Require Research Scientist at Sentiss Pharma # Click here for more details

Post : Research Scientist – Analytical Development (Technology Transfer)

Job Description
SUMMARY OF THE OVERALL JOB
• To execute Method Transfer activities, Routine Analysis, Stability Analysis, Analytical Method Development, Analytical Method Validation and responsible for the compliance of cGLP activities.

KEY FUNCTIONS / RESPONSIBILITIES
• To execute Method Transfer Activities of Raw Material and Finish Products.
• To perform analysis of raw materials and API as per pharmacopeias / vendors methods.
• To analyse the samples of finished products as per test procedure and prepare certificate of analysis.
• To develop and validate analytical methods for the testing of formulations/ finished products using techniques such as HPLC/UV/GC/wet chemical methods etc.
• To perform all analytical activities in compliance with cGLP.
• Any other responsibilities assigned from time to time.

Additional Information
Experience : 4-6 years
Qualification : MSc./ M.Pharm (Pharmaceutical Chemistry)
Location : Baddi
Industry Type : Pharma
Salary: INR 3,50,000 - 5,50,000 P.A.
Functional Area : Analytical Development (Technology Transfer)
End Date : 20th December, 2018

Senior Executive in Medical Affairs required at Sentiss Pharma

Sentiss is committed to providing the best quality pharmaceutical products primarily in the Ophthalmic, ENT and Inhalation segments. Over the past 25 years, by exhibiting commitment and showcasing our winning culture, Sentiss has evolved tremendously and is recognized as the third best Ophthalmic Company (IMS 2015) in Russia. Sentiss’ footprint on the world map is a testimony to its quality philosophy and practice of product differentiation. Sentiss strives to be a global leader in its core segment and continues to expand its operations in Russia, CIS, Europe, USA and Indian markets. Sentiss has a quality workforce of 700+ people across multiple geographies. Sentiss is recognized as one of the Top 100 Great Places to Work in India in 2015.

Post : Sr. Executive – Medical Affairs

Job Description

• To prepare and review documents related to regulatory submission viz non-clinical and clinical modules, PSURs, SmPC and PIs for different regulatory authorities
• To help in assessment of reported ADRs.
• To provide Pharmacokinetic and ADR profile based on the literature after finalizing the product.

Require Research Scientist at Sentiss Pharma

Established in the early 90's, this organization has emerged as an integrated pharmaceutical company offering products to the global market. Headquartered at Delhi NCR, India and plant in North India, the Company develops, manufactures and markets a wide range of quality products in diverse area of treatment.Over the years, the organization has positioned itself as a significant player in the Russian and CIS markets and has expanded its foothold in the US, Europe, India and other markets. The key competitive advantage lies in having the Research & Development centre together with the world class manufacturing facility that has enabled it to provide end-to-end solutions from product development to marketing. The manufacturing facilities are approved by many regulatory bodies including EUGMP and WHOGMP thereby allowing the company to reach International markets.

Post : Research Scientist