West Pharmaceutical Services logo

Quality Engineer

West Pharmaceutical Services

Williamsport, PAOnsitePosted 42 days ago
Full TimeMid LevelQuality (QA / QC)Medical Device
Original posting ↗

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 plant's relations with its customers and suppliers. Perform all duties associated with the auditing and documentation of compliance related items against ISO standards.

Job description

Essential Duties and Responsibilities

  • 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/KPI's in the improvement of Cost of Poor Quality and Yield Opportunity to 100%
  • Other duties as assigned

Education

Bachelor's 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 company's safety policy at all times
  • Able to comply with the company's quality policy at all times.

License and Certifications

Manufacturing\Six Sigma Green Belt Certification Upon Hire preferred and Manufacturing\Lean 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

Requirements

  • Bachelor's degree preferably in technical discipline; Science, Engineering, Quality Assurance, or a related field.
  • 3+ Years as a quality or engineering professional in a manufacturing environment.
  • Background in SPC, Root Cause and Corrective Action.
  • Strong knowledge, understanding of statistics and use of Minitab.
  • Must be able to use the various pieces of measuring / testing equipment (calipers, micrometers, comparators, height gages, vision and data collection systems).
  • Excellent communications (including both written & oral methods), interpersonal, problem solving, planning/organizational, negotiating and computer skills required (especially MS Office applications & statistical analysis systems).
  • General understanding of manufacturing and plant operations.
  • Strong customer facing experience.
  • Familiarity with SAP, Master Control or similar systems and databases, a plus.
  • Manufacturing\Six Sigma Green Belt Certification Upon Hire preferred.
  • Manufacturing\Lean Six Sigma Black Belt with DOE experience. Upon Hire preferred.

Benefits

  • Health benefits
  • Professional development
  • Growth opportunities
  • Inclusive community

Company overview

West Pharmaceutical Services, Inc. is a global leader in the design and manufacture of innovative, high-quality injectable pharmaceutical packaging and delivery systems. Founded in 1923 and headquartered in Exton, Pennsylvania, the company serves as a trusted partner to both established and emerging drug developers, ensuring the safe, effective containment and delivery of life-saving and life-enhancing medicines for patients worldwide. With approximately 10,000 team members across 50 sites globally, West delivers billions of components and devices annually, supporting pharmaceutical companies in their mission to bring critical therapies to market. The company operates as a publicly traded entity on the New York Stock Exchange (NYSE: WST) and is included in the S&P 500 index, generating approximately $2.95 billion in net sales in fiscal year 2023. West specializes in pharmaceutical packaging systems and delivery systems, focusing on injectable drug containment solutions that meet stringent regulatory requirements and quality standards.

Explore more jobs of your matchFind more biopharma roles with GetBioJob.