Senior Executive & QA Inspector

jamjoompharma/careers; Jeddah; On-site; SAR 150,000 - 200,000; Full time

Job summary

A leading pharmaceutical company in Jeddah is seeking a Quality Control Specialist to oversee production processes and ensure quality standards are met. The ideal candidate will have a Bachelor's Degree in Life Sciences, Biochemistry, or Pharmacy, along with a minimum of three years' experience in the pharmaceutical industry. The role involves line clearance, stability monitoring, and compliance with quality regulations. Strong communication and data analysis skills are essential.

Qualifications

• Minimum of 3 years’ experience in the pharmaceutical industry or related operations.

Responsibilities

• Oversee the entire production process ensuring quality standards.
• Conduct line clearance approval and In-process Checks.
• Monitor ongoing stability plan and retain sample management.
• Manage quality events and deviations.
• Ensure cGMP compliance.

Skills

Interactive communication skills

Data analysis

Good observation capabilities

Education

Bachelor's Degree in Life Sciences, Biochemistry or Pharmacy

Job description

Jamjoom Pharma has in a very short span of time emerged, as one of the leading pharmaceutical companies in the Afrasia region. The geographical focus of the company is on countries in the Middle East, Africa, and CIS regions. Strategic focus on selected therapeutic categories has contributed to the rapid growth, market acceptance, and overall success of the company.

Role Summary:

• Overseeing the entire production process, looking out for specific problems, minutely observing the units of goods produced for visible defects.
• Ensuring that the units produced adhere to an established quality standard.
• Performing various tests (IPC) on the samples drawn, noting down observations, samples inspections, and stability studies samples collection

Responsibilities:

• Line clearance approval and In-process Checks
• Monitoring of Ongoing stability plan (Exhibit/Validation)
• Retain sample Management
• Quality Event and Deviation Management
• Sampling
• cGMP compliance

Qualifications:

• Bachelor's Degree in Life Sciences, Biochemistry or Pharmacy
• A minimum of 03 years’ experience in the same pharmaceutical industry / In Process Quality Operation / Manufacturing Function.
• Interactive communication skills and computer skills.
• Data analysis and good observation capabilities