• Manage the day-to-day activities of CHAMPS’ integrated maternity care team initiative. • Coordinate meetings, develop agendas, take minutes. • Collect and manage data. • Help to develop training materials and set up staff and community trainings. • Conducting literature reviews. • Contribute to the preparation reports, presentations and manuscripts for publication. • Attending CHEER meetings and helping to draft agendas and minutes. • Maintain records, reports and files as required. • Participating in national and BMC-based groups that CHEER is a member of. • Maintain departmental policies and procedures, objectives, quality assurance programs, safety, environmental and infection control standards.

Role Description The Staff Technical Operations Scientist for Beckman Coulter Diagnostics is responsible for ensuring the successful establishment of Beckman Coulter products being manufactured in India by an OEM partner. The role will include aspects of Quality Assurance, Design Transfer, Test Method Transfer, and the setup and validation of equipment and manufacturing processes. This position is part of the Made in India transfer team located at the OEM manufacturing site. In this role, you will have the opportunity to: - Support the technical transfer activity for a multi-phase and multi-year project to transfer programs into a third-party contract manufacturing facility in India. - Provide technical direction and support for third-party manufacturing activities including coordination of activities with cross-functional roles from Quality, Regulatory, Development, Project Management, Supply Chain, Procurement, and Validation. - Be involved in the full project life cycle - successful project completion will include full implementation from initiation to deployment for multiple products, including equipment setup validation, manufacturing process transfer and validation, test method transfer and validation, and post-launch support. - Support activities to ensure continuity of supply of product to the market and ensure projects are effectively set up and meet their timelines. - Use of DBS tools and techniques to streamline processes e.g., SW, TPI, VPM, Daily Management, etc. - Responsible for driving and implementing the Supply Chain Activities in compliance with the local and global design change process and relevant procedures. - Coordinate with relevant groups across the company to ensure that procedures/specifications, raw materials, resources, and facilities are in place to support the contractor manufacturing activities. - Ensure that all these activities are performed in a manner that ensures compliance with the relevant policy, procedures, regulatory authorities, and GMP. Qualifications - Bachelor’s degree with 9+ years experience OR Master’s degree with 7+ years experience. - Proven problem investigation and problem-solving skills are essential. - Demonstrated ability to effectively prioritize and lead a team to deliver on commitments and meet the needs of the business. - Prior experience managing strategic Supply Chain projects. - A good working understanding of cGMP and ISO/FDA requirements. Benefits - Flexible, remote working arrangements for eligible roles. - Enriching careers, no matter the work arrangement.

Role Description The Staff Technical Operations Scientist for Beckman Coulter Diagnostics is responsible for ensuring the successful establishment of Beckman Coulter products being manufactured in India by an OEM partner. The role will include aspects of Quality Assurance, Design Transfer, Test Method Transfer, and the setup and validation of equipment and manufacturing processes. This position is part of the Made in India transfer team located in India and will be located at the OEM manufacturing site. In this role, you will have the opportunity to: - Support the technical transfer activity for a multi-phase and multi-year project to transfer programs into a third-party contract manufacturing facility in India. - Provide Technical direction and support for third party manufacturing activities including coordination of activities with cross-functional roles from Quality, Regulatory, Development, Project Management, Supply Chain, Procurement, and Validation. - Be involved in the full project life cycle - successful project completion will include full implementation from initiation to deployment for multiple products, including equipment setup validation, manufacturing process transfer and validation, Test method transfer and validation, and post launch support. - Support activities to ensure continuity of supply of product to the market and ensure projects are effectively set up and meet their timelines. - Use of DBS tools and techniques to streamline processes eg SW, TPI, VPM, Daily Management, etc. - Responsible for driving and implementing the Supply Chain Activities in compliance with the local and global design change process and relevant procedures. - Coordinate with relevant groups across the Company to ensure that procedures/specifications, raw materials, resources, and facilities are in place to support the contractor manufacturing activities. - Ensuring that all these activities are performed in a manner that ensures compliance with the relevant policy, procedures, regulatory authorities, and GMP. Qualifications - Bachelor’s degree with 9+ years experience OR Master’s degree with 7+ years experience. - Proven problem investigation and problem solving skills are essential. - Demonstrated ability to effectively prioritize and lead a team to deliver on commitments and meet the needs of the business. - Prior experience managing strategic Supply chain projects. - A good working understanding of cGMP and ISO/FDA requirements. Benefits - This position is eligible for a remote work arrangement in which you can work remotely from your home. - Flexible, remote working arrangements for eligible roles. - Commitment to providing enriching careers, no matter the work arrangement.

• Lead the analytical development and quality control strategy for one or more programs, setting the technical direction for method development, validation, and lifecycle management to ensure robust, phase-appropriate control of product quality. • Partner with CDMO and contract laboratory partners as the primary technical point of contact, driving resolution of complex analytical or method-related issues and holding partners accountable to scientific and quality standards. • Lead drug substance (API) analytical method development, qualification, and validation, including forced degradation, related substances/impurity profiling, and physicochemical characterization to support process understanding and specification setting. • Perform in-depth review and interpretation of analytical data (HPLC/UPLC, Dissolution, KF, GC, etc) across release and stability programs, and personally lead the resolution of the most complex or ambiguous data issues. • Identify subtle trends, shifts, or outliers in complex data sets that may impact product quality, method robustness, or long-term stability, and translate findings into program-level risk assessments and recommendations for leadership. • Serve as the technical lead and final scientific authority during OOS, OOT, and atypical result investigations, driving root cause determination and ensuring scientifically sound, defensible conclusions. • Own preparation and technical accuracy of the analytical development and quality control data packages supporting regulatory submissions, and author the CMC analytical sections of regulatory documents (e.g., NADA/INAD filings, briefing documents, and responses to health authority questions), ensuring data and method documentation are complete, scientifically sound, and submission-ready. • Mentor and provide technical guidance to junior scientists and analysts, building analytical capability across the team.