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2.0 - 6.0 years
0 Lacs
karnataka
On-site
As a QA Officer specializing in Oral Solid Dosage (OSD) pharmaceutical manufacturing at [Company Name], your role will be crucial in ensuring compliance with regulatory standards, maintaining quality systems, and overseeing manufacturing processes to uphold consistent product quality. Key Responsibilities: - Implement and monitor adherence to GMP and SOPs for OSD manufacturing. - Conduct in-process quality checks for tablets, capsules, and other forms. - Review and approve batch manufacturing records and validation protocols. - Assist in internal and external audits, including regulatory inspections. - Provide training to production staff on quality and compliance standards. - Participate in...
Posted 2 days ago
5.0 - 9.0 years
0 Lacs
telangana
On-site
As a QA Chemist at Sinterx Pharma Private Limited, you will play a crucial role in ensuring that all API intermediate manufacturing operations adhere to established quality standards, GMP requirements, and regulatory guidelines. Your responsibilities will include: - Reviewing and approving GMP documentation such as BMRs, BPRs, SOPs - Overseeing batch records, managing deviations, and CAPA - Conducting internal audits and ensuring compliance throughout the production lifecycle Qualifications required for this role include: - Bachelor's or Master's Degree in Chemistry, Pharmaceutical Sciences, or Life Sciences - 5 to 8 years of experience in Quality Assurance within the API or API Intermediate...
Posted 2 weeks ago
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