Validation Specialist

Azzur COD is looking for A Validation Specialist II who will provide validation services. Ensures compliance with relevant regulatory agencies in all activities, under some supervision, and may begin to supervise others at Azzur Clean Rooms On Demand (COD) locations.

• Writes procedures, investigations, protocols, reports, change controls, etc. to support the Maintenance and Engineering, Validation, Quality, and Regulatory departments. Documents are reviewed.
• Generates validation 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 or 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.
• Responsible for writing investigations, deviations, CAPAs and Change Controls with supervision.

• Performs on site or support work under some supervision, including but
  not limited to:
• Validation protocol execution for FAT/SAT/IQ/OQ/PQ
• Equipment Qualification test execution
• Investigations and deviations
• Risk analysis and/or Data integrity assessments and review of client data
• Executes protocols, helps resolve deviations/discrepancies, analyzes study data, and writes summary reports under supervision.
• Provides solutions to routine technical problems of limited scope with supervision. Supports the resolution of regulatory observations or manufacturing site issues.
• Responsible for tracking time to budget and notifying supervisors of any issues with deliverables.

• Bachelor’s Degree in engineering, science, or a similar field or equivalent experience.

• 2-3 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 Kaye Validator, Sensitech Temptale and other dataloggers.

•  Familiarity with aspects of Validation
•  Strong GMP and GDP
•  Kaye AVS software

• Working knowledge of FDA and cGMP regulations and documentation practices
• Familiarity with temperature mapping
• Familiarity with executing protocols, including systems such as Process Validation, utilities,
  manufacturing equipment and basic knowledge of laboratory validation

Benefits

Fulltime Employment with Azzur can offer you:

• Flexible PTO
• Training and Development Opportunities
• 401(k) match
• Bonus Eligibility
• Medical Benefits
• Paid Holidays
• Company provided laptop

Who we are:

Azzur Group is dedicated to providing clients with efficient, innovative quality and compliance solutions from Discovery to Delivery™. With more than 500 industry partners, including 80% of the top pharma/biotech manufacturers in the U.S., Azzur Group provides carefully calibrated and efficiently executed project management, process engineering, and compliance services. As one of the fastest-growing private companies in America, Azzur Group provides clients with consulting, facility solutions, engineering, validation, IT, technical, training, COD, laboratory services, and solutions they need to remain innovative and competitive.

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