Immunologist Project Manager
Bedford County, PA
Employment Type: Permanent (Shift: Days)
Job description
Responsible for oversight of the Polyclonal, monoclonal, and Pharmacokinetic departments and processes, in accordance with client specifications and/or work orders with the goal of providing consistent, high-quality products and services to our customers with complete, accurate documentation.
Responsibilities include (but are not limited to):
Listing and collaborating with external entities
Attending and participating in project team meetings and coaching research associates
Write and revise Standard Operating Procedures (SOPs) and Batch Records (BR) as needed.
Attend Client Meetings for new development of business
Collaborating with team members to design experiments and playing a creative role in problem-solving
Compliance with all Standard Operating Procedures (SOPs) in relation to project management
Providing routine project updates to internal and external clients for all projects currently being performed
Perform work in accordance with good manufacturing practices (cGMP) or Good Laboratory Practices (GLP) dependent upon study requirements.
Creating project reports/laboratory reports and maintaining records as needed
Assist in the preparation of investigation reports as part of the Corrective and Preventative Action (CAPA) program.
Implement additional training materials and marketing materials for Sales and Marketing.
Implement and update pricing models as required
Oversight of all project schedulers in the company in the Polyclonal, Monoclonal, and Parmacokinetic studies
Maintain knowledge of the latest developments in the immunology field.
Listing and collaborating with external entities
Attending and participating in project team meetings and coaching research associates
Write and revise Standard Operating Procedures (SOPs) and Batch Records (BR) as needed.
Attend Client Meetings for new development of business
Collaborating with team members to design experiments and playing a creative role in problem-solving
Compliance with all Standard Operating Procedures (SOPs) in relation to project management
Providing routine project updates to internal and external clients for all projects currently being performed
Perform work in accordance with good manufacturing practices (cGMP) or Good Laboratory Practices (GLP) dependent upon study requirements.
Creating project reports/laboratory reports and maintaining records as needed
Assist in the preparation of investigation reports as part of the Corrective and Preventative Action (CAPA) program.
Implement additional training materials and marketing materials for Sales and Marketing.
Implement and update pricing models as required
Oversight of all project schedulers in the company in the Polyclonal, Monoclonal, and Parmacokinetic studies
Maintain knowledge of the latest developments in the immunology field.