R&D Assistant Manager Job at HRLeverage
- Sagamu, Ogun State
- Permanent
- Full-time
- 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.
- 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.
- 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.
Interested and qualified candidates should send their CV and Cover Letter to:
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