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Remote Pharma Technical Mgr

Key Facts

Remote From: 
Full time
Senior (5-10 years)
English

Other Skills

  • โ€ข
    Analytical Thinking
  • โ€ข
    Quality Assurance
  • โ€ข
    Decision Making
  • โ€ข
    Physical Flexibility

Roles & Responsibilities

  • 8+ years of experience in the DS (drug substance) manufacturing or development environment
  • Bachelor's degree in Science/Engineering/Operations or a related field
  • Experience with lifecycle management for commercial products
  • Knowledge of Good Manufacturing Practices (GMPs)

Requirements:

  • Support process change activities for drug substances, intermediates and raw materials
  • Support or lead investigations and resolve discrepancies in a timely manner
  • Work closely with DS manufacturing team to understand the capabilities, capacity availability and constraints at the CMOs
  • Provide technical oversight during GMP manufacturing campaigns

Job description

Remote Pharma Technical Mgr needs 8+ years of experience in the DS (drug substance) manufacturing or development environment

Remote Pharma Technical Mgr requires:

Bachelor's degree in Science/Engineering/Operations or a related field

Experience with lifecycle management for commercial products

Knowledge of Good Manufacturing Practices (GMPs)

Strong technical writing and analytical problem-solving capabilities

Exercise good judgment and make decision that is appropriate for the organization

Results-driven, take initiative and ownership to accomplish work

Ability to demonstrate flexibility and embrace change in a dynamic, rapidly growing environment

Remote Pharma Technical Mgr duties

Support process change activities for drug substances, intermediates and raw materials

Support or lead investigations and resolve discrepancies in a timely manner

Work closely with DS manufacturing team to understand the capabilities, capacity availability and constraints at the CMOs, develop plans to secure capacity appropriately

Provide technical oversight during GMP manufacturing campaigns

Work closely with Quality Assurance, Regulatory Affairs, Supply Chain, and external manufacturing partners to ensure alignment on timelines and deliverables

Ability to work independently with minimal guidance

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