Packaging Engineer & Projects Lead — Drug Product

Verista; Indianapolis (IN); On-site; USD 70,000 - 103,000; Full time

Benefits offered by this job

Competitive pay

Medical, Dental & Vision

401(k) with company match

Paid Time Off

Tuition Reimbursement

Life & Disability Insurance

Job summary

Verista in Indianapolis is seeking a Packaging Engineer to develop primary and secondary packaging for drug products and to lead process development activities. You will work with internal and external stakeholders to advance projects from clinical development through commercialization, ensuring regulatory readiness. Onsite five days per week in Indianapolis.

The role requires a B.S. in Engineering (or related) and 1–3 years in pharma/medical device environments; strong cross-functional

Qualifications

• Bachelor of Science in Engineering or related field; 1–3 years pharma/medical device experience may substitute.
• Ability to lead cross-functional projects and influence decisions.
• Strong interpersonal skills and teamwork in a diverse network.
• Onsite requirement: 5 days per week in Indianapolis.

Responsibilities

• Plan and execute activities to design, qualify packaging components and container-closure systems.
• Collaborate with internal and external stakeholders to drive project progression.
• Lead studies to develop packaging specifications and filling profiles.
• Support regulatory and quality documentation and technical transfer activities.

Skills

Quality mindset

Project leadership

Cross-functional collaboration

Interdisciplinary teamwork

Education

B.S. in Engineering

Materials Science

Industrial Design

Job description

Verista in Indianapolis is seeking a Packaging Engineer to develop primary and secondary packaging for drug products and to lead process development activities. You will work with internal and external stakeholders to advance projects from clinical development through commercialization, ensuring regulatory readiness. Onsite five days per week in Indianapolis.

The role requires a B.S. in Engineering (or related) and 1–3 years in pharma/medical device environments; strong cross-functional