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Mgr. Sterility Assurance


Education and/or Special Training EDUCATION:
• Bachelor of Science degree in Biology, Microbiology or a closely related life science. Prefer Master’s Degree.
Job Description JOB DESCRIPTION:
• Lead Sterility Assurance team to ensure compliance to ANSI/AAMI/ISO, FDA Quality System Regulation, ISO13485 related to medical device sterilization, microbiology and related product and manufacturing process controls.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Manage the Sterility Assurance team to drive compliance to applicable FDA, ISO, ANSI/AAMI and Company requirements, including all safety, quality and operational documentation and practices
• Provide knowledge and recommendations for processing products through gamma irradiation, ethylene oxide, hydrogen peroxide gas plasma and both moist and dry heat forms of sterilization
• Merge cGLP, CGMP, ANSI, AAMI, ISO, FDA, EPA and USP guidelines with actual bioburden, cytotoxicity and bacterial endotoxin test results to create knowledge that is capable of innovatively advancing quality improvement initiatives that address sterility concerns on orthopedic devices
• Review/approve product and sterilization process change control documentation and specifications
• Actively participate in cross-functional projects that develop and improve manufacturing processes for existing and new products
• Benchmark and evaluate customer needs
• Manage all sterilization validations, dose audits, customer inquiries specific to sterilization and cleaning, residual evaluations, and all other processes that have the potential of negatively impacting product quality from a sterility, cleanliness or biocompatibility view point
• Provide vision, guidance and effective communication to all team members to ensure the team’s understanding and achievement of Quality, Cost, Delivery, Safety and Talent objectives
• Manage, coach, mentor, and develop the performance of team to drive and support a high performance work culture; includes writing and delivering performance appraisals, administering disciplinary action, providing positive recognition, liaising with Human Resources to ensure consistency in administration and compliance with Company policies, focusing on the development of high-potential employees and crafting succession plans, and establishing a collaborative environment that encourages and supports employee engagement
• Develop and manage the departmental budget
• Ensure employees are provided with proper training and development
• Build a strong, talented team through active participation in employee selection and recruiting activities
• Ensure provision of a clean, safe and environmentally compliant work environment
• Develop and foster relationships with peers, other internal customers (Mfg., QA, IT, Finance, etc.) and external customers/vendors to gain perspective and identify opportunities for improvement and efficiency when dealing with business issues
Qualifications/Work Experience QUALIFICATIONS:
• 7+ years of medical device or pharmaceutical microbiological or biological testing, or research and development experience that includes product sterilization
• 2+ years of direct management over microbiologists or other technicians in the field of life science
• Prefer experience in a medical device manufacturing environment
• Applied knowledge of microbiological and sterilization concepts, practices, and procedures
• These include gamma irradiation, ethylene oxide, hydrogen peroxide gas plasma, and both moist and dry heat forms of sterilization
• Demonstrated knowledge of endotoxin and bioburden testing
• Advocate for product excellence and quality
• Demonstrated ability to multi-task
• Ability to cross-reference and keep current on relevant ANSI, AAMI, ISO, USP, EPA, EU and related guidelines
• Demonstrated ability to work on cross-functional teams
• Prefer experience leading project teams and using project management tools
• Demonstrated problem-solving skills, and ability to troubleshoot and organize priorities
• Ability to learn quickly and respond to the urgent needs of the team, ensuring all deadlines are met
• Prefer knowledge in analytical chemistry and cleaning validations
• Demonstrated leadership, interpersonal and influence skills, with the proven ability to teach and coach individuals from diverse backgrounds with varying communication and technical skills
• Demonstrated ability to implement performance measures, drive team effectiveness and productivity, while maintaining high levels of employee engagement and morale
• Demonstrated presentation and communication skills (written and verbal)
• Individual will present at all levels of the company
• Demonstrated proficiency in MS software, including Word, Excel, PowerPoint, Outlook, MS Project and Visio
Percent Travel Required <10%

contact
jamie@pharmasearchpartners.com



Additional Information
Position Type: Employee  
Ref Code: jr006

Contact Information
Jamie Riley
Jamie@Pharmasearchpartners.com?subject=jr006
Pharma Search Partners Inc
951 sandfield rd
Blythewood SC 29016
803-691-6867 ext:
803-691-6765