Vital Therapeutics & Formulations Pvt. Ltd., a fast-growing pharmaceutical company in Hyderabad, is hosting a Walk-In Interview for Analytical Research & Development (AR&D), Formulation Research & Development (FR&D), Development Quality Assurance (DQA), and Regulatory Affairs (RA) roles on 3 May 2025.
With over 15 years of expertise in contract manufacturing, vitamins, nutraceuticals, and animal health products, Vital Therapeutics is a trusted partner to global MNCs like Pfizer and Dr. Reddy’s, operating a USFDA, WHO-GMP, ISO 9001, and FSSC 22000-certified facility. Join us in Cherlapally, Hyderabad, to advance your career in the pharmaceutical industry.
Job Openings Overview for AR&D, FR&D, DQA, and Regulatory Affairs Roles
We are hiring for the following positions at our Research and Development Center in Cherlapally, Hyderabad:
Analytical Research & Development (AR&D)
- Designation: Officer/Executive/Sr. Executive
- Qualification: M.Pharm, M.Sc, Ph.D
- Experience: 2–10 years in Formulations
Formulation Research & Development (FR&D)
- Designation: Officer/Executive/Sr. Executive
- Qualification: M.Pharm, M.Sc, Ph.D
- Experience: 2–10 years in Formulations
Development Quality Assurance (DQA)
- Designation: Officer/Executive
- Qualification: B.Pharm, M.Pharm, M.Sc
- Experience: 2–6 years in Formulations
Regulatory Affairs (RA for ROW Markets)
- Designation: Officer/Executive
- Qualification: M.Pharm (Regulatory Affairs)
- Experience: 2–6 years in Formulations
Work Location: Cherlapally (near Habsiguda, ECIL, Kushaiguda), Hyderabad, Telangana
Interview Date: Saturday, 3 May 2025
Interview Time: 10:30 AM
Interview Venue: Vital Therapeutics and Formulations Pvt. Ltd., Plot No: 47 B/2, St. No. 4, Phase-I, IDA, Cherlapally, Secunderabad, Telangana
Job Description for AR&D, FR&D, DQA, and Regulatory Affairs Roles
Qualifications
- AR&D: M.Pharm (Pharmaceutical Analysis), M.Sc (Analytical Chemistry), Ph.D in related fields.
- FR&D: M.Pharm (Pharmaceutics), M.Sc (Chemistry), Ph.D in related fields.
- DQA: B.Pharm, M.Pharm (Quality Assurance), M.Sc (Chemistry, Biotechnology).
- RA: M.Pharm (Regulatory Affairs).
- Strong academic records from recognized institutions are required.
Experience
- AR&D/FR&D: 2–10 years in formulation development or analytical research for pharmaceuticals or nutraceuticals, preferably in OSD, liquids, or injectables.
- DQA/RA: 2–6 years in development quality assurance or regulatory affairs for formulations, with exposure to USFDA, EMA, or ROW markets (Asia, LATAM, Africa, CIS, Middle East).
Skills
Analytical Research & Development (AR&D):
- Expertise in Analytical Research Method Development (ARMD) and method validation using HPLC, GC, and wet analysis.
- Proficiency in implementing Good Laboratory Practices (GLP) and Good Documentation Practices (GDP).
- Knowledge of ICH guidelines for analytical method development and validation.
- Familiarity with software like Empower or Chromeleon for analytical data management.
Formulation Research & Development (FR&D):
- Skills in designing, developing, and optimizing formulations for pharmaceuticals (e.g., tablets, capsules, liquids) or nutraceuticals.
- Expertise in Quality by Design (QbD) implementation for formulation development.
- Ability to prepare technical documents (e.g., formulation protocols, reports).
- Strong collaboration with AR&D and DQA teams to ensure regulatory compliance.
Development Quality Assurance (DQA):
- Proficiency in leading QA activities for product development, including design, testing, and validation.
- Knowledge of FDA, EMA, and GMP regulatory guidelines.
- Skills in developing quality control procedures and implementing QbD systems.
- Expertise in risk assessment, continuous improvement, and QMS (e.g., Change Control, CAPA).
- Ability to collaborate with R&D and AR&D to address quality issues.
Regulatory Affairs (RA for ROW Markets):
- Strong knowledge of ICH guidelines, CTD formats, and country-specific regulations for Asia, LATAM, Africa, CIS, and the Middle East.
- Expertise in dossier preparation, submission management, and post-approval changes.
- Proficiency in regulatory databases and submission tools.
- Skills in regulatory risk assessment and mitigation strategies.
- Excellent communication, project management, and leadership abilities.
Responsibilities
Analytical Research & Development (AR&D):
- Develop and validate analytical methods using HPLC, GC, and wet analysis for formulations.
- Ensure compliance with GLP, GDP, and ICH guidelines during method development.
- Prepare and review validation protocols, reports, and SOPs.
- Support stability studies and method transfer to quality control.
Formulation Research & Development (FR&D):
- Design and optimize formulations for pharmaceuticals or nutraceuticals using QbD principles.
- Prepare formulation protocols, development reports, and technical documents for regulatory submissions.
- Collaborate with AR&D, DQA, and production teams to ensure scalability and compliance.
- Conduct pre-formulation studies and process optimization for new products.
Development Quality Assurance (DQA):
- Oversee quality assurance during product development, ensuring compliance with FDA, EMA, and GMP standards.
- Develop and implement quality control procedures and QbD systems for new products.
- Conduct risk assessments and manage QMS activities (e.g., Deviations, CAPA).
- Support R&D and AR&D teams in resolving quality issues and preparing for audits.
Regulatory Affairs (RA for ROW Markets):
- Develop regulatory filing strategies for ROW markets (Asia, LATAM, Africa, CIS, Middle East).
- Prepare and review CTD dossiers and country-specific submissions for product approvals.
- Manage post-approval changes and ensure compliance with ICH and regional regulations.
- Assess regulatory risks and provide mitigation strategies to ensure timely approvals.
Walk-In Interview Details for Pharmaceutical Jobs
Join us to explore these pharmaceutical career opportunities and meet our recruitment team:
- Date: Saturday, 3 May 2025
- Time: 10:30 AM
- Venue: Vital Therapeutics and Formulations Pvt. Ltd., Plot No: 47 B/2, St. No. 4, Phase-I, IDA, Cherlapally, Secunderabad, Telangana
Documents to Bring:
- Latest copy of resume
- Offer letter, increment letter
- Last 3 months’ payslips and bank statement
- Previous company service letters
- All educational certificates (M.Pharm, M.Sc, B.Pharm, Ph.D)
- Aadhar and PAN card copies
Contact:
- Email: hr@vitalpharma.in
- Phone: 9666 977 644
Note: Immediate joiners are preferred. Vital Therapeutics & Formulations Pvt. Ltd. does not charge any fees for recruitment. Beware of fraudulent offers requesting payments and report suspicious activities to hr@vitalpharma.in.
How to Apply for AR&D, FR&D, DQA, and Regulatory Affairs Jobs
Candidates can attend the walk-in interview with the required documents or apply online:
- Email: Send your CV to hr@vitalpharma.in with the subject line “Application for [Department Name] – Hyderabad Walk-In 3 May 2025.”
- Website: Visit www.vitalpharma.in for more details about Vital Therapeutics & Formulations Pvt. Ltd. and career opportunities.
Why Join Vital Therapeutics & Formulations for Your Pharmaceutical Career
Vital Therapeutics & Formulations Pvt. Ltd., based in Hyderabad, is a leading contract manufacturing organization with a 10 crore tablet/month capacity and expertise in oral solids, liquids, and nutraceuticals. Certified by USFDA, WHO-GMP, ISO 9001, and FSSC 22000, we serve global MNCs like Pfizer and Dr. Reddy’s. By joining our Cherlapally team, you will:
- Work in a USFDA-approved R&D facility with advanced instrumentation and exposure to global standards.
- Contribute to innovative formulations for pharmaceuticals, nutraceuticals, and animal health products.
- Benefit from a collaborative culture rated 3.8/5 for work environment (based on employee reviews).
- Gain hands-on experience in AR&D, FR&D, DQA, and Regulatory Affairs with opportunities for skill development.
- Be part of a company committed to quality assurance and customer delight in over 60 countries.
Don’t miss this opportunity to advance your career in pharmaceutical R&D jobs, quality assurance jobs, or regulatory affairs jobs with Vital Therapeutics & Formulations Pvt. Ltd. We look forward to meeting you at the walk-in interview on 3 May 2025 in Cherlapally, Hyderabad!
