of production scientists and operators in the scale-up, technology transfer, and execution of cGMP manufacturing. Develop employees...+ years of manufacturing experience in a cGMP setting. 1+ years of Management, Supervisory, or Lead experience. Preferred...
, a leading contract development and manufacturing organization (CDMO) and a recognized Center of Excellence for antibody-drug... conjugate (ADC) manufacturing. We are seeking passionate and enthusiastic professionals to contribute to our innovative...
. External applicants must be eligible to work in the US. Your Role: At MilliporeSigma, as the Manufacturing Technician 4... approaches, and perform support operations in a cGMP regulated environment for the support of API (Active Pharmaceutical...
of GMP regulations in a cGMP manufacturing environment. Proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint...Job Title: QC Supervisor Job Description As a QC Supervisor, you will lead a team of six QC Scientists responsible...
manufacturing for commercial product and stability testing. Prior experience in a cGMP environment is required. Responsibilities... and required instrumentation such as HPLC, UPLC, CGE, iCE, UV, pH, Osmolality, and cell-based bioassays. Knowledge of GMP regulations in a cGMP...
for an API Contract Manufacturing Organization. You will lead the Validation team to ensure the execution of validation... with Manufacturing, Project Management, Process & Analytical Development, Quality Control, Quality Assurance, Packaging, Materials...
manufacturing for commercial product and stability testing. Prior experience in a cGMP environment is required. Responsibilities... and required instrumentation such as HPLC, UPLC, CGE, iCE, UV, pH, Osmolality, and cell-based bioassays. Knowledge of GMP regulations in a cGMP...
machinery, pumps, valves, piping and cGMP's desirable. Previous experience working in a chemical manufacturing environment... sealer & other equipment and conveyors associated with the line Notify supervisor or other authorized personnel of the need...
and/or electronic records as required by management (i.e. cGMP or ISO procedures). Is responsible for keeping equipment and surrounding... work area clean at all times. Under the direction and monitoring of the department supervisor, I am responsible for the...
supervisor or other authorized personnel of the need for packaging supplies or other materials for the packaging line... as required. ⦁ Under the direction and monitoring of department supervisor, must be capable of training a replacement...
of results during a manufacturing operation Notify supervisor of critical in-process decisions based on analytical data... site performs manufacturing and cleaning operations in a facility which produces Active Pharmaceutical Ingredients (APIs...
product and service solutions around the globe. Position Summary: Based at the chemical manufacturing site, the Utility... to: aisle ways stairways lavatories lunchroom general manufacturing areas plant office floors parking lots stairways...
and/or electronic records as required by management (i.e. cGMP or ISO procedures). Is responsible for keeping equipment and surrounding... work area clean at all times. Under the direction and monitoring of the department supervisor, I am responsible for the...
Manufacturing Practice guidelines (ICHQ7) and Drug Products. This position reports to QC supervisor. You will be responsible..., calculation spreadsheets, audit trails, and time-of-use logs on cGMP instrumentation. Ensure laboratory testing complies...
to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume... drug manufacturing facility with around 1k employees. The GMP facility focuses on cell process development for clinical...