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Sr Process Engineer jobs at West Pharma

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76 jobs found
23.11.2025
WP

West Pharma Senior Process Engineer United States, Pennsylvania

Limitless High-tech career opportunities - Expoint
Initiate, lead and coordinate improvements of existing processes globally on quality, service, HSE and cost within the standard known/approved process frame and using best practice knowledge. Strongly support the implementation...
Description:
Essential Duties and Responsibilities
  • Initiate, lead and coordinate improvements of existing processes globally on quality, service, HSE and cost within the standard known/approved process frame and using best practice knowledge
  • Strongly support the implementation / roll-out of automation and new innovative processes and technologies in joint cooperation with the automation, engineering- and quality assurance teams and the plants.
  • Manage the development of robust process for final industrial production in targeted plants.
  • Assess current process status in all relevant West locations globally, define best practices, perform a gap analysis and manage the harmonization of this best practice to all sites involved.
  • Engage in solutioning product or process related issues as needed.
  • Support the introduction, start-up and validation of new equipment in the local sites.
  • Support process or technology or product transfer projects between plants from a process stand-point.
  • Evaluate and approve all change requests globally.
  • Utilize six sigma tools in minimizing process variation and improving the quality of product produced.
Education
  • Bachelor's or Master's Degree in Engineering or another scientific area or equivalent experience required
Work Experience
  • Minimum 3 years experience in a similar position within the manufacturing industry required
  • Experience in Project Management preferred
Preferred Knowledge, Skills and Abilities
  • Good knowledge of LEAN and Six Sigma manufacturing principles (Green Belt certification)
  • Knowledge of MS Office, statistical tools and Minitab
  • cGMP knowledge
  • Fluent English and German skills
  • Self motivated, result- and solution-oriented personality
  • Excellent communication skills
  • Ability to successfully collaborate with teams across different countries and organizational levels
Physical Requirements
Light-Exerting up to 20lbs/9kg of force frequently, and/or negligible amount of force frequently constantly to move objects.
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23.11.2025
WP

West Pharma Sr Manager Operational Excellence United States, North Carolina

Limitless High-tech career opportunities - Expoint
Oversee the planning, execution, and delivery of all transformation projects, ensuring they are completed on time, with scope and within budget. Establish clear metrics and KPI’s for each transformation initiative,...
Description:
Job Summary

In this role you will coordinate business unit lean savings, goals and objectives through the use of statistical techniques by planning, scheduling, and executing process projects. You will communicate project status, and define and shape strategic planning efforts, including critical goal and objective development that identifies and improves critical processes necessary to achieve annual targets, including waste reduction to drive technical and operational improvement. This role will focus on coordinating, managing, and driving all transformation initiatives across site, ensuring alignment with both site’s and operational goals and the corporate stakeholders’ broader strategic objectives.

Essential Duties and Responsibilities
  • Oversee the planning, execution, and delivery of all transformation projects, ensuring they are completed on time, with scope and within budget.
  • Establish clear metrics and KPI’s for each transformation initiative, regularly tracking and reporting on progress to SLT and key stakeholders.
  • Participate in the development and support of the West Business System (WBS), with the goal of sustaining operational standards on the site.
  • Develop and communicate a comprehensive transformation strategy that aligns with the site growth targets, technical & operational capability imperatives, operational excellence objectives and the Operating Units vision.
  • Provide thought leadership and direction for all transformation activities, ensuring they are prioritized, scheduled, and executed effectively.
  • Create strategic plans to eliminate waste within the business unit by utilizing lean processes, key performance indicators, metrics, cost savings, best demonstrated practices and enterprise resource management.
  • Create and execute a robust change management framework that prepares the site and its employees for upcoming changes, minimizes resistance, and maximizes adoption of new processes and technologies.
  • Ensures that all transformation initiatives are supported by effective communication plans that keep all stakeholders informed and engaged.
  • Develop robust, capable systems necessary to achieve the strategic goals and objectives and drive excellence through the manufacturing operations; assure that production processes are repeatable and capable of meeting specifications, by ensuring the consistent and uniform application of OPEX tools.
  • Provide leadership on lean thinking and lean processes to ensure established goals and objectives are met and provide methods to monitor processes to assure they remain in control.
  • Assist in the training and guidance for lean champions and team members to develop and implement Lean action plans and transfer lean initiatives to other West plants.
Education
  • Bachelor’s in engineering, Statistics or recognized equivalent required
  • Master’s Degree in related field preferred
Work Experience
  • Minimum 10 years (Sr Mgr) in related field required
  • At least 5 years of experience in a manufacturing/production environment required
  • Must possess a Six Sigma Green Belt certification and have at least 5 years of experience demonstrating and using Six Sigma/Lean tools and methodologies required
  • Medical Device industry experience preferred
Preferred Knowledge, Skills and Abilities
  • Must have good interpersonal/leadership skills and be able to interface with all departments and team member levels.
  • Must have excellent organizational, interpersonal and problem-solving skills and be able to interface with employees at all levels of the organization.
  • 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.
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
  • Safely work in construction environments
  • Noise level in the work environment while on the production floor is usually moderate to loud. Hearing protection is required.
  • Must follow and comply with Plant’s Dress and Hygiene Code (SOI)
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22.11.2025
WP

West Pharma Tooling Engineer United States, Arizona, Tempe

Limitless High-tech career opportunities - Expoint
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...
Description:
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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22.11.2025
WP

West Pharma Process Engineer United States, Pennsylvania, Williamsport

Limitless High-tech career opportunities - Expoint
Interacts with all departments pertaining to implementation of statistically established studies either for process improvements or establishment thereof. Ensure quality of all materials used in the process by developing and...
Description:
Essential Duties and Responsibilities
  • Interacts with all departments pertaining to implementation of statistically established studies either for process improvements or establishment thereof.
  • Ensure quality of all materials used in the process by developing and implementing effective reliable testing techniques.
  • Ensure continued reliability of testing techniques by maintaining current knowledge of all technical and analytical information.
  • Write technical reports as required to defend or support decisions concerning material acceptability.
  • Establish and implement reliable procedures to ensure compliance with good manufacturing practices.
  • Provide project leadership for materials / process related projects by coordinating the efforts of the various departmental disciplines for the successful completion according to plan and budget.
  • Support the efforts of production in materials related areas as a technical advisor.
  • Reviews data using InTouch and eDart software, for investigation of problems.
  • Take appropriate action to ensure compliance with all safety, health and hazardous communication standards.
  • Ensures that established policies, rules and regulations, and procedures are followed.
  • Actively participate and comply with all West HSE programs and regulations.
  • Maintain a neat and orderly work environment in accordance with West 6S program.
  • Other duties as assigned.
Education
  • Associate or Bachelor’s Degree or equivalent on the job experience in a technical discipline to include manufacturing, industrial, materials or plastics.
Work Experience
  • Experience: 3-5 years of job-related experience
  • Knowledge of the basic principles of injection molding, systematic molding, mold design, mold assembly, and machine operations.
Preferred Knowledge, Skills and Abilities
  • Must have excellent interpersonal & problem-solving skills & be able to interface with employees at all levels of the organization; must possess good organization, time-management, negotiating & conflict resolution skills.
  • Must be familiar with computers and various software programs.
  • Familiarity with SAP, Master Control or similar systems and databases, a plus.
  • Knowledge of statistical tools and Minitab.
  • 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 preferred
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
  • While performing the duties of this job, the employee is regularly required to, sit, stand, walk, talk, hear, see and use hands and fingers to operate office equipment (ie phones, computers, copies, etc.).
  • Sitting and/or standing for extended periods may occur as well as getting to and from offices and building sites.
  • The ability to be able to lift and carry various items up to 40 pounds.
  • The employee is occasionally exposed to wet and/or humid conditions and fumes or airborne particles.
  • The employee occasionally works near moving mechanical parts and or equipment.
  • The employee occasionally works in clean room environments requiring special gowning and training to operate in these environments.
  • The noise level in the office work environment is usually quiet. The noise level in the manufacturing work environment is moderate to loud. Hearing protection is required as posted in the manufacturing work environment.
  • Job requires mental skill or ability such as communication, decision making (sometimes quick), interpreting data, reading, or writing, organization, problem solving, understand direction, etc.
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22.11.2025
WP

West Pharma Senior Quality Engineer United States, Arizona, Tempe

Limitless High-tech career opportunities - Expoint
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...
Description:
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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22.11.2025
WP

West Pharma Sr Automation Engineer United States, Arizona, Tempe

Limitless High-tech career opportunities - Expoint
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...
Description:
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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22.11.2025
WP

West Pharma Supervisor Process Engineering United States, Pennsylvania

Limitless High-tech career opportunities - Expoint
Support the plant’s continuous improvement efforts with the development and improvement of products and processes assuring the plant’s competitive position. Ensure compliance with cGMPs. Guide, coordinate, or perform modifications, improvements...
Description:
Job Summary

In this role, you will organize, coordinate, or perform modifications, validations, and enhancements of processes, equipment, and tooling to new and existing products to ensure safety, maximum yields, quality, cost effectiveness and throughput of our processes.

Essential Duties and Responsibilities
  • Support the plant’s continuous improvement efforts with the development and improvement of products and processes assuring the plant’s competitive position.
  • Ensure compliance with cGMPs
  • Guide, coordinate, or perform modifications, improvements or validations of existing or new products, processes, tooling, equipment, and related research and development activity.
  • Provide training and guidance to production engineering personnel.
  • Plan, schedule, or perform projects within the approved time schedules and budgets
  • Keep Engineering Manager advised of any unusual situation which may impair or affect production or assigned projects
  • Keep BOM and routes current
  • Review procedures to ensure they reflect the most effective means and contain the most current and correct information
  • Maintain engineering records and documents as required
  • Lead the way in supporting the plant’s efforts in meeting the corporate and plant goals
  • Review processes continually to ensure their quality
  • Safeguard confidential information and maintain effective team member relations
  • Performs other duties as assigned based on business needs as directed by Area Manager(s), Production Manager and/or Director, Ops.
  • 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 Engineering or another scientific area or equivalent experience required
Work Experience
  • 5-8 Years of experience
  • Lean/Six Sigma Training/Certification Preferred
Preferred Knowledge, Skills and Abilities
  • 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 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
Light-Exerting up to 20lbs/9kg of force frequently, and/or negligible amount of force frequently 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, solve problems, and prioritize
  • Must 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
  • Observe and interpret situations
  • Work under deadlines with shifting priorities
Show more

These jobs might be a good fit

Limitless High-tech career opportunities - Expoint
Initiate, lead and coordinate improvements of existing processes globally on quality, service, HSE and cost within the standard known/approved process frame and using best practice knowledge. Strongly support the implementation...
Description:
Essential Duties and Responsibilities
  • Initiate, lead and coordinate improvements of existing processes globally on quality, service, HSE and cost within the standard known/approved process frame and using best practice knowledge
  • Strongly support the implementation / roll-out of automation and new innovative processes and technologies in joint cooperation with the automation, engineering- and quality assurance teams and the plants.
  • Manage the development of robust process for final industrial production in targeted plants.
  • Assess current process status in all relevant West locations globally, define best practices, perform a gap analysis and manage the harmonization of this best practice to all sites involved.
  • Engage in solutioning product or process related issues as needed.
  • Support the introduction, start-up and validation of new equipment in the local sites.
  • Support process or technology or product transfer projects between plants from a process stand-point.
  • Evaluate and approve all change requests globally.
  • Utilize six sigma tools in minimizing process variation and improving the quality of product produced.
Education
  • Bachelor's or Master's Degree in Engineering or another scientific area or equivalent experience required
Work Experience
  • Minimum 3 years experience in a similar position within the manufacturing industry required
  • Experience in Project Management preferred
Preferred Knowledge, Skills and Abilities
  • Good knowledge of LEAN and Six Sigma manufacturing principles (Green Belt certification)
  • Knowledge of MS Office, statistical tools and Minitab
  • cGMP knowledge
  • Fluent English and German skills
  • Self motivated, result- and solution-oriented personality
  • Excellent communication skills
  • Ability to successfully collaborate with teams across different countries and organizational levels
Physical Requirements
Light-Exerting up to 20lbs/9kg of force frequently, and/or negligible amount of force frequently constantly to move objects.
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