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דרושים Sr Specialist Supply Management Global Logistics ב-West Pharma ב-United States, West Whiteland Township

מצאו את ההתאמה המושלמת עבורכם עם אקספוינט! חפשו הזדמנויות עבודה בתור Sr Specialist Supply Management Global Logistics ב-United States, West Whiteland Township והצטרפו לרשת החברות המובילות בתעשיית ההייטק, כמו West Pharma. הירשמו עכשיו ומצאו את עבודת החלומות שלך עם אקספוינט!
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West Whiteland Township
43 jobs found
23.11.2025
WP

West Pharma Senior Regulatory Affairs Specialist United States, Pennsylvania, West Whiteland Township

Limitless High-tech career opportunities - Expoint
Develop and implement medical device regulatory strategies for West’s administration and safety system product portfolio with an emphasis on gaining regional regulatory approval/clearance/licensure for medical devices in an efficient, compliant...
Description:

Job Summary

The Sr. Specialist, Regulatory Affairs, Medical is responsible for influencing department regulatory processes and procedures, developing strategies, authoring, reviewing, and supporting global registrations, including Premarket Notifications, China NMPA Registrations, Technical Documentation for CE Marking, and technical packages. The Sr. Specialist ensures timely and high-quality execution of all regulatory deliverables.  In addition, the Sr. Specialist mentors team members and ensures compliance with West Pharmaceutical Services, Inc. (West) and government requirements. This position includes supporting internal and external customer regulatory requests.

Essential Duties and Responsibilities
  • Develop and implement medical device regulatory strategies for West’s administration and safety system product portfolio with an emphasis on gaining regional regulatory approval/clearance/licensure for medical devices in an efficient, compliant manner.
  • Author and review US, EU, and additional international submissions with guidance for new products and product changes as required to ensure content accuracy, compliance with applicable regulations, and timely approvals for market release.
  • Provide technical review of data and or reports to be incorporated into regulatory submissions to ensure scientific rigor, accuracy, and clarity of presentation.
  • Provide leadership to cross functional teams for regulatory issues and questions.
  • Compile and maintain regulatory documentation databases or systems as well as technical documentation required for new or modified products.
  • Create documentation in response to customer regulatory requests which includes regulatory letters, technical packages, etc.
  • Clearly and effectively communicate team/project progress/status, decisions, timelines, etc. to RA management, internal and external customers.
  • Develop specific objectives and manage work assignments, with minimal guidance to achieve personal objectives in conformance with overall business goals
  • Adhere to all applicable government and West regulations, practices, and procedures to maintain compliance
  • Maintain working knowledge of computer software packages including MS Word, MS Excel, MS Teams, MS PowerPoint, Master Control, Adobe, SharePoint, and others as required
Education
  • Bachelor’s degree or equivalent experience is required
  • Master’s degree or PhD in science, math, engineering, or related discipline preferred
Work Experience
  • Minimum 5 years of relevant experience
  • 2+ years of medical device regulatory experience preferred
  • Experience with US FDA regulations (Title 21CFR820), EU MDD (93/42/EEC) and EU MDR (2017/745)
  • History of successful international device registration,EU MDR technical documentation and/or US 510(K) authoring experience
  • Advanced knowledge of ISO 13485
  • Advanced knowledge of product life cycle, product development process, design control and change control
  • Experience interacting with government agencies
  • Excellent oral communication, technical writing, and decision-making skills
Preferred Knowledge, Skills and Abilities
  • Attention to detail with planning, time management and organizational skills
  • Regulatory compliance competency including Quality Systems
  • Experience with administration and safety systems preferred
  • Ability to triage and manage work priorities and to follow established processes while identifying areas for process improvement.
Additional Requirements
  • Ability to comprehend principles of math, science, engineering, and medical device use.
  • Ability to handle technical reports, drawings, specifications, regulatory and quality documentation with a high degree of confidentiality.
  • Ability to research, read, analyze, and interpret regulatory literature and documentation, regulations, technical standards, guidance documents, test reports, clinical/medical terminology, technical product information, and complex documents.
  • Ability to review, collate, describe, and summarize scientific and technical data.
  • Ability to organize complex information and combine pieces of information to form general rules or conclusions.
  • Ability to utilize judgment and make decisions considering the relative risks and benefits of potential actions to choose the most appropriate one.
  • Ability to assess, plan, schedule and manage multiple long-term and short-term projects, tasks, responsibilities and/or priorities in a concurrent fashion with several parallel deliverables and execute deliverables to time-line commitments.
  • Ability to be an effective team member and work well with others in a team environment on cross-functional and/or matrix teams.
  • Ability to be flexible with changing priorities and comply with constantly changing regulatory procedures.
  • Ability to build strong relationships both internally and externally. Ability to work in a fast-paced environment.
  • Ability to comprehend and apply language skills to the degree required to perform the job based upon the job requirements listed above.
  • Ability to verbally communicate ideas and issues effectively to other team members and management.
  • Ability to write and record data and information as required by procedures.
  • Proficiency in the use of personal computers and computer programs, particularly, Microsoft Office Suite: Excel, Word, PowerPoint, and Adobe Acrobat (or equivalents if changed by the Company).
License and Certifications
  • Regulatory Affairs Certifications (RAC)-RAPS R.A.C certification(s) 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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23.11.2025
WP

West Pharma Senior Specialist Supplier Quality United States, Pennsylvania, West Whiteland Township

Limitless High-tech career opportunities - Expoint
Establish and successfully executesupplier management planswhich will align to overall business objectives. Maintain a strong collaborativepartnership. supplier performanceincluding incoming failures, manufacturing yields and field failures to drive Supplier Corrective Action...
Description:
Job Summary

In this role you will be responsible for performing Supplier Quality activities associated with external suppliers. This role performs activities to ensure West supplier’s maintain compliance with West’s procedures and policies. You will interface with R&D, Sourcing, Design Quality, Regulatory and Operations Quality to drive improved supplier quality performance.

Essential Duties and Responsibilities
  • Establish and successfully executesupplier management planswhich will align to overall business objectives

  • Maintain a strong collaborativepartnership

Additional Responsibilities
  • supplier performanceincluding incoming failures, manufacturing yields and field failures to drive Supplier Corrective Action Reports (SCARs)

  • ExecuteSupplier Corrective Action Requests(SCAR) with suppliers, ensuring effective and timely closure

  • Work with suppliers, R&D, and Sourcing on continuous improvement of supplier performance includingsupplier changerequest.

  • Evaluate potential new or future suppliers and support supplierselection processwith the cross-functional team

  • Participate in cross-functional teams of design engineering and quality engineering to work with suppliers duringproduct developmentand ensures agreement for manufacturable, cost-effective designs

  • Approves components for use in products by drivingProduct Approvalactivities with the suppliers

  • Supports Supplier evaluation,auditmanagement and related records

  • Supports the evaluation and development ofQuality Agreements and purchasing specificationswith suppliers

  • Support the development of anIncoming Inspection strategyon purchased products


Education
  • Bachelor's Degree In Engineering or Science required
  • Master's Degree In Engineering or Science preferred
Work Experience
  • Minimum 5 years of quality related experience with preferred experience in pharmaceutical and/or medical device industry

  • Experience working with suppliers and supplier engagement activities

Preferred Knowledge, Skills and Abilities
  • Knowledge of sterilization process is preferred

  • Knowledge of cGMP, cGDP, relevant ISO standards, medical device requirements and other international regulations

  • Familiarity with MasterControl, SAP and working knowledge of statistical data analysis

  • Fluent in English

  • Thorough understanding of validation activities and risk management principles and techniques

  • Strong problem-solving and critical thinking skills

  • Negotiation skills and collaborating with suppliers

  • Ability to work under high volume production and fast changing environment

  • Willingness to work in a cross-functional team with different time zones

  • Able to comply with the company’s safety policy at all times.
Physical Requirements
Sedentary-Exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time.
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23.11.2025
WP

West Pharma Director Enterprise Risk Management United States, Pennsylvania, West Whiteland Township

Limitless High-tech career opportunities - Expoint
Direct and maintain the ERM program and strategy, ensuring alignment with Committee of Sponsoring Organizations' (COSO) ERM Framework and the latest professional standards, and publish/update ERM policies and procedures. Establish...
Description:

Essential Duties and Responsibilities
  • Direct and maintain the ERM program and strategy, ensuring alignment with Committee of Sponsoring Organizations' (COSO) ERM Framework and the latest professional standards, and publish/update ERM policies and procedures.
  • Establish and lead an Enterprise Risk Governance Council and promote ERM activities and visibility within the Executive Leadership Team and across departments, operating units, and business functions.
  • Provide expert risk consulting and advice to all levels of management and business units to ensure comprehensive, high-quality risk reporting and early identification of risk trends.
  • Facilitate and coordinate requests for information from auditors, regulators, and collaborate with Financial, Legal, Compliance, Information Technology, Internal Audit, and Operations teams.
  • Lead scheduled enterprise risk reporting and presentations for Executive Management, the Audit Committee, and the Board of Directors.
  • Review key risk and performance indicators/metrics to assist in early risk trend identification and manage risk self-assessments with business unit management.
  • Build strong internal and external alliances to positively influence risk identification and resolution.
  • Provide risk support for major initiatives, including M&A activities, related integrations, vendor management projects, and large system/process improvements.
  • Direct enterprise risk communication to stakeholders through targeted correspondence and internal networks and oversee the development and delivery of ongoing ERM training programs.
  • Assure quality control of enterprise risk-related databases and risk registers and facilitate development and maintenance of department-level risk registers and dashboards in company databases.
Education
  • Master's Degree Business Administration, Finance, Accounting, or related field. preferred
  • Bachelor's Degree Business Administration, Finance, Accounting, or related field. required
Work Experience
  • Minimum 10 years of experience in enterprise risk management, audit, project management, or related field, including 5-7+ years in ERM process development and operation required
Preferred Knowledge, Skills and Abilities
  • Strong knowledge of COSO ERM framework and other internal control standards.
  • Proficiency in risk quantification methods and systems.
  • Ability to maintain ERM training and certifications to leverage current experience and enhance the ERM program.
  • Strong interpersonal skills with the ability to build relationships across all levels of the organization, including the Board of Directors.
  • Consistently demonstrate high standards, professional ethics, integrity, and trust.
  • Positive and resourceful with an inquisitive nature, proactively seeking out information to drive successful ERM initiatives.
  • Must be able to operate across different geographic time zones.
  • Excellent communication and influence skills, including report writing, presentations, and group facilitation.
  • Demonstrated executive presence and ability to work independently in a dynamic environment.
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 Director Elastomers & Primary Containment Capital Management United States, Pennsylvania, West Whiteland Township

Limitless High-tech career opportunities - Expoint
Ensure Budget and Strategic Plan capital alignments are completed for EPC. Develop and support capital plans focused on large-scale programs and projects. Lead the development of asset management plans to...
Description:

This is a hybrid position requiring the employee to be onsite a minimum of 3 days per week

Job Summary

In this role, the Director of Elastomers & Primary Containment (EPC) Capital Management will spearhead the capital process for function. This will include prioritization for EPC projects, developing and updating strategic plans, budgets, and supporting the forecasting process. You will play a crucial role in formulating capital plans focused on substantial growth initiatives and asset replacements. Enhancing and refining systems for improved accuracy in capital reporting will be a core responsibility. You will liaise with senior management to deliver comprehensive updates on budgets, and year-to-date capital expenditures, while ensuring that Project Expenditure Requests (PERs) comply with both Finance and Global standards.

Essential Duties and Responsibilities

Capital Prioritization and Management:

  • Ensure Budget and Strategic Plan capital alignments are completed for EPC.
  • Develop and support capital plans focused on large-scale programs and projects.
  • Lead the development of asset management plans to include site facility plans and asset replacement plans.
  • Manage the execution of capital plans by leading site review meetings and operation management meetings
  • Review project plans to ensure alignment with Global Engineering and Finance guidelines. Project plans also must be aligned with capital budgets and forecasts.

Project and Capital Database Management:

  • Maintain an EPC project database ensuring all prioritizations are met and managed efficiently.
  • Regularly update and monitor the execution of capital forecasting to meet annual spending requirements.

PER Review and Forecasting:

  • Establish and lead PER reviews for EPC, ensuring KPIs such as ROIC, timeline, and payback periods are embedded and reviewed before management oversight.
  • Develop comprehensive site forecasts for future project needs in collaboration with site and global engineering teams.
  • Collaborate with Finance to manage CAPEX for EPC.
  • Other duties as assigned
Education
  • Bachelor’s degree with preference in Engineering
Work Experience
  • Minimum 10 years of experience; preference for
  • Good understanding of general manufacturing and related project management
  • Strong expertise of tools like Excel and MS Project.
Preferred Knowledge, Skills and Abilities
  • 8-10 years’ experience in managing all aspects of complex technical projects to include analytics and scheduling
  • Strong capability to manage through influence and across functions
  • Strong leadership and strategic thinking, global mindset; anticipates risks, can successfully navigate ambiguity
  • High sense for the business; strong business acumen
  • Strong coordination and Project Management skills
  • Engages others, builds relationships, and creates networks outside team. Checks in with different people to understand the bigger picture.
  • Ability to perform root cause analysis and corrective action solutions. Follows through on actions.
  • Is curious, agile, engages in new experiences and looks for different perspectives
  • 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 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.
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
  • Proven ability to work in a virtual environment in a global organization and to effectively prioritize and execute tasks in a high-pressure environment
  • Make independent and sound judgments.
  • Multitask, work under time constraints, problem solve, and prioritize.
  • Excellent communicator with ability to maintain confidentiality and resolve conflicts and ambiguity.
  • Use written and verbal communication skills effectively.
  • Read and interpret data, information and documents to analyze and solve problems.
  • Learn and apply new information and new skills.
  • Proven ability to work in a virtual environment in a global organization and to effectively prioritize and execute tasks in a high-pressure environment
  • Make independent and sound judgments.
  • Multitask, work under time constraints, problem solve and prioritize.
  • Excellent communicator with ability to maintain confidentiality and resolve conflicts and ambiguity.
  • Use written and verbal communication skills effectively.
  • Read and interpret data, information and documents to analyze and solve problems.
  • Learn and apply new information and new skills.
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22.11.2025
WP

West Pharma Senior Specialist Product Development R&D United States, Pennsylvania, West Whiteland Township

Limitless High-tech career opportunities - Expoint
In depth collaboration with internal stakeholders to deliver, drive and execute on ESG goals including Climate strategy; Waste in operations; R&D for the environment; Responsible supply chain. Serve as the...
Description:
Job Summary

The Sr Manager, ESG Strategy & Support will act as a key strategic partner in leading and shaping the Environmental, Social, and Governance (ESG) program at West. This pivotal role involves embedding ESG considerations into West's business processes while aligning with its Mission, Vision, and Values. Responsibilities include ensuring compliance with ESG-related laws and regulations such as CSRD, CDP, EU Deforestation, SBTi, CBAM and GRI. The role functions to support the ESG program and involves close collaboration with team members to establish strategies and devise global, regional, and local plans that align with West's Global ESG goals.

Essential Duties and Responsibilities
  • In depth collaboration with internal stakeholders to deliver, drive and execute on ESG goals including Climate strategy; Waste in operations; R&D for the environment; Responsible supply chain
  • Serve as the “go-to” ESG subject matter expert for assigned business functions, which may include operations, commercial, supply chain, and research & development projects.
  • Champion the creation and release of the annual ESG report, working with Communications and Data Collection and Reporting teams.
  • Drive the Science-Based Target Initiative (SBTi) strategy.
  • Ensure conformity to global ESG-related laws and regulations (voluntary and mandatory) reporting standards while spearheading program enhancements and monitoring ESG reporting best practices and evolving legislative/regulatory regimes.
  • Establish robust procedures and systems for dialogues with internal and external stakeholders concerning ESG issues, including assessment and development of ESG policies, processes, and systems where appropriate.
  • Proven track record in analyzing and communicating complex ESG data to a wide variety of stakeholders, delivering strategic insights to senior executives.
  • Augment engagement with primary customers and investors, ensuring timely and effective responses to all ESG-related inquiries.
  • Tackle other role-related tasks as necessitated by the organization, strictly observing all organizational guidelines, policies, and safety regulations.
  • Other duties as assigned.
Education
  • Bachelor's degree in environmental or other sciences, or related fields (required).
  • Master’s degree in business, environmental sciences or related fields (preferred)
Work Experience
  • Minimum 10 years in ESG or sustainability-related roles, with preferred experience in SBTi and emissions calculations (required).
Preferred Knowledge, Skills and Abilities
  • Familiarity with or experience implementing operational and / or supplier environmental and human rights risk analysis and due diligence processes.
  • Experience using and / or implementing Product Carbon Footprint (ISO 14067, PATH) / LCA.
  • Demonstrated ability to engage R&D organizations to implement sustainability-related considerations into product development / stage gate processes.
  • Have an established network within the ESG community to engage with thought leaders and regulatory bodies.
  • Experience with SBTi and Scope 1, 2 and 3 emissions calculations.
  • Experience with ESG reporting software such as NASDAQ OneReport, Metrio.
  • Advanced knowledge of the depth and breadth of sustainability-related ranking organizations such as UN Sustainable Development Goals, CDP, and SASB reporting requirements.
  • Advanced level skill in MS Excel, Power Point, Word, and Outlook.
  • Advanced knowledge of the depth and breadth of sustainability-related ranking organizations such as DJSI and CDP.
  • Extremely detail-oriented and deadline driven, with proven track record.
  • Excellent communication skills, both written and oral, with proven track record.
  • Excellent organizational, administrative, and time-management skills with the ability to work effectively under pressure.
  • Exceptional ability to immediately establish credibility with senior executives.
  • Ability to independently manage projects and solve problems quickly and effectively.
  • Proven ability to cultivate teamwork and fill knowledge or skill gaps where needed.
  • Ability to build and maintain strong relationships with customers, business partners, resource managers, and other senior-level executives.
  • 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.
  • Ability to manage multiple tasks/projects/priorities and simple systems simultaneously.
  • Ability to exercise good judgment and maintain a high level of integrity.
  • Ability to comply with the company’s safety and quality policy at all times.
Physical Requirements
Sedentary-Exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time.
Additional Requirements
  • Communication, quick decision making based on logic, circumstances and data at hand, interpreting data, reading or writing, public speaking - must be able to express or exchange ideas with team members.
  • Must be able to understand direction and adhere to established procedures.
  • Must be able to communicate effectively, speak in front of groups, express & exchange ideas and understand direction.
  • Maintain the ability to work well with others in a variety of situations.
  • Able to learn and apply new information or new skills.
  • Read, interpret and analyse data, information and documents.
  • Must be able to multi-task, work under time constraints, problem solve and prioritize.
  • Must be resilient.
  • Demonstrates enthusiasm, takes accountability, is “self-started” and takes initiative for all work and is results driven.
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22.11.2025
WP

West Pharma Project Specialist Metrology United States, Pennsylvania, West Whiteland Township

Limitless High-tech career opportunities - Expoint
Create and maintain the yearly WSS CAPEX program schedule for all items approved for the CAPEX budget. Hold regular project meetings with cross-functional stakeholdersCreate and maintain detailed project schedules (Gantt...
Description:
Job Summary

The Project Specialist, Metrology is responsible for managing the West Services and Solutions (WSS) CAPEX program from planning and initiation through asset registration and implementation. You will be responsible for identifying and aligning stakeholders from cross-functional teams, creating, maintaining, and reporting project schedules, forecasting, updating, and reporting on financials associated with each project, and coordinating the WSS CAPEX items within the overall Global Quality Laboratory CAPEX budget. Responsible for driving projects to completion based on timelines, budget, and resources.

Essential Duties and Responsibilities
  • Create and maintain the yearly WSS CAPEX program schedule for all items approved for the CAPEX budget
  • Hold regular project meetings with cross-functional stakeholdersCreate and maintain detailed project schedules (Gantt or similar)
  • Facilitate alignment of timelines, responsibilities, and deliverables in accordance with procedures
  • Follow escalation procedure for delayed/impacted projects and Track project milestones
  • Report project status highlighting risks and opportunities for improvement
  • Track and report financials associated with each CAPEX project
  • Coordinate with WSS Lab Purchasing, WSS Metrology, Global Technical Projects, Global Finance, and Quality Laboratory to establish and provide accurate
    • forecasting and closure of projects
    • Track and report budget adherence
    • Manage resource allocation and communication for the program
  • Ensure appropriate resources have been committed to each project working with management when there are conflicts
  • Maintain a clear and unambiguous communication plan with all stakeholders and management for expectations, commitments, timelines, deliverables, responsibilities, and status
  • Proactively identify and facilitate resolution of all project-related issues
  • Management/initiation of associated administrative details: initiating change controls assigning tasks, resources, and timelines, requesting the initiation of required documents, general administrative tasks to keep the projects on track
  • Implement change management processes, when needed, to align with shifting requirements and priorities
  • Support the WSS Metrology team with routine tasks, as needed
Basic Qualifications
  • Bachelor's Degree in a related area or equivalent experience
  • Minimum 2 years of experience in metrology/analytical instrumentation in a cGMP environment, preferred
  • Minimum 2 years of experience in project management, preferred
Preferred Knowledge, Skills and Abilities
  • Demonstrated ability to multi-task and manage multiple projects simultaneously
  • Strong understanding of a cGMP environment
  • Experience with Quality Management Systems
  • Dependable, highly organized, detail oriented, able to think creatively under pressure and work in a fast-paced, constantly changing environment
  • Excellent written and verbal communication skills
  • Familiarity with SAP
  • Experience with project management tools such as MS Project
  • Able to comply with the company’s safety and quality policies at all times
Additional Requirements
  • 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 & write, speak in front of groups, express & exchange ideas, understand direction and adhere to procedures
  • Organizational skills will enable planning, prioritization & achievement of goals especially of importance for the successful execution of related activities
License and Certifications
  • Project Management Certificate, such as CAPM, 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 Specialist Cost Accountant United States, Pennsylvania, West Whiteland Township

Limitless High-tech career opportunities - Expoint
Prepare journal entries related to manufacturing accounting and inventory reserves to support accurate and timely financial statements in accordance with US GAAP and corporate financial policies. Process manufacturing orders as...
Description:
Essential Duties and Responsibilities
  • Prepare journal entries related to manufacturing accounting and inventory reserves to support accurate and timely financial statements in accordance with US GAAP and corporate financial policies
  • Process manufacturing orders as part of the month-end close process
  • Participate in other monthly close activities for plants in area of responsibility
  • Prepare account reconciliations to ensure proper balance sheet valuation
  • Calculate standard costing of products in SAP as part of new product workflow
  • Monitor variances to standard cost and correct any erroneous errors
  • Support the periodic cycle count process
  • Reconcile 3rd party warehouses
  • Ensure appropriate controls and compliance with US GAAP
  • Support and assist other functions within the business as required
Education
  • Bachelor's Degree Accounting or Business with concentration in Accounting/Finance or equivalent experience required
Work Experience
  • Minimum 3 years Accounting required
Preferred Knowledge, Skills and Abilities
  • Accounting experience, preferable in a manufacturing environment using SAP or other ERP
  • Understanding of GAAP and internal control principles
  • Highly proficient in written and spoken English
  • Working knowledge of MS Office or the willingness to learn it quickly with highly proficient Excel skills
  • Strong communication skills
  • Strong people skills – approachable, good listener, empathetic
  • Strong learning capacity
  • Ability to work independently in global environment
  • Able to be aware of all relevant SOPs as per Company policy as they are related to the position covered by this Job Description
  • Able to comply with the company’s safety and quality policies at all times
Additional Requirements
  • Must be able to understand direction and adhere to established procedures
  • Must be able to communicate effectively, speak in front of groups, express and exchange ideas and understand direction
  • Maintain the ability to work well with others in a variety of situations
  • Able to learn and apply new information or new skills
  • Read and interpret data, information and documents
  • Must be able to multi-task, work under time constraints, problem solve, and prioritize
  • Ability to make independent and sound judgments
  • Demonstrates enthusiasm, takes accountability and drives for results
  • #LI-JJ1 #LI-HYBRID
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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Limitless High-tech career opportunities - Expoint
Develop and implement medical device regulatory strategies for West’s administration and safety system product portfolio with an emphasis on gaining regional regulatory approval/clearance/licensure for medical devices in an efficient, compliant...
Description:

Job Summary

The Sr. Specialist, Regulatory Affairs, Medical is responsible for influencing department regulatory processes and procedures, developing strategies, authoring, reviewing, and supporting global registrations, including Premarket Notifications, China NMPA Registrations, Technical Documentation for CE Marking, and technical packages. The Sr. Specialist ensures timely and high-quality execution of all regulatory deliverables.  In addition, the Sr. Specialist mentors team members and ensures compliance with West Pharmaceutical Services, Inc. (West) and government requirements. This position includes supporting internal and external customer regulatory requests.

Essential Duties and Responsibilities
  • Develop and implement medical device regulatory strategies for West’s administration and safety system product portfolio with an emphasis on gaining regional regulatory approval/clearance/licensure for medical devices in an efficient, compliant manner.
  • Author and review US, EU, and additional international submissions with guidance for new products and product changes as required to ensure content accuracy, compliance with applicable regulations, and timely approvals for market release.
  • Provide technical review of data and or reports to be incorporated into regulatory submissions to ensure scientific rigor, accuracy, and clarity of presentation.
  • Provide leadership to cross functional teams for regulatory issues and questions.
  • Compile and maintain regulatory documentation databases or systems as well as technical documentation required for new or modified products.
  • Create documentation in response to customer regulatory requests which includes regulatory letters, technical packages, etc.
  • Clearly and effectively communicate team/project progress/status, decisions, timelines, etc. to RA management, internal and external customers.
  • Develop specific objectives and manage work assignments, with minimal guidance to achieve personal objectives in conformance with overall business goals
  • Adhere to all applicable government and West regulations, practices, and procedures to maintain compliance
  • Maintain working knowledge of computer software packages including MS Word, MS Excel, MS Teams, MS PowerPoint, Master Control, Adobe, SharePoint, and others as required
Education
  • Bachelor’s degree or equivalent experience is required
  • Master’s degree or PhD in science, math, engineering, or related discipline preferred
Work Experience
  • Minimum 5 years of relevant experience
  • 2+ years of medical device regulatory experience preferred
  • Experience with US FDA regulations (Title 21CFR820), EU MDD (93/42/EEC) and EU MDR (2017/745)
  • History of successful international device registration,EU MDR technical documentation and/or US 510(K) authoring experience
  • Advanced knowledge of ISO 13485
  • Advanced knowledge of product life cycle, product development process, design control and change control
  • Experience interacting with government agencies
  • Excellent oral communication, technical writing, and decision-making skills
Preferred Knowledge, Skills and Abilities
  • Attention to detail with planning, time management and organizational skills
  • Regulatory compliance competency including Quality Systems
  • Experience with administration and safety systems preferred
  • Ability to triage and manage work priorities and to follow established processes while identifying areas for process improvement.
Additional Requirements
  • Ability to comprehend principles of math, science, engineering, and medical device use.
  • Ability to handle technical reports, drawings, specifications, regulatory and quality documentation with a high degree of confidentiality.
  • Ability to research, read, analyze, and interpret regulatory literature and documentation, regulations, technical standards, guidance documents, test reports, clinical/medical terminology, technical product information, and complex documents.
  • Ability to review, collate, describe, and summarize scientific and technical data.
  • Ability to organize complex information and combine pieces of information to form general rules or conclusions.
  • Ability to utilize judgment and make decisions considering the relative risks and benefits of potential actions to choose the most appropriate one.
  • Ability to assess, plan, schedule and manage multiple long-term and short-term projects, tasks, responsibilities and/or priorities in a concurrent fashion with several parallel deliverables and execute deliverables to time-line commitments.
  • Ability to be an effective team member and work well with others in a team environment on cross-functional and/or matrix teams.
  • Ability to be flexible with changing priorities and comply with constantly changing regulatory procedures.
  • Ability to build strong relationships both internally and externally. Ability to work in a fast-paced environment.
  • Ability to comprehend and apply language skills to the degree required to perform the job based upon the job requirements listed above.
  • Ability to verbally communicate ideas and issues effectively to other team members and management.
  • Ability to write and record data and information as required by procedures.
  • Proficiency in the use of personal computers and computer programs, particularly, Microsoft Office Suite: Excel, Word, PowerPoint, and Adobe Acrobat (or equivalents if changed by the Company).
License and Certifications
  • Regulatory Affairs Certifications (RAC)-RAPS R.A.C certification(s) 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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בואו למצוא את עבודת החלומות שלכם בהייטק עם אקספוינט. באמצעות הפלטפורמה שלנו תוכל לחפש בקלות הזדמנויות Sr Specialist Supply Management Global Logistics בחברת West Pharma ב-United States, West Whiteland Township. 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.