Arene Lifesciences Limited, a Hyderabad-based, EU-GMP compliant pharmaceutical company specializing in Active Pharmaceutical Ingredients (APIs) and intermediates, is hosting a walk-in interview for R&D and AR&D positions. With state-of-the-art manufacturing facilities approved by global regulatory bodies like FDA, ANVISA, WHO, Council of Europe (EDQM), CFDA, and OGYEI, we are committed to delivering high-quality, cost-effective pharmaceutical products worldwide. Join our dynamic team to drive innovation in the API bulk drug industry
Event Details
- Dates: April 19 & 21, 2025 (Note: No interviews on Sundays)
- Time: 9:00 AM to 3:00 PM
- Venue: Arene Lifesciences Pvt. Ltd., Corporate Office, SR Chambers, Plot No: 3-58, Ramachandrapuram (RC Puram), Patancheru (M), Sangareddy (D), Telangana – 502032
- Work Location: Sangareddy, Telangana
Open Positions
We are seeking passionate professionals with experience in API bulk drug development to join our Research & Development (R&D) and Analytical Research & Development (AR&D) teams. Candidates with a strong foundation in pharmaceutical research are highly preferred.
R&D Responsibilities and Requirements
- Qualification: B.Sc/M.Sc/B.Tech/M.Tech (Chemistry, Organic Chemistry, or related fields)
- Experience: Freshers or 1-5 years in API bulk drug R&D
- Responsibilities:
- Develop efficient processes and novel chemistry for API synthesis.
- Conduct experiments to optimize reaction conditions and scale-up processes.
- Collaborate with cross-functional teams to support product development.
- Document experimental data and prepare technical reports.
- Requirements:
- Experience in API bulk drug research is advantageous.
- Strong knowledge of organic chemistry and process development.
- Ability to work in a fast-paced, innovation-driven environment.
AR&D Responsibilities and Requirements
- Qualification: B.Sc/M.Sc/B.Tech/M.Tech (Analytical Chemistry, Chemistry, or related fields)
- Experience: 2-5 years in API bulk drug AR&D
- Responsibilities:
- Develop and validate analytical methods for API characterization.
- Perform stability studies and quality control testing using HPLC, GC, and other techniques.
- Review and approve analytical data to ensure compliance with regulatory standards.
- Support regulatory submissions with accurate documentation.
- Requirements:
- Hands-on experience with analytical techniques (HPLC, GC, etc.) in API bulk drug analysis.
- Familiarity with pharmacopeial standards and ICH guidelines.
- Strong attention to detail and problem-solving skills.
How to Apply
Interested candidates should:
- Attend the walk-in interview with an updated resume, passport-sized photographs, and relevant documents.
- Send their CV to careers@arenelife.com prior to the interview.
- Contact: +91 7989746454 for inquiries.
- Visit https://www.arenelifesciences.com/ for more information about our company.
Additional Information
- Note: Experience in API bulk drug development is highly preferred. Arene Lifesciences is proud to hold certifications from FDA, ANVISA, WHO Prequalification of Medical Products, Council of Europe (EDQM), CFDA, and OGYEI, ensuring compliance with global regulatory standards.
- Benefits: Work in a certified, world-class environment with opportunities for professional growth and collaboration with a 50-member strong in-house R&D team.
Contact Us
For inquiries, reach out via email at careers@arenelife.com or call +91 7989746454.
Join Arene Lifesciences and contribute to improving global access to life-saving medications through innovation and quality!