Validation Engineer I

South San Francisco, CA 94080 | Contract

Post Date: 08/07/2018 Job ID: 4590 Industry: Quality

Our client is a leading biotechnology company that discovers, develops, manufactures and commercializes medicines to treat patients with serious or life-threatening medical conditions. They are among the world' s leading biotech companies, with multiple products on the market and a promising development pipeline.

 

Duties:
  • This entry level position is for a Validation Contractor for the Validation Engineering group in South San Francisco Production (SSFP). 
  • The candidate will be responsible for supporting validation activities.
  • This includes supporting Periodic Reviews of validated equipment in SSFP, which entails review of change records for validation impact, through the TrackWise system.
  • The Periodic Review will also include review of monitoring data trends and validation lifecycle documents.
  • These reviews will be compiled in a Periodic Review summary report.
  • The contractor may support revalidation execution on equipment to ensure the equipment has been operating in a validated state, Cleaning Validation activities, New Product Introduction (NPI), and qualification of changes to GMP equipment. 
  • Activities may include but are not limited to protocol generation, execution of protocols, swab and rinse water sampling, data analysis, reviewing worksheets, obtaining batch records and QC results, and summary report authoring.
  • The contractor will be expected to work effectively with customers (System Owner and Technical SME and Quality) to complete these validation activities.
  • Contractor must follow all safe work practices including use of appropriate Personal Protective Equipment and  ensure training is up to date.

 

 

 

 

 

Skills:

  • The candidate must be highly self-motivated, have excellent organization and communication skills, be willing and able to work independently or as part of a multi-disciplinary team.  
  • Attention to detail is essential for a successful candidate. 
  • Experience in a GMP regulated environment and use of quality systems and processes such as change control and discrepancy / deviation processes is desirable, but not required.

 

Education:

  • A B.S. or higher in Engineering or Science discipline with 0-3 years of relevant experience.
Apply Online

Not ready to apply?

Send an email reminder to:

Share This Job:

Related Jobs: