Title: Sr. Specialist, Audit Program
Requisition ID: 66894
Date: Sep 13, 2024
Location: Scottsdale, Arizona, US
Department: Quality
Job Summary: In this role, you will support the external (customer, regulatory, and corporate) and internal audit programs for a medical device manufacturing facility. Assists in establishing systems to support the audit programs at the facility and to drive continuous improvements and minimize audit observations. Maintains the internal and external audit schedule. Preps for and hosts audits. Creates the responses to audit reports. Ensures completion of auditing corrections. Performs all duties associated with compliance-related items for ISO standards and cGMPs.
Essential Duties and Responsibilities:
- Maintain the internal and external audit schedule. Coordinate customer and regulatory audits as needed throughout the year. Ensure internal audits are performed on time.
- Ensures the site is prepared for each audit. Ensures requested documents are prepared and the facility is audit ready.
- Acts as audit host. Gives site visitor presentation. Conducts facility tour with auditor. Is Front Room lead during audit. Main point of contact with auditor prior to, during, and after the audit.
- Receives audit reports and is responsible for coordinating the audit responses. Works with management and technical staff in performing root cause analysis and implementing corrective and preventive actions to preclude recurrence. Ensures responses are sent by the due date required.
- Coordinates with observation owners to ensure corrections to audit observations are performed by the due date.
- Hosts near-miss meetings with site SMEs post-audit to prevent future findings.
- Provide training to site employees on regulatory/ISO/GMP/GDP standard requirements, as needed.
- Maintains audit databases and ensures they are up to date.
- Ensures audit KPIs are monitored and in compliance with internal requirements. Performs tracking and trending of audit metrics.
- Utilizes knowledge of International Standards and Federal Regulations (i.e. ISO 13485/21 CFR 820/EU MDR) to maintain the quality management system.
- May work with supplier onboarding process and PO generation, as needed.
- May execute internal audits following ISO 13485/21 CFR 820/EU MDR standards and internal procedures.
- Conforms with and abides by all regulations, policies, work procedures, instruction, and all safety rules.
- Exhibits regular, reliable, punctual and predictable attendance.
- Other duties as assigned.
Basic Qualifications:
- Strong analytical thinking and complex problem-solving skills.
- Bachelor’s degree in engineering or similar degree, or equivalent work experience.
- ISO 13485 Lead Auditor certified.
- Experience working within FDA CFRs, ISO 13485, EU MDR or other regulated environments.
- Experience completing CAPAs and/or complex investigations.
Preferred Knowledge, Skills and Abilities:
- EU MDR auditor certified.
- CQA/ASQ certified.
- Able to interface with customers and meeting customer expectations.
- Experience operating within the Medical Device regulations.
- Ability to work with interdisciplinary teams.
- Experience with Project Management tools and able to provide support and contribute in Lean Sigma programs and activities towards delivery of the set target.
- Willingness to learn manufacturing procedures and aid with improvements via Quality Management.
- 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.
Travel Requirements: None.
Physical and Mental Requirements:
- Need to have extreme attention to detail.
- Ability to work in an office and/or manufacturing environment. May need to stand or sit for extended periods of time.
- Medical component and device manufacturing require strict adherence to standards. Must be able to tolerate fumes from various manufacturing processes, also subject to heat and cold, as well as, loud noise.
- Strong communication and technical writing skills, interpretation of data, interpersonal skills, ability to work on and lead teams.
- Use written and oral communication skills.
- 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 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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West embraces diversity and equality of opportunity. We foster an environment where all individuals are safe, treated fairly, valued and respected. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, disability status or other applicable legally protected characteristics. Where permitted by law, employment with West Pharmaceutical Services, Inc. or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of post-offer background screening and/or drug screening.
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