
Packaging Process Engineer II
- Petersburg, VA
- Permanent
- Full-time
- Management of equipment vendors including the execution of FAT & SAT, on-site maintenance visits, management of continuous improvement projects & spare parts criticality assessments.
- Complete FAT, SAT, Commissioning and Engineering Studies.
- Support Validation activities such as IQ, OQ, and PQ.
- Prepare the required cGMP documentation to support production operations.
- Coordinate technical deliverables across all business functions to support successful processes and product launches.
- Lead and participate in cross-functional teams to troubleshoot and resolve technical issues, drive continuous improvement, and process optimization using tools such as DMAIC and FMEA.
- Ability to quickly adapt and adjust priorities in response to unforeseen disruptions in operations.
- Manage changes for responsible equipment as per site change control procedures.
- Participate in regulatory inspections (e.g. FDA, DEA audits).
- Lead improvement of equipment reliability through CI and TPM processes to support the transition from project level to sustainable manufacturing/ramp up production.
- Exposure to pharmaceutical manufacturing and operations including pen assembly, packaging equipment, and line-level serialization systems preferred.
- Strong interpersonal and communication skills, both written and verbal.
- Ability to quickly adapt and adjust priorities.
- Project management experience.
- Ability to work effectively with outside suppliers.
- Knowledge of Lean/Six Sigma methodologies.
- Strong problem-solving skills.
- Strong mechanical aptitude and hands-on approach.
- Familiarity with engineering and architectural/construction drawings is highly advantageous.
- Demonstrated ability and willingness to accept ownership of new technical challenges and assigned projects. Passion for Civica's mission to provide affordable quality generic medicines that are accessible to all.
- 5+ years of experience within the discipline is required.
- B.S. in Engineering or Science discipline required.
- Experience working in a cGMP environment preferred.
- Ability to manage teams to execute activities on the manufacturing floor.
- Experience in a data-driven approach to root cause analysis and prioritization of continuous improvement initiatives (e.g., Six Sigma, 5-why, fishbone diagram).
- Ability to adapt to changing priorities as project demands and business needs change.
- CQV experience and greenfield facility start-up experience preferred.
- Ability to explain complex technical issues to external customers/agencies.
- Demonstrated excellence in planning and organizational skills