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United States
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Tempe
25 jobs found
21.09.2025
WP

West Pharma Quality Auditor Assembly United States, Arizona, Tempe

Limitless High-tech career opportunities - Expoint
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 to include laser...
Description:

This shift is Monday - Friday 8:00 AM - 4:30 PM.

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 to include laser micrometer, optical comparator and other equipment as applicable
  • 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
  • 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
  • Print documents from Master Control, shopfloor or other software program and manages documents related to the Quality System
  • Segregate nonconforming product and handle quarantined product and raw materials as applicable by site
  • Generate rejection and deviation reports as directed by site
  • 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
  • Minimum one year manufacturing experience required
Preferred Knowledge, Skills and Abilities
  • Must poses an acute attention to detail
  • Basic computer skills
Travel Requirements
None: No travel required
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.
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21.09.2025
WP

West Pharma Production Operator Fixed Term Assignment United States, Arizona, Tempe

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Under the supervision of a trainer or supervisor perform the following duties... process trimmed product through washing and drying process per site SOI’s and work instructions. Ensure that the equipment...
Description:
Essential Duties and Responsibilities
  • Under the supervision of a trainer or supervisor perform the following duties...
  • process trimmed product through washing and drying process per site SOI’s and work instructions.
  • Ensure that the equipment is set up accurately.
  • Ensure continual flow of product through the module from the mold press thru the trim press.
  • Operate a mold press to produce molded panels of product following site SOI’s and work instructions.
  • Operate a manual / automatic trim press as needed following site SOI’s and work instructions.
  • Process product through any required special treatments such as sort, silicone, chlorination, etc.
  • As needed, set up pack scales for weighing and packing of finished product and prepare carton labels for boxing and shipping.
  • Alert the Area Supervisor to conditions that may prevent meeting production and quality expectations.
  • Accurately maintain all required documentation and paperwork to ensure product traceability.
  • Inspect molded/trimmed work to ensure quality product is being produced.
  • Move materials into and out of the area as required.
  • Properly clean and prep assigned workstations/equipment during and prior to the next available shift.
  • 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.
  • Performs other duties as assigned based on business needs.
Education
  • High School Diploma or GED Required
Work Experience
  • No min required
Preferred Knowledge, Skills and Abilities
  • Must possess an acute attention to detail
  • Basic computer skills, i.e. use a mouse/keyboard.
  • Ability to apply Good Manufacturing Practices (GMP)
  • General use of computer work station and ability to use SAP commands is preferred
  • Must be willing and able to work as a team member and make general decisions within authorized job responsibilities
  • Must be able to train and guide others as required.
  • Must be able to read and write in English
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.
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20.09.2025
WP

West Pharma Sr Business Systems Analyst United States, Arizona, Tempe

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Designing and implementing Business Intelligence (BI) solutions throughout the organization. Establishing and developing relationships with key internal stakeholders to understand the distinct BI needs across all business departments and support...
Description:
Essential Duties and Responsibilities
  • Designing and implementing Business Intelligence (BI) solutions throughout the organization.
  • Establishing and developing relationships with key internal stakeholders to understand the distinct BI needs across all business departments and support the service delivery.
  • Building and preserving productive relationships with a broader business network, IT associates, and vendors, while addressing and resolving potential issues.
  • Aiding in the creation of a uniform approach towards the execution of BI projects.
  • Overseeing multiple BI projects, ensuring smooth progression from inception to completion.
  • Offering maintenance services for existing BI solutions and serving as the primary escalation point for issues related to BI projects.
  • Bridging the gap between business necessities and technical considerations, negotiating solutions, and encouraging creativity when feasible.
  • Contributing to the ongoing growth and delivery of BI services, inclusive of projects, while ensuring constant protection and security of business data.
  • Define and translate business rules and processes into S4 Hana data solutions
  • Lead projects impacting data integration for manufacturing KPI’s
  • Providing guidance, templates, reporting and instructions to Supply Chain, Operations, Quality, Warehousing and Finance regarding the required maintenance of Master Data and transactions.
    • E.g. Tier meeting dashboards, reports such as OEE, scrap, sales & absorption
  • Supporting equipment interfacing needs.
    • E.g. Intouch & Edart MRP’s
  • Supports and continuously improves procedures and processes related to but not limited SAP S4 Hana & Power Bi.
  • Other duties as assigned.
Education
  • Bachelor's degree in computer science, business or related field; or equivalent work experience.
Work Experience
  • Related SAP & Power BI Work Experience: Minimum 5 years of experience
  • A minimum of 5 years’ experience in a Business Analyst role or a similar position with relevant experience.
Preferred Knowledge, Skills and Abilities
  • Experience in delivering or managing BI projects.
  • Familiarity with high-volume manufacturing operations.
  • Proven ability to manage multiple projects simultaneously, demonstrating excellent multitasking and prioritization skills.
  • Proficiency in translating technical language into comprehensible terms.
  • Experience in implementing, configuring, and testing BI solutions.
  • Experience in developing within the Microsoft Power Platform environment, with a focus on Power BI, Power Automate, and Power Apps.
  • Working knowledge of Microsoft Power BI Desktop, management of Microsoft Teams groups, OneDrive storage, and Microsoft SharePoint.
  • Proficiency in using Microsoft 365 applications, with an understanding of its interconnections with Microsoft SharePoint and Microsoft Power Platform.
  • Experience in data extraction, cleansing, and integration.
  • Understanding of Lean Manufacturing principles, such as Value Stream Maps, Continuous Improvement, and Kaizen.
  • Ability to accurately document work performed.
  • Ability to work independently on own projects while working concurrently with all departments.
  • Awareness of all relevant SOPs as per Company policy as they are related to the position covered by this Job Description
  • 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 within 1 Year required
Physical Requirements
Sedentary-Exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time.
Additional Requirements
  • Self-motivated, results- and solution-oriented personality
  • Very good organizational and project management skills
  • Highly analytical and structured way of working
  • Ability to successfully collaborate with teams across different countries and organizational levels
  • Fluent in English
  • Proficient in Microsoft based programs
  • Ability to assert technical solutions and standards in an international environment
  • Excellent communication skills and ability to collaborate well with people across different countries
  • Manage working with colleagues in different time-zones
  • Able to routinely use standard office equipment such as computers, phones, photocopiers, filing cabinets and fax machines. Position operates in a professional office environment. May stand or sit for extended periods of time
  • Must be able to communicate effectively with written and oral skills, make quick decisions, interpret data, read and write, speak in front of groups, express and exchange ideas, understand direction and adhere to procedures
  • Organizational skills will enable planning, prioritization and achievement of goals especially of importance for the successful execution of related activities
  • Read and interpret data, information and documents
  • 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
  • Ability to make independent and sound judgments
  • Observe and interpret situations, analyze and solve problems
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13.09.2025
WP

West Pharma Quality Auditor Supervisor United States, Arizona, Tempe

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Able to train, provide trouble shooting guidance/feedback, and problem resolutions on metrology equipment including but not limited to CMM’s (Coordinate Measurement Machine), Vision Systems, and manual gaging. Proactively analyze data...
Description:
Job Summary

In this role, you will monitor and control the daily activities of quality inspection, testing, documentation review, and calibration in support of Operations and product release. This role is on-site (Monday through Friday) from 10:00 pm to 6:00 am.

Essential Duties and Responsibilities
  • Able to train, provide trouble shooting guidance/feedback, and problem resolutions on metrology equipment including but not limited to CMM’s (Coordinate Measurement Machine), Vision Systems, and manual gaging.
  • Proactively analyze data and interpret results for any trending or OOS (out of specification) events.
  • Provides direct supervision, resolves personnel issues, conducts performance evaluations and performs supervisory discipline as necessary.
  • Exhibit a strong “quality first” mentality and ensure that product and process quality are held to the highest standard.
  • Ensures compliance with quality system documents, cGMPs, ISO standards and FDA regulations.
  • Schedule and prioritize quality inspection, testing, documentation review, and calibration to support Operations and release of product.
  • Identifies and develops opportunities to improve existing processes and procedures.
  • Support quality assurance improvement activities by evaluating products, processes or materials in order to develop control or improvement strategies intended to improve the customer’s experience.
  • Work with technical staff in performing root cause failure analysis and implementing corrective and preventive actions to eliminate recurrence.
  • Assist in and manage the verbal communications and visual checks of work activity to ensure quality requirements are met. Ensure proper corrective actions, discrepancy reports and follow up activities are accomplished. Advise on equipment condition, test method, etc. to aid in the course of action when components do not meet specifications. Responsible for quality inspection and verification.
  • Reviews documentation and records for accuracy. Determines if product is impacted, can be released, or if Non‐Conformance Report is required.
  • Assist in developing documentation and procedures during the qualification of new equipment/inspection methods.
  • Performs other duties as assigned based on business needs.
  • Conforms with and abides by all regulations, policies, work procedures, instruction, and all safety rules.
  • Exhibits regular, reliable, punctual and predictable attendance .

Education or Equivalent Experience: Associate’s Degree in Technical or Engineering

Work Experience
  • 5+ years experience in regulated Quality Assurance and or metrology and Document/Configuration Control (or a formal education equivalent) required.
  • Experience with Medical Device Product Development Life Cycle Activities, Verification / Validation Activities, Metrology/Manufacturing background and Risk Management preferred.
  • Experience with quality systems such as ISO 13485 and 21 CFR 820 preferred.
  • Experience with MasterControl, SAP, and SharePoint preferred.
  • Experience with customer interface and meeting customer expectations preferred.
  • 3+ years of supervisor experience preferred.
Preferred Knowledge, Skills and Abilities
  • Ability to work independently, multi-task and thrive in fast-paced environment.
  • Excellent written and verbal communication skills.
  • Proficient in statistical software, Windows OS, Microsoft Office Suite including Word, Excel, and PowerPoint.
  • Proven knowledge and understanding of the Food and Drug Administration (FDA) 21 CFR 820 and International Organization for Standardization (ISO) ISO 13485.
  • Familiarity with root cause analysis tools.
  • Working knowledge of MasterControl and SAP.
  • Support and contribute in Lean Sigma programs and activities towards delivery of the set target.
  • Ability to make and implement decisions based on experience and facts as well as provide direction to peers or less experienced team members.
  • Able to be aware of all relevant SOPs as per Company policy and Quality Manual.
  • Able to comply with the company’s safety policy at all times.
Physical Requirements
Sedentary-Exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time.
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.
  • 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.
  • Maintain high attention to detail, accuracy, and overall quality of work.
  • Effectively communicate and interface with various levels internally and with customers.
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12.09.2025
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West Pharma Production Line Lead United States, Arizona, Tempe

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Assist and directs the activities and resources of daily production assigned to the work group including;interviewing, work assignments, break scheduling and relief, and shipping and packing label generation. Maintains a...
Description:


Job Summary:
In this role, you will be able to be a Self‐directed operator with good leadership skills and the ability to assist the
Production Shift Supervisor in the daily scheduling, operation and evaluation of production staff assigned to their
work group. Coordinates and or assists in all materials, production, quality and documentation of raw materials and
finished parts with Supervisors, Material Handlers, and Production Engineering. Assists the Supervisor in training,
coaching and performance evaluations.

Assists as needed in the Supervisor’s absence.Essential Duties and Responsibilities:


• Assist and directs the activities and resources of daily production assigned to the work group including;
interviewing, work assignments, break scheduling and relief, and shipping and packing label generation.
• Maintains a clean, orderly and safe workstation and environment at all times.
• Establishes team objectives and measurements for production, calculates and compares production
results with daily production reports, and enter results in ERP system.
• Coordinates with other departments to ensure variety of production necessities such as; documentation,
labeling, packaging, part quality, equipment control(s) are set and functioning correctly, and line changes
are completed for changes in production and/or customer specifications.
• Coordinates with the other Production Leads and Shift Supervisor on all production and personnel
matters as needed to meet work objectives.
• Lead continuous process improvement efforts to reduce scrap, cycle times, improve efficiency, and
eliminate waste within the production environment.
• Follows all applicable SOPs, GMPs, and DOIs.
• Contributes to continuous process improvement efforts to reduce scrap, cycle times, improve efficiency,
and eliminate waste.
• Supports and contributes in Lean Sigma programs and activities towards delivery of the set target.
• Provides a “Customer Service” attitude when interacting with internal and external customers while
accomplishing work, production, and achieving quality standards.
• Conforms with and abides by all regulations, policies, work procedures, instruction, and safety rules.
• Complies with the company’s quality policy at all times
• Maintains a clean, orderly and safe workstation and environment at all times.
• Ensures Daily, Weekly, and Monthly cleanings are performed, and documented per procedure.
• Exhibits regular, reliable, punctual and predictable attendance.
• May be required to work mandatory overtime and/or irregular hours and/or on irregular days to
complete assignments and meet business needs.
• Performs other duties as assigned.


• Minimum 18 years of age
• Able to read, verbalize, and understand procedures, safety sheets, instructions, and policies in English
• Experience: 1-3 years of experience, ideally in manufacturing and/or clean room environment
• Experience in manufacturing as a competent operator/inspector.
Preferred Knowledge, Skills and Abilities:
• Education: High School Diploma or GED
• Experience with cGMP practices, ISO, and medical device manufacturing

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12.09.2025
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West Pharma Sr Manager Supply Chain Operations United States, Arizona, Tempe

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Strategically develop production plans in coordination with the Regional Planner/s and direct plant personnel in the execution of the approved plans --- following their review and approval at the monthly...
Description:
Job Summary
Manages all aspects of site supply chain function, including procurement, production planning, warehouse management (shipping, receiving, transportation and inventory) and database coordination while optimizing the use of resources to achieve established delivery, lead-time, inventory, and cash flow objectives
Essential Duties and Responsibilities
  • Strategically develop production plans in coordination with the Regional Planner/s and direct plant personnel in the execution of the approved plans --- following their review and approval at the monthly Sales and Operations Planning (S&OP) meeting.
  • Directs the teams that develop and executes production, inventory, and material plans.
  • Adheres to monthly S&OP schedule in providing inputs & managing outputs and participates in all required production and supply chain/customer meetings.
  • Collaborates with the regional planner & demand analyst to understand customer demand (inter-company included) and market drivers to facilitate a balancing of capacity (tool, machine and labor), inventory and delivery lead-time in the development of the production plan.
  • Partners with the regional planner to aggregate the plant Master Production Schedule (MPS), incorporate forecast & market demand and develop a production plan (VOLUME).
  • Implements and oversees vendor managed inventory (VMI) programs.
  • Executes Rough Cut Capacity Planning (RCCP) for key resources (tools, machine, labor and material) to establish that the Production Plan is achievable and to recommend the need for additional resources.
  • Works with the strategic supply planner to develop and maintain a program to manage raw material sourcing routine for an optimal balance between inventory, cash flow and transportation cost.
  • Provides strategic direction and guidance in planning for conversations related to purchasing of raw materials.
  • Manages the customer order cycle and communication between plants, headquarters and the customer.
  • Monitors manufacturing lead times and delivery performance to assure targeted customer service levels are being achieved.
  • Provides oversight and strategic leadership on slow moving and obsolete inventory.
  • In the absence of packaged solutions, develops and implements PC/Microsoft based tools.
  • Leads effective product transfer plans and supports database coordinator to ensure the integrity and accuracy of the ERP and MES data.
  • Develops and manages the training, growth, development, and succession planning for the Supply Chain Department
  • Support and contribute to Lean/Six Sigma programs and activities
  • Conforms with and abides by all regulations, policies, work procedures, instruction, and all safety rules.
  • Performs other duties, as assigned based on business needs.
Education
  • Bachelor's Degree Supply Chain, Engineering, Finance, or Business required
  • Master's Degree MBA preferred
Work Experience

Minimum 10 years (Sr Mgr)experience in operational management in the medical device/pharma/plastics injection industry,Prior manufacturing experience in an industrial /cGMP setting andExperience in lean manufacturing systems and costs savings programs which affect company financial and growth plans are Required.


License and Certifications
  • Manufacturing\Certified in Logistics, Transportation, and Distribution (CLTD)-APICS preferred
  • Manufacturing\Certified in Production and Inventory Management (CPIM)-APICS preferred
Physical Requirements
Sedentary-Exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time.
Additional Requirements
  • Able to sit and/or stand for extended periods
  • Able to be able to lift and carry various items up to 40 pounds
  • Able to climb stairs and ladders
  • Must be able to multi-task, work under time constraints, problem solve, and prioritize.
  • Must also be able to maintain confidentiality and resolve conflicts.
  • Ability to make independent and sound judgments.
  • Read and interpret data, information, and documents
  • Analyze and solve problems and interpret situations
  • Work under deadlines with constant interruptions
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04.09.2025
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West Pharma Tool Room Lead United States, Arizona, Tempe

Limitless High-tech career opportunities - Expoint
Production & Scheduling. Work closely with production staff to establish daily and weekly tooling priorities. Schedule tool room work for optimal flow, aligning with production floor needs and priorities. Adjust...
Description:
Job Summary

The Tool Room Lead is responsible for coordinating daily tool room activities to support production priorities, tool maintenance, and continuous improvement initiatives. This role serves as the key link between production staff, tooling engineers, and the Tooling Engineering Manager. The Tool Room Lead ensures that tool room work is scheduled for best flow, jobs are prioritized correctly, and communication remains clear and consistent.

Essential Duties and Responsibilities
  • Production & Scheduling
  • Work closely with production staff to establish daily and weekly tooling priorities.
  • Schedule tool room work for optimal flow, aligning with production floor needs and priorities.
  • Adjust schedules based on urgent or changing production requirements.
  • Provide clear daily job assignments and direction to mold makers.
  • Communication & Reporting
  • Issue daily shop updates on job status, progress, and issues to the Tooling Engineers and Tooling Engineering Manager.
  • Act as the primary communication point between the Mold Makers, Production staff, and Tooling engineers.
  • Escalate critical or urgent tooling issues promptly to the Tooling Engineering Manager.
  • Provide both positive and constructive feedback on Mold makers and Tooling Engineers to the Tooling Engineering Manager, supporting staff development and accountability.
  • Collaboration & Continuous Improvement
  • Collaborate with Tooling Engineers on production repairs and improvement projects.
  • Work jointly with Tooling Engineers and the Tooling Engineering Manager on steel evaluations, mold health reviews, and repair planning.
  • Support implementation of standardized work instructions and best practices across the tool room.
  • Shop & Team Leadership
  • Maintain a clean, organized, and safe tool room environment.
  • Lead, coach, and provide feedback to Mold Makers.
  • Ensure all repair and maintenance work is documented accurately and completed to high quality standards.
  • Coordinate with Tooling Engineers on spare parts requirements and availability.
Education
  • High School Diploma with 10-15 years related manufacturing (precision machining) experience required or
  • Associate's Degree with 5-10 years related manufacturing experience (or equivalent education / training / experience); required or
  • Bachelor's Degree with 5+ years manufacturing experience required
Work Experience

Minimum 5 years (Sr Assoc) 5 years supervisory or leadership experience in a machine shop environment.

Must have effective problem solving and interpersonal skills, both written and verbal.

Must be able to manage resources effectively & efficiently.

Ability to work through problems and develop appropriate, successful solutions.

Able to exercise independent judgment with limited instruction and guidance.

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
  • Frequent standing, twisting, bending, reaching, pushing, pulling and walking.
  • Must have excellent organizational interpersonal and problem-solving skills and be able to interface with employees in all levels of the organization and in a variety of situations.
  • Effective personal time management skills and must be able to multi-task, work under time constraints, and prioritize with constant interuptions.
  • Must have the cognitive ability to plan, execute to goal, supervise and coordinate the work of a team in area of responsibility.
  • Ability to quickly adapt to changes in a dynamic environment.
  • Must be able to maintain confidentiality and effectively resolve conflicts.
  • Able to routinely use standard office equipment such as computers, phones, photocopiers, filing cabinets and fax machines. Position operates in a professional office environment. May stand or sit for extended periods of time.
  • Leadership skills and must be able to communicate effectively with written and oral skills, make quick decisions, interpret data, read and write, speak in front of groups, express and exchange ideas, understand direction and adhere to procedures.
  • Read and interpret data, information and documents.
  • Observe and interpret situations, analyze and solve problems.
  • Ability to make independent and sound judgments with guidance from management as needed.
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Limitless High-tech career opportunities - Expoint
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 to include laser...
Description:

This shift is Monday - Friday 8:00 AM - 4:30 PM.

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 to include laser micrometer, optical comparator and other equipment as applicable
  • 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
  • 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
  • Print documents from Master Control, shopfloor or other software program and manages documents related to the Quality System
  • Segregate nonconforming product and handle quarantined product and raw materials as applicable by site
  • Generate rejection and deviation reports as directed by site
  • 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
  • Minimum one year manufacturing experience required
Preferred Knowledge, Skills and Abilities
  • Must poses an acute attention to detail
  • Basic computer skills
Travel Requirements
None: No travel required
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.
Show more
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