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Quality Auditor Molding - Fixed Term Contract

West Pharmaceutical Services

Tempe, AZOnsitePosted 11 days ago
ContractEntry LevelQuality (QA / QC)Medical Device
Original posting ↗

Summary

The role is essential in ensuring in-process and finished products meet customer specifications. This role provides total manufacturing quality inspection services including quality inspection, quality control, sampling inspection, documentation and record keeping. Adhering to Good Documentation Process (GDP) is essential to maintain all documentation necessary to ensure conformity to specifications and traceability of records.

Job description

Job Summary

The role is essential in ensuring in-process and finished products meet customer specifications. This role provides total manufacturing quality inspection services including quality inspection, quality control, sampling inspection, documentation and record keeping. Adhering to Good Documentation Process (GDP) is essential to maintain all documentation necessary to ensure conformity to specifications and traceability of records.

Essential Duties and Responsibilities

  • Perform sampling, inspections, and testing of in-process and finished goods products per applicable procedures and AQL plans, utilizing both visual means as well as calibrated test equipment that includes CMMs, Vision Systems, and manual gaging.
  • Release acceptable in-process and finished goods product for further processing and/or shipping as applicable per site
  • Understand and follow applicable ISO standards requirements and follow good documentation practices
  • Perform review of inspection records to assure product conforms to specifications and proper documentation practices
  • Retains sample of finished products and maintains all applicable documents to form batch records and ensures appropriate batch records disposition (i.e., filing, scanning etc.) as necessary
  • Segregate nonconforming product and handle quarantined product and raw materials as applicable by site
  • Escalate "out of specification" events
  • Perform trace back investigation of nonconforming raw material and product as directed by site
  • Promotes and supports a Lean environment.
  • Conforms with and abides by all corporate and site-specific regulations, policies, work procedures, instruction, and all safety rules
  • Exhibits regular, reliable, punctual and predictable attendance
  • Other duties as assigned

Education

High School Diploma or GED Required.

Work Experience

1 year manufacturing experience preferred

Preferred Knowledge, Skills and Abilities

  • Must possess an acute attention to detail
  • Basic computer skills
  • Able to be aware of all relevant standard operating procedures as per Company policy
  • Possess ability to work independently and as part of a team with self-motivation, adaptability, and a positive attitude
  • Willingness to learn new and review new analytical techniques

Travel Requirements

None: No travel required

Physical Requirements

Light-Exerting up to 20lbs/9kg of force frequently, and/or negligible amount of force frequently constantly to move objects.

Additional Requirements

  • Ability to learn, understand, and remember normal tasks.
  • Ability to hear, speak, and understand conversation in English.
  • 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.
  • Read and interpret data, information and documents
  • Work under deadlines with constant interruptions

Requirements

  • High School Diploma or GED Required
  • 1 year manufacturing experience preferred
  • Must possess an acute attention to detail
  • Basic computer skills
  • Able to be aware of all relevant standard operating procedures as per Company policy
  • Possess ability to work independently and as part of a team with self-motivation, adaptability, and a positive attitude
  • Willingness to learn new and review new analytical techniques
  • Ability to learn, understand, and remember normal tasks
  • Ability to hear, speak, and understand conversation in English
  • 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
  • Read and interpret data, information and documents
  • Work under deadlines with constant interruptions

Benefits

  • Training
  • Full time hours
  • Bonus
  • Health programs
  • Financial health support

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.

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