Scientist Job at Syngene | MPharm Graduates Apply Now
Syngene International Ltd., a leading global contract research, development, and manufacturing organization (CRDMO), is inviting applications for the role of Associate Scientist – Bioanalytical at its Discovery Services Division in Bangalore. This Scientist Job is a great opportunity for M.Pharm professionals passionate about analytical science, LCMS/MS, and bioanalysis in a world-class R&D environment.
- Job Title: Bioanalytical Scientist
- Job Location: Bangalore, KA, IN, 560099
About Syngene
Syngene is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply.
At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit.
Responsibilities of the Scientist Job
- Overall adherence to safe practices and procedures of oneself and the teams aligned.
- Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company’s integrity & quality standards.
- Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times.
- Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace.
- Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self.
- Compliance to Syngene’s quality standards at all times.
- Hold self and their teams accountable for the achievement of safety goals.
- Govern and Review safety metrics from time to time.
Purpose of the MPharm Job
- To participate in sample processing for PK, ADME assays and handling of LCMS/MS. Ability to adapt to the dynamic team environment.
- Processing of different matrices samples of PK studies.
- Optimization of test compounds manually as well as automated on LCMS/MS.
- Develop methods with the team lead.
- Independently handling of HPLC for UV based samples analysis.
- Documenting the lab note books online and compound management.
Education
- M. Pharm in Pharmaceutical sciences, Pharmaceutical Analysis who has interest and passion for LC/MS related bioanalysis.
Experience for the MPharm Job
- Minimum 3-5 years of experience in analysis of ADME assays using HPLC and LCMS/MS.
Skills and Capabilities
- Expertise in column selection, mobile phase selection, solvent preparations and sample processing techniques such as protein precipitation, liquid-liquid extraction and solid phase extraction is mandatory.
- Sample processing of New chemical entities from various in-vitro and in-vivo studies executed in Preclinical discovery by using appropriate extraction methods.
- Should be able to develop and validate LC-MS based qualitative/quantitative methods and apply them in routine analysis.
- Should be well versed with internet-based literature search and capable of implementing the Learnings as and when required.
- Candidate is expected to have basic understanding in interpretation of Mass/UV Spectra.
- Should ensure preventative maintenance and calibration schedules of HPLC & mass spec by coordinating with vendor and support staff.
- General understanding of Drug metabolism and Pharmacokinetics.
- Should be able to deliver scientific presentation in departmental journal club and write official Project reports.
