Website:
tirupatigroup.co.in
Job details:
Company Description Tirupati Group is a healthcare-focused organization founded in 2005 with a mission to make healthcare accessible and affordable for all. The company has grown into one of India’s largest and fastest-growing pharmaceutical leaders, with a global presence across 11 countries and 145 clients. With advanced R&D capabilities, Tirupati Group combines cutting-edge biotechnology and innovation to deliver novel, best-in-class solutions in pharmaceuticals, nutraceuticals, Ayurveda, and sports nutrition. Its state-of-the-art facilities at the foothills of Himachal Pradesh, India, are known for efficient end-to-end manufacturing and rigorous GLP-compliant quality standards. The company is committed to enhancing quality of life through high-quality solutions delivered with integrity.
Role Description The Qualification Validation Executive is responsible for supporting and executing qualification and validation activities for equipment, utilities, and processes within Tirupati Group’s manufacturing facilities. This full-time, on-site role is based in Paonta Sahib and involves preparing and reviewing qualification protocols, validation plans, and related documentation in line with regulatory and internal quality standards. The role includes coordinating and performing validation tests, documenting results, identifying deviations, and supporting corrective and preventive actions. The executive will collaborate closely with Quality Assurance, Production, Engineering, and R&D teams to ensure compliance, continuous improvement, and readiness for internal and external audits. Day-to-day tasks also include maintaining validation records, tracking validation status, and contributing to risk assessments and change control activities.
Qualifications
- Strong understanding of qualification and validation principles for pharmaceutical, nutraceutical, or related manufacturing environments, including equipment, utilities, and processes.
- Knowledge of GLP, GMP, and relevant regulatory guidelines (national and international) and ability to apply them to routine validation activities.
- Experience with documentation practices, including drafting, reviewing, and maintaining protocols, reports, SOPs, and validation-related records.
- Analytical and problem-solving skills for interpreting validation data, identifying deviations, and supporting root cause analysis and CAPA implementation.
- Effective communication and collaboration skills for working with cross-functional teams such as QA, Production, Engineering, and R&D.
- Attention to detail, organizational skills, and ability to manage multiple validation tasks and deadlines in a fast-paced environment.
- Proficiency with basic computer applications and data handling tools relevant to validation and quality documentation.
- Bachelor’s degree in Pharmacy, Life Sciences, Biotechnology, or a related field; prior experience in a regulated manufacturing setup is an advantage.
- Willingness to work on-site in Paonta Sahib and adhere to safety, quality, and compliance standards at all times.
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