibodies (mAbs), ... primary packaging to enable phase appropriate regulatory filings for large molecule sterile products. -These sterile products include those administered via… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionPrincipal Scientist - Mixed Modalities, Sterile Product DevelopmentThe Mixed Modalities team within Sterile Product Development is responsible for ... formulation scientist responsible for the design and development of sterile products across injectable, implantable, ophthalmic, and inhaled dosage forms.Provide… more
- Merck & Co. (Rahway, NJ)
- …Practice (GMP) clinical supply manufacturing facility in Rahway, New Jersey.The Sterile Process Engineer role at the Associate Director level will leverage ... GMP standard operating procedures and protocols in support of sterile clinical drug product operations. This individual will leverage...on-site, based in New Jersey and reports to the Sterile Process Engineering Lead of the FLEx GMP facility… more
- Merck & Co. (Rahway, NJ)
- …Rahway, NJ FLEx (Formulation, Laboratory & Experimentation) center, primarily for sterile operations under the remit of Our Company's Research Labs Pharmaceutical ... group (Pharm Ops Engineering). The role is on-site and reports to the Sterile Pharm Ops Engineering Lead of the FLEx GMP facility within Pharmaceutical Operations… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …both clinical and commercial requirements in either a Grade C or sterile cGMP environment.Key Responsibilities Oversee cell therapy production and ensure safe and ... to cGMP requirements.Lead a ~250+ organization responsible for either the non- sterile or sterile manufacturing processes in a 24/7 operation and be responsible… more
- Merck & Co. (Durham, NC)
- …technical skills to contribute to the design, development and manufacturing of sterile products, making accessible our company's next generation of Vaccines and ... and teamwork skillsPreferred Experience and Skills:cGMP experience in a sterile bulk, biologics or pharmaceutical environment, operations, technical services, supply… more
- Aequor (Athens, GA)
- …Tasks to be completed may include aseptic filling of vials under sterile conditions, vial preparation and sterilization, capping of vials under non- sterile ... conditions, and general support activities related to filling. Operates general manufacturing equipment in strict accordance with SOPs to complete tasks as noted above. Brings deviations in process protocols to supervisors attention. Maintains all associated… more
- Aequor (Framingham, MA)
- …of projects in 's biologics pipeline. Key responsibilities will include sterile cell culture techniques with suspension cultures, pool and clone generation, ... cell line generation processes. Perform mammalian cell culture techniques: sterile technique, cell counting, passaging, cryopreservation, etc. Perform basic… more
- Merck & Co. (Durham, NC)
- …maintenance and spare parts procurement systemscGMP experience in a sterile , bulk or finished pharmaceutical environmentExperience authoring PM/calibration job plans ... and management of spare partsInstallation, operation, maintenance and/or troubleshooting experience with utility and Clean utility equipment such as boilers, chillers, Cooling towers, air compressors, waste deactivation systems, HVAC, clean steam, WFI.Ability… more
- Merck & Co. (Durham, NC)
- …troubleshooting and maintenance support to VMF Operations areas ( sterile supply, weigh/dispense, media, stabilizer/prep, thaw/pool, filling, capping/inspection, ... clean utilities etc.) located in aseptic and clean room environments.- Works within a team to perform maintenance and troubleshooting activities.- Completes complex maintenance tasks, resolves deviations and evaluates equipment performance.- Follows proper… more
- Merck & Co. (Millsboro, DE)
- …This position is responsible for overseeing late-shift activities to support the Sterile operations and Logistics Integrated Process Team (IPT) up to and including ... Central Services, Media Preparation, and Warehouse activities.Primary Responsibilities: Supervision of facilities, equipment and personnel, cross train across departments including coordination of additional labor, such as temporary employees or other… more
- Merck & Co. (Durham, NC)
- …troubleshooting and maintenance support to VMF Operations areas ( sterile supply, weigh/dispense, media, stabilizer/prep, thaw/pool, filling, capping/inspection, ... clean utilities etc.) located in aseptic and clean room environments.- Works within a team to perform maintenance and troubleshooting activities.- Completes complex maintenance tasks, resolves deviations and evaluates equipment performance.- Follows proper… more
- Merck & Co. (Rahway, NJ)
- …platforms.Deep understanding of clinical and commercial manufacturing requirements for sterile drug products, as well as combination product assembly ... processes.Extensive knowledge of US and global medical device and healthcare regulations, including FDA combination products cGMP, Quality System Regulation, FDA Human Factors guidance, ISO 14971, 11608 and 11040, EN 62366, Council Directive 93/42/EEC,… more
- Merck & Co. (Durham, NC)
- …amounts of data (ex. PowerApps, Spotfire)cGMP experience in a sterile , bulk or finished pharmaceutical environment.Mechanical functionality and reliability knowledge ... (asset management)Certified Maintenance Professional (CMRP, CRL, etc.)Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only:Our company is committed to inclusion, ensuring that candidates can engage in a hiring… more
- Merck & Co. (Durham, NC)
- …amounts of data (ex. PowerApps, Spotfire)cGMP experience in a sterile , bulk or finished pharmaceutical environment.Mechanical functionality and reliability knowledge ... (asset management)Certified Maintenance Professional (CMRP, CRL, etc.)#MSJR EBRG VETJOBSCurrent Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only:Our company is committed to inclusion, ensuring that candidates can… more
- Merck & Co. (Durham, NC)
- …maintenance and spare parts procurement systemscGMP experience in a sterile , bulk or finished pharmaceutical environmentExperience in automation and manufacturing ... execution systems (MES), process modeling and process improvement.Mechanical functionality and reliability knowledge (asset management)Experience working in a clean room or GMP/regulated manufacturing environmentExperience with formal problem-solving… more
- Insmed Incorporated (San Diego, CA)
- …knowledge to include performing western blots.Perform cell culture, sterile technique, and transfection.Qualifications:Bachelor's degree in Biology, Chemistry, or ... related field required. Graduate degree holders are encouraged to apply.Excellent communication skills with ability to interact professionally with colleagues and present research results in written reports and team presentations.Willingness to learn new… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …a personalized cell therapy to support both clinical and commercial requirements in a sterile cGMP environment. Job duties will be performed within a team based on ... an assigned production shift schedule.Shift Schedule: Sunday - Wednesday 2nd Shift (1PM-12:30AM)Key Responsibilities Support process operations by performing support specific and real-time floor service tasks (ie, kitting and kit cleaning, inventory management… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment. This role will serve as the business process owner ... for the Corrective and Preventive Actions (CAPA) process and is responsible for ensuring compliance within quality systems processes.Key Responsibilities Provide oversight to the CAPA program for the CAR-T manufacturing site.Oversee metrics, trending, and… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …manufacturing plant to support both clinical and commercial requirements in a sterile GMP environment. This role will also provide oversight of technical, ... qualification, and validation activities including data or document review and approval as needed. This role will be responsible for reviewing and approving qualification protocols, reports, risk assessments, technical studies, and any associated documentation… more
Related Job Searches:
Central Sterile Processing Technician,
Certified Sterile Processing Tech,
Certified Sterile Processing Technician,
Medical Supply Technician Sterile,
Sterile Processing,
Sterile Processing Tech,
Sterile Processing Tech II,
Sterile Processing Technician,
Sterile Processing Technician II,
Supervisor Sterile Processing