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Senior Manager Drug Substance Technology & Engineering

Job in Thousand Oaks, Ventura County, California, 91362, USA
Listing for: Initial Therapeutics, Inc.
Full Time position
Listed on 2026-06-24
Job specializations:
  • Engineering
    Operations Manager, Regulatory Compliance Specialist
  • Management
    Operations Manager, Regulatory Compliance Specialist, Program / Project Manager
Salary/Wage Range or Industry Benchmark: 130000 - 160000 USD Yearly USD 130000.00 160000.00 YEAR
Job Description & How to Apply Below

Senior Manager Drug Substance Technology & Engineering

Amgen is seeking a Senior Manager to join the Drug Substance Technology & Engineering (DSTE) team at our Thousand Oaks, California site. In this onsite leadership role, you will oversee downstream purification manufacturing support unit operations supporting both clinical and commercial biologics drug substance, lead a team of downstream process engineers, and play a key role in early phase technology transfer and the manufacturing execution, process optimization, and strategic improvement initiatives across all phases of development and the commercialization lifecycle.

Location:

Thousand Oaks, CA
Travel:
Up to 10% domestic and international travel

Key Responsibilities
  • Support the development, scale‑up, tech transfer and manufacturing execution of cGMP clinical and commercial downstream purification processes including harvest, clarification, chromatography (Protein A, AEX, CEX, etc.), viral filtration, UF/DF, and sterile filtration.
  • Apply engineering principles and statistical analysis to: identify, develop and implement downstream process improvements into the manufacturing facility; resolve technical issues observed during scale‑up and/or manufacturing execution of purification processes.
  • Manage escalation and on‑floor support as required to achieve successful scale‑up and manufacturing objectives.
  • Interface with process development teams to ensure processes are robust and designed to deliver all quality attributes and enable manufacturing success.
  • Collaborate with Process Development, Quality, Manufacturing, Regulatory, Validation and Supply Chain to drive continuous improvements into our business processes.
  • Lead site activities for continuous process verification, process monitoring, optimization, complex investigation, and product life‑cycle management.
  • Ensure safety and compliance of process development activities.
  • Collaborate with other site‑functions and network drug substance teams in delivering plant goals.
  • Lead cross‑functional teams to resolve complex problems while meeting quality, schedule, and cost objectives.
  • Ensure manufacturing operations are aligned with the registered process.
  • Provide support for regulatory filing, inspection, and other CMC activities.
  • Serve as member of the ATO DSTE leadership team utilizing network thinking and innovative approaches to advance the drug substance organizational capabilities.
Supervising Others / Team Experience
  • Create multi‑year technical strategies for advancing business performance.
  • Ensure safe practices are followed.
  • Provide mentoring and expertise to staff on the downstream team.
  • Motivate, develop, and coach staff while promoting team collaboration.
  • Apply effective management practices in the direction and development of others.
Leadership and Influence
  • Identify and negotiate resources and develop timelines for project activities.
  • Collaborate within the department and interdepartmentally.
  • Provide scientific and technical leadership.
  • Ensure department staff are adequately developed and trained.
  • Provide adequate feedback through coaching and effective performance appraisal and development planning.
  • Initiate and encourage scientific collaboration with groups outside the department.
  • Manage project resources (material, labor, time, etc.) and elevate relevant issues to project lead and line‑management.
  • Build and maintain effective collaborations with partner organizations.
Decision Making and Judgment
  • Anticipate, proactively detect, and address problems related to departmental and interdepartmental activities.
  • Inform and consult department head and senior staff appropriately.
Qualifications Basic Qualifications
  • Doctorate degree and 2 years of biologics process development or commercial‑scale technical support experience, OR
  • Masters degree and 6 years of biologics process development or commercial‑scale technical support experience, OR
  • Bachelors degree and 8 years of biologics process development or commercial‑scale technical support experience, OR
  • Associates degree and 10 years of biologics process development or commercial‑scale technical support experience, OR
  • High school diploma / GED and 12 years of biologics process…
Position Requirements
10+ Years work experience
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