Piramal Pharma Solutions is a global contract development and manufacturing organization (CDMO) known for delivering high-quality pharmaceutical products and services. With a strong focus on innovation and compliance, Piramal Pharma Solutions supports pharmaceutical companies worldwide in bringing medicines to market efficiently and safely. The Pithampur site is a key manufacturing and quality control hub specializing in Oral Solid Dosage (OSD) formulations.
Job Description: RM Analyst – QC Department
Position: RM Analyst – QC Department
Location: Piramal Pharma Solutions, Pithampur Site
Experience Required: Minimum 5 years in a regulated pharmaceutical environment
Department: Quality Control (QC)
Key Responsibilities:
- Conduct thorough raw material analysis to ensure compliance with quality standards.
- Perform testing and validation of raw materials used in OSD formulation.
- Maintain documentation and records in accordance with regulatory requirements.
- Collaborate with cross-functional teams to support quality assurance and regulatory audits.
- Ensure adherence to Good Manufacturing Practices (GMP) and company SOPs.
- Troubleshoot and resolve quality issues related to raw materials.
Key Requirements:
- Strong knowledge and hands-on experience in raw material analysis.
- Proven expertise in OSD formulation within a regulated pharmaceutical environment.
- Familiarity with regulatory guidelines and quality standards.
- Excellent analytical and problem-solving skills.
- Ability to work effectively in a team and communicate clearly.
Why Join Piramal Pharma Solutions?
- Work with a globally recognized pharmaceutical company.
- Opportunity to grow your career in a regulated and innovative environment.
- Be part of a team committed to quality and compliance.
- Competitive salary and benefits package.
How to Apply
If you meet the above criteria and want to be part of a leading pharma company, send your updated CV to: