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Associate Scientist, Formulation Development / Research & Development Pharm at Hikma Pharmaceuticals PLC

, , Egypt -

Full Time

Start Date

Immediate

Expiry Date

26 Jun, 26

Salary

0.0

Posted On

28 Mar, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Formulation Development, Product Development, Literature Survey, Pre-formulation, Formulation Trials, Documentation, Reporting, Laboratory Instruments Operation, GMP Standards, SOPs, Stability Studies, Bio-equivalence Studies, Pilot Batches, Scaling Up, Validation Batches, Tech Transfer

Industry

Description

Job Purpose: To implement activities related to product development including formulations development, analysis and reporting any faced issues to achieve product development in a timely manner with considerations for scaleup and tech transfer. Duties & Responsibilities: Literature survey and performing pre-formulation & formulation trials for any of the new products to fulfill the company’s research objectives. Documentation and reporting all formulation trials observation and results according to the predetermined procedures. Operate the laboratory instruments and equipment according to their SOPs and Complying to the GMP standards and procedures after having the necessary training. Prepare samples for stability & Bio-equivalence studies. Performing pilot, scaling up & validation batches and preparing the required documents. Complying with the occupational safety and waste procedures in Hikma. To perform any other task related to the job description or nature Job Location: Six October City, Giza Qualifications: Bachelor’s degree in Pharmacy with grade Very good or Excellent Minimum Experience: 0-1 years of experience in same field Fluency in English, both written and verbal

Responsibilities

The role involves implementing product development activities, including formulation development, analysis, and reporting observations from literature surveys and formulation trials to meet research objectives. Duties also include operating lab equipment under GMP standards, preparing samples for stability studies, and performing scaling up and validation batches.