The Training and Development effort at Colgate-Palmolive is a direct outcome of the Individual Development Plan and the Business need. The business critical and individual specific needs are identified every year and a training needs inventory is drawn up. Colgate's leadership position in the global marketplace is directly linked to the skill of our employees. Practical learning and professional growth are critical to our continued success. We invest generously in the training and education of Colgate people.
Post : Research Scientist
Job Description:
• Responsible for Oral Care and Personal care stability programs, Physical and Chemical evaluation of Cosmetic products and Oral pharmaceutical products/ Raw materials.
• Responsible for various Analytical instruments and stability chambers and ovens for Performance qualifications, Validations, Calibrations and Preventive maintenance.
• Good troubleshooting skills on analytical instrumentation.
• Collaborate and participate in Cross functional Teams ( I&S and micro) to provide requisite support on key business programs
• Implement best practices for cGMP/ FDA protocols. Ensure compliance to 21CFR part 11 guidelines. MUST have worked in a laboratory adhering to 21CFR guidelines and compliance and a Subject matter expert in cGMP protocols and cGLP practices.
• Responsible for analysis of water testing.
• Well versed with cGLP and Good documentation practices and procedures.
• Develop, optimize and validate analytical methods.
• Effectively collaborate and communicate with global customers
• Responsible for Oral Care and Personal care stability programs, Physical and Chemical evaluation of Cosmetic products and Oral pharmaceutical products/ Raw materials.
• Responsible for various Analytical instruments and stability chambers and ovens for Performance qualifications, Validations, Calibrations and Preventive maintenance.
• Good troubleshooting skills on analytical instrumentation.
• Collaborate and participate in Cross functional Teams ( I&S and micro) to provide requisite support on key business programs
• Implement best practices for cGMP/ FDA protocols. Ensure compliance to 21CFR part 11 guidelines. MUST have worked in a laboratory adhering to 21CFR guidelines and compliance and a Subject matter expert in cGMP protocols and cGLP practices.
• Responsible for analysis of water testing.
• Well versed with cGLP and Good documentation practices and procedures.
• Develop, optimize and validate analytical methods.
• Effectively collaborate and communicate with global customers
Additional Information:
Location: Mumbai
Functional linkages:
Internal: Micro, PD/I&S
External: Global analytical group, Regulatory authorities, Manufacturing plants within and Outside India
Functional Area: R&D
Location: Mumbai
Functional linkages:
Internal: Micro, PD/I&S
External: Global analytical group, Regulatory authorities, Manufacturing plants within and Outside India
Functional Area: R&D
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