Are you an experienced professional in pharmaceutical quality control? Piramal Pharma Solutions, a global leader in pharmaceutical manufacturing, is hiring an RM Analyst for the QC Department at our state-of-the-art Pithampur site. This is your chance to join a dynamic team driving innovation in oral solid dosage (OSD) formulation. If you have expertise in raw material analysis and a passion for excellence in a regulatory environment, apply today to advance your career with a trusted name in the pharma industry.
Job Responsibilities
As an RM Analyst in the Quality Control (QC) Department at Piramal Pharma Solutions, you will play a critical role in ensuring product quality and compliance. Your key responsibilities include:
- Conducting raw material analysis to ensure compliance with regulatory standards.
- Performing quality control tests for OSD formulation products.
- Maintaining accurate documentation in line with Good Manufacturing Practices (GMP).
- Collaborating with cross-functional teams to support production and regulatory audits.
- Troubleshooting analytical issues and implementing corrective actions.
- Ensuring adherence to safety and environmental protocols in the lab.
Qualifications
To succeed as an RM Analyst, you should meet the following criteria:
- Experience: Minimum of 5 years in a regulated pharmaceutical company, with expertise in raw material analysis.
- Technical Skills: Strong knowledge of OSD formulation and quality control processes.
- Regulatory Knowledge: Proven experience in a regulatory environment, familiar with GMP and ICH guidelines.
- Education: Bachelor’s or Master’s degree in Pharmacy, Chemistry, or a related field.
- Soft Skills: Analytical mindset, attention to detail, and excellent communication skills.
Benefits
Joining Piramal Pharma Solutions offers you:
- Career Growth: Opportunities to advance in a leading pharmaceutical company.
- Competitive Salary: Attractive compensation package with performance-based incentives.
- Work Environment: Collaborative and innovative workplace at the Pithampur site.
- Health & Wellness: Comprehensive health insurance and wellness programs.
- Learning Opportunities: Access to training and development programs to enhance your skills.
How to Apply
Ready to take the next step in your pharmaceutical career? Send your updated CV to Anuj.yagik@piramal.com with the subject line “RM Analyst Application – Pithampur.” Ensure your CV highlights your experience in raw material analysis and OSD formulation. Applications are reviewed on a rolling basis, so apply by October 3, 2025, to be considered.
FAQs
Q: What is the application deadline for the RM Analyst position?
A: Applications are accepted until October 3, 2025. Early submissions are encouraged as reviews are conducted on a rolling basis.
Q: What qualifications are most important for this role?
A: A minimum of 5 years of experience in raw material analysis and expertise in OSD formulation within a regulated environment are critical.
