Vital Therapeutics Walk-In (Hyderabad) for R&D, F&D, QA, RA

Vital Therapeutics and Formulations Pvt. Ltd., a Research and Development Center, is conducting a Walk-In Interview in Hyderabad on Friday, May 3rd, 2025, for experienced professionals in various departments including Research & Development (R&D), Formulation & Development (F&D), Quality Assurance (DQA), and Regulatory Affairs (RA) for Row Markets. If you have the relevant qualifications and experience in the pharmaceutical industry, we encourage you to attend.

Career Opportunities at Vital Therapeutics – Walk-In on May 3rd

Join Vital Therapeutics and contribute to our research, development, and quality assurance processes. This walk-in interview provides an excellent opportunity to explore diverse roles within our organization and advance your career in the pharmaceutical sector.

About Vital Therapeutics and Formulations Pvt. Ltd.

Vital Therapeutics and Formulations Pvt. Ltd. is a Research and Development Center focused on [Insert brief description of the company if known – e.g., developing innovative pharmaceutical formulations and ensuring high-quality standards]. We are committed to [Insert company’s mission or values if known – e.g., advancing healthcare through research and development].

Walk-In Interview Details

Date & Time

Date: 3^rd May’2025
Time: 10:30 AM

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.

Open Positions

Department: R&D

**Qualification:** M. Pharmacy / M.Sc / Ph.D
**Experience:** 2 to 10 Years of formulations analytical research (method development and method validation as per HPLC, GC and wet analysis).
**Key Skills:** Analytical research (method development and method validation as per HPLC, GC and wet analysis).

Department: F&D

**Qualification:** M. Pharmacy / M.Sc / Ph.D
**Experience:** 2 to 10 Years of formulations development.
**Key Skills:** Design, develop, and optimize formulations for pharmaceutical or nutraceuticals etc. Implementation of QbD. Prepare technical documents, including formulation protocols and reports. Collaborate with cross-functional teams such as ARD, DQA etc to ensure compliance.

Department: DQA (Quality Assurance)

**Qualification:** B. Pharmacy / M. Pharmacy / M.Sc
**Experience:** 2 to 6 Years of formulations.
**Key Skills:** Lead quality assurance activities for product development, including design, testing, and validation stages. Ensure compliance with regulatory guidelines and quality standards (e.g., FDA, EMA, GMP). Develop and implement quality control procedures for new product development. Collaborate with R&D and F&D to resolve quality issues. Manage risk assessment processes and ensure continual improvement in quality systems. Should have knowledge in QbD system for product development.

Department: RA (Regulatory Affairs for Row Market)

**Qualification:** M. Pharmacy (Regulatory)
**Experience:** 2 to 6 Years
**Key Skills:** Develop and implement regulatory filing strategies for row markets. Strong knowledge of ICH guidelines, GMP formats, country-specific regulations in Asia, Latam, Africa, CIS, and the Middle East. Expertise in dossier preparation, submission management, and product approval changes. Excellent communication, project management, and leadership skills. Expertise in regulatory database and submission tools. Assess regulatory risks and provide mitigation strategies. Oversee the preparation, review, and submission of CTD (Common Technical Document) and country-specific dossiers.

How to Apply

Interested candidates with the relevant experience and qualifications are invited to attend the Walk-In Interview at the specified venue and time. Please bring copies of your updated resume and relevant documents for the interview process.

For any queries, you can reach out via email to [email protected] or call HR at 9666 977 644.