Bristol Myers Squibb
Join to apply for the
Process Engineer
role at
Bristol Myers Squibb Direct message the job poster from Bristol Myers Squibb Duration: 3 months (possibility of conversion to FTE or extension for the right candidate) Pay Rate: $48.76 to $61.93/hr on W2 50% onsite required Work Schedule: Mon- Fri (normal business hours) Job Description: The Technical Project Manager, Cell Therapy Technical Operations is responsible for planning and delivery of Cell Therapy Tech Transfer projects. The Technical Project Manager will serve in a multi-faceted role providing technical direction to drug product technology transfers as well as coordinating project details and progress. The role reports to the Technical Operations tech transfer lead. This role will operate within a larger project management structure to ensure technology transfer and operational readiness sub-teams are progressing toward overall goals. This role will also contribute directly to technical deliverables that enable the technology transfer of drug product processes. The Technical Project Manager will partner with cross-functional business teams including Technical Operations, Quality, Supply Chain, Regulatory as well as with external partners to coordinate execution deliverables, document technology transfer activities, build detailed project schedules, and manage and mitigate risks and issues. Responsibilities: Collaborate with cross-functional teams within client and external partners to support drug product technology transfers Develop content for technical team including risk mitigation plans, procedures, risk assessment and process models Contribute to authoring, review and execution of protocols for characterization, tech transfer and validation of drug product operations. Facilitate evaluation process changes, coordinating with change owners, suppliers and development teams to generate required data Author project charters including definition of high-level timelines and budget needs by consulting with project team, SMEs, and other stakeholders as necessary Define and manage detailed project schedule including routine communication of progress, risks, and issues Manages project/program activities including kick-off meetings, recurring status meetings, reporting, risk tracking, and conflict resolution. Manage risks and issues, including leading creation of mitigation plan and/or escalation as required Coordinates logistics for complex document approval and test results approval Develop and deliver stakeholder communications including regular project status updates Manage project change control for changes in scope and timeline Develop and implement tools to streamline project communication and status evaluation Work creatively and analytically to solve problems demonstrating teamwork and innovation Develop and deliver progress reports, proposals, requirements documentation, presentations, and risk assessments Lead process improvements within the Technical Operations team applying lessons learned, best practices, and innovations to mature project management processes, tools, and methodologies Knowledge & Skills: Basic understanding of cell culture, cryopreservation, purification, and aseptic processing or lab technique Knowledge of cGMP/FDA regulated industry Technical writing capability Experience successfully supporting biotechnology/cell therapy projects and/or programs Experience in SDLC Methodologies, Agile, SCRUM, SDLC/Waterfall preferred Leadership, diplomatic and motivational skills including the ability to work and drive issues to resolution cooperatively in a diverse group Knowledge of applications such as Microsoft Office Suite, Smartsheet, Microsoft Project or similar project management software, etc. Qualifications: Required Bachelors degree in Biology, Engineering, science or technical discipline. 2+ years of experience in Cell therapy of Biopharmaceutical operations. 2+ years experience in project/program management of complex projects involving cross-functional teams. Minimum 5 years of professional experience Demonstrated knowledge of, and competency in, project management processes, including planning, resource planning and allocation, and risk and issue management. PMP certification highly desirable. Familiarity with financial principles, core business concepts, and business and operations management. Ability to travel up to 20% within US Equal Opportunity Employer ASK Consulting is an equal opportunity employer and does not discriminate against employees or applicants based on race, religion, color, sex, national origin, age, sexual orientation, gender identity, genetic information, disability, veteran status, or any other classification protected by federal, state, or local laws.
#J-18808-Ljbffr
Process Engineer
role at
Bristol Myers Squibb Direct message the job poster from Bristol Myers Squibb Duration: 3 months (possibility of conversion to FTE or extension for the right candidate) Pay Rate: $48.76 to $61.93/hr on W2 50% onsite required Work Schedule: Mon- Fri (normal business hours) Job Description: The Technical Project Manager, Cell Therapy Technical Operations is responsible for planning and delivery of Cell Therapy Tech Transfer projects. The Technical Project Manager will serve in a multi-faceted role providing technical direction to drug product technology transfers as well as coordinating project details and progress. The role reports to the Technical Operations tech transfer lead. This role will operate within a larger project management structure to ensure technology transfer and operational readiness sub-teams are progressing toward overall goals. This role will also contribute directly to technical deliverables that enable the technology transfer of drug product processes. The Technical Project Manager will partner with cross-functional business teams including Technical Operations, Quality, Supply Chain, Regulatory as well as with external partners to coordinate execution deliverables, document technology transfer activities, build detailed project schedules, and manage and mitigate risks and issues. Responsibilities: Collaborate with cross-functional teams within client and external partners to support drug product technology transfers Develop content for technical team including risk mitigation plans, procedures, risk assessment and process models Contribute to authoring, review and execution of protocols for characterization, tech transfer and validation of drug product operations. Facilitate evaluation process changes, coordinating with change owners, suppliers and development teams to generate required data Author project charters including definition of high-level timelines and budget needs by consulting with project team, SMEs, and other stakeholders as necessary Define and manage detailed project schedule including routine communication of progress, risks, and issues Manages project/program activities including kick-off meetings, recurring status meetings, reporting, risk tracking, and conflict resolution. Manage risks and issues, including leading creation of mitigation plan and/or escalation as required Coordinates logistics for complex document approval and test results approval Develop and deliver stakeholder communications including regular project status updates Manage project change control for changes in scope and timeline Develop and implement tools to streamline project communication and status evaluation Work creatively and analytically to solve problems demonstrating teamwork and innovation Develop and deliver progress reports, proposals, requirements documentation, presentations, and risk assessments Lead process improvements within the Technical Operations team applying lessons learned, best practices, and innovations to mature project management processes, tools, and methodologies Knowledge & Skills: Basic understanding of cell culture, cryopreservation, purification, and aseptic processing or lab technique Knowledge of cGMP/FDA regulated industry Technical writing capability Experience successfully supporting biotechnology/cell therapy projects and/or programs Experience in SDLC Methodologies, Agile, SCRUM, SDLC/Waterfall preferred Leadership, diplomatic and motivational skills including the ability to work and drive issues to resolution cooperatively in a diverse group Knowledge of applications such as Microsoft Office Suite, Smartsheet, Microsoft Project or similar project management software, etc. Qualifications: Required Bachelors degree in Biology, Engineering, science or technical discipline. 2+ years of experience in Cell therapy of Biopharmaceutical operations. 2+ years experience in project/program management of complex projects involving cross-functional teams. Minimum 5 years of professional experience Demonstrated knowledge of, and competency in, project management processes, including planning, resource planning and allocation, and risk and issue management. PMP certification highly desirable. Familiarity with financial principles, core business concepts, and business and operations management. Ability to travel up to 20% within US Equal Opportunity Employer ASK Consulting is an equal opportunity employer and does not discriminate against employees or applicants based on race, religion, color, sex, national origin, age, sexual orientation, gender identity, genetic information, disability, veteran status, or any other classification protected by federal, state, or local laws.
#J-18808-Ljbffr