Pharmaceutical Industry

Cyprus

Mundipharma Pharmaceuticals Ltd 

Mechanical Engineers

Electrical / Electronics Engineers

Chemical Engineers

Mundipharma Pharmaceuticals Ltd is a rapidly growing company in the pharmaceutical CMO (Contract Manufacturing Organization) sector, dedicated to providing high-quality pharmaceutical manufacturing and distribution services in Cyprus and in more than 50 countries worldwide. We are looking for an engineer to join the Validation Team as a Validation Officer.&nbsp;Location:&nbsp;Dali Industrial Area, NicosiaWorking hours:&nbsp;38 hours/ week. Monday - Thursday 08:00-16:30, Friday 08:00-15:45.&nbsp;Duties &amp; Responsibilities include but are not limited to (training will be provided for all tasks):<ul><li>Performing analytical work in support of validation projects that cover product process improvements, introduction of new material and equipment.</li><li>Collaborates with all relevant departments to ensure that all manufacturing processes and analytical methods are validated, and all relevant documents are updated accordingly.</li><li>Assists with training of relevant personnel in handling validated procedures and methods.</li><li>Actively looking for solutions for quality problems</li><li>Ensures all equipment and buildings are appropriately qualified for use in the manufacture of pharmaceutical products.</li><li>Approves and monitors any external contractor related to validation activities.</li><li>Collaborates with the Production and Quality Personnel on the setting up, revision and maintenance of Batch Manufacturing and Packaging Instructions, and other written procedures.</li><li>Collaborates with the Production and Quality personnel relating to the monitoring and control of the manufacturing environment, plant hygiene, training needs, the approval and monitoring of suppliers of materials the designation and monitoring of storage conditions for materials and products, the retention of records, and self-inspections.</li><li>Maintain accurate written records and reports in accordance with GMP/GLP.</li><li>Independently carries out all aspects of analysis to provide right first-time quality results.</li><li>Accurately reports analysis status to ensure the effective continuation of work across shifts.</li></ul>Who we're looking forEducation and Experience<ul><li>University degree in mechanical, chemical, or electrical engineering&nbsp;</li><li>Working experience in validation, and laboratory instrumentation preferable but not required</li><li>Experience with analytical investigations, change control and documentation management preferred</li><li>Excellent knowledge of Greek and English language (verbal and written)</li><li>Strong Computer skills including MS Office, QA applications, and Databases&nbsp;</li><li>Solid Experience in effective usage of data analysis tools and statistical analysis</li></ul>The remuneration package includes 13th salary, provident fund, private medical insurance,&nbsp;company doctor services, a good working environment, etc.&nbsp;&nbsp;&nbsp;&nbsp;

Location:&nbsp;Dali Industrial Area, Nicosia<div style="text-align: justify;"> </div>Working hours:&nbsp;38 hours/ week. Monday - Thursday 08:00-16:30, Friday 08:00-15:45.<div style="text-align: justify;"> </div>Mundipharma Pharmaceuticals is looking for an engineer to join its Validation Team as a Validation Officer.<div style="text-align: justify;"> </div>Duties &amp; Responsibilities include but are not limited to (training will be provided for all tasks):<div style="text-align: justify;"> </div><ul style="text-align: justify;"><li>Performing analytical work in support of validation projects that cover product process improvements, introduction of new material and equipment.</li><li>Collaborates with all relevant departments to ensure that all manufacturing processes and analytical methods are validated, and all relevant documents are updated accordingly.</li><li>Assists with training of relevant personnel in handling validated procedures and methods.</li><li>Actively looking for solutions for quality problems</li><li>Ensures all equipment and buildings are appropriately qualified for use in the manufacture of pharmaceutical products.</li><li>Approves and monitors any external contractor related to validation activities.</li><li>Collaborates with the Production and Quality Personnel on the setting up, revision and maintenance of Batch Manufacturing and Packaging Instructions, and other written procedures.</li><li>Collaborates with the Production and Quality personnel relating to the monitoring and control of the manufacturing environment, plant hygiene, training needs, the approval and monitoring of suppliers of materials the designation and monitoring of storage conditions for materials and products, the retention of records, and self-inspections.</li><li>Maintain accurate written records and reports in accordance with GMP/GLP.</li><li>Independently carries out all aspects of analysis to provide right first-time quality results.</li><li>Accurately reports analysis status to ensure the effective continuation of work across shifts.</li></ul><div style="text-align: justify;"> </div>Who we're looking for<div style="text-align: justify;"> </div>Education and Experience<div style="text-align: justify;"> </div><ul style="text-align: justify;"><li>University degree in mechanical, chemical, or electrical engineering&nbsp;</li><li>Working experience in validation, and laboratory instrumentation preferable but not required</li><li>Experience with analytical investigations, change control and documentation management preferred</li><li>Excellent knowledge of Greek and English language (verbal and written)</li><li>Strong Computer skills including MS Office, QA applications, and Databases&nbsp;</li><li>Solid Experience in effective usage of data analysis tools and statistical analysis</li></ul><div style="text-align: justify;"> </div>The remuneration package includes 13th salary, provident fund, private medical insurance,&nbsp;etc.&nbsp;&nbsp;<div style="text-align: justify;"> </div>Interested applicants should apply to&nbsp;<a href="mailto:hr@mundipharma.com.cy">hr@mundipharma.com.cy</a>&nbsp;stating the position applied. Please note that only the selected candidates will be contacted. All applications will be handled in strict confidence.The company is an equal opportunities employer.

Problem-solving 

Writing reports 

MS Office

Validation Officer

Validation Officer

Validation Officer

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