Macleods Pharmaceuticals, India’s fastest growing company was established in 1986. Ranked amongst the top 10 pharma companies with a strength of 20000 employees, operating in 140+ countries. Our bioequivalence centre was established in 2005 and is responsible for conducting studies for filing product registrations with various regulatory authorities. They have held valid accreditation and are routinely inspected by various Indian & international regulatory bodies and institutions such as CDSCO, DSIR-India and NABL, USFDA, UK MHRA, NPRAMalaysia and WHO. The centre is equipped to work across clinical, bioanalytical, pharmacokinetic functions and statistical, quality assurance and data protection, each integral to the organization.
We are looking for Fresher
Associate Project Management:
Roles and Responsibilities
- Project Monitoring, Execution, and coordination with the internal Department.
- Team Management, Managing and tracking the ongoing projects for timely
completion. - Finalization of Project strategies and scheduling.
- Co-ordination with internal departments R&D, Regulatory, QA/QC, Marketing, Procurement, etc.
We are looking for Fresher B.Pharm + MBA Candidates only can apply.
Please forward us your updated CV on vishalb@macleodspharma.com / poojat@macleodspharma.com
Research Associate- PDR MDI
We are looking for PHD Pharmaceutics candidates.
Please forward us your updated CV on vishalb@macleodspharma.com / poojat@macleodspharma.com
Roles and Responsibilities
- Candidate should perform literature search as per Regulator.
- Should have some basic understanding of patent and generic formulation development.
- Characterization of marketed product wrt market requirements.
- Pre formulation development.
- Evaluation/optimization of Excipients and primary packaging Materials.
- Basic knowledge of documents Master formula card, Bill of Material, stability protocol.
- Should possess basic manufacturing process during development.
- Knowledge of ICH stability conditions and compilation of analytical data.
- Preparation of various documents like PDR, stability protocol, development report writing FDR/PDR.
- Lab management system.
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