Validation Engineer

Azzur is a GxP compliance and consulting organization dedicated to providing high quality, expertly backed, assistance that drives life science companies to success. We are seeking highly motivated and talented individuals to join our incredible team of skilled problem solvers. Qualified candidates must have a desire to learn, apply, engage, and adapt in the ever-changing healthcare field while simultaneously and organically exuding Azzur’s core values:

Put Others First, Courage to Take Action, Take Personal Responsibility and Have Fun!

Responsibilities:

• Writes procedures, investigations, protocols, reports, change
  controls, etc. to support the Maintenance and Engineering, Validation,
  Quality, and Regulatory departments. 
• Generates validation life cycle documentation (FAT, SAT, IOQ,
  PQ) for cleaning, sterilization, shipping, and processes validation and
  facilities, utilities, systems, equipment qualification/requalification.
• Writes and revises a variety of Installation, Operation and
  Performance qualification/verification related documents, including any of
  all of the following: SOPs, validation/verification master plans, guidelines
  and execution plans, automation test plans, engineering design reviews,
  commissioning, qualification or other technical documents, user
  requirement specifications (URS), functional requirement specifications
  (FRS), detailed design specifications, factory acceptance test documents
  (FAT), and/or commissioning test procedures.
  
• Performs on site or support work for a client under supervision, including
  but not limited to:
• Validation protocol execution for FAT/SAT/IQ/OQ/PQ, thermal
  mapping of temperature controlled chambers, warehouses, and
  sterilization processes
• Equipment Qualification test execution
• Investigations and deviations
• Risk analysis, and/or
• Data integrity assessments and review of client data
• Executes protocols and helps resolve deviations/discrepancies,
  analyze study data and write summary reports, under supervision of
  senior consultants.

Qualifications and Experience:

• Bachelors Degree in engineering, science, or similar field or equivalent experience; Preferred Education: Masters Degree in engineering, science, or similar field
• 2-8 years experience in validation services in a regulated, manufacturing environment within the biotechnology, pharmaceutical, or medical device industry
• Experience in executing protocols including systems such as Process Validation, utilities, manufacturing equipment and basic knowledge of laboratory validation
• Experience with temperature mapping
• Experience with many aspects of validation
• Working knowledge of FDA and cGMP regulations and documentation practice
• Ability to read and interpret Piping and Instrument Diagrams (P&IDs), and electrical diagrams

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