About Company:
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.
Website
https://vitalpharma.in/
Vacancy Details:
Job Description:
RESEARCH AND DEVELOPMENT CENTER (R&D) VITAL THERAPEUTICS AND FORMULATIONS PVT.LTD WALK IN INTERVIEWS ON 3RD MAY 2025 @HYDERABAD.
1.DEPARTMENT: AR&D
QUALIFICATION: M. PHARMACY/MSC/PH.D
EXPERIENCE: 2 TO 10 YEARS OF FORMULATIONS
KEY SKILLS: ANALYTICAL RESEARCH METHOD DEVELOPMENT (ARMD) AND METHOD VALIDATION AS
HPLC, GC, AND WET ANALYSIS, IMPLEMENT GLP & GDP PRACTICES.
2.DEPARTMENT: FR&D
QUALIFICATION: M. PHARMACY/MSC/PH.D
EXPERIENCE: 2 TO 10 YEARS OF FORMULATIONS
KEY SKILLS:
A) DESIGN, DEVELOP, AND OPTIMIZE FORMULATIONS FOR PHARMACEUTICAL OR NUTRACEUTICALS ETC. IMPLEMENTATION OF QBD
B) PREPARE TECHNICAL DOCUMENTS, INCLUDING FORMULATION PROTOCOLS AND REPORTS.
C)COLLABORATE WITH CROSS-FUNCTIONAL TEAMS SUCH ARD, DQA ETC TO ENSURE COMPLIANCE.
3.DEPARTMENT: DQA
QUALIFICATION: B. PHARMACY/M. PHARMACY/MSC
EXPERIENCE: 2 TO 6 YEARS OF FORMULATIONS
KEY SKILLS:
A) LEAD QUALITY ASSURANCE ACTIVITIES FOR PRODUCT DEVELOPMENT, INCLUDING DESIGN, TESTING, AND VALIDATION STAGES.
B) ENSURE COMPLIANCE WITH REGULATORY GUIDELINES AND QUALITY STANDARDS (E.G., FDA, EMA, GMP).
C)DEVELOP AND IMPLEMENT QUALITY CONTROL PROCEDURES FOR NEW PRODUCT DEVELOPMENT.
D) COLLABORATE WITH R&D, ARD TO IMPLEMENT THE QUALITY ISSUES.
E) MANAGE RISK ASSESSMENT PROCESSES AND ENSURE CONTINUOUS IMPROVEMENT IN QUALITY SYSTEMS.
F) SHOULD HAVE KNOWLEDGE IN QBD SYSTEM FOR PRODUCT DEVELOPMENT.
4.DEPARTMENT: RA (REGULATORY AFFAIRS FOR ROW MARKET)
QUALIFICATION: M. PHARMACY (REGULATORY)
EXPERIENCE: 2 TO 6 YEARS OF FORMULATIONS
KEY SKILLS:
A) DEVELOP AND IMPLEMENT REGULATORY FILING STRATEGIES FOR ROW MARKETS
B) STRONG KNOWLEDGE OF ICH GUIDELINES, CTD FORMATS, COUNTRY-SPECIFIC REGULATIONS IN ASIA, LATAM, AFRICA, CIS, AND THE MIDDLE EAST.
C) EXPERTISE IN DOSSIER PREPARATION, SUBMISSION MANAGEMENT, AND POST-APPROVAL CHANGES.
DJEXCELLENT COMMUNICATION, PROJECT MANAGEMENT, AND LEADERSHIP SKILLS.
E) PROFICIENCY IN REGULATORY DATABASES AND SUBMISSION TOOLS.
F) ASSESS REGULATORY RISKS AND PROVIDE MITIGATION STRATEGIES
G) OVERSEE THE PREPARATION, REVIEW, AND SUBMISSION OF CTD (COMMON TECHNICAL DOCUMENT) AND COUNTRY-SPECIFIC DOSSIERS.
HOW TO APPLY?
DATE: 3RD MAY 2025
TIME: 10:30AM
WORK LOCATION: CHERLAPALLY (NEARBY HABSIGUDA, ECIL, KUSHAIGUDA)
INTERVIEW VENUE: VITAL THERAPEUTICS AND FORMULATION PVT. LTD. PLOT NO:47 B/2, ST.NO.4, PHASE-I, IDA, CHERLAPALLY, SECUNDERABAD.
E-MAIL ID: HR@VITALPHARMA.IN
HR: 9666 977 644
