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Extruding Compounding Operator jobs at West Pharma

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45 jobs found
23.11.2025
WP

West Pharma Operator Production HOR United States, Pennsylvania, West Whiteland Township

Limitless High-tech career opportunities - Expoint
Overall ownership and accountability for developing, leading and driving new business development for DDD OU product platforms for identified strategic accounts to achieve revenue growth targets for commercial and product...
Description:
Essential Duties and Responsibilities
  • Overall ownership and accountability for developing, leading and driving new business development for DDD OU product platforms for identified strategic accounts to achieve revenue growth targets for commercial and product development sales.
  • Advance the vision for strategic partnerships and customer opportunities as the SME for device services offerings, for all direct assigned accounts and regions. Establish business development programs including early adopter customers, target service levels, and CDAs (Customer Development Agreements).
  • Responsible for driving the prospecting and lead development, monitoring sales and funnel performance. Lead and support customer facing teams in key customer interactions/strategic partnerships throughout the selling journey including critical customer/strategic collaboration, presentations, post-sales leadership and problem solving to deliver on revenue and growth targets.
Education
  • Bachelor's in Engineering, Science or Business-related discipline
Work Experience
  • Minimum 15 years of experience in B2B, Combination Products, Business Development, Product/Program Management.
  • Indepth knowledge and experience in pharmaceutical/medical device technical development, sales, marketing or related business.
  • Experience in successfully leading global multi-functional or cross-functional teams, in developing cohesive relationships and producing strong business results.
  • Excellent communication/negotiation/influencing skills and strong customer focus.
  • Excellent commercial and financial acumen.
  • Self-starter, highly motivated and ability to work independently with little or no daily supervision.
Preferred Knowledge, Skills and Abilities
  • MBA or master’s degree preferred
  • Background with a good technical understanding and knowledge of Combination products, medical device qualification, primary packaging, Regulatory requirements and Program Management.
  • Significant leadership team experience and executive leadership exposure.
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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23.11.2025
WP

West Pharma Production Operator- Hour Night Shift United States, Pennsylvania

Limitless High-tech career opportunities - Expoint
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.
Education
  • High School Diploma or GED required
Work Experience
  • 1-3 years manufacturing experience preferred

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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23.11.2025
WP

West Pharma Production Operator United States, Arizona, Tempe

Limitless High-tech career opportunities - Expoint
Identify problems by reading schematics/prints, where available, and make necessary repairs on the equipment or system to ensure safe operation of the machine or system. Respond to production maintenance request...
Description:

This position is Monday - Friday 7:00 AM - 3:30 PM

Job Summary

Management and implementation of facility projects and support in holistic building management. Perform a wide variety of mechanical, as well as pneumatic maintenance activities and some basic electrical activities on various pieces of equipment to maintain safe operations of equipment while maintaining production goals and quality standards. Other responsibilities include sourcing parts for obsolete parts and ordering them, documenting all the maintenance activities performed, PM's, installation, and validations of equipment. Will support and help other groups like Process Engineering, QA, and Facilities in resolving problems, improvements, investigations etc. In this role you will service/maintain several machines, while learning the others in the department. Work from prints, sketches, sample parts, verbal or written instructions. Interpret drawings, select material plan, and layout work in proper operational sequence. Maintain and setup vision systems during production.

Essential Duties and Responsibilities
  • Identify problems by reading schematics/prints, where available, and make necessary repairs on the equipment or system to ensure safe operation of the machine or system.
  • Respond to production maintenance request and any unscheduled down time.
  • Troubleshoot and adjust or repair ancillary equipment like blow overs, bulb pullers, and heaters.
  • Changeovers and setups on Vision Systems, make minor adjustments as required.
  • Perform ink mixing as well as disposing of procedure as per set Safety/QS guidelines for printing machines.
  • Perform necessary oil changes on machine gear boxes and dispose of used oil per established procedure.
  • Rebuild/retrofit machine or machine components as per specifications.
  • Perform installation, replacement or decommissioning of equipment.
  • Perform validations as necessary for equipment.
  • Work with training department to train new mechanics on machine repair, setup and related plant procedures.
  • Complete PM's on or before the due date and communicate to proper authority of job completion.
  • Source obsolete parts for equipment and make them stock item.
  • Identify and locate parts in the stock room through MP2 or other such system.
  • Participate in various company run programs like Continuous Improvement, Safety initiatives, audits, investigations etc.
  • Support projects and improvement initiatives from engineering, process, QA, Safety and Operations groups.
  • Document performed tasks for the day into the maintenance log before the end of each shift.
  • Safeguard all corporate or plant confidential information.
  • Use good housekeeping practices to maintain safe, (safe is always first) clean, orderly work area.
  • Upgrade technical skills by various educational workshops, on-site or off-site trainings supported by WEST.
  • Follow engineering department guidelines and procedures.
  • Conforms with and abides by all safety rules, regulations, policies, work procedures and all instructions.
  • Exhibits regular, reliable, punctual and predictable attendance.
  • Implementation and collaboration of facility projects
Education
  • High School Diploma Or GED required
Work Experience
  • 3 years manufacturing maintenance experience
Preferred Knowledge, Skills and Abilities
  • Experience with plastic injection molding preferred.
  • Experience with robots and pick in place robots.
  • Experience with ISO 9000 standards and GMP’s.
  • Excellent communication and interpersonal skills.
  • Experience with SAP or similar software for maintenance tracking.
  • Agile working style.
  • Ability to work weekends and overtime as required
Travel Requirements
None: No travel required
Physical Requirements
Heavy-Exerting up to 100lbs/45kg of force occasionally and/or up to 50lb/22kg of force frequently, and/or up to 20lbs/9kg of force constantly to move objects.
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22.11.2025
WP

West Pharma Cell Operator United States, Florida, Saint Petersburg

Limitless High-tech career opportunities - Expoint
Complete all pertinent documentation as required by SOIs and WIs. Perform sampling inspections and use measuring equipment per plant procedures. Fill hoppers, remove finished goods and in process and place...
Description:
Job Summary

In this role, you willoperate One Piece Flow Machine (assembly machine/ press); collect product samples and inspect product from belt and cartons for various defects outlined subsequent to and during training periods.

Essential Duties and Responsibilities
  • Complete all pertinent documentation as required by SOIs and WIs.
  • Perform sampling inspections and use measuring equipment per plant procedures.
  • Fill hoppers, remove finished goods and in process and place on skids or conveyor.
  • Follow schedules and operate presses.
  • Monitor statistical process control (SPC) charts to assure product is within specifications.
  • Perform clean out and line clearances.
  • Remove all finished goods from Production floor as needed.
  • Provide all paperwork/materials to assembly floor for “next order”.
  • Obtain raw materials from warehouse for new orders. Provide to appropriate machine areas as needed.
  • Remove trash and scrap from assembly area and place in appropriate containers/receptacles.
  • Scan labels on WIP and Finished Good product as required.
  • Guide and function as a coach for the work of new or less experienced operators and support personnel while working in a team-oriented fast paced environment.
  • Relieve operations of areas through directed break schedules.
  • Work with Quality team to ensure accurate and timely batch record review and provide feedback to necessary parties.
  • Adhere to all company policies.
  • Must observe all good housekeeping practices.
  • 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 .
  • Safety glasses, hairnet, face/beard cover, gloves, safety shoes and hearing protection as required.
Education
    • Education: High School or equivalent
    • Experience:1year of experience
    • Must possess an acute attention to detail and be able to communicate
    • Proficient in West’s Shop Floor applications and Microsoft Office
    • Willing to work overtime as needed
Work Experience
  • No min required
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.

Physical Requirements
Medium-Exerting up to 50lb/22kg of force occasionally and/or up to 20lbs/9kg of force frequently, and/or up to 10lbs/4kgs of force constantly to move objects.
Additional Requirements
  • Must be able to distinguish colors and fine print.
  • Must be able to distinguish defective parts.
  • Must be able to lift 35 lb. box and move a distance of 10 yards
  • Manufacturing environment
  • Must be able to express and exchange ideas with employees
  • Must be able to build strong relationships with direct reports and peers
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22.11.2025
WP

West Pharma Production Operator United States, Arizona, Scottsdale

Limitless High-tech career opportunities - Expoint
Perform analysis using various established or experimental techniques, instrumentation, and/or test methods while following standard operating proceedures (SOPs). Uses critical thinking skills to analyze field failures to identify the root...
Description:
Job Summary

In this role, you will be responsible for performing testing of products for internal and external customers using a variety of analytical techniques. You may be assisting in developing procedures for instrumentation, test instructions, and test reports. You may coordinate the day-to-day receipt and shipment of samples in the laboratory and support the Laboratory team in administration and quality systems.

Essential Duties and Responsibilities
  • Perform analysis using various established or experimental techniques, instrumentation, and/or test methods while following standard operating proceedures (SOPs).
  • Uses critical thinking skills to analyze field failures to identify the root cause and documents findings per procedures. Is familiar with and utilizes a variety of root cause analysis methodologies to assess technical problems.
  • Uses software tools (Salesforce, MasterControl, Microsoft Office Suite) to document and manage investigations.
  • With guidance, assist in completing projects from protocol to final report.
  • Uses strong technical writing skills to communicate findings in a technical, concise, and effective manner.
  • Train new analysts as appropriate.
  • Exercises creativity in developing new test / debugging methods.
  • Keep current with new analytical techniques and technology.
  • Assist in preparation of technical reports, work instructions, SOPs, qualification documentation, lab study design and preparation in study plans and protocols.
  • Apply internal QA procedures and perform lab investigations, OOS, and OOT as required.
  • Actively participate in and complete all appropriate training tasks in a timely manner and meet individual and departmental goals as required.
  • Work independently and collaboratively with other technical experts, and laboratory management, making rational and sound decisions with self-motivation, adaptability, and a positive attitude.
  • Support laboratory management in data quality-documentation, and archiving.
  • Maintain compliance to cGMP and ISO requirements and established safety procedures.
  • May utilize various inputs to schedule work, use Sharepoint, SAP, Excel files, and Word documents. Proficiently use MS Office products for data gathering, reporting, and data entry.
  • May handle Test Requests – write, review, and approve, and maintain traceability of samples.
Education
  • Bachelor's Degree in Biology, Chemistry or a relevant scientific field preferred
  • High School Diploma required
Work Experience
  • 0 - 3 years of experience required
  • Experience working in a laboratory or cGMP/pharmaceutical environment preferred
  • Laboratory administrative/Coordinator/Analyst role preferred
Preferred Knowledge, Skills and Abilities
  • Support and contribute to Lean Sigma programs and activities towards delivery of the set target
  • Knowledge of one of these skills: Container Closure Integrity, Physical / Mechanical testing such as Instron / Zwick, Particle Testing (HIAC, particle isolation, filtration and microscopy), Dimensional analysis (Smartscope or optical comparators)
  • Method development and validation
  • Willingness to learn and apply new analytical techniques
  • Proficient in Microsoft Office tools and capable to learn other software programs
  • Able to review regulatory code and learn safety standards
  • 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
  • Able to comply with the company’s safety and quality policies at all times
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 be able to stand for long periods of time
  • Use hands to finger, handle, feel or operate objects, tools or controls and reach with hands and arms
  • Physical ability and willingness to wear proper gowning for work in an ISO 5 compliant particulate cleanroom environment
  • 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 follow directions, 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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22.11.2025
WP

West Pharma Manager Compounding & Dimensioning Equipment Lead United States, North Carolina

Limitless High-tech career opportunities - Expoint
Inspire and guide the Global Compounding & Dimensioning Equipment SME team (up to 3 FTE) towards achieving organizational goals. Develop a high-performing team through mentoring and professional development. Lead engineering,...
Description:
Job Summary

As the Global Equipment Compounding & Dimensioning Subject Matter Expert (SME) Leader, you will set the strategic direction and lead a team responsible for specifying, implementing, and improving equipment for weighing, mixing, and dimensioning processes in our global elastomer production facilities. You will cultivate a collaborative environment, align with cross-functional engineering teams, and drive our company’s vision for innovation and standardization in equipment processes.

Essential Duties and Responsibilities
  • Inspire and guide the Global Compounding & Dimensioning Equipment SME team (up to 3 FTE) towards achieving organizational goals. Develop a high-performing team through mentoring and professional development.
  • Lead engineering, management, plant operations and global team members while working with vendors to develop engineering specifications for new equipment or required improvements on existing.
  • Shape and communicate a clear vision for advancing equipment processes, leading efforts to standardize and harmonize production equipment and associated documentation globally.
  • Proactively map out and oversee team workload and project timelines to drive efficient execution of objectives, with a focus on resource optimization for new projects, corrective action/preventive action (CAPA) initiatives, and equipment development.
  • Foster a culture of collaboration across various departments by working closely with Process Engineering and production teams. Facilitate the identification of innovative solutions to enhance existing systems and solve design challenges.
  • Keep up to date on new and future equipment standards and trends in the market and identify value-added improvement which may be beneficial.
  • Work independently, and with vendors, to understand root cause of failures, propose design or component changes, and implement and validate equipment modifications.
  • Take the lead in systematic problem-solving activities if the manufacturing plants need support.
  • Coordinate and/or execute all necessary GMP related validations and/or process engineering evaluations as needed for manufacturing equipment.
  • Guide vendors through clear communication and task assignments. Maintain oversight on deliverables ensuring completion of Factory Acceptance Testing (FAT), Site Acceptance Testing (SAT), Installation/Operational Qualifications (IOQ), and more.
  • Champion the establishment of equipment standards aligning with global best practices to achieve unparalleled quality, efficiency, cost reduction, and safety.
  • Project Management: Take the lead on equipment project management from the URS issue to PQ by applying current project managements practices including the needed GMP conform documentation.
  • Research and analyze data such as vendor design proposal, specifications, and manuals to determine feasibility of design or application.
  • Collaborate with cross-functional teams to follow equipment related corporate goals.
  • Ensure all equipment aligns with the latest Safety Regulations.
Education
  • Bachelor’s or Master’s degree in Science or Engineering (Electrical, Mechanical, or Industrial preferred).
Work Experience
  • Over 8 years of leadership experience in the pharmaceutical or manufacturing environments, specifically within equipment management and improvement.
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
  • Proven track record of successful equipment project management, from specification to qualification.
  • Strong engineering and trouble shooting skills.
  • Proven working experience in project management.
  • Demonstrated ability to manage projects in a dynamic environment with minimal direction.
  • Excellent written and verbal communication skills (English & preferably a 2nd language)
  • Strong strategic thinking capabilities with the ability to drive innovation and embrace change.
  • Ability to drive changes and to think outside the box.
  • Track record of project management excellence and great ability to perform in dynamic, autonomous environments.
  • Exceptional communication skills, both in client-facing scenarios and within internal teams.
  • Strong in Project and Time Management.
  • Outstanding leadership and organizational skills.
  • Working experience with Microsoft office products, Power BI, SolidWorks and/or other CAD systems.
  • Able to comply with the company’s safety policy at all times.
  • Able to comply with the company’s quality policy at all times.
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22.11.2025
WP

West Pharma Production Operator - Overnight United States, Florida, Saint Petersburg

Limitless High-tech career opportunities - Expoint
Job Title:Production Operator. Available Shift:. 3rd Shift (10:20 PM – 6:30 AM, Monday-Friday). Location:St. Petersburg, FL. Pay:Startingat $19.06/hour + $1.00 / Shift Differential = $20.06/hour. Training:Mandatory training will be provided...
Description:

Position Overview

  • Job Title:Production Operator
  • Available Shift:
    • 3rd Shift (10:20 PM – 6:30 AM, Monday-Friday).
  • Location:St. Petersburg, FL.
  • Pay:Startingat $19.06/hour + $1.00 / Shift Differential = $20.06/hour
  • Training:Mandatory training will be provided for 6-12 weeks on 1st Shift (6:20AM-2:30PM).
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.
Show more

These jobs might be a good fit

Limitless High-tech career opportunities - Expoint
Overall ownership and accountability for developing, leading and driving new business development for DDD OU product platforms for identified strategic accounts to achieve revenue growth targets for commercial and product...
Description:
Essential Duties and Responsibilities
  • Overall ownership and accountability for developing, leading and driving new business development for DDD OU product platforms for identified strategic accounts to achieve revenue growth targets for commercial and product development sales.
  • Advance the vision for strategic partnerships and customer opportunities as the SME for device services offerings, for all direct assigned accounts and regions. Establish business development programs including early adopter customers, target service levels, and CDAs (Customer Development Agreements).
  • Responsible for driving the prospecting and lead development, monitoring sales and funnel performance. Lead and support customer facing teams in key customer interactions/strategic partnerships throughout the selling journey including critical customer/strategic collaboration, presentations, post-sales leadership and problem solving to deliver on revenue and growth targets.
Education
  • Bachelor's in Engineering, Science or Business-related discipline
Work Experience
  • Minimum 15 years of experience in B2B, Combination Products, Business Development, Product/Program Management.
  • Indepth knowledge and experience in pharmaceutical/medical device technical development, sales, marketing or related business.
  • Experience in successfully leading global multi-functional or cross-functional teams, in developing cohesive relationships and producing strong business results.
  • Excellent communication/negotiation/influencing skills and strong customer focus.
  • Excellent commercial and financial acumen.
  • Self-starter, highly motivated and ability to work independently with little or no daily supervision.
Preferred Knowledge, Skills and Abilities
  • MBA or master’s degree preferred
  • Background with a good technical understanding and knowledge of Combination products, medical device qualification, primary packaging, Regulatory requirements and Program Management.
  • Significant leadership team experience and executive leadership exposure.
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.
Show more
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