Commissioning, Qualification, and Validation Engineer

At AST, we enhance the efficiency, productivity, and safety of flexible  aseptic manufacturing processes  for the worldwide Life Science Industry by offering innovative products, services, and solutions.  Do you want to contribute to a shared vision and mission?

Would you like to bring your unique talents to have a significant impact at a growing company?

At AST we strive to build a workplace that enables every team member to meet and exceed their capabilities.

We set our expectations high and provide the environment and resources necessary to bring out the very best.

AST is proud of our team.

Providing challenging and rewarding work, with opportunities for personal / professional development is our key to this longevity.

AST is an equal opportunity employer.  Compensation range for onsite WA applicants is $90,000 to $140,000.

All applicants are welcome to apply.   Employee benefits include :

• Medical (HSA & PPO), Dental, Vision, Long / Short term disability, HSA account with employer contribution, 401(K) (Traditional & Roth options) with up to 5% company match, Education Assistance, Paid Time Off (PTO), Paid Holiday, and bonus potential.  What will I be doing?
• AST is seeking a Commissioning, Qualification, and Validation (CQV) Engineer to join our Research and Development Team.
• The CQV Engineer will play an active role in spearheading and developing AST’s CQV initiatives and services.
• You will work cross functionally to contribute and execute AST’s strategic vision on products, services, and customer experiences.
• This role reports to the Principal CQV Engineer and is a full-time position that is located onsite in Tacoma, Washington.
• If the CQV Engineer position aligns with your goals and you share our passion for AST’s Mission, Vision, Purpose, Values and Key Behaviors, we want to hear from you.

Responsibilities :

50% travel required.

Qualifications :

At least 4 years of hands-on experience commissioning, qualifying, and validating filling and isolator systems in biotech / pharma manufacturing environments.   Proficient in validation lifecycle documentation :

Eligibility Requirements :