Quality Assurance Engineer – Process & Validation

Essential Duties and Responsibilities

• Work with validation and engineering teams to provide Quality oversight for validation and qualification activities and ensure work is performed in a compliant and controlled manner.
• Participate in Quality Risk Management and analysis.
• Maintain current knowledge of local and international regulatory and legislative requirements and trends to ensure that expert advice and appropriate technical support on all quality related matters is provided to the site.
• Support product process transfers, including validation, from and/or to other manufacturing sites.
• Support activities related to product introduction to the site.
• Support aseptic process simulations.
• Support quality processes and systems across the product lifecycle including, but not limited to, change control, CAPA, deviations and investigations, laboratory control, Annual Product Quality Review (APQR), and management notification.
• Provide quality review and support for laboratory method validation/verification and laboratory information management system (LIMS).
• Provide support to equipment, facilities and utilities qualification as needed.
• Work collaboratively to resolve problems by taking risk-based and compliant approaches to solutions.
• Promote a quality mindset and quality excellence approach to all activities.
• Promote a safety mindset and focus on safety for all operations activities. Travel (up to 5%) may be required

• Bachelor’s degree in a scientific discipline with 4+ years Quality/cGMP experience in the pharmaceutical industry.
• Experience in process and cleaning validation, LIMS systems, Aseptic Process Simulations and Quality Risk Management.
• Knowledge in 21
  
  CFR Part 11, Electronic Records and Signatures and data integrity is required.
• Participation and leading activities to support regulatory agency inspections required.
• Project management, organization, and execution skills are required.
• Ability to apply technical expertise to solve problems and issues.
• Participating in and leading activities that support regulatory agency inspections is required.
• Excellent interpersonal and written communication skills and experience using various software/electronic applications required.
• Self-motivated, flexible, and able to work in a small, fast-paced, dynamic, environment.
• Ability to work autonomously and within established guidelines, procedures, and practices.
• Committed to delivering high quality results, working with others to overcome challenges, and focusing on what matters.
• Continuously looking for opportunities to learn, build skills, and share knowledge with others.

• Technical expertise in sterile pharmaceutical isolator technology, combination product and medical devices.

Gravity IT Resources is an Equal Opportunity Employer. We are committed to creating an inclusive environment for all employees and applicants. We do not discriminate on the basis of race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, disability, genetic information, veteran status, or any other legally protected characteristic. All employment decisions are based on qualifications, merit, and business needs.