Associate Director, Analytical Sciences
Company: Bristol-Myers Squibb
Position Summary
The Associate Director, Analytical Sciences will oversee performance, execution, and compliance of the QCEAS HYD team. Reporting to the HYD Global Quality Lead, you will work closely with the QCEAS team leaders to deliver compliant, accurate, timely and efficient project and standard work activities in accordance with QCEAS expectations. The role will manage a team based in Hyderabad, India that supports all QCEAS activities, overseeing performance, execution, and compliance of the QCEAS team in Hyderabad.
Key Responsibilities
- Provide strategy, oversight and tactical support of the Commercial analytical Sciences activities including method data trending, method qualification activities, instrument lifecycle management, stability operations and data trending, document & knowledge management, and analytical quality assurance.
- Report to the Senior Director, Head of Global Quality Capability Center, Hyderabad. Work closely with the Global team for QCEAS and associated data, systems and processes for BMS products.
- Lead the Hyderabad QCEAS team members to deliver robust and timely processing of all QCEAS activities to meet enterprise and global regulatory requirements.
- Accountable for HYD QCEAS team delivery of performance and compliance requirements.
- Communicate continuously and effectively with management (Senior Director, Head of Global Quality Capability Center, Hyderabad as appropriate) and key QCEAS stakeholders on QCEAS related matters. Escalate system performance issues to QCEAS Support for expedited resolution.
- Grow, develop, engage and empower team through existing BMS tools such as Workday – inclusive of performance management, development plans and objectives as per BMS Workday system.
- Manage employee related activities for the department (hires, trains, appraises, mentors, motivates, disciplines).
- Support health and performance of associated electronic management systems in compliance with procedural guidelines.
- Manage stakeholder needs in balance to priorities and execution of document procedural adherence.
- Provide leadership and coaching in relation to the HYD QCEAS team.
- Manage risk and uncertainty, and anticipate the need for and implement contingency plans.
- Lead team to meet goals while resolving complex issues.
- Exercise sound judgment, using a risk-based approach, to ensure compliance with procedural document regulations, practices, and policies.
- Develop, adjust, and monitor key performance indicators to identify and mitigate risk to business objectives.
- Collect metrics to identify trends and take appropriate action.
- Communicate up-to-date status to impacted business units.
Qualifications & Experience
- Fluent in English, with proven professional working proficiency in English for reading, writing, and speaking, including the ability to deliver clear and articulate presentations.
- Minimum of a bachelor’s degree and 10 years industry experience; 7 years as a people leader.
- Commitment to quality.
Candidate Rights
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
Equal Opportunity Employment
Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.
Data Protection
We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.