Contract: CDD
Education: Degree in Pharmaceutical Sciences, Chemistry, Biology, or a related field.
Experience: 0–3 years of experience in a pharmaceutical QA role or GMP-regulated environment.
Languages: Good written, spoken, and reading proficiency in Arabic, English, and French.
Professional Knowledge:Strong understanding of cGMP, GLP, GDP, ICH, and WHO guidelines.
Familiarity with QA documentation practices and regulatory inspection requirements.
Knowledge of Pharmacopeial standards (USP, EP, BP, etc.).
Awareness of quality risk management and change control principles.
Experience with documentation systems and electronic quality systems is a plus.
Personal Traits:
Why Join Us?
By joining our team, you'll become part of a dynamic, growth-oriented company that values knowledge, motivation, and attitude. You'll have the chance to significantly impact our success, while working in an environment that encourages continuous learning and career advancement.
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Alger, Algérie
Secteur d'activité
Industries
Date d'expiration
10 juillet
Niveau de poste
Débutant / Junior | Confirmé / Expérimenté
Nombre de postes
1 poste ouvert
Type de contrat
CDD Ou Mission
Niveau d'étude (diplome)
Licence (LMD), Bac + 3
We are looking for a dedicated and detail-oriented Quality Assurance (QA) Officer who will ensure compliance with regulatory standards and support quality systems to maintain the highest levels of product safety, efficacy, and consistency throughout the pharmaceutical manufacturing process.
Your Responsibilities:
Ensure all production and testing activities comply with cGMP, GLP, and company SOPs.
Review and approve batch manufacturing records, analytical reports, and deviations.
Support internal audits, self-inspections, and regulatory inspections.
Investigate and document non-conformances, deviations, and complaints.
Participate in risk assessments, CAPA implementation, and continuous improvement initiatives.
Collaborate with cross-functional teams including Production, QC, and Regulatory Affairs.
Assist in the development, review, and maintenance of SOPs, policies, and quality documentation.
Monitor and enforce good documentation practices and data integrity principles.
Provide training on QA procedures and GMP compliance to relevant staff.
Qualifications & Skills:
Contract: CDD
Education: Degree in Pharmaceutical Sciences, Chemistry, Biology, or a related field.
Experience: 0–3 years of experience in a pharmaceutical QA role or GMP-regulated environment.
Languages: Good written, spoken, and reading proficiency in Arabic, English, and French.
Professional Knowledge:
Personal Traits:
Why Join Us?
By joining our team, you'll become part of a dynamic, growth-oriented company that values knowledge, motivation, and attitude. You'll have the chance to significantly impact our success, while working in an environment that encourages continuous learning and career advancement.
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