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Quality Systems Specialist

West Pharmaceutical Services
Irelandfull_timeVerifiedPosted 21 Nov 2023

About the role


At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?  

 

There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.  

 

We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.  

 

Job Summary:

This role is responsible for the coordination of West’s customer notification process which includes documentation and communication of West’s changes to Customers.  Management of Change Control Review Board activities across cross functional teams for elastomer and medical device business units. This role will also be responsible for providing guidance, support, and training on West’s change control procedures and systems.

 

Essential Duties and Responsibilities:

  • Perform activities for creation, issuance and review of customer notifications relating to West change controls. 
  • Coordinate customer notification process across cross functional teams, which includes direct communication with change owners to define appropriate change notification information, impacted customers and customer approval process, if needed.
  • Manage activities of Change Control Review Board(s)(CCRB) and Medical Device Change Control Review Board (MDCCRB). This includes facilitating cross functional team discussions and documentation of meeting details and outcome.
  • Engage with cross functional teams during change initiation to ensure information relating to customer notification/engagement is evaluated during change execution.
  • Support West customer facing teams to provide support on Customer Notifications/ communication of change.
  • Hold monthly change meetings with customers, as applicable, to communication information on upcoming changes. Provide feedback to change owners and update customer notifications, as needed.
  • Maintain CCRB and MDCCRB metrics and customer notification metrics for trending, analysis, and reporting.
  • Maintain the change control customer notification history, records and documentation to demonstrate compliance to regulations and company policies, procedures and requirements.
  • Assist areas for training on change control and customer notification procedures and key compliance requirements as applied to West products and processes.
  • Support initiatives for the development of digital strategies to enhance change control and customer notification processes.
  • Support corporate harmonization initiatives as they pertain to the quality management system.
  • As appropriate, use knowledge and experience to identify initiatives to improve the effectiveness and/or efficiency of systems.
  • Work independently with supervision.
  • Act in accordance with the company’s Guiding Principles and adherence to the corporate Code of Conduct.
  • Other duties as assigned.

 

 

Basic Qualifications: 

  • Education: Bachelor or Master’s degree in science preferred or equivalent experience in related discipline
  • Experience: Minimum 3 years of quality related experience with preferred experience in Medical Device / pharmaceutical industry.

 

Preferred Knowledge, Skills and Abilities:

  • Experience in regulated industry such as pharmaceutical or medical device.
  • In depth knowledge of cGMP, cGDP, relevant ISO standards
  • Experience with SAP systems
  • Familiarity with document management databases, particularly MasterControl.
  • 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 policy at all times
  • Able to comply with the company’s quality policy at all times
  • Support and contribute to Lean Sigma programs and activities towards delivery of the set target

 

 

Travel Requirements:

  • Must be able to travel up to 5% of the time


West embraces diversity and equality of opportunity. We foster an environment where all individua

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Company

West Pharmaceutical Services

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