Process Engineer III - Serialization

Resilience is a technology-focused biomanufacturing company changing the way medicine is made. We are building sustainable, high‑tech, end‑to‑end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need.

Process Engineer III – Serialization serves as the subject matter expert (SME) for serialization systems while providing engineering support for a designated low‑volume pharmaceutical production line. This role ensures reliable operation, compliance, and continuous improvement of serialization processes in alignment with regulatory requirements, driving performance, quality, and efficiency on the assigned manufacturing line.

• Project & Technical Leadership
  • Lead small‑to‑medium engineering projects, including equipment upgrades and process improvements
  • Support new product introductions (NPI) and technology transfers into manufacturing
  • Interface with external vendors and integrators for system support and enhancements
  • Mentor junior engineers and provide technical guidance across the team
• Serialization Systems SME
  • Act as the site SME for serialization systems, including aggregation, vision systems, and data management platforms
  • Troubleshoot serialization equipment and software issues, coordinating with vendors and IT as needed
  • Lead and support serialization‑related deviations, CAPAs, and change controls
  • Develop and maintain SOPs, work instructions, and training materials related to serialization processes
  • Support audits and inspections by regulatory agencies and clients
• Manufacturing Line Support
  • Provide daily engineering support for an assigned low‑volume production line
  • Troubleshoot equipment and process issues to minimize downtime and maintain production schedules
  • Lead or support root cause investigations and implement corrective actions
  • Drive continuous improvement initiatives focused on safety, quality, and efficiency
  • Collaborate with Operations, Quality, Maintenance, and Supply Chain to ensure smooth execution of production
  • Support process validation activities, including IQ/OQ/PQ and continued process verification

• Hands‑on experience with serialization systems (e.g., vision systems, aggregation, Level2/3 systems)
• Strong knowledge of GxP environments and regulatory requirements (FDA, EMA)
• Experience with validation (IQ/OQ/PQ), change control, and deviation management
• Experience with automated inspection/packaging equipment (preferred)
• Ability to analyze data and implement process improvements

• Bachelor’s degree in engineering (Mechanical, Chemical, Biomedical, or related field)
• Experience in contract manufacturing organization (CMO/CDMO) environments
• 5–8+years of experience in pharmaceutical or medical device manufacturing (contract manufacturing preferred)
• Familiarity with serialization platforms (e.g., Systech)

Work authorization sponsorship or support for visas is not available for this position.

Resilience is an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, physical or mental disability, genetic information, or characteristic, or other non‑job‑related characteristics or other prohibited grounds specified in applicable federal, state, and local laws.

Requests for reasonable accommodation can be made at any stage of the recruitment process.

Benefits include an annual cash bonus program, a 401(k) plan with a generous company match, comprehensive health coverage (medical, dental, vision), family building benefits, life and disability insurance, paid vacation, paid holidays, additional paid leaves of absence, tuition reimbursement, and caregiving support. The target base pay range for this position is $80,000.00 – $ per year, dependent on location, experience, and qualifications.