
Senior Manager Quality Control
- Hyderabad, Telangana
- Permanent
- Full-time
- Daily management of the Quality Control Technical Resources team
- Responsible for organizing team resources to ensure that agreed upon due dates are met for QC Network requests
- Responsible for creating and maintaining business processes and tools that will facilitate the management and visibility of QC network requests
- Responsible for ensuring that the Technical Resources team has access to the required laboratory information management and enterprise systems needed to carry out document management tasks (for example, LIMS, electronic laboratory notebook).
- Responsible for leading issue resolution and problem-solving exercises within the team and cross-functionally, as needed
- Support staff training, career development and performance management
- Responsible for ensuring compliance with safety guidelines, cGMPs and other applicable regulatory requirements.
- Participate in Amgen global network teams
- Establish and enable LEAN principles across area of responsibility
- Establish and enable department goals, strategies and KPIs
- Champion site and QC global process improvements
- Interfaces with management on significant matters, often requiring the coordination of activity across organizational units
- Plans and organizes project assignments of substantial variety and complexity
- Translates complex data into actionable information and applies strong technical knowledge to meet business objectives
- Identifies process gaps, introduces innovative solutions, and leads operational excellence projects to improve efficiency and productivity, while decreasing expense/operating costs.
- Leads root cause analysis discussions for more complex problems to develop and efficiently implement effective permanent solutions.
- Master’s degree with 12-16 years of Pharma and Biotech commercial or clinical manufacturing Quality Control experience
- 5 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources
- Experience working and leading teams in a cGMP laboratory environment.
- Strong technical writing skills within a highly regulated environment.
- Working knowledge of cGMP regulations, practices, and trends pertaining to Quality Control.
- Experience managing staff and/or leading teams, projects, programs or directing the allocation of resources.
- Track record of building or participating as a member of high performing team.
- Experience with various laboratory computer systems and applications.
- Strong leadership and negotiation skills with a demonstrated ability to influence different styles.
- Demonstrated innovative thinking and ability to transform work organizations.
- Exposure to Operational Excellence initiatives.
- Understanding of quality management systems and quality control processes related to drug substance and drug product for clinical and commercial operations.
- Demonstrated ability to navigate through ambiguity and provide structured problem solving.
- Demonstrated ability to coordinate multi-functional project teams and deliver on schedule.
- Demonstrated ability to coordinate and lead cross-functional teams.
- Demonstrated ability to find opportunities and implement new technologies and services to transform the business into a more agile, efficient and effective organization.
- Demonstrated skills in staff motivation, coaching/mentoring and professional development.
- Great teammate who can collaborate and provide leadership through influence to achieve the required results.