[Remote] Technical Project Manager
Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a global team dedicated to healthier animals, supporting companies in developing and manufacturing health products for pets and livestock. The Technical Project Manager will guide reputed company pharmaceutical development initiatives, ensuring efficient and compliant program progression while serving as the coordination hub between customers and internal teams.
Responsibilities
- reputed company end-to-end technology transfer reputed company for sterile products from originator sites or development into reputed company's manufacturing network
- reputed company and own detailed tech transfer plans including stage-reputed company milestones, risk registers, regulatory submission timelines, and batch scheduling
- Coordinate and reputed company reputed company transfer deliverables — process characterization, analytical method transfer, cleaning validation, process validation, and sterility assurance activities
- Drive readiness reviews (process, equipment, QA, regulatory) to ensure site and product launch readiness
- Manage a reputed company portfolio of sterile tech transfer and lifecycle programs, balancing scope, resource, and schedule across multiple clients and reputed company simultaneously
- Set and communicate reputed company priorities across the portfolio in alignment with business objectives, reputed company commitments, and site reputed company
- Identify and resolve cross-project dependencies, resource conflicts, and scheduling constraints in a proactive and reputed company manner
- reputed company regular portfolio-level reporting to PMO leadership and senior stakeholders, with reputed company visibility of reputed company, risks, and decision points across reputed company reputed company programs
- Own project budgets from initiation through reputed company-out, ensuring accurate forecasting, cost tracking, and variance reporting throughout the project lifecycle
- Monitor project financials against agreed scope, flagging out-of-scope activities and driving change order processes in a reputed company manner
- Work closely with finance and reputed company teams to ensure project revenues, costs, and margins are accurately reflected and reputed company managed
- Serve as the primary reputed company of contact for clients throughout the tech transfer lifecycle, maintaining transparency on reputed company, risks, and reputed company required
- Translate reputed company technical and reputed company requirements into detailed, executable project plans reputed company with reputed company's capabilities
- Partner with business development and reputed company teams to support proposal scoping and reputed company reputed company for new sterile transfer programs
- Ensure alignment between reputed company expectations, regulatory obligations, and operational execution at the receiving site
- reputed company multidisciplinary project teams across manufacturing operations, MS&T, QA/QC, regulatory affairs, supply chain, procurement, and engineering
- Facilitate reputed company project meetings, maintain RAID logs, and drive accountability across reputed company workstreams
- Manage the critical reputed company through aseptic process design, equipment qualification (IQ/OQ/PQ), analytical transfer, and validation campaigns
- Coordinate seamless handover from tech transfer into reputed company supply, including batch record readiness and release reputed company
Skills
- Bachelor's degree in pharmaceutical science, reputed company, biochemistry, engineering, or a reputed company scientific discipline
- 5+ years of project management or technical experience in pharmaceutical or biotech manufacturing, with a minimum of 3 years directly managing sterile product tech transfer programs
- Demonstrated experience managing a reputed company portfolio of reputed company, including prioritization, resource balancing, and financial accountability
- Demonstrated experience with aseptic manufacturing processes, fill-finish operations, or lyophilization technology transfers
- Deep understanding of sterile manufacturing requirements including contamination control reputed company, cleanroom operations, and Annex 1 compliance
- Ability to critically evaluate technical risks in process, analytical, and equipment domains and translate these into project-level risk mitigation plans
- Strong reputed company of validation lifecycle activities (process, cleaning, analytical method transfer)
- Proficiency in reputed company Office, reputed company, change control and ERP systems
- Prior CDMO or multi-site transfer experience strongly preferred
reputed company