We are seeking an experienced and detail-oriented Quality Assurance Manager to join our Formulation Development team. The ideal candidate will play a pivotal role in ensuring that our pharmaceutical formulations meet the highest quality standards and regulatory requirements. The Quality Assurance Manager will be responsible for overseeing all aspects of quality assurance in the formulation development process, from initial research to product commercialization. Key Responsibilities: - Develop and implement quality assurance policies and procedures for the formulation development department, ensuring compliance with regulatory guidelines. - Collaborate with cross-functional teams, including Research & Development, Manufacturing, and Regulatory Affairs, to establish and maintain quality standards throughout the product development lifecycle. - Conduct risk assessments and identify areas of improvement in the formulation development process, implementing corrective and preventive actions as needed. - Lead the preparation and execution of quality audits, both internal and external, ensuring adherence to Good Manufacturing Practices (GMP) and other regulatory requirements. - Review and approve documentation related to formulation development, including batch records, protocols, and reports. - Provide training and mentorship to team members on quality assurance principles and best practices. - Investigate and resolve quality-related issues, deviations, and non-conformances, implementing effective corrective actions. - Stay up-to-date with industry trends and regulatory changes, ensuring continuous improvement in quality systems and processes. Qualifications: - Bachelor\'s degree in Pharmacy, Chemistry, or related field; Master\'s degree preferred. - Minimum of 7 years of experience in pharmaceutical quality assurance, with a focus on formulation development. - In-depth knowledge of regulatory requirements, including GMP, FDA, and other relevant guidelines. - Strong leadership and communication skills, with the ability to work collaboratively in a cross-functional team. - Excellent problem-solving and analytical abilities. - Detail-oriented with a commitment to maintaining the highest quality standards. - Prior experience in conducting quality audits is a plus. - Regulatory certifications (e.g., RAC) are desirable. To apply, please submit your resume and cover letter to hr@microtheraps.com or What\xe2\x80\x99s app to 9500112999/9361746519 Job Type: Full-time Salary: \xe2\x82\xb9600,000.00 - \xe2\x82\xb91,000,000.00 per year Schedule:

• Day shift

Education:

• Bachelor\'s (Preferred)

Experience:

• total work: 7 years (Required)

Ability to Commute:

• Chennai, Tamil Nadu (Required)

Ability to Relocate:

• Chennai, Tamil Nadu: Relocate before starting work (Required)

Work Location: In person Speak with the employer
+91 9361746519