We are seeking a technical resource to
support
Sterile Manufacturing Operations
, with a focus on
inspection
engineering activities and parenteral inspection technologies
, supporting
ongoing operations, product transfers, and continuous improvement initiatives.

Key Responsibilities

• 
  Lead
  inspection
  engineering activities
• 
  Develop
  and implement
  new inspection technologies
• 
  Provide
  support for
  product transfers
• 
  Deliver
  operational support of inspection systems
  for sterile/biologic
  products
• 
  Lead
  process
  improvements
• 
  Execute
  validation and line trials
• 
  Troubleshoot
  inspection equipment
• 
  Manage
  inspection-related projects
  to ensure compliance, quality, and
  efficiency

Collaboration

• 
  Collaborate
  cross-functionally with
  manufacturing, engineering, quality, and
  validation teams
• 
  Ensure
  alignment with
  site priorities and regulatory requirements

Requirements

Qualifications / Requirements

• 
  Problem-solving
  capabilities
• 
  Experience
  in
  pharmaceutical sterile manufacturing environments
• 
  Scientist with experience in the inspection of serialized liquid parenteral products.
• 
  Experience with syringe inspection systems and processes.
• 
  Strong technical knowledge of inspection technologies and processes applied to liquid pharmaceutical products.
• 
  Fully Bilingual (English & Spanish)

Education & Experience (Inferred Based on Industry
Standards)

• 
  Bachelor’s
  degree in Engineering (Mechanical, Electrical, Industrial, Chemical, or
  related field) or applied sciences
• 
  Approximately
  5–10+ years of experience
  in sterile/biologic inspection systems
  or inspection technologies
• 
  Experience
  with validation, equipment troubleshooting, and implementation of
  inspection technologies