Tirane, ofroj vend pune
Tirane
Tipi
me orar te plote
Fusha | Profili i punes
Farmaceutik
Gjuha
anglisht
Eksperienca
vetem me eksperience
Qualified Person - Quality Control
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 good command 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 in English, no later than Friday, 18 July, 2025.
Contact details:
+355 069 799 4434
Cel. : +355 0697994434
WhatsApp
Tirane
Tipi
me orar te plote
Fusha | Profili i punes
Farmaceutik
Gjuha
anglisht
Eksperienca
vetem me eksperience
Qualified Person - Quality Control
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 good command 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 in English, no later than Friday, 18 July, 2025.
Contact details:
+355 069 799 4434
Cel. : +355 0697994434