At West were 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 Wests indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future
Theres 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
Plan schedule execute & communicate all items regarding quality issues complaints validations & other projects to QA Manager and/or other interested parties. Provide technical assistance for developing and maintaining measurement routines for the various vision measuring system. Provide quality assistance in support of new product development and validation. Support customer complaint process. Provide quality assistance including SPC support with facility manufacturing engineering maintenance shipping and warehouse functions. Be a quality resource in the improvement of all aspects of plant operations and in the plants relations with its customers and suppliers. Perform all duties associated with the auditing and documentation of compliance related items against ISO standards.
Essential Duties and Responsibilities
- Provides technical and quality support by:
- Assisting facility and design development personnel as needed for engineering/projects.
- Providing guidance and training to all QA personnel about new operation and programming of vision system equipment.
- Providing backup support to QA Manager and/or QA Supervisor as needed.
- Assisting in the investigation of customer complaints to ensure timely response.
- Assisting in maintenance and improvement of facility required quality systems including ISO 13485 and HACCP.
- As required work with Manufacturing Engineering Sales the Customers and Suppliers to resolve issues on new products. (This may require travel.)
- Become knowledgeable in all areas of the Q.A. Department and work with the various functions within Q.A. to resolve internal issues as they arise.
- Perform audits of the various departments / functions as directed by the Q. A. Manager.
- As required participate and or lead Customer meetings / audits Supplier meetings / audits and corporate audits.
- Work with management and technical staff in performing root cause failure analysis and implementing corrective and preventative actions to preclude recurrence (CAPA).
- Ability to closely interact with customers to understand and integrate those requirements into West manufacturing and quality system requirements
- Work independently and with project teams to develop design control deliverables including quality plans manufacturing and inspection documentation test methods and any necessary records for filing tooling product history files
- Complete dimensional analysis for OQ & PQ as needed to include capability normality and transformation of data when required.
- Create validation protocols (IQ OQ & PQ) and obtain customer approval when applicable.
- Complete validation reports and submit to internal and external teams as applicable.
- Aid in validating and reviewing validations of equipment products and processes.
- Developing and execute Gauge R&R studies to ensure confidence in defined measuring techniques. When applicable work with QA Supervisor to develop/execute plan for improvements (equipment training etc.).
- Assist Measuring Techs in the evaluation of and possible improvements to defined measurement routines fixtures and troubleshooting of problems related to the vision measuring system.
- As directed by the QA Manager represent the facility QA engineering and manufacturing groups for new products. As a member ensure plant S.O.I.s and Corporate G.O.P.s are being followed and ensure all necessary testing and evaluations have been completed prior to completion and final approval.
- Drive site and departmental goals/KPIs in the improvement of Cost of Poor Quality and Yield Opportunity to 100%
- Other duties as assigned
Additional Responsibilities
Education
- Bachelors degree preferably in technical discipline; Science Engineering Quality Assurance or a related field.
Work Experience
- Background in SPC Root Cause and Corrective Action (Exposure to 8D or A3 methodology preferred).
- Experience: 3 Years as a quality or engineering professional in a manufacturing environment.
Preferred Knowledge Skills and Abilities
- Must be familiar with computers and various software programs.
- Strong knowledge understanding of statistics and use of Minitab.
- Must be able to use the various pieces of measuring / testing equipment. (I.e. calipers micrometers comparators height gages vision and data collection systems.)
- Excellent communications (including both written & oral methods) interpersonal problem solving (including root cause failure analysis methods) planning/organizational negotiating and computer skills required (especially MS Office applications & statistical analysis systems); general understanding of manufacturing and plant operations are also required.
- Strong customer facing experience
- Background in plastics is preferred.
- Familiarity with SAP Master Control or similar systems and databases a plus.
- Able to be aware of all relevant standard operating procedures as per Company policy as they are related to the position covered by this Job Description
- Support and contribute to Lean Sigma programs and activities towards delivery of the set target
- Able to comply with the companys safety policy at all times
- Able to comply with the companys quality policy at all times.
License and Certifications
- ManufacturingSix Sigma Green Belt Certification Upon Hire preferred and
- ManufacturingLean Six Sigma Black Belt with DOE experience. Upon Hire preferred
Travel Requirements
10%: Up to 26 business days per year
Physical Requirements
Medium-Exerting up to 50lb/22kg of force occasionally and/or up to 20lbs/9kg of force frequently and/or up to 10lbs/4kgs of force constantly to move objects.
Additional Requirements
- Must maintain the ability to work well with others in a variety of situations.
- Must be able to multi-task work under time constraints problem solve and prioritize.
- Self-motivated with the ability to make independent and sound judgments.
- Read and interpret data information and documents
- Learn and apply new information or skills
West embraces diversity and equality of opportunity. We foster an environment where all individuals are safe treated fairly valued and respected. We do not discriminate on the basis of race religion color national origin gender sex gender identity sexual orientation age marital status veteran status disability status or other applicable legally protected characteristics. Where permitted by law employment with West Pharmaceutical Services Inc. or any of its subsidiary or affiliate companies is contingent upon the satisfactory completion of post-offer background screening.
#LI-9394
Required Experience:
IC
At West were 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...
At West were 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 Wests indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future
Theres 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
Plan schedule execute & communicate all items regarding quality issues complaints validations & other projects to QA Manager and/or other interested parties. Provide technical assistance for developing and maintaining measurement routines for the various vision measuring system. Provide quality assistance in support of new product development and validation. Support customer complaint process. Provide quality assistance including SPC support with facility manufacturing engineering maintenance shipping and warehouse functions. Be a quality resource in the improvement of all aspects of plant operations and in the plants relations with its customers and suppliers. Perform all duties associated with the auditing and documentation of compliance related items against ISO standards.
Essential Duties and Responsibilities
- Provides technical and quality support by:
- Assisting facility and design development personnel as needed for engineering/projects.
- Providing guidance and training to all QA personnel about new operation and programming of vision system equipment.
- Providing backup support to QA Manager and/or QA Supervisor as needed.
- Assisting in the investigation of customer complaints to ensure timely response.
- Assisting in maintenance and improvement of facility required quality systems including ISO 13485 and HACCP.
- As required work with Manufacturing Engineering Sales the Customers and Suppliers to resolve issues on new products. (This may require travel.)
- Become knowledgeable in all areas of the Q.A. Department and work with the various functions within Q.A. to resolve internal issues as they arise.
- Perform audits of the various departments / functions as directed by the Q. A. Manager.
- As required participate and or lead Customer meetings / audits Supplier meetings / audits and corporate audits.
- Work with management and technical staff in performing root cause failure analysis and implementing corrective and preventative actions to preclude recurrence (CAPA).
- Ability to closely interact with customers to understand and integrate those requirements into West manufacturing and quality system requirements
- Work independently and with project teams to develop design control deliverables including quality plans manufacturing and inspection documentation test methods and any necessary records for filing tooling product history files
- Complete dimensional analysis for OQ & PQ as needed to include capability normality and transformation of data when required.
- Create validation protocols (IQ OQ & PQ) and obtain customer approval when applicable.
- Complete validation reports and submit to internal and external teams as applicable.
- Aid in validating and reviewing validations of equipment products and processes.
- Developing and execute Gauge R&R studies to ensure confidence in defined measuring techniques. When applicable work with QA Supervisor to develop/execute plan for improvements (equipment training etc.).
- Assist Measuring Techs in the evaluation of and possible improvements to defined measurement routines fixtures and troubleshooting of problems related to the vision measuring system.
- As directed by the QA Manager represent the facility QA engineering and manufacturing groups for new products. As a member ensure plant S.O.I.s and Corporate G.O.P.s are being followed and ensure all necessary testing and evaluations have been completed prior to completion and final approval.
- Drive site and departmental goals/KPIs in the improvement of Cost of Poor Quality and Yield Opportunity to 100%
- Other duties as assigned
Additional Responsibilities
Education
- Bachelors degree preferably in technical discipline; Science Engineering Quality Assurance or a related field.
Work Experience
- Background in SPC Root Cause and Corrective Action (Exposure to 8D or A3 methodology preferred).
- Experience: 3 Years as a quality or engineering professional in a manufacturing environment.
Preferred Knowledge Skills and Abilities
- Must be familiar with computers and various software programs.
- Strong knowledge understanding of statistics and use of Minitab.
- Must be able to use the various pieces of measuring / testing equipment. (I.e. calipers micrometers comparators height gages vision and data collection systems.)
- Excellent communications (including both written & oral methods) interpersonal problem solving (including root cause failure analysis methods) planning/organizational negotiating and computer skills required (especially MS Office applications & statistical analysis systems); general understanding of manufacturing and plant operations are also required.
- Strong customer facing experience
- Background in plastics is preferred.
- Familiarity with SAP Master Control or similar systems and databases a plus.
- Able to be aware of all relevant standard operating procedures as per Company policy as they are related to the position covered by this Job Description
- Support and contribute to Lean Sigma programs and activities towards delivery of the set target
- Able to comply with the companys safety policy at all times
- Able to comply with the companys quality policy at all times.
License and Certifications
- ManufacturingSix Sigma Green Belt Certification Upon Hire preferred and
- ManufacturingLean Six Sigma Black Belt with DOE experience. Upon Hire preferred
Travel Requirements
10%: Up to 26 business days per year
Physical Requirements
Medium-Exerting up to 50lb/22kg of force occasionally and/or up to 20lbs/9kg of force frequently and/or up to 10lbs/4kgs of force constantly to move objects.
Additional Requirements
- Must maintain the ability to work well with others in a variety of situations.
- Must be able to multi-task work under time constraints problem solve and prioritize.
- Self-motivated with the ability to make independent and sound judgments.
- Read and interpret data information and documents
- Learn and apply new information or skills
West embraces diversity and equality of opportunity. We foster an environment where all individuals are safe treated fairly valued and respected. We do not discriminate on the basis of race religion color national origin gender sex gender identity sexual orientation age marital status veteran status disability status or other applicable legally protected characteristics. Where permitted by law employment with West Pharmaceutical Services Inc. or any of its subsidiary or affiliate companies is contingent upon the satisfactory completion of post-offer background screening.
#LI-9394
Required Experience:
IC
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