Description:

• BSc/BEng plus previous experience in CQV field or equivalent combination of education and experience.
• Experience in pharmaceutical/biopharmaceutical industry or related industry/manufacturing environment.
• Areas of experience: plant utilities, clean utilities, CIP, SIP, Fill Finish, HVAC, Filling lines, CTUs, component prep equipment, formulation.
• Well-developed communication skills, both verbal and written.

Essential Duties and Responsibilities:

• Writes and executes commissioning, qualification, & validation protocols for facilities utilities, equipment, and computerized systems
  Writes final reports
  Resolves protocol discrepancies and deviations
  Reviews vendor generated validation protocol packages
  Responsible for the generation of complex protocols using a risk-based approach that meets current regulatory requirements and industry practices

Other Skills and Abilities:

• Excellent oral and written communication
  Ability to effectively manage time and prioritize tasks independently
  Excellent organizational skills
  Ability to manage day-to-day operations in a fast-paced environment
  Ability to effectively manage several tasks simultaneously
  Must be self-motivated and have a proven ability to work in a team environment

Local candidates only Areas of experience: plant utilities, clean utilities, CIP, SIP, Fill Finish, HVAC, Filling lines, CTUs, Free parking onsite Top must-have skills: - Validation experience specific to pharma or biotech - 4 years of experience, willing to accept more years of experience.