3574 QC Analyst II
This is an onsite business critical position contingent worker will be working onsite in Oceanside and required to take a mandatory weekly COVID test. SummaryConduct routine and non-routine analysis of manufacturing environment and in process commercial products according to standard operating procedures.Responsible for collecting, processing and reporting data.Apply knowledge of […]
3439 Manufacturing Technical Specialist II
Duties:In this position, you will need to work effectively as part of a team responsible for ensuring successful and efficient pilot plant upstream/downstream operations and support of the site launching capability for the production of marketed recombinant proteins and their respective tech transfers.The group conducts hands-on small scale and pilot […]
3336 Organizational Change Manager II (part-time)
Purpose:Organizational Change Management Expert for the project ‘Global Release Execution System’; Global Quality in Pharma Technology (PT). The goal of the project is to Improve Efficiency and Compliance of Batch Release globally.Provides Project Management expertise utilizing standard tools and consistent methodology. Job Description:Organizational change management (OCM): Assess and manage stakeholders, […]
3078 MRO Parts Technician
Summary:Responsible for maintaining & purchasing inventory of equipment parts and consumable materials in support of maintenance, manufacturing, quality control, and process development groups.Responsible for assisting MRO Parts Technicians and other storeroom staff. Job Responsibilities:Manage inventory of equipment parts and consumable materials in support of process development, maintenance, manufacturing, quality control […]
3079 Automation Engineer IV
Duties:Perform automation and instrumentation and control engineering design services for existing facility projects, including upgrades and capacity expansions, equipment upgrading and replacement.Produce and review design drawings and specification documents (URS, FS, DS, etc.).Generate, execute, and review design testing, generate and participate in functional specification testing, and perform field inspection services.Generate, […]
3114 Technical Change Management Documentation Specialist
Duties:Coordinate and document technical changes for Technical Transfer projects in Trackwise.Coordinate and execute document changes for Technical Transfer projects.Coordinate, execute and document Design Qualification for Technical Transfer projects.Draft change records and document deliverables in Trackwise.Execute document changes in Syncade and Condor.Manage, generate, modify, and support GMP documentation and drawing changes.Update/report […]
3077 Manufacturing BioProcess Technician
Duties:Responsible for producing innovative biotherapeutic medicine by interfacing with highly automated production systems and controls in cGMP manufacturing environments, and maintaining areas in high state of inspection preparedness.Operates production equipment for cell culture or purification that may include culture growth, process monitoring, sampling, harvesting, purification, formulation, freeze thaw and transfer.Performs […]
1647 Change Management Associate
Duties:Looking for a person interested in a development opportunity in change management.Lead communication and organization change management on Site Transformation and network IT/OT Transformation efforts.Provide support where needed in site initiatives and COVID-19 Incident Management Team (IMT).Prior communication and change management experience.Prior experience with being part of a major change/transformation […]
3080 QC Analyst II
Duties: Conduct routine and non-routine analysis of manufacturing environment and in process commercial products according to standard operating procedures. Responsible for collecting, processing and reporting data. Apply knowledge of good manufacturing practices and good laboratory practices on a daily basis. Compile data for documentation of test procedures and prepare reports […]
8048 QC Analyst II
Duties:Perform chemical testing in support of manufacturing operations, lot release and validation in accordance with standard operating procedures.Collect, process, and report data.Apply knowledge of good manufacturing practices and good laboratory practices on a daily basis.Conduct routine and non-routine analysis of manufactured products.Calibrate and maintain laboratory and instrumentation equipment.Revise and update […]