Job Description

Overview:

We are seeking a skilled and experienced Manufacturing Chemist with expertise in Formulation & Development (F&D) specifically for Injection Liquids. The ideal candidate will play a pivotal role in our pharmaceutical manufacturing operations, contributing to the formulation, development, and production of high-quality injectable liquids.

Key Responsibilities:

Formulation Development:

Lead the formulation development activities for injectable liquids, ensuring compliance with regulatory standards and guidelines.

Conduct feasibility studies, stability testing, and process optimization to ensure robust formulations.

Process Development:

• Design and optimize manufacturing processes for injectable liquids, focusing on efficiency, scalability, and quality.
• Collaborate with cross-functional teams to implement new technologies and improvements in production processes.

Quality Assurance and Control:

• Oversee quality control measures throughout the manufacturing process to maintain product integrity and compliance with regulatory requirements.
• Conduct investigations and implement corrective actions for any deviations or non-conformities.

Regulatory Compliance:

• Stay updated with regulatory requirements and guidelines related to injectable liquids.
• Prepare and review documentation for regulatory submissions and inspections.

Project Management:

• Manage projects related to formulation development and process optimization, ensuring timelines and milestones are met.
• Coordinate activities with internal departments and external partners as necessary.

Training and Development:

• Train and mentor junior staff members in formulation techniques, process development, and regulatory compliance.

Qualifications & Skills :

• Bachelor's or Master's degree in Pharmacy, Pharmaceutical Sciences, Chemistry, or related field.
• Above 10 years of experience in pharmaceutical manufacturing, with a focus on injectable liquids.
• Proven experience in formulation development and process optimization.
• Strong knowledge of regulatory guidelines (FDA, EMA,EU etc.) and GMP requirements.
• Excellent project management skills with the ability to manage multiple projects simultaneously.
• Effective communication and interpersonal skills, with the ability to work collaboratively in a team environment.

Job Types: Full-time, Permanent

Work Location: In person