R&D Assistant Manager

Job Description

• We are seeking a highly motivated and experienced R&D Assistant Manager to join our Research and Development team at our pharmaceutical factory.
• The R&D Assistant Manager will play a key role in supporting the development and optimization of pharmaceutical formulations, processes, and analytical methods.

Key Responsibilities

• Collaborate with R&D team members to design and execute experiments for the development and optimization of pharmaceutical formulations, processes, and analytical methods.
• Perform laboratory experiments, analyze data, and interpret results to support product development and process optimization efforts.
• Assist in the preparation and review of technical documents, including study protocols, reports, and regulatory submissions.
• Maintain accurate records of experimental procedures, results, and observations in accordance with Good Laboratory Practices (GLP) and regulatory guidelines.
• Coordinate with cross-functional teams, including Quality Assurance, Regulatory Affairs, and Manufacturing, to ensure alignment and compliance with project timelines and regulatory requirements.
• Stay informed about industry trends, scientific advancements, and regulatory updates relevant to pharmaceutical research and development.
• Contribute to a culture of innovation, collaboration, and continuous improvement within the R&D team and across the organization.

Qualifications

• Bachelor's Degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Chemical Engineering, or related field. Advanced degrees (e.g., Master's or PhD) are preferred.
• Minimum of [3] years of experience in pharmaceutical research and development, with a focus on formulation development and process optimization.
• Strong knowledge of pharmaceutical dosage forms, drug delivery systems, and analytical techniques commonly used in pharmaceutical R&D.
• Experience with laboratory equipment, instrumentation, and software for formulation development, characterization, and analysis.
• Familiarity with regulatory requirements from agencies such as the FDA, EMA, and ICH guidelines.
• Excellent communication skills, both verbal and written, with the ability to effectively communicate technical information to cross-functional teams.
• Strong organizational skills, attention to detail, and ability to manage multiple projects simultaneously.
• Ability to work independently as well as part of a team in a fast-paced, collaborative environment.