Research Associate II/III - FR&D (OSD & Injectable)

Why This Role Matters
The Research Associate II/III – FR&D (OSD & Injectable) role at Jodas Expoim is critical in driving innovation in pharmaceutical development. This position supports the formulation research and development (FR&D) of both oral solid dosage (OSD) and injectable products. By contributing to pre-formulation, formulation design, process optimization, and dossier preparation, the role ensures that high-quality, safe, and effective medicines are developed for global markets. Professionals in this position play a pivotal role in accelerating product development timelines while maintaining regulatory compliance.

Job Description
The Research Associate II/III – FR&D will be responsible for the design, development, and scale-up of pharmaceutical formulations for both OSD and injectable products. This role involves conducting experimental work, analyzing results, and preparing regulatory-ready documentation. You will work closely with cross-functional teams including analytical development, quality assurance, and manufacturing to ensure the smooth transition of products from lab to commercial scale.

Key Features of the Role:
• Work on innovative pharmaceutical products, including oral solid dosage and injectables
• Involvement in pre-product development strategy and literature review
• Exposure to formulation optimization, process characterization, and scale-up
• Preparation of dossier-ready documentation for regulatory submissions
• Collaborative environment with experienced R&D and QA professionals
• Opportunity to gain expertise in both OSD and sterile injectable formulations
• Hands-on experience in experimental design and problem-solving in a lab setting

Responsibilities:
• Conduct literature and patent reviews to support pre-product development strategies
• Execute experimental work and accurately report observations
• Compile pre-formulation data for active pharmaceutical ingredients and excipients
• Prepare tentative and final input specifications for formulations
• Develop master formula records, process characterization protocols, and reports
• Prepare product development reports and related regulatory documentation for dossier filing
• Execute process evaluation, optimization, and scale-up activities for new and modified products
• Develop exhibit batches for testing and validation
• Collaborate with analytical, QA, and manufacturing teams to ensure smooth technology transfer
• Maintain accurate records and adhere to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP)

Core Competencies:
• Knowledge of OSD and injectable formulation principles
• Understanding of pre-formulation, formulation development, and process scale-up
• Familiarity with regulatory requirements for dossier submission
• Strong analytical and problem-solving skills
• Attention to detail and ability to maintain high-quality documentation
• Effective communication and teamwork skills
• Ability to work independently and manage multiple projects in parallel

Required Qualifications:
• B.Pharm / M.Pharm / M.Sc in Chemistry or Pharmaceutics
• 3–6 years of experience in formulation R&D, including OSD and injectable products
• Experience in process optimization, scale-up, and experimental design
• Familiarity with regulatory documentation, master formula records, and product development reports

Experience and Skills:
• Proven experience in pharmaceutical formulation R&D for OSD and injectables
• Knowledge of excipient compatibility, pre-formulation, and process characterization
• Hands-on laboratory skills and ability to execute experiments independently
• Ability to compile and maintain comprehensive regulatory documentation
• Understanding of Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP)
• Strong technical writing and reporting skills

Salary Insights:
• Competitive and commensurate with experience

Number of Positions:
• 02 – OSD formulation
• 05 – Injectable formulation

Company Overview:
Jodas Expoim is a leading pharmaceutical organization specializing in the development of oral and injectable formulations. Known for its focus on innovation, quality, and regulatory compliance, the company serves both domestic and international markets. With advanced R&D and manufacturing capabilities, Jodas Expoim is committed to delivering high-quality medicines that improve patient outcomes globally.

FAQs:
• What is the required experience?
– 3–6 years in FR&D for OSD and injectable formulations

• What qualification is required?
– B.Pharm, M.Pharm, or M.Sc in Chemistry or Pharmaceutics

• What products will I work on?
– Oral solid dosage forms and sterile injectable formulations

• Is regulatory knowledge important?
– Yes, experience in preparing master formula records, product development reports, and dossiers is essential

• Is lab work required?
– Yes, hands-on execution of experiments and formulation work is a core responsibility

Application Tips:
• Highlight experience in OSD and injectable formulation development
• Showcase familiarity with pre-formulation studies, excipient compatibility, and scale-up processes
• Emphasize regulatory documentation experience for dossier filing
• Demonstrate problem-solving, analytical, and technical reporting abilities
• Include experience in master formula preparation, process characterization, and optimization