Müsahibə əsasında
Vakansiya haqqında
Key Responsibilities:
- Expand the existing quality system to include cGMP requirements and create/update necessary SOPs, forms, and documents.
- Maintain the assigned QMS system up-to-date and follow up the in-progress system’s activities, postpone and record closure as per the procedural timeline.
- Lead investigations for site non-conformity issues.
- Maintain the Site documentation updated, reviewed/approved, distributed to the required end users and archived.
- Escalate to the Quality Manager any situation that poses risk to the QMS system implementation, product quality and patient safety.
- Support internal and external audits by preparing documentation, leading audits, writing reports, agreeing on CAPAs, and ensuring effective follow-up.
- Perform trending of QMS modules including exception management, supplier assessment, annual product review and quality council reporting.
- Maintain self-training according to training plan and stay updated with the pharmaceutical guidelines.
- Review, criticize and approve GxP documentation from different departments including but not limited to BMR, validation documentation, different studies, specifications, BOM, testing methods.
- Control and organize the site document Archive and the retained sample area.
Requirements:
- Bachelor’s degree in chemistry or a related field
- Strong knowledge of MS Office programs
- Excellent documentation and report preparation skills
- Familiarity with quality assurance systems (GMP, ISO, CAPA, Deviation, Change Control, etc.)
- Minimum 2–3 years of experience in quality assurance in the pharmaceutical or manufacturing industry
- Strong analytical thinking and problem-solving skills
- Ability to work in a team and manage projects
- Good command of English (written and spoken)
- Ability to adapt quickly to a dynamic work environment and shifting priorities
Benefits:
- Shuttle bus
- Lunch
- Pasha Insurance
- Pasha Life (Endowment insurance)
Working Conditions:
- Working Hours: 5 days a week, from 09:00 to 18:00.
- Workplace: Hokmali village, Absheron district, 15 km from the Baku-Shamakhi highway.
Interested candidates can directly send their CV via LinkedIn or to the e-mail address in the Apply for job button and indicate in the subject line that they are applying for the position of “Quality Assurance Specialist”.
Note: Applications from candidates who do not meet the job requirements, do not follow the above-mentioned instructions, or apply after the specified deadline will not be considered.
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