Step into the Senior Associate, Investigations role at Jubilant HollisterStier. Your focus on deviation management and CAPA will ensure compliance with critical GMP standards.
As part of a dedicated team, you will coordinate investigation activities in manufacturing and quality assurance, emphasizing thorough documentation and adherence to best practices. Your analytical skills are pivotal in identifying trends and solving recurring issues, thereby supporting continuous improvement initiatives within the company.
Key Responsibilities:
• Coordinate deviation documentation procedures
• Conduct comprehensive root cause analyses
• Oversee the development of CAPA strategies
• Ensure all records meet regulatory standards
• Facilitate effective communication with team contributors
Requirements:
• 3-5 years in quality assurance or related fields
• Experience with root cause analysis techniques
• Knowledge of GMP regulations
• Background in sterile manufactur...