Skills Required المهارات المطلوبة
R&D/Science
Analyst/Research
Pharmaceutical
Pharmaceutical
Research
Formulation
English
Microsoft Office
Pharmacy
Science
Computer Skills
R&D
Troubleshooting
GMP
Leadership
Development
ctd
Management
Job Description الوصف الوظيفي
We Are Hiring: Formulation Section Head
We are looking for a Formulation Section Head to join our team. The selected candidate will lead the formulation development team responsible for designing, developing, and optimizing pharmaceutical formulations for different dosage forms.
Job Responsibilities:
Lead the investigation into complex formulation failures, stability issues, or out-of-specification
(OOS) results during development
Supervise the transition of products from the R&D pilot scale to full-scale production, ensuring
successful process validation.
Assist in checking the maintenance of the department, premises, and equipment.
Ensure that R&D investigation results are properly documented.
Proposal for specifications of starting materials, packaging materials, and intermediate, bulk, and
finished products in relation to their stability recommendations with the QC staff.
Co-ordinate new methods of analysis, Validation, and stability study required for new products under registration. With QC staff.
Co-ordinate with the QA validation team to begin validation processes according to the schedule
Assist with production for the first three production batches.
Help the existing formulation team in collecting all the required tasks concerning the new product developments.
Solve troubleshooting problems when occurred in the minimized time.
Help in the revision of the sent Certificates of Analysis (COAs) of Active Pharmaceutical Ingredients (APIs) and excipients.
Update and revise Common Technical Document (CTD) files.
Manage multiple projects simultaneously, prioritizing tasks.
Provide technical guidance and expertise in formulation development, formulation optimization, and scale-up.
Collaborate with cross-functional teams, including the R&D analytical team, production, and regulatory affairs.
Ensure accurate and timely documentation of formulation development activities, including reports, protocols, and Standard Operating Procedures (SOPs).