Junior Officer

Accent Biosciences; Bharuch District; Vor Ort; INR 350.000 - 550.000; Vollzeit

Zusammenfassung

Accent Biosciences is seeking a capability-driven R&D professional in Gujarat, India. The role covers end-to-end R&D, from formulation development to process optimization, with emphasis on documentation and compliance.

Ideal candidates have up to 3 years in R&D/product development, strong analytical abilities, and familiarity with GMP/ISO standards. The position involves lab trials, tech transfer activities, and collaboration with QC and production teams.

Qualifikationen

• Fresher to 3 years of experience in R&D, Product Development, or Process Development.
• Knowledge of GMP/ISO requirements.
• Excellent documentation and record-keeping skills.
• Proficiency in MS Office (Word, Excel, PowerPoint).

Aufgaben

• Conduct research and development activities as per project requirements.
• Develop new products, formulations, and manufacturing processes.
• Perform laboratory trials and pilot-scale studies.
• Optimize existing products and processes for improved efficiency and quality.
• Evaluate raw materials and alternative sources.
• Prepare and maintain R&D reports, protocols, and records.
• Prepare product development reports and technical documents.
• Maintain laboratory notebooks and trial records.
• Assist in scale-up activities from laboratory to production.
• Coordinate technology transfer activities with Production and QA departments.
• Provide technical support during commercial manufacturing.
• Follow GMP, GLP, and company safety requirements.
• Ensure proper handling and storage of chemicals and samples.
• Maintain cleanliness and organization of the laboratory.
• Participate in audits and regulatory inspections.

Kenntnisse

Product development

Process optimization

Laboratory practices

Documentation skills

GMP/ISO knowledge

MS Office

Analytical and problem solving

Communication and teamwork

Ausbildung

B.Sc./M.Sc. (Chemistry)

B.Pharm./M.Pharm.

B.E./B.Tech. (Chemical Engineering)

Or equivalent qualification

Jobbeschreibung

Research & Development

• Conduct research and development activities as per project requirements.
• Develop new products, formulations, and manufacturing processes.
• Perform laboratory trials and pilot-scale studies.
• Optimize existing products and processes for improved efficiency and quality.
• Evaluate raw materials and alternative sources.

Documentation

• Prepare and maintain R&D reports, protocols, and records.
• Prepare product development reports and technical documents.
• Maintain laboratory notebooks and trial records.
• Support preparation of SOPs, specifications, and validation documents.

Testing & Analysis

• Coordinate with QC department for analytical testing.
• Analyze test results and prepare conclusions.
• Investigate product and process-related issues.
• Support troubleshooting during manufacturing.

Technology Transfer

• Assist in scale-up activities from laboratory to production.
• Coordinate technology transfer activities with Production and QA departments.
• Provide technical support during commercial manufacturing.

Compliance & Safety

• Follow GMP, GLP, and company safety requirements.
• Ensure proper handling and storage of chemicals and samples.
• Maintain cleanliness and organization of the laboratory.
• Participate in audits and regulatory inspections.

Educational Qualification

• B.Sc./M.Sc. (Chemistry)
• B.Pharm./M.Pharm.
• B.E./B.Tech. (Chemical Engineering)
• Or equivalent qualification

Experience

• Fresher to 3 years of experience in R&D, Product Development, or Process Development.

Skills Required

• Knowledge of product development and process optimization.
• Good laboratory practices and documentation skills.
• Knowledge of GMP/ISO requirements.
• Strong analytical and problem-solving skills.
• Proficiency in MS Office (Word, Excel, PowerPoint).
• Good communication and teamwork abilities.

Key Performance Indicators (KPIs)

• Timely completion of R&D projects.
• Successful product development and scale-up.
• Accuracy of documentation.
• Compliance with quality and safety requirements.
• Reduction in process costs and improvement in product quality.