Research Associate- In vitro ADME

Job Description

Designation: Research Associate In vitro ADMEJob Location: BangaloreDepartment: Discovery BiologyAbout SyngeneIncorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation.Job PurposeLooking for a highly motivated, enthusiastic and result-oriented individual who will lead a team of scientists, interface with the client on project deliverables and be accountable for all the activities in DMPK and Assay Biology Group. S/he should comply with the company safety, quality and regulatory standards. The candidate will be involved in guiding the team towards planning and delivery of the projects with the required quality and on-time delivery metrics. The ideal candidate will be responsible for the operational and scientific management of the group and will also actively participate in the implementation of enabling technologies and automation.Key Responsibilities:

• Scientifically contributing and leading client projects with regular updates and timely communications to internal and external customers on the progress of the project
• Scheduling and preparing project execution plans based on resource allocation (people, equipment)
• Ensuring that implementation of projects is conducted in an efficient and timely manner.
• Scientific execution of lab-work (hands-on whenever required), troubleshooting technical problems, data analysis and presentation. Developing efficient semi-throughput processes is desirable.
• Supervise, assist, and mentor scientists on bioanalysis, pharmacokinetic analysis; data interpretation and report writing.
• Manage a team of Scientists- Masters and PhD [includes goal setting, understanding developmental needs, assigning responsibilities in the laboratory activities, critically assessing their performance and providing timely feedback]
• Maintain efficient lab operations and improve lab workflow
• Active participation in Data Integrity and Safety trainings and initiatives.
• Review of ELNs, raw data and study report to ensure data integrity for self and reporting team is maintained, complying ALCOA+ principles.
• Technical data presentation in internal and client meetings.
• Maintains compliance with all company policies and procedures.
• Take complete responsibility of the safety, compliance and productivity output of the team.
• Follow environment, health, and safety (EHS) guidelines in the workplace, ensuring that it is adhered to by self and the team, to maintain highest lab safety standards at-all-times

Educational Qualification:

• MSc (Chemistry/Biological Sciences)/M. Pharm from reputed University + Ph.D. Postdoctoral experience preferred.

Technical/functional Skills:

• A track record of scientific accomplishments and project leadership in in-vitro ADME, in-vivo pharmacokinetics, in-vitro and in-vivo toxicology studies and bioassays, as evidenced by peer-reviewed publications/patents.
• 5+ years of managing a high-performing team in industry with a focus on design and conduct of bioanalysis ADME studies, cell-based assays, pharmacokinetic/ toxicokinetic analysis.
• Experience with increasing productivity through automation is preferred
• Ability to inspire and grow a high-performing team, chart and set team goals into action, and build team credibility by managing timely execution of client projects with highest quality standards.

Experience:

• 9 to 15 years of experience post Ph.D.

Behavioral Skills:

• Ability to manage a team of scientists to deliver quality work within the time frame, train and coach junior scientists, inculcate good work ethics.
• Ability to work with co workers and peers professionally and tactfully.
• Excellent verbal/written communication and ability to communicate effectively to client with high transparency is essential.
• Interpersonal skills with an emphasis on working in a team environment to accomplish impactful results.

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.,

Keyskills :
documentationhplcresearchin vitrocalibrationanimal healthvalidationdata analysis