Sr. Associate Scientist, Formulation Development

Hikma Quality

JOB PURPOSE:

To conduct scientific studies and experiments to develop new products and technologies and improve existing ones.

Key Responsibilities:

• Follows all relevant departmental policies, processes, standard operating procedures, and instructions so that work is carried out in a controlled and consistent manner during Day-to-day operations.
• Follows the day-to-day operations related to own job to ensure continuity of work Job Specific Accountabilities
• Implements all analytical research activities including initiation, designs, routine procedures, and reports on any faced issues to support product development efficiently.
• Conducts the development activities for basic pharmaceutical formulations including initiation and reporting any faced obstacles to support product development in a timely manner with considerations for scale-up/ tech-transfer.
• Demonstrates excellent oral and written communication skills with the ability to present results through written reports, publications, and related documentation.
• Summarizes and critically evaluates the study results in order to develop and test new hypotheses, execute experiments and author technical reports.
• Participates in the development and scale-up processes from bench top to pilot scale to assist in technology transfer to commercial plants.
• Establishes a knowledge base by actively seeking out technologies and tracking publications in relevant fields to keep the company informed of research and industry developments.
• Gathers and provides new perspectives, arriving at solutions based on multiples sources of information to evaluate and solve complex technical challenges that arise on both internal and external projects.
• Analyses and evaluates test results to make well-reasoned strategic recommendations that inform future R&D decisions at the company.
• Collaborates and gains commitment with stakeholders internally and externally to achieve project objectives in support of product development and approval Continuous Improvement
• Contributes to the identification of opportunities for continuous improvement of processes and practices considering international best practice , improvement of business processes, cost reduction and productivity improvement Reporting.
• Assists in the preparation of timely and accurate reports of Research & Development to meet company and department requirements, policies and standards Safety, Quality & Environment
• Complies with all relevant safety, quality and environmental management policies, procedures, and controls to ensure a healthy and safe work environment. Related Assignments
• Performs other related duties or assignments as directed.

Qualifications:

We are looking for candidates whose experience and skills align closely with the qualifications outlined below:

Experience:

• 1 3 years of relevant experience in pharmaceutical industry in research & development or a laboratory setting.
• Any previous pharmaceutical research experience is a plus

Education:

• Bachelor s degree in Pharmacy or related scientific field with a Masters/PHD preferred.

Language:

• Advanced-level English (written and spoken).

Required Skills:

• Proficiency in MS Office (Word, Excel, PowerPoint).
• Familiarity with SAP (preferred).
• Ability to work independently and manage multiple tasks.
• Strong teamwork and collaboration skills.
• Knowledge of FDA Current Good Manufacturing Practices (cGMP).
• Quick learner with flexibility and adaptability.
• Active listening and strong motivation.