Complycraft, a growing regulatory consulting and compliance organization, is hiring a Regulatory Affairs Executive for its on-site office in Pimpri, Maharashtra. This opportunity is ideal for B.Pharm, M.Pharm, or Life Sciences graduates seeking hands-on exposure in regulatory documentation, compliance, and dossier preparation across pharmaceutical and healthcare domains.
This role offers direct interaction with regulatory frameworks, internal stakeholders, and regulatory authorities, making it a strong career-building position for professionals aiming to grow in Regulatory Affairs, CDSCO, and global compliance pathways.
🧪 Key Responsibilities – Regulatory Affairs Executive
As a Regulatory Affairs Executive at Complycraft, your core responsibilities will include:
- Preparation, compilation, and review of regulatory documentation and dossiers
- Ensuring compliance with applicable regulatory requirements and guidelines
- Monitoring and interpreting updates in Indian and global regulatory regulations
- Supporting regulatory submissions and approval processes
- Coordinating with internal departments to ensure regulatory readiness
- Liaising with regulatory authorities to facilitate timely approvals
- Maintaining accurate regulatory records and documentation systems
- Assisting senior regulatory consultants on client projects
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🎓 Qualifications & Eligibility Criteria
To be considered for this Regulatory Affairs Executive role, candidates should meet the following criteria:
- Bachelor’s degree in Pharmacy, Life Sciences, or related discipline
- Knowledge of regulatory affairs processes and regulatory requirements
- Proficiency in regulatory documentation and compliance activities
- Strong analytical, organizational, and problem-solving skills
- Prior experience in pharmaceutical, healthcare, or regulatory consulting is an added advantage
- Ability to work collaboratively in an on-site, fast-paced environment
💼 Salary & Benefits
- Estimated Salary Range: ₹3,00,000 – ₹5,00,000 per annum (CTC)
- Full-time, on-site employment
- Exposure to real-world regulatory submissions and compliance projects
- Opportunity to work with experienced medical device and regulatory consultants
- Strong learning curve in Indian and international regulatory frameworks
- Career growth in Regulatory Affairs, CDSCO, ISO, and global compliance domains
📍 Job Location
Pimpri, Maharashtra, India
(On-site role)
📥 How to Apply
info@complycraft.in
