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HomeCompaniesCareers Westpharma ComPrincipal Engineer, Quality Automation & Inspection

Principal Engineer, Quality Automation & Inspection

Careers Westpharma Com · Eschweiler, NW, DE · Hybrid · Deleted · SAP SuccessFactors RMK / CSB

Job facts

FieldValue
CompanyCareers Westpharma Com
TitlePrincipal Engineer, Quality Automation & Inspection
Normalized title-
Department / team-
LocationThis is an position requiring the team member to be 3 days a week. Who We Are: At West, United States
Work modelHybrid / Hybrid
Employment type-
Salary-
Statusdeleted
ATS providerSAP SuccessFactors RMK / CSB
Posted / first seen2026-06-01 / 2026-06-01
Changed / last seen2026-06-06 / 2026-06-04

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PageWhat it containsOpen
Company jobsActive postings from Careers Westpharma Com.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through SAP SuccessFactors RMK / CSB.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in This is an position requiring the team member to be 3 days a week. Who We Are: At West.Open
Work model jobsActive Hybrid postings.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyCareers Westpharma Com
Sourcefccd5700-9e1b-48bc-b9ef-338ff84622ba
ATS providerSAP SuccessFactors RMK / CSB

Description

This is an hybrid position requiring the team member to be onsite 3 days a week. Who We Are: At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future? There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families. We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts. Job Summary This role will drive technical transformation within manufacturing and quality operations by implementing automated inspection processes within Quality Assurance. This role is key to implementing new technology, developing and introducing process improvements, managing equipment life cycle, and executing validation. This person will provide the company with the technical and quality resources to manage deliverables focused on metrology for elastomer and primary containment pharmaceutical products. With a global mandate and scope, this person will have the opportunity to drive the implementation of innovative processes and technologies in cooperation with the engineering, operations, IT, and quality assurance teams and the plants. Essential Duties and Responsibilities Lead the identification, testing, design, and development of innovative automation solutions to measure product dimensions & inspect for defects. Lead the move to integrate inspection equipment into automated production lines Scale developed solutions to production. Initiate, lead, and coordinate improvements and lean waste reduction of existing processes. Work with site SMEs to validate solutions, including the preparation of validation documentation, execution of validation protocols, and triaging of unexpected events. Ensure that procedures and systems are in place to introduce new processes and equipment. Support training and development of personnel on new processes and systems. Harmonize best practices by assessing current process status in all relevant West locations globally, defining best practices, performing gap analyses, and managing the harmonization. Interface with customers and suppliers on new and existing inspection & quality projects. Support global Data Integrity alignment projects for inspection equipment Work with interdisciplinary teams to perform root cause analysis and implement corrective and preventive actions. Conduct data trend analysis to identify short and long-range patterns to support continuous improvement initiatives. Participate in budgeting and business planning activities Prepare data/presentations and attend quality review meetings with senior leadership. Ensure compliance with cGMPs, FDA and other regulations as necessary. Abide by all regulations, policies, work procedures, instruction, and all safety rules. Education BS degree preferably in a technical discipline such as engineering or equivalent experience required Work Experience Minimum 5 years of experience in technical or engineering field. Must have a very good knowledge of manufacturing automation and the development of quality plans for high-speed manufacturing. Knowledge of machine control systems and integrated manufacturing control. Excellent interpersonal skills: good team player and individual contributor as well. Strong problem solving and critical thinking skills to troubleshoot issues and identify root causes. Experience in automation industry Preferred Knowledge, Skills and Abilities Knowledge of ISO/ASME GD&T requirements, interpreting 2D engineering drawings, and 3D models Proven experience of statistical methods (Measurement System Analysis (MSA), Equivalence, Design of Experiments) Experience using Six Sigma & SPC tools and techniques Experience with ISO 9000 standards and GMPs. ASQ certification highly desired. Green Belt or Black Belt certification. Graduate degree (MS). Knowledge of AI-based vision tools and deep learning defect detections Experience with AI/ML- based vision systems Able to be aware of all relevant SOPs as per Company policy as they are related to the position covered by this Job Description License and Certifications Engineering - General\ASQ Certified Quality Engineer (CQE or CQA) Upon Hire preferred and Manufacturing\Six Sigma Green Belt Certification Upon Hire preferred or Manufacturing\Lean Six Sigma Black Belt Upon Hire preferred Travel Requirements 20%: Up to 52 business days per year Physical Requirements Light-Exerting up to 20lbs/9kg of force frequently, and/or negligible amount of force frequently constantly to move objects. Additional Requirements Adaptable to changes in the work environment, manage competing demands and deal with frequent change, delays or unexpected events. Must maintain the ability to work well with others in a variety of situations Maintain high attention to detail, accuracy, and overall quality of work Must be able to multi-task, work under time constraints, problem solve, and prioritize Ability to make independent and sound judgments Observe and interpret situations, analyze and solve problems Effectively communicate and interface with various levels internally and with customers #LI-DJ1 #LI-HYBRID

Full job record

Job ID3afc1aed337021648b85ed8666701489b3745fd7
Org IDbfeb37f8-d5cb-48f4-a736-2f8adc37d306
Source IDfccd5700-9e1b-48bc-b9ef-338ff84622ba
Board IDfccd5700-9e1b-48bc-b9ef-338ff84622ba
Providersuccessfactors_rmk
Provider Job Key1399317433
TitlePrincipal Engineer, Quality Automation & Inspection
Normalized Title
Statusdeleted
Activeno
Location TextEschweiler, NW, DE
Department
Team
Employment Type
Workplace Typehybrid
Remote Policyhybrid
CountryUnited States
Region
CityThis is an position requiring the team member to be 3 days a week. Who We Are: At West
Salary RawThis is an hybrid position requiring the team member to be onsite 3 days a week. Who We Are: At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future? There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families. We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts. Job Summary This role will drive technical transformation within manufacturing and quality operations by implementing automated inspection processes within Quality Assurance. This role is key to implementing new technology, developing and introducing process improvements, managing equipment life cycle, and executing validation. This person will provide the company with the technical and quality resources to manage deliverables focused on metrology for elastomer and primary containment pharmaceutical products. With a global mandate and scope, this person will have the opportunity to drive the implementation of innovative processes and technologies in cooperation with the engineering, operations, IT, and quality assurance teams and the plants. Essential Duties and Responsibilities Lead the identification, testing, design, and development of innovative automation solutions to measure product dimensions & inspect for defects. Lead the move to integrate inspection equipment into automated production lines Scale developed solutions to production. Initiate, lead, and coordinate improvements and lean waste reduction of existing processes. Work with site SMEs to validate solutions, including the preparation of validation documentation, execution of validation protocols, and triaging of unexpected events. Ensure that procedures and systems are in place to introduce new processes and equipment. Support training and development of personnel on new processes and systems. Harmonize best practices by assessing current process status in all relevant West locations globally, defining best practices, performing gap analyses, and managing the harmonization. Interface with customers and suppliers on new and existing inspection & quality projects. Support global Data Integrity alignment projects for inspection equipment Work with interdisciplinary teams to perform root cause analysis and implement corrective and preventive actions. Conduct data trend analysis to identify short and long-range patterns to support continuous improvement initiatives. Participate in budgeting and business planning activities Prepare data/presentations and attend quality review meetings with senior leadership. Ensure compliance with cGMPs, FDA and other regulations as necessary. Abide by all regulations, policies, work procedures, instruction, and all safety rules. Education BS degree preferably in a technical discipline such as engineering or equivalent experience required Work Experience Minimum 5 years of experience in technical or engineering field. Must have a very good knowledge of manufacturing automation and the development of quality plans for high-speed manufacturing. Knowledge of machine control systems and integrated manufacturing control. Excellent interpersonal skills: good team player and individual contributor as well. Strong problem solving and critical thinking skills to troubleshoot issues and identify root causes. Experience in automation industry Preferred Knowledge, Skills and Abilities Knowledge of ISO/ASME GD&T requirements, interpreting 2D engineering drawings, and 3D models Proven experience of statistical methods (Measurement System Analysis (MSA), Equivalence, Design of Experiments) Experience using Six Sigma & SPC tools and techniques Experience with ISO 9000 standards and GMPs. ASQ certification highly desired. Green Belt or Black Belt certification. Graduate degree (MS). Knowledge of AI-based vision tools and deep learning defect detections Experience with AI/ML- based vision systems Able to be aware of all relevant SOPs as per Company policy as they are related to the position covered by this Job Description License and Certifications Engineering - General\ASQ Certified Quality Engineer (CQE or CQA) Upon Hire preferred and Manufacturing\Six Sigma Green Belt Certification Upon Hire preferred or Manufacturing\Lean Six Sigma Black Belt Upon Hire preferred Travel Requirements 20%: Up to 52 business days per year Physical Requirements Light-Exerting up to 20lbs/9kg of force frequently, and/or negligible amount of force frequently constantly to move objects. Additional Requirements Adaptable to changes in the work environment, manage competing demands and deal with frequent change, delays or unexpected events. Must maintain the ability to work well with others in a variety of situations Maintain high attention to detail, accuracy, and overall quality of work Must be able to multi-task, work under time constraints, problem solve, and prioritize Ability to make independent and sound judgments Observe and interpret situations, analyze and solve problems Effectively communicate and interface with various levels internally and with customers #LI-DJ1 #LI-HYBRID
Salary Min
Salary Max
Salary Currency
Salary Periodday
Source URLhttps://careers.westpharma.com/job/Eschweiler-Principal-Engineer%2C-Quality-Automation-&-Inspection-NW/1399317433/
Apply URL/talentcommunity/apply/1399317433/?locale=en_US
First Seen At2026-06-01 14:18:31Z
Last Seen At2026-06-04 12:53:20Z
Last Checked At2026-06-06 13:46:55Z
Last Changed At2026-06-06 13:46:55Z
Inactive At2026-06-06 13:46:55Z
Source Posted At2026-06-01 00:00:00Z
Source Updated At
Raw Payload Uris3://bluework-jobs-prod-raw-590183727216/raw/provider=successfactors_rmk/board=careers.westpharma.com/date=2026-06-04/2026-06-04T12-52-47-034Z-5fd957194798a795acf53e92ea1c92d45cbbdc7765fe6e93402b735ea2f3a2b1.json
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