Baxter International Inc.
Senior Manager, Plastics Engineering
Baxter International Inc., Skaneateles Falls, New York, us, 13153
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Senior Manager, Plastics Engineering
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Baxter International Inc. Our Mission to Save and Sustain Lives drives Baxter's culture of courage, trust, and collaboration. The Senior Manager – Plastics Engineering is a key role in the Plastics Engineering department within Global Engineering in Integrated Supply Chain. The group provides subject matter expertise in Tooling & Molding, including Injection Molding, Blow Molding & Extrusion. The incumbent is expected to have strong technical knowledge of tools, tool design, machines, technologies and suppliers in these areas. Experience in Medical Device New Product Development is required. Experience with a Structured Phase Gate Development approach is a plus, combined with application of DFM (Design for Molding & Design for Manufacturing) & DFA (Design for Assembly) principles is a must. Ability and mindset to train and develop junior team members is required. Manage financials and project timelines, including holding tooling vendors responsible for tool build quality and capability of molded products." What you will be doing
Lead & manage high profile, high complexity projects, including capacity expansion or replacement, new technology, and platform design & development projects. Manage technical design aspects of part design, tool design, capacity analysis, capital budget requirements, approvals, and broader molding & tooling strategy for internal manufacturing as well as Direct Procurement. Extensive & in‑depth knowledge of hot runner tool design and its application in high cavitation tools. Strong knowledge of Scientific Injection Molding Process Development utilizing statistical software and analysis techniques. Fundamental knowledge of resins, raw materials and their application in medical device design V&V. Experience with tooling & molding suppliers, their strengths and capabilities over time, including tool pricing structures and estimates for new tools and refurbishment. Ability to recommend and make decisions on tool builds and repairs. Strong knowledge of quality standards and requirements applicable to Medical Device Design & Manufacturing, including IQ/OQ/PQ and capability requirements for DFSS and large-scale production platforms. Knowledge of various resins and their processing characteristics is a plus. Perform supplier capability assessments and/or audits related to process controls, manufacturing capabilities, and lean maturity. Publish assessment reports outlining non-conformities and opportunities for improvement, and work with suppliers to plan and implement corrective actions. Maintain relationships with key external suppliers/partners and internal collaborators/customers, promoting collaboration and cross-functional problem solving to drive results. Drive supply base improvement for Baxter manufacturing facilities and external contract manufacturers, including reviewing supplier performance and working with suppliers to achieve quality, delivery and cost improvements. Identify critical processes, adhere to ethics and compliance, simplify ways of working, and manage multiple projects to drive efficient workflow. Balance process-centric and results-driven behaviors; navigate a highly matrixed, global organization and foster collaboration. Flexibility to travel 25% to 50%. What do you bring
Bachelor’s or Master’s degree in Plastics Engineering or relevant engineering/technology training and/or certification. Minimum 15 years of experience in plastics engineering, tool design & development, tools build, medical device production & supply chain. Experience in plant operations is required; 3+ years in plant operations preferred. Proven ability to lead cross-functional teams and manage projects. Strong understanding of functional areas such as Manufacturing, Quality, Regulatory Compliance, Supply Chain, and Supplier Quality. Experience in a large-scale and global medical device or highly regulated environment; Automotive/Aerospace is a plus. Strong knowledge of quality systems and practices (ISO13485, APQP, FMEA, Control Plan, MSA, IQ/OQ/PQ Validation). Proven experience in technical problem solving and continuous improvement using tools such as 8D, 5 WHYs, PDCA, OEE, DMAIC. Six Sigma Green or Black Belt preferred. Excellent written and verbal communication and presentation skills; ability to communicate clearly at all levels. Strong program management skills and ability to navigate a matrix, global organization. We understand compensation is important. Baxter offers a base salary range of $144,000 to $198,000, plus annual incentive bonus, and equity target. Actual salary may vary based on factors including skills, experience, and location. Applicants must be authorized to work in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time. US Benefits and Equal Employment Opportunity
Baxter offers comprehensive benefits, including medical and dental coverage from day one, life and disability insurance, retirement plans, and paid time off. Baxter is an equal opportunity employer and provides reasonable accommodations for applicants with disabilities. See Recruitment Fraud Notice for details. Seniority level
Director Employment type
Full-time Job function
Engineering and Information Technology Industries
Medical Equipment Manufacturing Pharmaceutical Manufacturing Hospitals and Health Care Referrals increase your chances of interviewing at Baxter International Inc. by 2x
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Senior Manager, Plastics Engineering
role at
Baxter International Inc. Our Mission to Save and Sustain Lives drives Baxter's culture of courage, trust, and collaboration. The Senior Manager – Plastics Engineering is a key role in the Plastics Engineering department within Global Engineering in Integrated Supply Chain. The group provides subject matter expertise in Tooling & Molding, including Injection Molding, Blow Molding & Extrusion. The incumbent is expected to have strong technical knowledge of tools, tool design, machines, technologies and suppliers in these areas. Experience in Medical Device New Product Development is required. Experience with a Structured Phase Gate Development approach is a plus, combined with application of DFM (Design for Molding & Design for Manufacturing) & DFA (Design for Assembly) principles is a must. Ability and mindset to train and develop junior team members is required. Manage financials and project timelines, including holding tooling vendors responsible for tool build quality and capability of molded products." What you will be doing
Lead & manage high profile, high complexity projects, including capacity expansion or replacement, new technology, and platform design & development projects. Manage technical design aspects of part design, tool design, capacity analysis, capital budget requirements, approvals, and broader molding & tooling strategy for internal manufacturing as well as Direct Procurement. Extensive & in‑depth knowledge of hot runner tool design and its application in high cavitation tools. Strong knowledge of Scientific Injection Molding Process Development utilizing statistical software and analysis techniques. Fundamental knowledge of resins, raw materials and their application in medical device design V&V. Experience with tooling & molding suppliers, their strengths and capabilities over time, including tool pricing structures and estimates for new tools and refurbishment. Ability to recommend and make decisions on tool builds and repairs. Strong knowledge of quality standards and requirements applicable to Medical Device Design & Manufacturing, including IQ/OQ/PQ and capability requirements for DFSS and large-scale production platforms. Knowledge of various resins and their processing characteristics is a plus. Perform supplier capability assessments and/or audits related to process controls, manufacturing capabilities, and lean maturity. Publish assessment reports outlining non-conformities and opportunities for improvement, and work with suppliers to plan and implement corrective actions. Maintain relationships with key external suppliers/partners and internal collaborators/customers, promoting collaboration and cross-functional problem solving to drive results. Drive supply base improvement for Baxter manufacturing facilities and external contract manufacturers, including reviewing supplier performance and working with suppliers to achieve quality, delivery and cost improvements. Identify critical processes, adhere to ethics and compliance, simplify ways of working, and manage multiple projects to drive efficient workflow. Balance process-centric and results-driven behaviors; navigate a highly matrixed, global organization and foster collaboration. Flexibility to travel 25% to 50%. What do you bring
Bachelor’s or Master’s degree in Plastics Engineering or relevant engineering/technology training and/or certification. Minimum 15 years of experience in plastics engineering, tool design & development, tools build, medical device production & supply chain. Experience in plant operations is required; 3+ years in plant operations preferred. Proven ability to lead cross-functional teams and manage projects. Strong understanding of functional areas such as Manufacturing, Quality, Regulatory Compliance, Supply Chain, and Supplier Quality. Experience in a large-scale and global medical device or highly regulated environment; Automotive/Aerospace is a plus. Strong knowledge of quality systems and practices (ISO13485, APQP, FMEA, Control Plan, MSA, IQ/OQ/PQ Validation). Proven experience in technical problem solving and continuous improvement using tools such as 8D, 5 WHYs, PDCA, OEE, DMAIC. Six Sigma Green or Black Belt preferred. Excellent written and verbal communication and presentation skills; ability to communicate clearly at all levels. Strong program management skills and ability to navigate a matrix, global organization. We understand compensation is important. Baxter offers a base salary range of $144,000 to $198,000, plus annual incentive bonus, and equity target. Actual salary may vary based on factors including skills, experience, and location. Applicants must be authorized to work in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time. US Benefits and Equal Employment Opportunity
Baxter offers comprehensive benefits, including medical and dental coverage from day one, life and disability insurance, retirement plans, and paid time off. Baxter is an equal opportunity employer and provides reasonable accommodations for applicants with disabilities. See Recruitment Fraud Notice for details. Seniority level
Director Employment type
Full-time Job function
Engineering and Information Technology Industries
Medical Equipment Manufacturing Pharmaceutical Manufacturing Hospitals and Health Care Referrals increase your chances of interviewing at Baxter International Inc. by 2x
#J-18808-Ljbffr