מציאת משרת הייטק בחברות הטובות ביותר מעולם לא הייתה קלה יותר
דרושים Tooling Engineer ב-West Pharma ב-United States, Tempe
מצאו את ההתאמה המושלמת עבורכם עם אקספוינט! חפשו הזדמנויות עבודה בתור Tooling Engineer ב-United States, Tempe והצטרפו לרשת החברות המובילות בתעשיית ההייטק, כמו West Pharma. הירשמו עכשיו ומצאו את עבודת החלומות שלך עם אקספוינט!
חברה (1)
אופי המשרה
קטגוריות תפקיד
שם תפקיד (1)
United States
אזור
Tempe
נמצאו 6 משרות
22.11.2025
WP
West Pharma Tooling Engineer United States, Arizona, Tempe
Provide engineering assistance to assure plant, machinery and processes are at an optimum level. Demonstrated experience in Metal Stamping and Progressive Die industry. Ensure plant is in compliance with OSHA...
תיאור:
Essential Duties and Responsibilities
- Provide engineering assistance to assure plant, machinery and processes are at an optimum level.
- Demonstrated experience in Metal Stamping and Progressive Die industry.
- Ensure plant is in compliance with OSHA and local, state and federal environmental regulations.
- Assist in Writing validation, user requirements, equipment specification and other documents as needed.
- Promote and support a Lean Manufacturing environment within the facility.
- Assist in process and procedure improvements to manufacture a quality product at a minimum cost.
- Assists in quoting new tooling/dies, engineering services, automation, etc. for new and existing customers. Helps Develop suppliers and maintain audit. Develops design concepts for new molds.
- Purchases tooling related equipment in accordance with the company policy.
- Provides a “Customer Service” attitude when interacting with internal and external customers while accomplishing work, production, and achieving quality standards.
- Maintain machine and plant equipment drawing for the Tool Room.
- Support in Developing initial project scope, timeline, savings and cost estimations.
- Write CER and project justification documents.
- Support in Developing equipment requirements.
- Research new technologies and methodologies to use in the plant.
- Present justification to management and/or customer to attain approvals.
- 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
- Bachelor's Degree in Mechanical Engineering, Manufacturing Engineering, or equivalent experience required
Work Experience
- Minimum 3 years of relevant experience. Prior manufacturing experience in an industrial setting (pharmaceutical industry experience preferred). required
- Advanced in using SolidWorks. required
- Excellent computer skills required including all MS Office applications. required
Preferred Knowledge, Skills and Abilities
- Good understanding in machining and fabrication equipment and methods (e.g. milling, turning, grinding, eroding, etc.).
- Familiar with cGMP, ISO, and FDA standards.
- Familiar with AutoCAD, Finite Element Analysis, Computational Fluid Dynamics, and PDM Pro.
- Able to be aware of all relevant SOPs as per Company policy as they are related to the position covered by this Job Description
- Support and contribute in Lean Sigma programs and activities towards delivery of the set target
- Able to comply with the company’s safety and quality policies 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
- Must be able to negotiate and effectively resolve conflicts when required
- 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
- Ability to quickly adapt to changes in a dynamic environment and must maintain the ability to work well with others in a variety of situations
- Effective personal time management skills. 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
- Must be able to speak English fluently
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משרות נוספות שיכולות לעניין אותך
22.11.2025
WP
West Pharma Senior Quality Engineer United States, Arizona, Tempe
Lead project planning activity and develop comprehensive project plans including scope, timelines, budget, resources, and project success criteria. Gain buy-in from project team and ensure an inclusive approach to project...
תיאור:
Job Summary
In this role, you will provide quality direction, governance, and Quality Management System best practices across the programs you support. This role oversees multiple concurrent projects to ensure regulatory and quality compliance is maintained throughout the product development lifecycle into manufacturing and sustainment.
Essential Duties and Responsibilities
- Lead project planning activity and develop comprehensive project plans including scope, timelines, budget, resources, and project success criteria. Gain buy-in from project team and ensure an inclusive approach to project planning. Proactively identify gaps and risks to project success and implement mitigation strategies to minimize impact.
- Collaborate with cross-functional teams, internal and external to the laboratory, to coordinate project execution and ensure that project objectives and success criteria are met.
- Provide Quality Engineering direction to multiple concurrent product development programs to ensure product and process compliance to all applicable regulatory and cGMP requirements, including ensuring all relevant safety procedures are employed.
- Author, review, and/or approve design history documentation and design manufacturing documentation (e.g., product specifications, design verification and validation activities, FMEA risk documents, test methods, protocols, reports, manufacturing records, etc.)
- Lead the development and maintenance of product or process risk and hazard analysis in accordance with West policies and procedures and ISO standards.
- Lead and manage QMS activities including CAPA, Failure Investigation, Non-Conformance assessment, audit findings, issue reviews, document control, change controls, configuration management, etc. Provide direction on any nonconformance, deviation, or excursion that may occur and drive to closure. Author and review product development QMS procedures and work instructions.
- Meet company and departmental goals in the continuous improvement of all products, services and processes, including the West QMS.
- May work independently and with project teams to develop design control deliverables including quality plans, manufacturing and inspection documentation, test methods, and any other necessary quality records. Provide quality reports and review trending on assigned areas of responsibility.
- May 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.
- May assumes responsibility for various assigned projects designed to improve product quality, reduce costs and/or validate facility products or processes, including development and implementation of any new or required inspection methods and in-process Statistical Process Control programs.
- May perform DOEs (Design of Experiments) to help improve and optimize new and/or existing plant processes or job protocols, and identify and remedy equipment and/or process documentation gaps and provide appropriate training where needed.
- May have people management responsibilities.
- Other duties as assigned.
Education
- Bachelor's Degree in Engineering or Science or equivalent experience required
Work Experience
- Minimum 5 years of experience in a regulated industry (e.g., Medical Device), including Product Development, Product Manufacturing, and Post Market Surveillance Activities required and
- Demonstrated experience (4+ years) independently defining, planning, and executing projects in highly regulated environments with a track record of success required and
- In-depth knowledge of cGMP regulations, ISO 17025, ISO 11040, ISO 13485, 21 CFR 820, ISO 14971 required and
- Proficiency in standard project management tools and software (e.g. Microsoft Project, Excel) for planning, tracking, and reporting project activities, and proficient in statistical software, Windows OS, Microsoft Office Suite including Word, Excel, and Power Point required and
Preferred Knowledge, Skills and Abilities
- Experience with MasterControl, SAP, Share Point, Teamcenter
- Experience with ISO 11040, ISO 11607
- Expertise in quality management tools. Standards, policies, and procedures – APQP, PPAP, MSA, SQC etc
- Strong working knowledge of quality systems of the respective ISO norms
- Working knowledge of supplier quality management from product development to mass production.
- Strong project management skills
- Proficient in computer system applications (SAP, master controls, etc) communication skills
- Excellent critical reading and writing skills
- Problem solving including root cause failure analysis methods
- Be aware of all relevant SOPs as per Company policy as they relate to this role
- Able to comply with the company’s safety and quality policies at all times
Additional Requirements
- Exhibit a strong “quality first” mentality and ensure that product and process quality are held to the highest standard.
- Excellent written and oral communication and interpersonal abilities, with the capacity to communicate complex technical concepts to diverse stakeholders.
- Ability to work independently, multi-task and thrive in fast-paced environment.
- Strong problem-solving skills including root cause failure analysis methods.
- 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.
- Critical reading skills and 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.
License and Certifications
- Manufacturing\Six Sigma Green Belt Certification or Black Belt Upon Hire preferred
- Quality\Certified Quality Technician-ASQ (CQE or CQA) Upon Hire preferred
- SO 17025 Auditor or Lead Auditor Training / Certification Upon Hire 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.
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משרות נוספות שיכולות לעניין אותך
22.11.2025
WP
West Pharma Sr Automation Engineer United States, Arizona, Tempe
Mentor and may lead engineering team to achieve site and department goals in a fast-paced environment. Collaborate with cross-functional teams to develop and implement sustainable manufacturing processes and systems. Technical...
תיאור:
Job Summary
In this role, you will effectively plan and guide Engineering team, ensuring quality product and operational efficiencies are met.
Essential Duties and Responsibilities
- Mentor and may lead engineering team to achieve site and department goals in a fast-paced environment.
- Collaborate with cross-functional teams to develop and implement sustainable manufacturing processes and systems.
- Technical and hands-on automated equipment troubleshooting, repair, and improvements.
- Perform and document engineering studies and evaluations.
- Analyze data to drive improvements, determine prioritization, and identify opportunities.
- Lead and provide mentorship in root cause and corrective action (RCCA).
- Assess and perform/schedule technical training, including electromechanical systems, pneumatics, servos, PLCs, schematic reading/interpretation, new technology, etc.
- Champion high-visibility projects. Develop project scope, timeline, savings, and cost estimations.
- Quote new automation lines, engineering services, etc. Develop design concepts for new automation.
- Write validation, user requirements, equipment specification, and other documents as needed.
- Establishes relationships with customer and automation suppliers in pursuit of win?win results and ongoing business.
- Provide engineering assistance to assure plant, machinery, and processes are at an optimum level.
- Routinely evaluate and review employee performance.
- Promote and support a Lean Manufacturing environment within the facility.
- Research new technologies and methodologies to use in the plant.
- Provide a “Customer Service” attitude when interacting with internal and external customers while accomplishing work, production, and achieving quality standards.
- Perform other duties as assigned based on business needs.
- Conform with and abides by all regulations, policies, work procedures, instruction, and all safety rules.
- Exhibit regular, reliable, punctual and predictable attendance.
- Other duties as assigned.
Education
- Bachelor's Degree In Engineering or Science field required
- Master's Degree In Engineering or Science field preferred
Work Experience
- Minimum 5 years 5-8 years of experience required and
- 2+ years of managerial or supervisory experience in manufacturing environment required and
- Strong automation background and experience with CAD and SAP systems a plus. preferred
Preferred Knowledge, Skills and Abilities
- Knowledge of manufacturing processes, workflows, production equipment and industrial techniques.
- Must have effective problem solving and interpersonal skills.
License and Certifications
- Manufacturing\Six Sigma Green Belt Certification Six Sigma green belt Upon Hire preferred or
- Manufacturing\Lean Six Sigma Black Belt Six Sigma black belt Upon Hire 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
- Must be able to perform job duties as required with limited physical demands.
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משרות נוספות שיכולות לעניין אותך
23.08.2025
WP
West Pharma Sr Quality Engineer United States, Arizona, Tempe
Lead project planning activity and develop comprehensive project plans including scope, timelines, budget, resources, and project success criteria. Gain buy-in from project team and ensure an inclusive approach to project...
תיאור:
Job Summary
In this role, you will provide quality direction, governance, and Quality Management System best practices across the programs you support. This role oversees multiple concurrent projects to ensure regulatory and quality compliance is maintained throughout the product development lifecycle into manufacturing and sustainment.
Essential Duties and Responsibilities
- Lead project planning activity and develop comprehensive project plans including scope, timelines, budget, resources, and project success criteria. Gain buy-in from project team and ensure an inclusive approach to project planning. Proactively identify gaps and risks to project success and implement mitigation strategies to minimize impact.
- Collaborate with cross-functional teams, internal and external to the laboratory, to coordinate project execution and ensure that project objectives and success criteria are met.
- Provide Quality Engineering direction to multiple concurrent product development programs to ensure product and process compliance to all applicable regulatory and cGMP requirements, including ensuring all relevant safety procedures are employed.
- Author, review, and/or approve design history documentation and design manufacturing documentation (e.g., product specifications, design verification and validation activities, FMEA risk documents, test methods, protocols, reports, manufacturing records, etc.)
- Lead the development and maintenance of product or process risk and hazard analysis in accordance with West policies and procedures and ISO standards.
- Lead and manage QMS activities including CAPA, Failure Investigation, Non-Conformance assessment, audit findings, issue reviews, document control, change controls, configuration management, etc. Provide direction on any nonconformance, deviation, or excursion that may occur and drive to closure. Author and review product development QMS procedures and work instructions.
- Meet company and departmental goals in the continuous improvement of all products, services and processes, including the West QMS.
- May work independently and with project teams to develop design control deliverables including quality plans, manufacturing and inspection documentation, test methods, and any other necessary quality records. Provide quality reports and review trending on assigned areas of responsibility.
- May 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.
- May assumes responsibility for various assigned projects designed to improve product quality, reduce costs and/or validate facility products or processes, including development and implementation of any new or required inspection methods and in-process Statistical Process Control programs.
- May perform DOEs (Design of Experiments) to help improve and optimize new and/or existing plant processes or job protocols, and identify and remedy equipment and/or process documentation gaps and provide appropriate training where needed.
- May have people management responsibilities.
- Other duties as assigned.
Education
- Bachelor's Degree in Engineering or Science or equivalent experience required
Work Experience
- Minimum 5 years of experience in a regulated industry (e.g., Medical Device), including Product Development, Product Manufacturing, and Post Market Surveillance Activities required and
- Demonstrated experience (4+ years) independently defining, planning, and executing projects in highly regulated environments with a track record of success required and
- In-depth knowledge of cGMP regulations, ISO 17025, ISO 11040, ISO 13485, 21 CFR 820, ISO 14971 required and
- Proficiency in standard project management tools and software (e.g. Microsoft Project, Excel) for planning, tracking, and reporting project activities, and proficient in statistical software, Windows OS, Microsoft Office Suite including Word, Excel, and Power Point required and
Preferred Knowledge, Skills and Abilities
- Experience with MasterControl, SAP, Share Point, Teamcenter
- Experience with ISO 11040, ISO 11607
- Expertise in quality management tools. Standards, policies, and procedures – APQP, PPAP, MSA, SQC etc
- Strong working knowledge of quality systems of the respective ISO norms
- Working knowledge of supplier quality management from product development to mass production.
- Strong project management skills
- Proficient in computer system applications (SAP, master controls, etc) communication skills
- Excellent critical reading and writing skills
- Problem solving including root cause failure analysis methods
- Be aware of all relevant SOPs as per Company policy as they relate to this role
- Able to comply with the company’s safety and quality policies at all times
License and Certifications
- Manufacturing\Six Sigma Green Belt Certification or Black Belt Upon Hire preferred
- Quality\Certified Quality Technician-ASQ (CQE or CQA) Upon Hire preferred
- SO 17025 Auditor or Lead Auditor Training / Certification Upon Hire 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
- Exhibit a strong “quality first” mentality and ensure that product and process quality are held to the highest standard.
- Excellent written and oral communication and interpersonal abilities, with the capacity to communicate complex technical concepts to diverse stakeholders.
- Ability to work independently, multi-task and thrive in fast-paced environment.
- Strong problem-solving skills including root cause failure analysis methods.
- 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.
- Critical reading skills and 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.
Show more
משרות נוספות שיכולות לעניין אותך
05.07.2025
WP
West Pharma Sr Tooling Engineer Global United States, Arizona, Tempe
Responsible for the project management of various highly skilled technical resources in providing tool design and manufacturing support to existing projects within operations. Successful management and delivery of tooling projects...
תיאור:
Job Summary:
Reporting to the Senior Manager for Global Tooling, the Senior Tooling Engineer will liaise with customers and suppliers in the support of tooling development, refurbishment and replacement for new and existing global programs within contract manufacturing. Responsibilities will include participation in vendor selection, conceptual design, selection of hot runner system, project management of tool fabrication and implementation into manufacturing. The Senior Tooling Engineer will demonstrate excellent attention to detail and manage their time efficiently.
Essential Duties and Responsibilities:
- Responsible for the project management of various highly skilled technical resources in providing tool design and manufacturing support to existing projects within operations.
- Successful management and delivery of tooling projects to agreed time scale and budget.
- Assist with the harmonization and implementation of Tooling Engineering standards and procedures across the CM Device Manufacturing Network based on current regulations, industry standards and industry practices permitting agility to meet the future needs of the business.
- Ensure suppliers meet customer and West tooling needs.
- Manage the successful handover of new validated tooling into production by liaising with customers, suppliers and internal West teams.
- Compile and deliver reports from critical tooling information gathered.
- Establish strong relationships with customers and suppliers in pursuit of continuous tooling improvements and on-going business development.
- Identify and implement continuous tooling improvements for future/repeat moulds.
- Manage the control of tool documentation, drawing and file management.
- Report/escalate all issues to Senior Manager, Global Tooling.
- Develop, review and revise tooling validation documentation.
- Attend internal meetings to establish priorities
- When required, support investigations and root cause analyses of major tooling issues.
- Liaise with external suppliers on the repair/replacement of tooling components and equipment
- Research and implement improvements to processes and procedures
- Work autonomously within established procedures and practices
- Comply to West Environmental, Health and Safety requirements, training and regulations
- Comply to all West company policies, procedures and corporate policies
- Act in accordance with West’s Guiding Principles and adheres to the Corporate Code of Conduct
- Perform additional duties at the request of the Senior Manager
Basic Qualifications:
- Engineering degree in Tool Design or related field preferably with practical experience working with injection moulds.
- Minimum 5 years of experience in the design, manufacture and project management of multi-cavity injection moulds.
- Extensive practical experience in Computer Aided Design
- Advanced and specialized tooling expertise, typically developed through a combination of job-related training and considerable on-the-job experience
- Demonstrate an in-depth knowledge of Statistical Process Control (SPC) and Design Of Experiments (DOE) within the Medtech industry
- Practical working knowledge and understanding of X Ray Computed Tomography (CT scanning) and 3D surface analysis using this technology
- Ability to work under pressure
- Must be able to organize and prioritise tasks for self
- Ability to build strong business relationships with all stakeholders
Preferred Knowledge, Skills and Abilities:
- Understand all relevant standard operating procedures as per Company policy as related to this position
- Toolmaking qualification ideally with time served producing injection moulds.
- Project management qualification i.e. PMP or equivalent
- Excellent written and verbal communication skills with the ability to accurately document work performed
- Knowledge of tooling servos, hydraulics, pneumatics and electrics
- Proficient IT skills, specifically Microsoft Office (Word, Excel, PowerPoint, Project and Outlook)
Travel Requirements:
- Must be available to travel to external toolmakers to assist in the design, development and testing of new tooling up to 25% of the time.
Physical and Mental Requirements:
- Physical requirements.
- Sedentary - exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to life, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time.
- Mental requirements.
- Ability to reason logically and make sound decisions, to consider alternative and diverse perspectives and to communicate effectively both orally and in writing,
- Ability to simultaneously address multiple complex problems.
- Ability to work as an integral part of a team.
- Ability to understand, remember and follow verbal and written instructions.
- Ability to complete assigned tasks without direct supervision.
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משרות נוספות שיכולות לעניין אותך
28.06.2025
WP
West Pharma Sr Spec Tooling Global Eng United States, Arizona, Tempe
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....
תיאור:
Job Summary
In this role, you will coordinate/assign work and provide operational support in your area of responsibility for the construction and/or repair of molds, dies, and/or ancillary equipment. Oversee the set-up, tooling, programming, and operation of CNC and/or manual milling, turning, and grinding machines that facilitate mold and die component manufacture/assembly. Schedule projects into suitable machines. Ensure inspection methodologies are appropriate, repeatable, and capable of maintaining specifications within tolerances. Assist in documenting new and existing procedures throughout the facility. Investigate, recommend and apply appropriate technology enhancements. May support in designing tools the manufacturing facilities require for production.
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
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.
Show more
משרות נוספות שיכולות לעניין אותך
Provide engineering assistance to assure plant, machinery and processes are at an optimum level. Demonstrated experience in Metal Stamping and Progressive Die industry. Ensure plant is in compliance with OSHA...
תיאור:
Essential Duties and Responsibilities
- Provide engineering assistance to assure plant, machinery and processes are at an optimum level.
- Demonstrated experience in Metal Stamping and Progressive Die industry.
- Ensure plant is in compliance with OSHA and local, state and federal environmental regulations.
- Assist in Writing validation, user requirements, equipment specification and other documents as needed.
- Promote and support a Lean Manufacturing environment within the facility.
- Assist in process and procedure improvements to manufacture a quality product at a minimum cost.
- Assists in quoting new tooling/dies, engineering services, automation, etc. for new and existing customers. Helps Develop suppliers and maintain audit. Develops design concepts for new molds.
- Purchases tooling related equipment in accordance with the company policy.
- Provides a “Customer Service” attitude when interacting with internal and external customers while accomplishing work, production, and achieving quality standards.
- Maintain machine and plant equipment drawing for the Tool Room.
- Support in Developing initial project scope, timeline, savings and cost estimations.
- Write CER and project justification documents.
- Support in Developing equipment requirements.
- Research new technologies and methodologies to use in the plant.
- Present justification to management and/or customer to attain approvals.
- 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
- Bachelor's Degree in Mechanical Engineering, Manufacturing Engineering, or equivalent experience required
Work Experience
- Minimum 3 years of relevant experience. Prior manufacturing experience in an industrial setting (pharmaceutical industry experience preferred). required
- Advanced in using SolidWorks. required
- Excellent computer skills required including all MS Office applications. required
Preferred Knowledge, Skills and Abilities
- Good understanding in machining and fabrication equipment and methods (e.g. milling, turning, grinding, eroding, etc.).
- Familiar with cGMP, ISO, and FDA standards.
- Familiar with AutoCAD, Finite Element Analysis, Computational Fluid Dynamics, and PDM Pro.
- Able to be aware of all relevant SOPs as per Company policy as they are related to the position covered by this Job Description
- Support and contribute in Lean Sigma programs and activities towards delivery of the set target
- Able to comply with the company’s safety and quality policies 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
- Must be able to negotiate and effectively resolve conflicts when required
- 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
- Ability to quickly adapt to changes in a dynamic environment and must maintain the ability to work well with others in a variety of situations
- Effective personal time management skills. 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
- Must be able to speak English fluently
Show more
משרות נוספות שיכולות לעניין אותך
בואו למצוא את עבודת החלומות שלכם בהייטק עם אקספוינט. באמצעות הפלטפורמה שלנו תוכל לחפש בקלות הזדמנויות Tooling Engineer בחברת West Pharma ב-United States, Tempe. בין אם אתם מחפשים אתגר חדש ובין אם אתם רוצים לעבוד עם ארגון ספציפי בתפקיד מסוים, Expoint מקלה על מציאת התאמת העבודה המושלמת עבורכם. התחברו לחברות מובילות באזור שלכם עוד היום וקדמו את קריירת ההייטק שלכם! הירשמו היום ועשו את הצעד הבא במסע הקריירה שלכם בעזרת אקספוינט.