All Jobs : (1-13 out of 13)

Essential Duties and Responsibilities:• Souring, Procurement and Supplier management of Finished Formulation from Third partypartners on P2P along with basic understanding for LL.• Spearhead partn

3 to 5 years of experience in Financial Reporting

Candidates should be good in preparing videos with 2D animation,audio / video effects and editingThe core area of this position is good knowledge of 3D software i.e 3Ds Max / Maya/Blender ( any one ).

Person should have good understanding of Pharma planning,manufacturing & distribution functionPerson should be proactive to foresee changes in market demand through close coordination with demand plan

Roles and Responsibilities 1. Effective business communication2. Analyzing the internal sales reports and deriving insights and assist business unit head to arrive to important and critical decisions3

Monitoring business performance and external environment via appropriate tools to deliver corrective action as required meeting business objectives

Ensure seamless experience for doctors and patients on platform with timely resolution of all queries and concernsto ensure best experience for doctors and patients with C2C platform

Ensure seamless experience for doctors and patients on platform with timely resolution of all queries and concernsto ensure best experience for doctors and patients with C2C platform

Guiding the ERP Team on HSN to be incorporated in Product / Service Masters for various Goods and Services being procured and for products being sold Education (Minimum Needed) : LLB,BCom,CA . . Good

Roles and Responsibilities . . . . A Recruitment Intern supports the recruiting team by ensuring that all the duties required are performed timeously and correctly

Minimum 5 years in Pharma Industry Experience

Minimum Exp 5-8 Years Position will require interacting with Vendors,Hotels,Airline,Travel company (FCM),Card Company. . Should have good knowledge of Excel and Powerpoint

Roles and Responsibilities :1. Clinical study report writing for regulatory like USFDA, MHRA, EU, BTIF etc.2. Making summary tables checking of all documents.3. Protocol & related document (ICF,CRF, a