After having met several important milestones including exciting clinical data, we are poised for new strategic objectives which will require significant new resources. Those new resources include a well-qualified QA Validation Specialist.

Provide QA oversight of Validation programs at Argos, including review and approval of IQ/OQ/PQ documentation. Ensures that all new or existing equipment, utilities, methods, and processes are adequately validated in accordance with company and regulatory requirements.


  • Provides QA oversight and/or review during the validation process
  • Supports the Validation Department in evaluating all tests needed to qualify critical equipment, utilities, methods, and processes
  • Performs Quality review and/or approval of Validation Protocols and Final Reports in support of validation efforts
  • Supports Quality review and/or approval of all applicable deviations, investigations, and CAPAs related to qualification and validation
  • Supports execution of FAT, SAT and equipment commissioning activities as required
  • Supports continuous improvements to Master Validation Plans, quality system practices, validation protocols and procedures and overall validation strategies
  • Develops and revises applicable SOPs and provides compliance oversight and support to other departments upon request
  • Supports and participates in the change control process for critical equipment, utilities, methods and processes
  • Completes appropriate documentation to assure compliance with GMP and Specifications
  • Supports established work priorities to meet targets and timelines
  • May participate in Core Member process teams, as needed
  • Other duties as required


  • Prefer Bachelors or Masters degree in a scientific, engineering discipline or equivalent
  • A minimum of five years industrial cGMP experience in an FDA regulated Biopharmaceutical
    environment with 3+ years QA validation experience
  • Solid knowledge of qualification/validation principals and their practical applications
  • Previous experience with the start-up and validation of a cGMP facility is preferred
  • Strong written and verbal communication skills
  • Strong computer skills (Word, Excel, PowerPoint, etc.)
  • Strong interpersonal communication skills
  • Demonstrated initiative and attention to detail
  • Demonstrated ability to multitask and meet deadlines
  • Ability and desire to work in cross-functional teams
  • Ability to work independently with minimal direction
  • Ability and willingness to be regularly, predictably and reliably at work

We offer a competitive compensation package along with outstanding benefits. For confidential consideration, please submit a resume with a cover letter and salary history.

No phone calls please.

Argos Therapeutics is an Equal Opportunity Employer.