Process Engineer II _ Automated Visual Inspection (544)

BioSpace; Petersburg (VA); On-site; USD 85,000 - 110,000; Full time

Job summary

Civica in Petersburg, Virginia is seeking a Process Engineer II, Automated Visual Inspection to advance packaging operations. You will coordinate vendor activities through design, fabrication, installation and qualification, and provide front-line technical support to Manufacturing.

The role requires 6+ years in process engineering, 3 years in automated vision systems, a BS in Engineering or Science, and experience with Six Sigma, DMAIC and FMEA.

Qualifications

• 6+ years of Process Engineering experience.
• 3 years of automated vision system experience.
• B.S. in Engineering or Science discipline.

Responsibilities

• Coordinate equipment vendor activities through design, fabrication, installation, and qualification.
• Provide front-line technical support to Manufacturing.
• Draft and execute engineering trials, DOEs, and cGMP documentation.
• Lead cross-functional teams to troubleshoot issues and drive process improvements.
• Manage changes per site change control procedures.
• Participate in regulatory inspections (e.g., FDA, DEA).

Skills

Process engineering

Project management

Root cause analysis

Six Sigma

Lean manufacturing

Vendor coordination

Education

Bachelor's degree in Engineering or Science

Job description

Job Description Essential Duties and Responsibilities: The Process Engineer II, Automated Visual Inspection, will be an integral part of the development of packaging operations at Civica's manufacturing facility in Petersburg, Virginia. Key duties include coordinating equipment vendor activities through design, fabrication, installation, and qualification; and serving as front-line technical support to Manufacturing. Responsible for automated visual inspection machines for vials, cartridges, and syringes, including de-nesting and re-nesting systems. The successful candidate will routinely interface with outside vendors, Manufacturing, Quality, Engineering, Supply Chain, and Maintenance. The essential functions include, but are not limited to the following:

• Management of equipment vendors including the execution of FAT & SAT, on-site maintenance visits, management of continuous improvement projects & spare parts criticality assessments.
• Support execution of the Commissioning & Qualification activities for responsible equipment including FAT, SAT, commissioning, IQ, OQ, and PQ.
• Responsible for drafting and executing engineering trials, DOEs, and preparation of required cGMP documentation for production operations.
• Draft risk assessments and specifications for defect kits to be utilized for equipment qualification.
• 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.
• 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.
• Prepare and update Preventative Maintenance (PM) tasks relating to production equipment maintenance needs.
• Lead and participate in investigations related to the equipment.

Basic Qualifications And Capabilities 6+ years of Process Engineering experience. 3 years of automated vision system experience. B.S. in Engineering or Science discipline. 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. Ability to explain complex technical issues to external customers/agencies. Demonstrated excellence in planning and organizational skills.Strong interpersonal and communication skills, both written and verbal. 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. Preferred Qualifications Experience working in a cGMP environment. CQV experience and greenfield facility start up experience. Physical Demands And Work Environment The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this position. Reasonable accommodation may be provided to enable individuals with disabilities to perform the functions. While performing the essential duties of this position, the employee is regularly required to speak or hear. The employee frequently is required to use hands or fingers, handle or feel objects, tools, or controls. The employee is occasionally required to stand; walk; sit; and reach with hands and arms. The employee must occasionally lift and/or move up to 25 pounds. The noise level in the work environment is usually low to moderate. The company is an Equal Opportunity Employer, drug free workplace, and complies with ADA regulations as applicable.