Open Vacancies At Kirovest Pharmaceutical Company

– About Kirovest

Kirovest Pharmaceuticals, located in Al-Obour City, is a leading name in the pharmaceutical industry, dedicated to producing high-quality medications. We are committed to maintaining the highest standards of quality and compliance and are seeking talented individuals to join our Quality Assurance team.

– Open Positions

QA Validation & Calibration Senior Specialist: Minimum 2 years of experience.
QA Validation & Calibration Supervisor: Minimum 5 years of experience with leadership abilities.
QA Documentation Section Head: Minimum 7 years of experience in QA documentation with proven leadership skills.
IPQA Senior Specialist: Minimum 3 years of in-process quality assurance experience.

– Key Responsibilities
For Validation & Calibration Specialists/Supervisors:
Prepare and update validation documents (SOPs, protocols, master plans).
Implement and review validation/revalidation protocols and calibration plans.
Collaborate with external agents for execution of validation activities and review related certificates and reports.
For Documentation Section Head:
Manage QA documentation (SOPs, batch records, protocols) and ensure compliance with regulatory standards.
Lead documentation audits and provide training on document control practices.
For IPQA Senior Specialist:
Monitor manufacturing activities, ensuring compliance with cGMP/GLP standards.
Address deviations in real time and prepare IPQA reports for audits.
– Requirements
Bachelor’s degree in Pharmacy or a related scientific field.
Strong knowledge of cGMP, GLP, and regulatory standards.
Excellent communication, organizational, and computer skills.
Experience requirements:
Validation & Calibration Senior Specialist: 3+ years.
Validation & Calibration Supervisor: 5+ years with leadership skills.
Documentation Section Head: 7+ years with team management experience.
IPQA Senior Specialist: 3+ years in pharmaceutical QA.
– To Apply
Send your updated CV to HR@kirovest.net with the subject line “QA – [Position Title]”.

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 Join Kirovest Pharmaceuticals – We’re Hiring Quality Control & Stability Specialists!

Kirovest Pharmaceuticals is a leading player in the pharmaceutical industry, committed to excellence, innovation, and the production of high-quality medications. As we continue to grow, we’re looking for experienced professionals to join our Quality Control and Stability teams.

🔬 Senior Quality Control Specialist
📌 Responsibilities:
✔ Conduct quality control testing on raw materials, in-process samples, and finished products.
✔ Analyze test results, investigate deviations, and implement corrective actions.
✔ Maintain compliance with GMP regulations and industry standards.

📌 Requirements:
✔ Bachelor’s degree in Pharmacy, Chemistry, or a related field.
✔ 3+ years of experience in pharmaceutical quality control.
✔ Strong knowledge of GMP, analytical techniques, and laboratory equipment.

🧪 Senior Stability Specialist
📌 Responsibilities:
✔ Develop and implement stability protocols for new and existing formulations.
✔ Conduct stability studies and analyze data to assess product shelf-life.
✔ Ensure compliance with ICH guidelines and regulatory requirements.

📌 Requirements:
✔ Bachelor’s degree in Pharmacy, Chemistry, or a related field.
✔ 3+ years of experience in pharmaceutical stability studies.
✔ Expertise in ICH guidelines and stability protocols.

💡 Why Join Kirovest?
✨ Competitive salary & benefits package.
✨ Career growth and development opportunities.
✨ A collaborative and innovative work environment.

Interested? Apply now by sending your CV to hr@kirovest.net with the subject line indicating the position you’re applying for.