Job
Description
Designation: Deputy Research Director Job Location: Bangalore Department: Veterinary Science About Syngene, Incorporated 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 Purpose: The Head of Veterinary Sciences will lead BBRC’s in vivo research operations within a 50,000 sq. ft. AAALAC-accredited facility, supporting diverse, multi-modality therapeutic and functional areas. This leadership role will report to BMS Veterinary Sciences leadership and is accountable locally to the Head of Site Operations serving as a key member of the BBRC Operations Leadership Team. The ideal candidate brings deep veterinary expertise, operational excellence, and a commitment to team development and scientific integrity. Key Responsibilities: Lead the Veterinary Sciences BBRC function, ensuring high-quality support for in vivo pharmacology, DMPK, toxicology, and translational research. Serve as a senior member of the Operations Leadership Team, collaborating with global stakeholders to align strategies across R&D sites. Accountable for alignment with BMS veterinary sciences practices and standards and the associated support of therapeutic area teams to facilitate cutting age research with innovation, speed and quality Develop long term strategy in developing capabilities and capacity in support of BMS’ drug discovery portfolio Lead, coach, and develop a multidisciplinary team to meet departmental objectives.Build a culture of excellence, collaboration, accountability, and continuous learning in the team. Oversee all local aspects of veterinary care, animal welfare, and vivarium operations, ensuring compliance with international regulations (AAALAC, CPCSEA, IAEC) and BMS standards Capable as acting or overseeing the Attending Veterinarian and contributing to institutional animal ethics committees (IAEC/IACUC). Drive excellence in animal care practices internally and with external CRO partners. Champion a culture of ethical responsibility, scientific rigor, collaboration, and continuous improvement. Promote the 3Rs (Replacement, Reduction, Refinement) and foster a strong Culture of Care. Develop and implement SOPs, training programs, and performance metrics. Collaborate with research, quality assurance, facilities, safety, and security teams. Provide veterinary input to study design, protocol development, and regulatory submissions. Travel domestically and internationally as required. Technical/functional Skills: Expertise across multiple species used in pharmaceutical research Strategic and operational acumen in managing vivarium and veterinary functions Strong interpersonal and communication skills, with a track record of cross-functional collaboration Familiarity with Lean, Six Sigma, or continuous improvement methodologies is a plus Experience with innovative facility design or vivarium integration is desirable Ability to manage multiple projects with resilience, accountability, and emotional intelligence Preferred Attributes: Operational leadership of multi-site or global veterinary functions Scientific innovation in developing or refining in vivo disease models Passion for ethical research, leadership, and high-performing team development Education Qualification: PhD in Veterinary Science is a plus Board certification in Laboratory Animal Medicine (e.g., ACLAM, ECLAM, ICLAM) or equivalent professional experience is preferred. Eligibility for veterinary licensure in India Experience: 15+ years in laboratory animal medicine, with leadership roles in pharmaceutical or research settings Proven success leading multidisciplinary teams in a global R&D environment Experience in both GLP and non-GLP studies; involvement in IND/CTA-enabling programs is advantageous Strong knowledge of global regulatory and accreditation frameworks (AAALAC, CPCSEA, OLAW, EU Directive 2010/63) 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.
