- Full Time
- Telangana

Website Sandoz
Job Title: Associate Scientist IVIVC (Biopharmaceutics)
Location: Telangana, India
Company: Sandoz
Join Sandoz – A Global Leader in Generics and Biosimilars!
About Sandoz
Sandoz has emerged as a standalone organization, moving forward from a position of strength as a global market leader in Generics and Biosimilar medicines. Be part of a transformative journey that will shape the future of healthcare, innovation, and culture at Sandoz. As we continue to impact millions of lives globally, this is your chance to embark on a career that truly makes a difference.
We are seeking passionate and talented individuals to join our team in shaping the future of Sandoz, driving innovation, and contributing to the growth of the company. This is an exciting opportunity for an Associate Scientist IVIVC (Biopharmaceutics) to be part of our dynamic team.
Job Summary:
As an Associate Scientist in IVIVC (Biopharmaceutics), you will be responsible for planning and conducting scientific experiments to support the development and delivery of drug products (DP). Working closely with a multifunctional project team, you will contribute to the design, optimization, and execution of scientific processes in accordance with regulatory standards. This role offers the opportunity to drive innovation in biopharmaceutics, delivering high-quality and stable dosage forms.
Key Responsibilities:
- Plan and perform scientific experiments, including pilot plant processes, for the development of drug products (DP).
- Develop and optimize biorelevant and discriminatory dissolution methods that mimic physiological conditions.
- Perform and document solubility experiments, dissolution method activities, and other characterization techniques such as DT, solubility, IDR, and viscosity.
- Analyze samples using analytical techniques like HPLC/UPLC and spectrophotometric methods, troubleshooting chromatographic challenges as needed.
- Design and manage experiments for low-complexity products under supervision, preparing scientific documentation.
- Collaborate with project teams to support the development of bioequivalent, stable, and cost-effective dosage forms.
- Assist with the preparation and review of the technological parts of dossiers.
- Provide support in developing in-silico tools like Gastroplus and Phoenix WinNonlin in collaboration with modeling experts.
Candidate Profile:
- Education: M.Pharm (Pharmaceutical Analysis, Pharmaceutics), MSc (Analytical Chemistry), or B.Pharm.
- Experience: 2-4 years in analytical development within the generic pharmaceutical industry.
- Skills:
- Strong experience in biopharmaceutics and dissolution method development.
- Proficiency in analytical techniques (HPLC/UPLC, spectrophotometry) and troubleshooting.
- Ability to work independently and collaboratively within a team.
- Strong written and oral communication skills.
- Familiarity with PBPK/IVIVC models is a plus.
Additional Information:
- Experience Required: 2-4 years
- Location: Telangana, India
- Industry Type: Pharma/Healthcare/Clinical Research
- Functional Area: Biopharmaceutics
- Application Deadline: 30th October 2024
Make a Real Impact at Sandoz!
Join us in our journey to deliver innovative healthcare solutions. Apply today and become part of a team that is shaping the future of Sandoz!
- For more articles, Kindly Click here
- For pharmaceutical jobs, follow us on LinkedIn
For more jobs, kindly visit our job section.
To apply for this job please visit novartis.wd3.myworkdayjobs.com.