Research Associate - Formulation R&D

Trikona Pharmaceuticals; Hyderabad; On-site; INR 500,000 - 900,000; Full time

Job summary

Trikona Pharmaceuticals in Hyderabad is seeking a formulation development professional to take projects from literature survey to commercialization. You will conduct literature and patent searches, prepare pre-product development strategies, and coordinate indents for raw materials and tooling.

You will execute experimental work, document results in lab notebooks, evaluate processes, optimize and scale-up, and ensure timely delivery of product development milestones while adhering to US FDA and

Qualifications

• 2-3 years of experience in production of semi solids, liquids or tablets/capsules.
• Acquaintance with USFDA & ICH guidelines.
• Ability to coordinate with all departments and meet product development timelines.

Responsibilities

• Develop a formulation from literature survey to commercialization.
• Literature, patent search & Preparation of Literature Survey Reports and patent search reports.
• Preparation of pre-product development strategy.
• Indent for raw materials, tooling etc.
• Execution of experimental work & documentation (Lab notebooks) and preparation of the reports.
• Execution of process evaluation, optimization, scale-up and exhibit batches.
• Meeting product development timelines.
• Acquainted knowledge in USFDA & ICH Guidelines.

Skills

Teamwork

Literature survey

Patent search

Process optimization

Scale-up

Documentation

Regulatory knowledge

Job description

• Work with a concept of teamwork (co-ordination and co-working with all departments).
• Development of a formulation from literature survey to commercialization.
• Literature, patent search & Preparation of Literature Survey Reports and patent search reports.
• Preparation of pre-product development strategy.
• Indent for raw materials, tooling etc.
• Execution of experimental work & documentation (Lab notebooks, log book entries) and preparation of the reports.
• Execution of process evaluation, optimization, scale-up and exhibit batches.
• Meeting product development timelines.
• Acquainted knowledge in USFDA & ICH Guidelines.
• 2-3 years of experience in production of semi Solids/ Liquids or tablets/capsules.