Vonco Products LLC
Integration (Process Validation) Engineer
Trevor, WI
Get past the screening software and onto a recruiter's desk
hirly rewrites your resume for this job — matching the keywords and skills in the posting, moving your most relevant experience to the top, and writing a cover letter to fit. About 30 seconds.
- Keywords matched to this posting
- Fit score before you apply
- Cover letter included
Matched against 2.4M live jobs from 200,000+ employers in 200+ countries.
Tailor my resume for this job →Apply from your AI assistant
Connect hirly to Claude and ask it to apply to this job. hirly tailors your resume, fills the employer’s form and asks before sending. ChatGPT: manual setup today.
Some employer sites stop an application at a CAPTCHA or sign-in and hand it back with a link. Applying needs a paid plan. Works with any assistant that supports MCP.
hirly's read of this role
- Seniority
- Mid level
- Country
- US
- Work mode
- On-site / unstated
- First seen by hirly
- 26 Sept 2026
Derived automatically from the posting. Upload your resume above to see how the role scores against it.
the posting
Description
Integration (Process Validation) Engineer
Medical Device Contract Manufacturer – Flexible Films & Packaging
Position Summary
The Integration (Process Validation) Engineer is responsible for leading and supporting process validation and manufacturing integration activities for medical device packaging, flexible film converting, and related manufacturing processes. This role ensures manufacturing processes are developed, validated, transferred, and maintained in compliance with FDA Quality System Regulation (21 CFR Part 820), ISO 13485, customer requirements, and internal quality standards.
The engineer will work cross-functionally with Operations, Quality, Design Engineering, and customers to support new product introductions, process improvements, equipment qualifications, and ongoing manufacturing validation activities.
Reporting Structure
Reports To: VP of Quality and Integration Engineering
Department: Integration Engineering
Essential Duties and Responsibilities
Develop and execute IQ, OQ, and PQ validation protocols and reports.
Lead validation activities for flexible film converting, RF welding, heat sealing, pouch manufacturing, printing, and labeling operations.
Perform process capability studies and statistical analysis to support validation activities.
Establish process windows, critical process parameters, and acceptance criteria.
Support new product introductions (NPI) from concept through commercial production.
Identify and implement process improvements focused on quality, efficiency, scrap reduction, and throughput.
Lead root cause investigations and corrective actions related to process performance.
Ensure compliance with FDA 21 CFR Part 820 / QMSR, ISO 13485, GMP requirements, and customer-specific quality requirements.
Support internal, customer, and regulatory audits.
Project Management & Customer Communication
Lead cross-functional project activities related to process validation, equipment implementation, and new product integration.
Develop and manage project timelines, deliverables, and validation schedules to support customer and internal milestones.
Coordinate activities between Engineering, Quality, Operations, Supply Chain, and customer teams to ensure successful project execution.
Serve as a primary technical point of contact for customers during new product introductions, validation activities, process transfers, and ongoing manufacturing support.
Communicate project status, technical risks, validation progress, and issue resolution plans to internal leadership and customers.
Facilitate customer meetings, technical reviews, and validation planning discussions.
Support quotation reviews and provide technical input related to manufacturability, process capability, and validation requirements.
Collaborate with customers to understand product requirements, critical-to-quality characteristics, and regulatory expectations.
Support customer visits, audits, factory acceptance activities, and production trials as needed.
Requirements
Required Qualifications
Bachelor’s degree in Engineering or related technical field required.
3+ years of engineering experience in a regulated manufacturing environment.
Experience with process validation in regulated manufacturing.
Working knowledge of IQ/OQ/PQ methodologies, statistical analysis, root cause analysis tools, and risk management methodologies.
Knowledge of FDA 21 CFR Part 820 and ISO 13485 requirements.
Strong technical writing and documentation skills.
Preferred Qualifications
Experience in flexible films, medical packaging, or converting operations.
Experience with RF welding, heat sealing, extrusion, laminating, pouch manufacturing, or printing technologies.
Experience supporting customer audits and regulatory inspections.
Experience with EQMS systems.
Key Competencies
Strong analytical and problem-solving skills
Project management and organizational skills
Attention to detail and documentation accuracy
Effective communication and collaboration skills
Ability to manage multiple priorities in a fast-paced manufacturing environment
Customer-focused mindset
Similar jobs
- FORCE INTEGRATION AND READINESS OFFICER TITLE 32 INDEFINITEArmy National Guard Units · Concord, New Hampshire, United StatesFirst seen today
- Integration and Automation Engineer Fullbay · Phoenix, Arizona, RemoteFirst seen todayremote
- Systems Integration EngineerContexture · Multiple Bases (Phoenix, Denver, or Grand Junction), ArizonaFirst seen today
- Workday Integrations Post Production Consultant ITopbloc · Chicago - IllinoisFirst seen today
- Workday Integrations Consultant ITopbloc · Chicago - IllinoisFirst seen today
Browse similar roles
Want this one?
Upload your resume and hirly rewrites it for this job and writes the cover letter — in about thirty seconds, before you sign up.
Tailor my resume for this job