Senior R&D Formulator

Basic Role Summary:

This is an excellent opportunity to join a dynamic team within our Veterinary Research and Development function. We are looking for an individual who will support and drive Chanelle Pharma’s vision to be the most valued global provider of high‑quality, competitively priced pharmaceutical products and to provide excellent services and support to our customers.

In this role, you will work closely with R&D Management and the wider team to support formulation development, scale‑up activities, and technical transfers. You will lead formulation development activities, oversee experimental design and execution, support manufacturing equipment setup and optimisation, and drive the successful transfer of products into commercial manufacture. You will report to the R&D Manager or designee.

Location: Onsite at our facility in Amman, Jordan.

As our Senior R&D Formulator Scientist, your key responsibilities will be as follows:

• Lead formulation development and scale‑up for solid, semi‑solid, and liquid dosage forms (sterile and non‑sterile), providing technical direction with minimal supervision.

• Optimise and oversee manufacturing equipment setup and operation to ensure efficient development and pilot‑scale execution.

• Plan, execute, and critically assess formulation trials, ensuring robust documentation and data integrity.

• Drive technology transfer activities, including process optimisation, pilot batch execution, and cross‑functional troubleshooting.

• Prepare, review, and approve scientific documentation such as batch records, protocols, technical reports, and validation‑related materials.

• Act as a key technical liaison with Production, Planning, Validation, Procurement, and Engineering to resolve challenges and maintain project timelines.

• Prepare and review technical documentation for regulatory submissions and provide scientifically robust responses to regulatory authority queries.

• Champion GMP, safety, and continuous improvement initiatives within the R&D environment.

• Lead or contribute to investigations, deviations, and change controls, ensuring timely and scientifically sound closure.

• Maintain high standards of housekeeping and equipment care across development areas.

• Represent R&D during internal and external audits, providing technical input and supporting corrective actions.

• Promote adherence to R&D procedures and identify opportunities for system and process optimisation.

Qualifications and Experience:

• Degree in Pharmaceutical Sciences or a related field.

• Significant experience in formulation development within a GMP manufacturing or R&D environment.

• Strong working knowledge of oral solid and/or liquid dosage manufacturing processes.

• Deep understanding of GMP and regulatory expectations.

Skills and Competencies:

• Strong technical competence with manufacturing equipment and ability to troubleshoot complex issues.

• Excellent attention to detail with strong data interpretation and decision‑making capability.

• Strong communication and collaboration skills, including the ability to guide and support junior team members.

• Proactive problem‑solver with a focus on continuous improvement.

• Strong organisational skills with the ability to manage multiple complex priorities.

• Demonstrates leadership, initiative, and commitment to high‑quality delivery.

• Proficiency in MS Office; experience with technical or data analysis tools is advantageous.

Applicants from diverse backgrounds, including those returning after a career break or with transferable skills from non‑traditional career paths, are encouraged to apply. We value varied experiences and are committed to fostering an inclusive environment that supports individuals with disabilities.