Manager/Sr. Manager, Drug Substance Contract Manufacturing

Location
San Diego, California
Posted
Jun 20, 2018
Required Education
Bachelors Degree
Position Type
Full time

Summary

The Manager is the lead technical chemist/engineer for commercial small molecule Drug Substance(s) and manages the activities at the corresponding contract manufacturing organizations (CMOs) within the supply chain network. The role provides technical and operational oversight of all cross-functional activities at the Drug Substance contract manufacturing sites, while ensuring that contractual commitments are honored. The role is accountable for the overall performance of assigned CMOs, including delivery, operational metrics, budget, and risk mitigation.

RESPONSIBILITIES:

  • Collaborates with internal cross-functional teams and CMOs to determine Drug Substance manufacturing requirements, identify and mitigate key risks, and ensure that manufacturing plans are executed as intended.
  • Ensures that synthetic processes are run according to the validated and approved process. In collaboration with CMC colleagues, identifies opportunities to optimize and improve the synthetic process.
  • Reviews pre- and post-production documents (e.g., master and executed batch records, protocols, technical reports), and manages the approval process for the same
  • Ensures on-time and predictable delivery of products and projects at assigned CMOs.
  • Manages stakeholder priorities across all commercial activities at Drug Substance CMOs.
  • Manages the operational activities (schedule, timelines, cost) of the CMOs, ensuring cost, quality, metrics, delivery and program objectives are met. Manages operational risk at the CMOs.
  • Provides Person-in-Plant coverage at assigned Drug Substance CMOs for critical production activities as and when needed.
  • Develops, executes and owns the supplier management process including relevant scorecards, to ensure appropriate controls, oversight and monitoring are in place
  • Supports the preparation and negotiation of RFQs, RFPs, Statements of Work (SOW), and Supply Agreements.
  • Supports validation activities for commercial products at assigned CMOs.
  • Partners with Quality Assurance to ensure CMOs are in compliance with all cGMP guidelines and SOP requirements
  • Supports the optimization of spend and resource allocation at the CMOs

 

Requirements:

  • Bachelor’s degree in Engineering, Science
  • Minimum of 5 Years of small molecule Drug Substance Manufacturing, Process Development or Engineering experience in the Pharmaceutical industry
  • Requires ability to travel minimum of 25% in North America, Europe and possibly other countries
  • Direct and proven CMO and Manufacturing Operations experience, including tech transfer, validation and commercial scale production of small molecule Drug Substances.
  • Demonstrated success in project planning, resource management, and collaboration with Development, Quality and development CMC.
  • Knowledge of how to negotiate and manage contracts, and establish and control budgets
  • Experience working in a cGMP-regulated environment, including knowledge of relevant US/EU regulatory and quality requirements, standards, and practices.
  • Strong knowledge of biotech/pharma small molecule manufacturing operations, and product and process development
  • Strong analytical and creative problem-solving skills.
  • Strong compliance orientation and attention to detail within a cGMP environment
  • Effective communicator at all levels; excellent written, oral and interpersonal communications and presentation skills.