About this opportunity
Merck & Co. lists this Associate Director, Validation opportunity in winston salem, North Carolina. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Winston-Salem, North Carolina, United States
Position Summary
The Sr. Manager of Validation will lead the Qualification and Validation, Cleaning, Sterility assurance and Computer System Validation (CSV) teams at the site. Serve as a member on project steering, value stream and quality systems performance teams. Establish operational objectives and systems to drive employee engagement and alignment with other departments. Deliver on site objectives while implementing harmonized engineering systems and processes. Provide leadership support to the other sites and validation initiatives as needed. Will lead system validation projects related to authoring and executing validation documentation for laboratory instruments/equipment and systems according to the ISPE GAMP 5 Validation Life Cycle as well as 21CFR Part11 and FDA’s guide to Computer Software Assurance. Documentation includes System Validation Plan, User Requirements, Risk Assessment, IQ, OQ, PQ, Test Scripts, Summary reports, Requirements Traceability Matrix (RTM), Periodic Review of Computer Systems, and Data Integrity Assessment.
The Sr. Validation Manager will be responsible for supporting the Validation/Qualification program by:
Provide leadership and direction to Validation team members, driving performance and value creation to the site function operational and strategic plans and tasks
Ensure adequate resourcing (capacity and capability) to accomplish site and OST objectives. Recommend solutions to alleviate constraints
Regularly interacts with senior management or executives on multi-department projects and challenges. Able to build coalitions for change.
Continuously improving the culture of the Validation team and the site
Represents Validation and Emergent during GMP and other regulatory agency inspections (CDC, OSHA, etc.)
Identify areas to drive down operations costs and improve project delivery efficiency. Develop specific investment strategies to realize these savings
Hands on troubleshooting and problem solving at the Gemba in support of engineering team members and operations
Develop and lead small and medium sized continuous improvement projects, remain involved in projects led by staff members
Direct support to OST head or lead annual OPEX budget for Validation department
Staff and System Development
Effective delegation and building confidence and competence within direct reports
Drive engagement in the technical and personal development of the Validation team and members
Develops strong relationships with partners (QA, Mfg., etc.) and cultivates these with all team members
Provide effective and collaborative cross functional leadership to facilitate development of the site strategy and delivery of site objectives
Improve the culture of the Validation team and the site
Qualifications
Education/Training Bachelor’s degree. Preferred Fields of Study: Life Sciences or Engineering with 10+ years work experience.
A minimum of 8 years of experience in a biopharmaceutical or related environment in an engineering or quality related role, with at least 3 years in a leadership role
Expert knowledge of GxPs, GAMP, CFRs/Annex 11, and Data Integrity requirements for laboratory systems and equipment (Understanding of data integrity principles and security controls including, but not limited to audit trail reviews, user access roles, disaster recovery, business continuity, system implementation, change control, archival, retirement, etc)
Strong understanding of Validation Lifecycle (GAMP 5) principles
Experience with calibration and maintenance management software
Knowledge of electronic document management systems
Experience with data integrity practices and compliance
Strong technical writing skills for qualification documents, SOPs, and work instructions
Ability to manage multiple projects simultaneously with minimal supervision
Detail-oriented with excellent verbal and written communication abilities
Ability to adapt to changing priorities in a deadline-oriented environment
Significant hands on experience and regulatory expectations knowledge with controls, automation and computer system validation.
Knowledge of pharmaceutical equipment, such as bioreactors, centrifuges, HVAC systems, building chillers, clean steam generators, and Temperature Controlled Units (e.g. refrigerators, freezers, and incubators) is an advantage.
Strong knowledge and experience in cGMP, root cause analysis, risk assessment and investigation tools/techniques.
Experience in writing computer system test scripts, validation protocols and summary reports
ProKidney is an equal employment opportunity employer and does not discriminate against any applicant because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, disability, genetic information, veteran status, military status, application for military service or any other class protected by state or federal law.
Applicants must be eligible to work in the United States without the need for work visa or residency sponsorship.
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Worksite address
winston salem, NC, 27104, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.