Team Lead Invitro Bioanalytical

As an in-vitro Bioanalytical Scientist at Syngene, your core purpose will be to provide expert DMPK support to multidisciplinary integrated Drug Discovery projects. Your responsibilities will include defining and implementing the DMPK strategy to expedite project progression, participating in capability building projects as per business requirements, and providing input into the design of experimental protocols and Bioanalytical procedures for the analysis of drug candidates in biological samples. Additionally, you will be expected to deliver scientific presentations in departmental journal clubs and write official project reports. Your role accountabilities will involve planning and supervising routine Bioanalytical workflow to ensure deliverables and productivity, verifying analytical study data for accuracy and integrity, mentoring and supervising fellow scientists for method development and troubleshooting, and playing a key role in evaluating and interpreting bioanalytical results. Troubleshooting LC-MS/MS based bioanalytical methods, having a basic understanding of interpreting Mass/UV Spectra, and ensuring preventative maintenance and calibration schedules of HPLC & mass spec will also be part of your responsibilities. In terms of leadership capabilities, you are expected to demonstrate skills in people management, strong communication, team building, problem-solving attitude, and interpersonal skills. You should consistently align with Syngene's core values of Excellence, Integrity, and Professionalism. As a Syngene leader, you will champion effective Environment, Occupational Health, Safety, and Sustainability (EHSS) practices for the company, oversee compliance within the Biologics business, and foster a corporate culture that promotes an EHSS mindset, quality, integrity, and compliance. People management, career planning, and talent retention will be key areas where you will provide clear, active leadership. Specific requirements for this role include a minimum of 10-15 years of experience in the relevant industry, with demonstrated capabilities in collaboration, leading teams, and Bioanalytical Excellence. The educational background required is an M. Pharm in Pharmaceutical sciences or Pharmaceutical Analysis with a minimum of 10 years of experience in handling ADME assays and HPLC and LCMS/MS, or a fresh Ph.D. in similar disciplines. Syngene is an Equal Opportunity Employer, and all employees are expected to uphold the company's values of Excellence, Integrity, and Professionalism in their daily work.,