Quality assurance Process validation Full Time

Company Description

Maya Biotech Private Limited is a distinguished pharmaceutical contract manufacturing company known for its commitment to quality, safety, and innovation. It is certified with WHO, GMP-GLP, and ISO 9001-2015, ensuring the highest standards in all its processes. Offering a diverse portfolio of products such as nasal sprays, metered dose inhalers, ophthalmic drops, and anaesthetic injections, the company has earned a reputation for excellence and reliability. Maya Biotech is a trusted partner for both manufacturing solutions and franchising opportunities, further solidifying its position in the pharmaceutical sector. The company operates with a keen focus on providing quality healthcare products that meet stringent industry benchmarks.

Role Description

This is a full-time, on-site role for a Quality Assurance Process Validation Specialist, located in Baddi. The role involves overseeing quality assurance processes, ensuring compliance with Good Manufacturing Practice (GMP), performing quality audits, and managing process validation activities to maintain the highest standards for pharmaceutical product manufacturing. The successful candidate will collaborate with cross-functional teams to ensure products meet regulatory and quality guidelines while driving continuous improvement in processes.

Qualifications

• Expertise in Quality Control and Quality Assurance to ensure adherence to established standards
• Strong knowledge of Quality Management systems and Good Manufacturing Practice (GMP)
• Proficiency in conducting Quality Audits to identify and address areas of improvement
• Experience in Process Validation and ensuring process compliance with industry standards
• Strong attention to detail and problem-solving skills
• Bachelor’s degree in Pharmaceutical Sciences, Chemistry, or a related field
• Prior experience in the pharmaceutical manufacturing sector is highly desirable
• Excellent communication and teamwork skills