Pharmaceutical Bioanalysis Specialist

Job Role : Analyst - Small Molecule Bioanalytical Laboratory

Job Location : Bangalore, India

About Company :

Syngene International Ltd. (BSE : 539268, NSE : SYNGENE, ISIN : INE398R01022), is an integrated research, development, and manufacturing solutions company serving the global pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical sectors. Syngenes 4500+ scientists offer both the skills and capacity to deliver great science, robust data management and IP security, and quality manufacturing at speed, to improve time-to-market and lower the cost of innovation. With a combination of 1.9 Mn sq ft of specialist discovery, development and manufacturing facilities, as well as dedicated research facilities for Amgen, Baxter, Bristol-Myers Squibb and Herbalife, Syngene works with biotech companies pursuing leading edge science as well as multinationals including GSK and Merck KGaA.

Role : Analyst for the Small Molecule Bioanalytical Laboratory is a technical role responsible for conducting BA / BE studies in the laboratory. Job responsibilities include performing critical method development and validation programs, technical and regulatory compliance of all studies.

This role requires an individual with a robust background in pharmaceutics, or other related life sciences, coupled with extensive experience in the bioanalytical field, particularly within small molecule bioanalysis.

This role demands an individual with a strong commitment to compliance, integrity, and excellence in bioanalytical research, particularly in small molecule analysis.

Key Responsibilities of the Role :

• Perform the bioanalytical work including sample processing for method development, method validation and study sample analysis as per the protocol in compliance with SOPs, STPs.
• Prepare STP, MV protocol and study sample analysis protocol.
• Coordinate with maintenance department for any problems related to utilities and equipment / instrument (e.G. LC-MS / MS, HPLC, etc) failures.
• Document data generated, entries in official documents.
• Ensure all studies adhere to regulatory guidelines and expectations set by GCP / GLP.
• Participate in all discussions on project-specific scientific details.

Education and Experience

Education

Masters in Pharmaceutics or other related life sciences from a reputed university.

Industry Experience

Equal Opportunity Employer

It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and / or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.