• Qualified Person - Quality Control

Tirane
Tipi
  1. me orar te plote
Fusha | Profili i punes
  1. Farmaceutik
  2. Mjekesi
Gjuha
  1. anglisht
Eksperienca
vetem me eksperience
Qualified Person - Quality Control
Job Description
The QP/QC is Responsible for overseeing all procedures in medical production

MINIMUM REQUIREMENTS:

  • Master of Sciences in Pharmacy (MPharm);
  • A minimum of 5 years prior working experience in the field of Pharmaceutical Manufacturing (the candidate shall have the right to receive a professional license in Pharmaceutical Manufacturing of drugs).
  • Language skills: very goodcommand of English, any other language is an asset;
  • Strong analytical skills, stress resistant;
  • Self-motivator, capable of leading and motivating people.
  • Good communication skills, both oral and written.
DUTIES
  • Certifies that each batch of medicinal products complies with marketing authorizations, GMP guidelines, and legal standards before release.
  • Ensure the pharmaceutical quality system (PQS) is robust and functioning correctly, including processes for deviations, out-of-specification results, and complaints.
  • Ensure that manufacturing and testing processes are validated and follow GMP principles.
  • Create and review batch records, validation protocols, and other GMP documentation.
  • Investigate and approve deviations from standard operating procedures.
  • Organize company and act as a liaison with regulatory bodies during inspections and audits.
  • Ultimately, is responsible for the final release of medicinal products.
  • Perform various tests on raw materials, in-process samples, and finished products to ensure they meet quality specifications.
  • Keep the testing equipment in a good working condition.
  • Ensures that all products and processes adhere to established quality standards and regulatory requirements.
  • Identify product defects and non-conformances.
  • Participates in investigations and corrective actions to address quality issues.
  • Collect, analyze, and interpret data to assess product quality.
  • Maintain accurate records of all testing and analysis activities.
  • Work closely with other departments, including production and engineering, to ensure product quality.
  • Communicate, provide information, and manage all requests from the group related to his activities.
  • Report periodically about his performance activities to his superior
NOTE:

This job description is not intended to be all-inclusive. Employee may perform other related duties as negotiated to meet the ongoing needs of the organization.
Employment contract and benefits according to the Labour Code of the Republic of Albania.
*All applications will be treated with complete confidentiality according to Law No. 124/2024 "On the Protection of Personal Data", Republic of Albania
The interested candidates are invited to apply online and send CV, no later than Friday, July 31, 2025.
Contact details:
E-mail: alb-i@web.de
Tel: +355 69 571 9787
 


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