Qa-Qms Manager
Job Description:
Job Description:
We are seeking a dedicated QMS professional to oversee and maintain the Quality Management System in compliance with cGMP and regulatory requirements. The role involves managing documentation, handling quality events, and supporting internal and external audits in an API manufacturing environment.
Key Responsibilities:
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Implement and maintain QMS processes in line with cGMP and ICH guidelines
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Manage documentation including SOPs, policies, and records
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Handle deviations, change controls, CAPA, and risk assessments
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Conduct internal audits and support regulatory inspections
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Facilitate training on quality systems and GMP practices
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Collaborate with cross-functional teams to ensure compliance and continuous improvement
Key Skills & Knowledge:
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Strong understanding of QMS principles and pharmaceutical regulations (ICH, WHO, USFDA, etc.)
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Experience in API manufacturing environment preferred
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Proficiency in handling deviation, CAPA, and change control systems
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Good communication and documentation skills
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Knowledge of data integrity and quality risk management
Company Profile
Our client is cGMP-compliant company focused on the manufacturing of niche Active ---ceutical Ingredients (APIs), in particu---r Hormones. Our manufacturing is done as per international regu---tory guidelines under strict quality control and oversight.
Our team has decades-long experience in ---ceutical APIs internationally which allows us to stay in an ever-evolving industry with core scientific strength, a deep insight into the sunrise technologies for API development, and evolving regu---tory requirements combined with our outreach in the international market, company offers unique partnership opportunities to ---ceutical formu---tion companies the world over.
Apply Now
- Interested candidates are requested to apply for this job.
- Recruiters will evaluate your candidature and will get in touch with you.