Piramal Pharma Solutions is a globally recognized Contract Development and Manufacturing Organization (CDMO) offering integrated services across the entire drug lifecycle—from discovery to commercialization.
With a strong presence across North America, Europe, and Asia, the company specializes in:
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Active Pharmaceutical Ingredients (APIs)
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Peptides & biologics
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Sterile fill/finish
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Antibody-drug conjugates (ADCs)
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Gene therapies and vaccines
Piramal is widely trusted by global innovators for its regulatory expertise, advanced technologies, and commitment to quality and compliance.
Piramal Pharma Solutions Hiring – Job Overview
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Position: Executive – Regulatory Affairs
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Location: Navi Mumbai, Maharashtra
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Qualification: Bachelor’s / Master’s in Chemistry or related field
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Experience: 1–5 Years (preferred)
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Industry: Pharmaceutical CDMO / API
This Piramal Pharma Solutions Hiring opportunity is ideal for candidates looking to build a strong career in regulatory affairs with global exposure.
Job Description
The role focuses on supporting regulatory submission processes and maintaining compliance with international standards such as FDA and CDSCO.
Key Responsibilities
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Maintain regulatory databases and submission tracking systems
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Compile regulatory dossiers (Applicant’s Part)
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Prepare Letters of Access (LoA)
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Support annual updates, amendments, and CEP submissions
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Coordinate with cross-functional teams for documentation
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Assist in FDA and CDSCO regulatory filings
Required Skills & Qualifications
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Strong knowledge of regulatory submissions (FDA/CDSCO)
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Understanding of API and peptide regulatory processes (preferred)
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Excellent documentation and data management skills
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Attention to detail and compliance mindset
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Good communication and coordination abilities
Why Choose Piramal Pharma Solutions?
Joining Piramal Pharma Solutions Hiring gives you access to:
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🌐 Global CDMO exposure
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🧬 Work on advanced APIs, peptides & biologics
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📈 Career growth in regulatory affairs
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🏆 Strong reputation in regulated markets
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🤝 Collaborative and inclusive work culture
How to Apply
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Apply via Piramal careers portal (Job ID: 10236)
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Or send your updated CV through official HR channels
👉 Ensure your resume highlights:
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Regulatory submission experience
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API/CDMO exposure
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Knowledge of FDA/CDSCO guidelines
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Piramal Pharma Career page.
Industry Insight
Regulatory Affairs professionals are critical in the pharmaceutical industry. According to global regulatory bodies like the U.S. Food and Drug Administration and Central Drugs Standard Control Organization, compliance and accurate documentation are essential for drug approvals and market access.
With increasing complexity in drug development (APIs, biologics, peptides), companies like Piramal are expanding regulatory teams to support global submissions efficiently.