GM/AVP - Formulation Development - Pharma

Company Profile: Our client is a mid-sized, leading Indian Pharma Manufacturing organisation - Leaders in their field. They have grown very rapidly since inception a decade ago by a group of young and experienced professionals with the specific objective to develop and produce complex, small volume, technology driven products at competitive prices. Around 7 to 8% of the turnover is spent on research and development. Our clients have filed more than 75 patents and 3 USDMFs and 1 EDMF so far. They have also filed a number of IDL Dossiers in China and Taiwan and dozens of products in Latin Market.

The Company's growth has largely been driven by exports. Today exports account for more than 75% of the Company's turnover. The state-of-the-art manufacturing facility at MIDC in the Central Suburbs (beyond Thane) and has been designed as per international guidelines to meet the standards of USFDA, EUGMP etc. The client is a private limited company and the company is held between 3 local promoters and an overseas investor.

Today, they export 80% of their APIs to companies in South America, Asia-Pacific, US and Europe.Our clients are looking for a GM/VP-Formulations to be based at the plant and reporting to the CEO. Our clients offer excellent salary/perks as per industry norms & commensurate with experience.

The position is expected to be closed by end-August.

We have the following vacancy:

GM/AVP -Formulation Development.

Reporting to CEO

Total Team- 35 and 4 people direct reportees

Based at their Research facility in Central Suburbs beyond Thane

B.Sc. / B.Pharm with Exp- 12 to 20 yrs of experience.

CTC- 35 L to 42 L

KRAs:

Experience in Formulation Research, Process Development, Technology Transfer and Overall Project Management of Pharmaceutical Dosage Forms leading to US - ANDA, Europe CTD fillings for Regulatory Markets.

Exposure to ANDA (inclusive of Para IV, FTF) includes Tablets (Immediate, & Modified release), Capsules, Dry Powder Suspension, Multiparticulate systems, Oral liquids & Suspension. Dry Powder injections.

Formulations include Antiretroviral, Antibiotic-Penicillin &Cephalosporins, Anti-hypertensive, Anti-diabetic, Anti-epileptic, Antidepressants, etc.

Good shop floor experience on Product/ Process Performance and Technology Transfer of oral Solid, Liquid Pharmaceutical Dosage Forms.

Well verse in developing stable, globally acceptable Bioequivalent, Validated generic Pharmaceutical Dosage Forms. Conceptualization of Non-Infringement Strategies.

Translate developmental plans to operational activities.

Provide broad expertise in area of responsibility at the interface between management and operations.

Impart training & mentoring to research manpower; recruit talent.

Establish and implement training and development plans.

Manage resource allocation and capacity to ensure timelines and key milestones are met.

Implement the relevant technologies and processes in the respective disciplines.

Please note: We will revert to you within 72 hours, if your CV & details match our client's requirement. Failing which, we will revert whenever we have a commensurate vacancy in future