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Technical Project Manager – Controls & Data Systems

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Tucker Parker Smith Group

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Location:
United States , Northridge

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Contract Type:
Not provided

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Salary:

78.00 USD / Hour

Job Description:

We are seeking a Technical Project Manager with a strong engineering background and proven project management experience to lead initiatives involving control systems, data acquisition, and pharmaceutical manufacturing processes. This role supports late-stage development, technical transfer, and commercialization, with a focus on execution, compliance, and client engagement.

Job Responsibility:

  • Lead technical projects from initiation through completion, ensuring alignment with scope, schedule, and budget
  • Develop and maintain project plans, risk assessments, and resource strategies
  • Coordinate cross-functional teams across R&D, Quality, Regulatory, and Operations
  • Ensure compliance with GMP, FDA, and regulatory requirements
  • Oversee design, implementation, and optimization of control systems and data acquisition platforms
  • Support technical transfer activities for pharmaceutical manufacturing programs
  • Guide system integration, testing, and validation efforts
  • Apply Quality by Design (QbD) principles and statistical tools (DoE, FMEA, Gage R&R)
  • Serve as the primary point of contact for clients throughout the project lifecycle
  • Lead project kick-offs, technical reviews, and issue resolution
  • Clearly communicate technical concepts to internal and external stakeholders
  • Support client audits and regulatory inspections
  • Identify opportunities to improve process robustness, product quality, and efficiency
  • Contribute to Lean initiatives and best practice implementation

Requirements:

  • Bachelor's or Master's degree in Engineering (Chemical, Mechanical, Electrical, Biomedical, or related)
  • PMP certification (or equivalent) required
  • 7 years of experience in pharmaceutical manufacturing
  • Experience managing technical projects in regulated or CDMO environments
  • Strong background in control systems, automation, and data acquisition
  • Knowledge of cGMP and regulatory requirements
  • Excellent communication, leadership, and stakeholder management skills

Nice to have:

  • Experience with transdermal patch or inhalation (MDI) manufacturing processes
  • Familiarity with coating, laminating, die-cutting, or filling/crimping operations
  • Experience supporting CMC documentation for regulatory submissions (NDA/ANDA)
  • Lean Six Sigma or continuous improvement certification

Additional Information:

Job Posted:
April 24, 2026

Employment Type:
Fulltime
Work Type:
On-site work
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