- Cipla (Fall River, MA)
- Job Title : Pkg. Documentation Specialist II FLSA Classification : Professional, Exempt Work Location : Fall River, MA Work Hours: General Shift: 8:30AM - 5:00PM ... Invagen Pharmaceuticals is searching for experienced candidates for the position of Documentation Specialist. The Documentation Specialist is responsible for the… more
- Christus Health (Beaumont, TX)
- …and completeness of the medical record documentation . The clinical documentation RN will provide support and expertise through comprehensive assessment ... Designs and implements in collaboration with physician leadership specific tools to support medical record physician documentation Develops and implements plans… more
- Aequor (Houston, TX)
- Role: Material Handler II Mon-Fri (Hours: 7:45am - 4:15pm CST) Location: Houston (100% on-site)*Ideal candidates will have Pharma manufacturing experience, SAP ... and 50% Production We're seeking driven and reliable individuals to join our Production Support team as a Material Handler. In this role, candidates will support … more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …the treatment of multiple myeloma.Legend Biotech is seeking a QA Change Control Specialist II as part of the Quality team based in Raritan, NJ.Role OverviewThe QA ... Change Control Specialist II role is an exempt level position with responsibilities...control process within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile… more
- Cipla (Central Islip, NY)
- …outside of Cipla's US Subsidiaries or Affiliates Job Title Warehouse Operator II Organization Name InvaGen Pharmaceuticals, Inc. Location Central Islip, NY locations ... schedule, pick list, or production record requirement. Make the necessary documentation entries. Deliver materials to specified locations in the warehouse. Load… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …the treatment of multiple myeloma.Legend Biotech is seeking a QA Shop Floor Specialist II /III as part of the Quality Operations team based in Raritan, New Jersey. ... of all aspects of the cell therapy clinical manufacturing process. Support manufacturing activities for cGMP compliance through spot checks/internal… more
- Cipla (Hauppauge, NY)
- …Cipla's US Subsidiaries or Affiliates. Job Title DPI Packaging Operator II Organization Name InvaGen Pharmaceuticals, Inc. Location Hauppauge, NY location Employment ... some combination thereof based on business needs. Responsibilities/ Accountabilities cGMP/ Documentation : Perform all functions according to current Good Manufacturing… more
- Cipla (Fall River, MA)
- Job Title : Manufacturing Operator II FLSA Classification : Full-Time, Non-Exempt/Hourly Professional Work Location : Fall River, MA Work Hours: First Shift: 7:00AM ... secondary requirement, this position will be expected to provide support to other operational functions to include but not...to batch and product to product change over. Online documentation and timely entries related to manufacturing and filling… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a Warehouse Associate II as part of the Technical Operations team based in Raritan, NJ.Role ... Operations team responsible for the production of a personalized cell therapy to support both clinical and commercial requirements in a sterile cGMP environment. Job… more
- Christus Health (Carrollton, TX)
- …for their journal entries and asking appropriate followup questions to ensure documentation is appropriate. In some cases, appropriate support will include ... as associated experience, then apply with your CV below. Summary: The Accountant II is responsible for preparing general ledger month-end journal entries relevant to… more
- Cipla (Central Islip, NY)
- …of Cipla's US Subsidiaries or Affiliates. Job Title Manufacturing Operator II Organization Name InvaGen Pharmaceuticals, Inc. Location Central Islip, NY Employment ... operate pharmaceutical production machinery independently and thoroughly complete required documentation (legible writing, accurate reporting, maintain and file, etc.)… more
- Insmed Incorporated (San Diego, CA)
- …science, we're in. Are you?About the Role:Insmed is seeking a Scientist II , Histologist with deep expertise in histology, molecular pathology, and translational ... science to support our gene therapy research and development programs. This...for morphological and pathology assessments. Analysis, Quality Control, and Documentation Examine slides under a microscope to evaluate tissue… more
- Shannon Health (San Angelo, TX)
- …Program of Study Required/Preferred High School Diploma or GED N/A Required or ( II ) RT, R (2141) Education Type Program of Study Required/Preferred High School ... not RCIS Certified prior to July 1, 2013 Experience Documentation of competency must be in education file for...manner on a regular or as needed basis. Level II Certification & Licensures (I) On-The-Job Training (2140) Certification/Licensure… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking CQV Specialist II as part of the Technical Operations team based in Raritan, NJ. Role ... position will be responsible for providing Commissioning, Qualification and Validation support to the cGMP Clinical and Commercial Cell Therapy Manufacturing plant.… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking QC Specialist, Lab Services, II /III as part of the Quality team based in Raritan, NJ. Role OverviewThe ... understanding of all Quality Control functions and business areas. May need supervision/ support to resolve some sophisticated issues. He/ She will serve as technical… more
- Aptyx (Charlotte, NC)
- …vendors on the sourcing of catheter materials, components, and processing Prepare documentation to support quality system for design functions (project plans, ... work on medical devices in the Development department in support of the department's objectives to provide goods and...equipment, including the creation of PM procedure as necessary Support of equipment maintenance, as appropriate for skills and… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …suites. Responsible for supporting production through on-floor knowledge and support , documentation to keep production running efficiently, supporting ... improvement initiatives and support colleagues Develop, write and support any documentation needed in the production as well as supporting trend reports… more
- Christus Health (Carrollton, TX)
- …their assigned applications in a timely and high-quality manner. The Systems Analyst II will provide application support and optimization. They work closely with ... Description Check all associated application documentation thoroughly before clicking on the apply button...bottom of this description. Summary: The Application System Analyst II serves as a liaison between system end-users (customers),… more
- BioAgilytix (Durham, NC)
- …keeping with regard to sponsor's samples, data, and reports ( documentation according to GxP guidelines)Additional Responsibilities:Other duties as neededMinimum ... federal, state, or local law.We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes,… more
- Caris Life Sciences (Phoenix, AZ)
- …than yourself, Caris is where your impact begins.** **Position Summary** The Technical Support Specialist II is responsible for the diagnosis, support , ... ensure hardware, software, and components for onsite and remote support Caris team members across the distributed environment are...a rapid growing fast paced environment. As a level II you will serve as a subject matter expert… more
