Overview

To draft, vet, negotiate, execute, file and maintain all the legal documents prepared / received by the Company in India and Overseas market:

All types of Contracts, Agreements, Legal Documentation including Memorandum of Understanding, Supplementary drafts, notices/letters, banking & financial documents, real estate / property documentation etc.
Power of Attorneys, Letter of Authority, Undertaking, Affidavits.
Term Sheets, Letter of Intent & Side letters, Opinions, Minutes of Meeting etc.
Negotiating with various law firms and external parties for the execution of the contracts listed above.
To conduct adequate research and take such opinions or do all such activities which are required for the valid execution of the documents.
To work on improvisation of systems and processes within the function that are required to increase the quality, efficiency and output of the assignments.
To work on any other assignment or profile as may be suggested by the immediate superior or as may be decided by the management from time to time.
Salary: INR 7,00,000 – 13,00,000 P.A

Industry: Pharma / Biotech / Clinical Research

Functional Area: Legal , Regulatory , Intellectual Property

Role Category: Other

Role: Legal Manager

Candidate must be excellent in communication.
Should have sound knowledge of documentation & complex drafting.
Should be conversant with Litigation, IPR and corporate compliance matters.
Education-

UG: LLB – Law

PG: LLM – Law

About Claris Injectables

Welcome!
Claris Injectables Limited, a wholly-owned subsidiary of Claris Lifesciences Limited - collectively β€˜Claris’, is a sterile injectables pharmaceutical company with its market presence across the world. Claris manufactures and/or markets products across multiple delivery systems, markets, and therapeutic segments, including anesthesia & analgesics, blood products, anti-infectives, critical care, and nephrology. A significant majority of these products are generic drugs, capable of being directly injected into the human body, predominantly used in the treatment of critical illnesses. Our customer base primarily includes government and semi-government institutions, group corporate hospitals, standalone prominent hospitals, and nursing homes.

With emphasis on quality, technology, and innovation, we offer a range of niche technology-driven injectables products across delivery systems, such as bags (PVC & NPVC), vials, ampoules, glass bottles, etc.

We have three manufacturing facilities at a campus located in Ahmedabad, India. Our sterile injectables facilities have been approved by regulatory authorities, including US FDA, MHRA (UK), TGA (Australia), MCC (South Africa), ANVISA (Brasil), INVIMA (Colombia), and GCC FDCA. Our manufacturing capabilities have enabled us earn several awards from prestigious institutions like IDMA (Indian Drug Manufacturers' Association) and Frost & Sullivan IMEA (India Manufacturing Excellence Award).

Our capabilities and experience span across several business verticals in the specialty injectables industry. We have a trained workforce extending over all the business functions, such as product development, regulatory affairs for obtaining product registrations, manufacturing, and sales & marketing.