August Bioservices-posted 3 months ago
Full-time • Mid Level
Nashville, TN
101-250 employees
Professional, Scientific, and Technical Services

Headquartered in Nashville, TN - one of the fastest-growing and most exciting cities in the United States - August Bioservices is a privately-owned, high-growth, and high-impact Contract Development Manufacturing Organization (CDMO). As a US-based outsourcing partner that provides a wide array of expert drug discovery, drug formulation, and drug manufacturing services to pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical industry. Our work is instrumental in helping to develop molecules today that can become the life-changing therapies of tomorrow. To support our growth plans, August is investing significant capital in a two-phase expansion project - including building a new state-of-the-art facility adjacent to our current facility. For those seeking dynamic opportunities, rewarding career paths and a chance to make a difference in global health, come grow with August! August Bioservices is looking for a Sr Validation Engineer team member that is passionate and driven regarding their work. August Bioservices needs a motivated individual to provide their expertise in the delivery of results for the company and its clients. Reporting to the Director of Validation and Metrology, the Sr Validation Engineer will be responsible for performing validation related tasks for the Nashville site. The Sr. Validation Engineer independently performs validation tasks to serve company and customer needs and to follow cGMPs.

  • Prepares validation protocols (IQ/OQ/PQ) and final reports for equipment and processes to assure they are in compliance with Code of federal regulations, (CFR), International Society for Pharmaceuticals Engineering (ISPE), and Aseptic Processing Guidance.
  • Will prepare and or review the User Requirement specifications, System Impact assessments, Design Specifications, Enhanced design reviews, and 21 CFR assessments.
  • Will be the validation lead for major site validation projects such as: equipment cleaning, cleanroom qualification, sterilizers, automated filling machines, utilities, WFI, and clean steam.
  • Will participate in Factory Acceptance testing and Site Acceptance testing.
  • Oversees and executes validation and re-validation studies.
  • Develops validation acceptance criteria.
  • Represents validation in agency and customer audits as an SME.
  • Writes and revises validation master plans, work instructions, and Standard Operating Procedures (SOPs).
  • Recommends validation procedural and test improvements.
  • Maintain current validation project schedules.
  • Provide training for both team validation members and contract validation personnel.
  • Review critical equipment drawings from a Validation perspective.
  • Review and summarize equipment history files to assess the validated state of equipment.
  • Proactively identifies potential obstacles to successful project completion.
  • Establishes remediation plans to overcome these obstacles.
  • Participates as validation representative on failure investigation teams.
  • BS in Biology, Biochemistry, Biotechnology, Microbiology, Chemical Engineering, Mechanical Engineering, Pharmaceutical Engineering or other related discipline.
  • 5+ years of experience with BS in Pharmaceutical, Biological or Biotech industry; hands-on experience in manufacturing operations or pilot lab / scale-up operations.
  • Excellent verbal and written communication skills.
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