MTech in any area of Life Sciences, Biotechnology, MSc degree in any allied area of Life Sciences, Biotechnology, BTech, BPharm, BE (4-years degree programme) in any allied area of Life Sciences/Biotechnology, BVSc, MBBS, with minimum 60% marks.

Masters/ Integrated Masters in Natural or Agricultural or Pharmaceutical Sciences/ MVSc/ Animal Sciences. OR Bachelors degree in Engineering or Technology or Medicine from a recognized University

Ph.D. in Chemistry plus 2-3 years postdoctoral experience in pharmaceutical solid-state chemistry, polymorph screening of APIs

1st class Masters degree in Life Sciences from a recognized University in the related field or 2nd class Masters Degree with Ph.D in relevant subject from a recognized University.

Masters degree in Biotechnology/Biochemistry/Microbiology Bioinformatics/ Biotechnology/ Life science/Biomedical Sciences/Bio-Engineering passed with minimum 55% marks.

Graduation in Science with PG Diploma in Clinical Research is mandatory. Candidates should have at least one-year experience

B.Pharm, M.Sc, B.Sc, ITI, Diploma, Pharmaceuticals Experience Only & Preferable Male Candidate Only

Analysis of RM / IP / FP samples, Operation and troubleshooting of instruments such as HPLC, UV, KF, IR, and Dissolution Apparatus.

Titan, an integrated Pharmaceutical Group which is backed by the holistic approach towards catering multifarious integrated services, which aims to meet the concept-to-commercialization needs of our customers while providing quality pharma and API products that serve for life saving medications.

Life Cycle management of branded portfolio from IP perspective including competition tracking. IP support for out-licensing projects.

Responsible for safety monitoring and evaluation of assigned GSK products. Conduct safety monitoring and evaluation for assigned products, including signal detection and risk assessment.

Responsible for performing the chemical and instrumentation analysis for In-process, raw materials, packing materials, intermediates and finished products to meet the dispatch timeline as per the monthly schedule received from PPIC.

Bachelors degree in Medical, Mechanical, Life Science or other healthcare related major. Works independently with general supervision on larger, moderately complex projects / assignments.

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. List knowledge, skills, and/or abilities required.

To handle process like manufacturing of liquid product including media, complex injectable and suspension manufacturing.

Plans, assigns and directs the Sales Managers to achieve top line and profitability in their respective Zones. Conducts performance evaluations and takes corrective action when deemed appropriate to do so.

Continually seek and implement means of improving processes to reduce study build cycle time, decrease work effort and enable the normalization of various sources of data into a common data repository in a way that allows for improved integration, consumption and downstream analysis

Prior pharma or CRO industry experience working on global clinical studies and projects or global process and system initiatives. Prior experience with Data Management.

Be a strong advocate for the Takeda ONE Oncology and R&D organizations in India in collaboration with India LOC; serve as local bridge for any future opportunities in engaging India innovation ecosystem.