Piper Companies is hiring a skilled Junior Filling CQV Engineer for an onsite, contract position based out of Indianapolis, IN. The Junior Filling CQV Engineer will be responsible for executing commissioning and qualification activities—including IOQ and airflow testing—for aseptic filling equipment, while supporting protocol development and collaborating with a small on-site team in a pharmaceutical manufacturing environment.

Responsibilities of the Junior Filling CQV Engineer:

• Execute commissioning and qualification (C&Q) activities, including IOQ and airflow testing, for aseptic filling equipment.
• Support protocol development by incorporating user requirements and component assessments.
• Collaborate with a small, high-performing team on-site to deliver project milestones within a parenteral manufacturing environment.
• Contribute to design qualification efforts as needed, ensuring compliance with regulatory and quality standards.
• Participate in ongoing site deployment and carryover projects beyond the initial 6-month term.

Qualifications for the Junior Filling CQV Engineer:

• 2-3 years of experience in Commissioning, Qualification, and Validation (CQV), particularly in pharmaceutical or biotech settings.
• Proven experience developing protocols and working with user requirements and component assessments.
• Strong understanding of aseptic filling systems; experience with Cytiva equipment is a plus.
• Ability to work effectively in a project-based role with minimal supervision and strong team collaboration.
• Bachelor’s degree in Engineering or equivalent relevant experience.

Compensation for the Junior Filling CQV Engineer:
-

Salary: $80,000-$90,000 USD/year

• Benefits: Medical, Dental, Vision, sick leave if required by law, and 401K

• Execute commissioning and qualification (C&Q) activities, including IOQ and airflow testing, for aseptic filling equipment.
• Support protocol development by incorporating user requirements and component assessments.
• Collaborate with a small, high-performing team on-site to deliver project milestones within a parenteral manufacturing environment.
• Contribute to design qualification efforts as needed, ensuring compliance with regulatory and quality standards.
• Participate in ongoing site deployment and carryover projects beyond the initial 6-month term