On-site
Part Time
Main Accountabilities:
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; highly recommended to be located on the shopfloor.
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.
Participating in internal and external audits and regulatory inspections providing support and documentation.
Developing and implementing risk management strategies to mitigate potential quality issues.
Fostering a culture of quality and continuous improvement across the organization.
Key Involvement in Decision Making Process
Key Roles (D,A,I):
Request corrections when GMP rules are not respected (D)
Prioritize quality and compliance objectives (A)
Proactively implement remediation action from findings from internal and external audits related to quality issues (D)
Request quality improvement initiatives and strategies (D)
Identify discrepancies and corrective/preventive actions that need to be taken (D)
Escalate to upper management any failure in GMP execution on shopfloor (I)
Inform relevant stakeholders and team members of quality performance, corrective actions, findings, and preventive measures (I)
Advise on how to present a topic and answer specific questions (A)
Advise on risk management strategies and plans (A)
Advise on initiatives to promote a quality-focused culture (A)
Requirements/Qualifications
Expected Experience
1-2 years experience in quality assurance within the pharmaceutical industry
Strong knowledge of Good Manufacturing Practices (GMP) and quality assurance principles
Expected Technical skills
Ability to analyze complex data and identify trends, issues, and solutions
High level of accuracy and attention to detail in all quality assurance activities
Strong verbal and written communication skills for effective interaction with team members and regulatory bodies
Proficiency in identifying problems and implementing effective corrective actions
Ability to manage multiple projects simultaneously, ensuring timely completion and adherence to quality standards
Language
Local language and English
Sanofi
Upload Resume
Drag or click to upload
Your data is secure with us, protected by advanced encryption.
Browse through a variety of job opportunities tailored to your skills and preferences. Filter by location, experience, salary, and more to find your perfect fit.
We have sent an OTP to your contact. Please enter it below to verify.
Instantly access job listings, apply easily, and track applications.
4.3 - 6.0 Lacs P.A.
greater rajkot area
Salary: Not disclosed
mumbai metropolitan region
Salary: Not disclosed
mumbai metropolitan region
Salary: Not disclosed
Salary: Not disclosed
madurai, chennai, coimbatore
2.0 - 6.5 Lacs P.A.
noida, uttar pradesh, india
Salary: Not disclosed
hyderabad, telangana, india
Salary: Not disclosed
pune, maharashtra, india
Salary: Not disclosed
1.44 - 1.8 Lacs P.A.
