With over 25 years of expertise, Vital Therapeutics & Formulations Pvt. Ltd. is a trusted leader in Animal Health, Pharmaceutical Contract Manufacturing, Human Nutrition and Formulation Development. Backed by a team of industry veterans and professionals, we are dedicated to delivering quality-driven solutions tailored to meet the diverse needs of our customers across domestic and international markets, including India, Africa, the Middle East, and South Asia. Our four key portfolios include:
🔹 Animal Health & Nutrition – Pioneering treatment, prevention, and nutritional solutions for poultry and ruminants, ensuring farmers maximize productivity with high-quality, research-backed products.
🔹 Pharmaceutical Contract Manufacturing – Specializing in oral liquid and powder formulations, catering to leading MNCs with state-of-the-art manufacturing, stringent quality control, and regulatory compliance.
🔹 Human Nutrition – Offering innovative stabilized formulations for pharmaceuticals, nutraceuticals, and food fortification.
🔹 Formulation & Innovation Centre – Focused on R&D, formulation development, technology transfer, and product commercialization across animal health, human nutrition, and pharmaceutical sectors. At Vital, we combine science and research to create affordable, high-quality, evidence-based solutions, ensuring product performance and customer satisfaction. Whether you’re looking for custom formulations, contract manufacturing, or innovative solutions, we are your trusted partner in quality and innovation.
DATE AND TIME:
- Date: 20th December’2025
- Time: 9:30am to 12:30pm
- Work Location: Cherlapally
(Nearby Factory location Habsiguda, ECIL, Kushaiguda, Uppal, Secunderabad) - Interview Venue: Vital Therapeutics and Formulations Pvt. Ltd. Plot No:47 B/2, St.No.4, Phase-I, IDA, Cherlapally, Secunderabad.
Contact :
- E mail: hr@vitalpharma.in
- HR: 9666 977 644
JOB DETAILS:
1. Department: QC – Male / Female
- Qualification: B. pharmacy / M. Pharmacy /MSc
- Experience: 2 to 3 years
- Skills: a) Handling of HPLC / RM Analysis / Finished Product Analysis / Stability Samples
b) Handling of Documentation like Spec & STP’s, SOP’s and other QMS activities.
2. Department: QA AQA – Male
- Qualification: MSc Analytical / M. Pharmacy
- Experience: 2 to 5 years
- Skills: – a) To assist the Management in executing all GMP / GLP related activities.
b) Handling of Market Complaints, Returns /Recall, Deviations, OOS, Validation report review.
c) To review and approve all specifications, STPs, SOPs, BMR, BPR, MFR.
d) To review and approve of all validation protocols and reports.
e) To ensure quality related complaints are investigated and resolved in coordination with QC, QA, and production departments.
f) To handle critical quality systems like deviations, change control, CAPA, training, OOS, validations and Qualifications.
g) To Review and approve Certificate of Analysis as per the customer requirement.
h) Excellent communication and writing skills
For More JOB Updates Join Our Whatsapp Group Click Here
