Home › Companies › Careers Westpharma Com › Principal Engineer, Quality Automation & Inspection
Principal Engineer, Quality Automation & Inspection
Careers Westpharma Com · Eschweiler, NW, DE · Hybrid · Deleted · SAP SuccessFactors RMK / CSB
Job facts
| Field | Value |
|---|---|
| Company | Careers Westpharma Com |
| Title | Principal Engineer, Quality Automation & Inspection |
| Normalized title | - |
| Department / team | - |
| Location | This is an position requiring the team member to be 3 days a week. Who We Are: At West, United States |
| Work model | Hybrid / Hybrid |
| Employment type | - |
| Salary | - |
| Status | deleted |
| ATS provider | SAP SuccessFactors RMK / CSB |
| Posted / first seen | 2026-06-01 / 2026-06-01 |
| Changed / last seen | 2026-06-06 / 2026-06-04 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from Careers Westpharma Com. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through SAP SuccessFactors RMK / CSB. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| City jobs | Active postings in This is an position requiring the team member to be 3 days a week. Who We Are: At West. | Open |
| Work model jobs | Active Hybrid postings. | Open |
| Lifecycle events | Open, update, close, and reopen events for this posting. | Open |
| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | Careers Westpharma Com |
| Source | fccd5700-9e1b-48bc-b9ef-338ff84622ba |
| ATS provider | SAP 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 ID | 3afc1aed337021648b85ed8666701489b3745fd7 |
| Org ID | bfeb37f8-d5cb-48f4-a736-2f8adc37d306 |
| Source ID | fccd5700-9e1b-48bc-b9ef-338ff84622ba |
| Board ID | fccd5700-9e1b-48bc-b9ef-338ff84622ba |
| Provider | successfactors_rmk |
| Provider Job Key | 1399317433 |
| Title | Principal Engineer, Quality Automation & Inspection |
| Normalized Title | — |
| Status | deleted |
| Active | no |
| Location Text | Eschweiler, NW, DE |
| Department | — |
| Team | — |
| Employment Type | — |
| Workplace Type | hybrid |
| Remote Policy | hybrid |
| Country | United States |
| Region | — |
| City | This is an position requiring the team member to be 3 days a week. Who We Are: At West |
| Salary Raw | 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 |
| Salary Min | — |
| Salary Max | — |
| Salary Currency | — |
| Salary Period | day |
| Source URL | https://careers.westpharma.com/job/Eschweiler-Principal-Engineer%2C-Quality-Automation-&-Inspection-NW/1399317433/ |
| Apply URL | /talentcommunity/apply/1399317433/?locale=en_US |
| First Seen At | 2026-06-01 14:18:31Z |
| Last Seen At | 2026-06-04 12:53:20Z |
| Last Checked At | 2026-06-06 13:46:55Z |
| Last Changed At | 2026-06-06 13:46:55Z |
| Inactive At | 2026-06-06 13:46:55Z |
| Source Posted At | 2026-06-01 00:00:00Z |
| Source Updated At | — |
| Raw Payload Uri | s3://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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