Jobs at PPC Industries Inc.

Lead a global application development organization for healthcare solutions, overseeing quoting, rapid prototyping, commercialization, and cross-functional alignment to drive customer-centric innovation, scalable processes, and profitable growth.

Lead portfolio strategy and pricing for cardiovascular and structural heart medical device products in a CDMO environment. Manage full product lifecycle, support manufacturing (extrusion, molding, assembly), provide market intelligence, enable sales with technical expertise, and drive cross-functional execution to grow profitability.

Technical leader supporting global medical tubing and flexible packaging extrusion and converting. Drives process improvement, scale-up, capital projects, V&V, quality investigations, training, and standardization across sites. Leads data-driven programs to improve OEE, yield, and cost savings; provides subject-matter expertise for new product introductions and manufacturing support; travels ~25% to support sites.

Serve as the site continuity lead for business systems and identity/access, ERP and IQMS support, vendor and carrier coordination, industrial VLAN oversight, licensing and endpoint management (Microsoft 365, Intune, Apple Business Manager), procurement support, and executive-ready decision briefs for multiple manufacturing sites.

Drive medtech sales growth across a Southwest territory by identifying opportunities, managing key accounts, developing sales strategies, conducting customer visits, negotiating deals, forecasting sales, and collaborating with cross-functional teams to expand market share and gather customer insights.

Lead end-to-end development of medical films and flexible packaging from concept to commercial launch. Responsibilities include polymer film and conversion process development, prototyping, pilot scale-up, validation (IQ/OQ/PQ), regulatory compliance (ISO 11607/13485, FDA), cross-functional project leadership, customer engagement, and continuous improvement using DOE/Minitab and risk management (FMEA).

Responsible for process control, risk management, and quality assurance for medical tubing extrusion and blown film. Manage CAPA, customer complaints, clean room operations, audits, SOPs, validations, and cross-functional quality improvements to ensure ISO and cGMP compliance.

Supervise production shift activities including safety, product quality, line operation, staffing, discipline, metrics collection, training, and cleanliness. Ensure GMP/ISO compliance, accurate production records, proper material usage, and act as IT point of contact. Support maintenance and provide regular shift performance reporting.

Manage manufacturing/production operations including assembly, machinery, processing, and packaging. Set production schedules, ensure quality and cost targets, train and lead line teams, resolve operational issues, and drive continuous improvement using Lean/Six Sigma methods.

Lead commercial responsibility for Bio Pharma Processing (BPP) key accounts on the East Coast, driving year-over-year profitable revenue growth. Develop customer relationships, identify and close new opportunities, manage pipeline, negotiate contracts, provide forecasting and budgeting, implement go-to-market strategies, liaise with manufacturing and internal teams, utilize Salesforce for account management, and cross-sell across divisions. Travel up to 50%.

Drive profitable revenue growth across assigned Western U.S. accounts for DuPont Healthcare Solutions Life Sciences division by developing new business, managing key accounts, forecasting, cross-selling, and coordinating with internal teams. Use Salesforce for pipeline management, support manufacturing transfers, negotiate contracts, attend trade shows, and provide market intelligence. Up to 50% travel.

Support New Product Development in converting by leading continuous improvement projects, assisting with process validation and equipment qualification, conducting investigations and data collection, reporting project updates, and providing general engineering support while collaborating cross-functionally in an ISO 13485 environment.

Support product stewardship and regulatory compliance for materials across Spectrum sites. Maintain regulatory records, manage customer inquiries, guide project teams on design and certification requirements (e.g., UL, REACH, RoHS, EU MDR), perform risk and data analyses, and review quality documentation to ensure compliance with global standards.

Create and maintain detailed asset-level production schedules and tactical raw material plans. Coordinate between manufacturing, supply chain, maintenance, and suppliers to ensure material availability, manage delivery and storage, resolve supply/demand imbalances, monitor production performance, and support inventory, quality, and order issue resolution.

Supervise end-to-end converting/sterile packaging shift operations in a cleanroom medical device environment. Ensure safety, GMP and ISO compliance, meet production and quality targets, manage staffing and schedules, train and develop operators, maintain documentation and metrics, support investigations and continuous improvement, and coordinate with Quality, Engineering, and Maintenance to resolve issues.

Support manufacturing engineering projects focused on extrusion processing, production, and validation. Participate in continuous improvement and Lean/Six Sigma initiatives, assist with process optimization, documentation, validation transitions to production, and partner with Quality Assurance on compliance and problem investigations.

Lead and deliver QMS and cross-functional projects to improve compliance with ISO 9001, FSSC 22000, and ISO 13485. Manage planning, governance, risk, stakeholder communication, audits, CAPA execution, and change implementation to drive operational excellence and audit readiness.