Piper Companies
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Filling CQV Engineer Jr.
role at
Piper Companies The
Filling CQV Engineer Jr.
will join a leading global pharmaceutical company that is rapidly expanding its international presence, with plans to double in both size and production in the coming years. This role supports a Manufacturing Facility in
Indianapolis, Indiana , and focuses on commissioning, qualification, and validation (CQV) of aseptic filling equipment. The
Filling CQV Engineer Jr.
will be responsible for protocol development, IOQ execution, and airflow testing, contributing to a high-performing team with a strong track record of success. Hours and Location
This position will follow standard hours: Monday through Friday, 8:00 AM to 5:00 PM, onsite in Indianapolis, Indiana. Responsibilities
Support CQV of a Cytiva Aseptic Filler (no upstream washer or tunnel). Execute IOQ protocols and airflow testing; potential involvement in design qualification. Collaborate on protocol development including user requirements and component assessments. Work with subject matter experts to ensure all inputs are captured for comprehensive protocol creation. Maintain high standards of quality, compliance, and execution in a regulated environment. Participate in continuous improvement initiatives and support site operations. Communicate effectively with stakeholders and contribute to team meetings and planning. Uphold all safety and environmental standards in daily operations. Qualifications
Bachelor’s Degree in Engineering or equivalent relevant experience. 2–3 years of CQV experience, including protocol development and component assessments. Strong understanding of user requirements and validation documentation. Familiarity with cGMP standards and regulated manufacturing environments. Excellent soft skills: hunger, motivation, and ability to thrive in a fast-paced, execution-heavy role. Strong analytical, problem‑solving, and organizational skills. Compensation & Benefits
Competitive hourly rate: $40–55/hr, based on experience. Full benefits package including Medical, Dental, Vision, 401K, PTO, Sick Leave, and Holidays. Key Words: Validation Specialist, CQV, IOQ, Protocol Development, Component Assessment, Aseptic Filling, cGMP Compliance, Root Cause Analysis, Change Control, Technical Documentation, Quality Assurance, Airflow Testing, Design Qualification If you are passionate about ensuring high standards in validation, compliance, and process improvement, we encourage you to apply today! This job opens for applications on 8/11. Applications for this job will be accepted for at least 30 days from the posting date.
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Filling CQV Engineer Jr.
role at
Piper Companies The
Filling CQV Engineer Jr.
will join a leading global pharmaceutical company that is rapidly expanding its international presence, with plans to double in both size and production in the coming years. This role supports a Manufacturing Facility in
Indianapolis, Indiana , and focuses on commissioning, qualification, and validation (CQV) of aseptic filling equipment. The
Filling CQV Engineer Jr.
will be responsible for protocol development, IOQ execution, and airflow testing, contributing to a high-performing team with a strong track record of success. Hours and Location
This position will follow standard hours: Monday through Friday, 8:00 AM to 5:00 PM, onsite in Indianapolis, Indiana. Responsibilities
Support CQV of a Cytiva Aseptic Filler (no upstream washer or tunnel). Execute IOQ protocols and airflow testing; potential involvement in design qualification. Collaborate on protocol development including user requirements and component assessments. Work with subject matter experts to ensure all inputs are captured for comprehensive protocol creation. Maintain high standards of quality, compliance, and execution in a regulated environment. Participate in continuous improvement initiatives and support site operations. Communicate effectively with stakeholders and contribute to team meetings and planning. Uphold all safety and environmental standards in daily operations. Qualifications
Bachelor’s Degree in Engineering or equivalent relevant experience. 2–3 years of CQV experience, including protocol development and component assessments. Strong understanding of user requirements and validation documentation. Familiarity with cGMP standards and regulated manufacturing environments. Excellent soft skills: hunger, motivation, and ability to thrive in a fast-paced, execution-heavy role. Strong analytical, problem‑solving, and organizational skills. Compensation & Benefits
Competitive hourly rate: $40–55/hr, based on experience. Full benefits package including Medical, Dental, Vision, 401K, PTO, Sick Leave, and Holidays. Key Words: Validation Specialist, CQV, IOQ, Protocol Development, Component Assessment, Aseptic Filling, cGMP Compliance, Root Cause Analysis, Change Control, Technical Documentation, Quality Assurance, Airflow Testing, Design Qualification If you are passionate about ensuring high standards in validation, compliance, and process improvement, we encourage you to apply today! This job opens for applications on 8/11. Applications for this job will be accepted for at least 30 days from the posting date.
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