Sanofi Inc. is looking to solve quality assurance issues in their manufacturing environment to deliver flawless healthcare solutions and protect people from infectious diseases.
Requirements
- Strong knowledge of Good Manufacturing Practices (GMP) and quality assurance principles
- Ability to analyze complex data and identify trends, issues, and solutions
- High level of accuracy and attention to detail in all quality assurance activities
- Proficiency in identifying problems and implementing effective corrective actions
- Ability to manage multiple projects simultaneously, ensuring timely completion and adherence to quality standards
- Accessing aseptic processing areas, sterile gowning, exceptional eye sight, sampling technique, detail oriented
- Experience with quality assurance systems and software
Responsibilities
- Ensuring that activities in his/her scope are conducted in compliance with applicable regulatory requirements
- Ensuring compliance with Good Manufacturing Practices (GMP) and other relevant regulations
- Conducting regular audits of production processes to identify and address potential quality issues
- Collaborating closely with production to ensure quality standards are maintained throughout the product lifecycle
- Managing and resolving quality-related issues in a timely and effective manner
- Monitoring and analyzing quality performance metrics, implementing corrective actions as needed
- Leading root cause analysis investigations for quality incidents and implementing preventive measures
Other
- Bachelor’s degree in science related field preferred
- Minimum of 2 years of experience within the pharmaceutical industry, Biotech, medical device, and lab environment
- Strong verbal and written communication skills for effective interaction with team members and regulatory bodies
- Ability to work in a team environment and collaborate with cross-functional teams
- Local language and English proficiency
