Senior Research Scientist

Ortiv-Q3 Research Pvt. Ltd.

Pharmaceutical enterprises worldwide benefit from the unique application know-how and experience of the Ortiv-Q3 Pharma Services team in solving the many issues related to dissolution and release testing from pharmaceutical dosage forms. Our staff, who specialises in in vitro dissolution testing, has a track record of determining the best technique for a wide range of goods, including implants, semi-solids, APIs, tablets, and many more. Situated in a US FDA-inspected facility, our staff's scientific experience combined with state-of-the-art instrumentation offers best-in-class services and ease of regulatory compliance for our customers. We operate in a cGMP-compliant setting with strong quality control standards.

offers a one-stop solution for In-vitro release and dissolution testing of pharmaceuticals. The team specializes in complex formulations and IVRT for regulated markets, particularly in the area of complex injections. Located in Ahmedabad, Ortiv-Q3 is known for its state-of-the-art infrastructure, providing high-quality, scientifically sound analytical and formulation services.

Role Description:

This is a full-time on-site role for an Assistant Manager/Senior Research Scientist/Research Scientist at Ortiv-Q3 Research Pvt. Ltd. located in Ahmedabad (Gujarat). The Assistant Manager/Senior Research Scientist/Research Scientist will be responsible for overseeing research projects, conducting experiments, data analysis, and interpretation. The role includes the formulation and development of complex products, preparing reports, and ensuring compliance with regulatory standards. The Assistant Manager will also be involved in mentoring junior scientists and collaborating with cross-functional teams.

Qualifications:

Experience in Nitrosamine Impurities, Genotoxic and NDSRI method development, validation and confirmatory.
Preparation and review of technical reports and Investigation reports.

Assist in planning and execution of LC-MS-MS activities.
Troubleshoot analytical equipment and ensure proper calibration.Strong analytical and problem-solving skills.

Excellent communication and documentation skills.
Strong research, experimental design, and data analysis skills.Experience in complex formulations and IVRT.Understanding of regulatory standards and compliance.Excellent written and verbal communication skills.Leadership and team management abilities.Experience in the pharmaceutical or related industry is a plus.

Experience: 08-10 Years
Qualification: MSc/ M. Pharm, Master's or Ph.D. in Chemistry, Pharmaceutical Sciences, or related field.Position: 01

Job Types: Full-time, Permanent

Pay: From ₹700,000.00 per year

Benefits:

• Food provided
• Health insurance
• Paid sick time
• Paid time off
• Provident Fund

Ability to commute/relocate:

• Sanathal, Ahmedabad, Gujarat: Reliably commute or planning to relocate before starting work (Preferred)

Application Question(s):

• Are you okay with 2.0 Years of bond ..?

Education:

• Master's (Preferred)

Experience:

• Clinical laboratory: 8 years (Preferred)

Language:

• English / Hindi (Preferred)

Location:

• Sanathal, Ahmedabad, Gujarat (Preferred)

Shift availability:

• Day Shift (Preferred)

Willingness to travel:

• 25% (Preferred)

Work Location: In person

Expected Start Date: 08/08/2025