Category
General
Publish Date
Tuesday 19-08-2025
Country
Egypt
Gender
any
Years Of Experience
6 - 9 Years
Salary
Negotiable
“AS&T Scientist “is required for a multinational Health Care company located in New Cairo
Responsibilities:
- Takes active role for Technology Transfer, ASQ (Alternative Supplier Qualifications), Capacity Expansions projects.
- Drives continuous improvement projects, analytical improvements, (remediation, development and validation) and responds to technical issues resulting from quality, manufacturing, and / or regulatory to ensure product reliability and cost leadership.
- Collaborates with Divisional MS&T and Regional MS&T Teams (APAC, LATAM, RUSSIA) to ensure providing technical support to METAP-CIS region, if needed.
- Participate and provide formulation and process-based guidance to validation studies examined for existing or new products manufactured by TPMs.
- Find a solution to manufacturing problems or any other issues to maintain a robust flow of finished products from TPM to avoid any potential back orders.
- Participate and monitor the validation studies of the new products, provide feedback and secure the compliance of the validated parameters.
- Review documentation / product samples shared by TPM and assess the risks associated with the manufacturing of the product under the Company Logo.
- Coordinates technical effort and update documents where required for regulatory agencies.
- Reviews and approves validation protocols/reports, technical development and justification reports.
Requirements:
- Bachelor’s degree in a scientific or technical field, preferably in Life Sciences, Pharmacy or Engineering.Master’s degree or PhD is preferred.
- 6+ years’ experience in the Pharmaceutical Industry, preferably in R&D and Quality Control is required.
- Excellent technical know-how on analytical method development and Test Method transfer.
- Competency in the operation and troubleshooting of HPLC, UPLC, LC-MS, GC or ICP-MS
- Excellent command on pharmacopoeias and ICH guidelines.
- Experience in support of marketed products and analytical studies
- Process and understanding of business needs and the ability to translate them into actions to meet timelines.
- Have a good knowledge of cGMP (Good Manufacturing Practices) and about product transfer, process validation activities.
- Fluent in English is a must.
