QC Compliance Officer

<p>Founded in 1969, <strong>Pharmathen</strong> has grown to become one of the largest, vertically integrated developers of complex drug delivery technologies and is among <strong>the top 50 pharmaceutical research companies</strong> in Europe.</p><p>The company has one of the most extensive and advanced pipelines of long acting injectables (LAI), sustained release and ophthalmic formulations.</p><p>Pharmathen’s highly diversified portfolio consists of <strong>over 90 commercialized products</strong>, which are produced in its US FDA and EU-approved manufacturing facilities in Greece, serving 250 customers and accessed by patients in more than 90 countries worldwide. </p><p>Pharmathen proudly employs more than <strong>1,600 people</strong> from over <strong>28 different nationalities</strong>, with 54% of its total workforce and 66% of its Research Operations Team being female. The company’s enduring success is attributed to a passion for creativity, strong ethics, and the dedication of its people, who share a commitment to the company's vision of making a difference in people’s lives.</p><p>Due to continuous growth and expansion, <strong>Pharmathen Pharmaceuticals</strong> offers a great opportunity for career development and is seeking to recruit <a rel="nofollow noreferrer noopener"></a>a <strong>QC Compliance Officer </strong>to join our <strong>Quality Control</strong> team at our premises in <strong>Sapes</strong>, Northern Greece.</p><p>As a <strong>QC Compliance Officer</strong>, the ideal candidate will lead laboratory investigations and/or resolution of Deviations, OOS, OOT and be responsible for GMP Compliance in the Quality Control.</p><p>More particularly:</p><p><strong>Requirements</strong></p><p><strong>What you will do: </strong></p><ul> <li>Analyze and investigate all Deviations, OOS &amp; OOT incidents to Quality Control</li> <li>Be Responsible for GMP Compliance in the Analytical Laboratory</li> <li>Apply Regulatory Requirements for Quality Control (EU/US)</li> <li>Draft or revise Standard Operating Procedures of Quality Control</li> <li>Apply Statistical Control in analytical results of Quality Control and identify trends</li> <li>Supervise of Control and Assurance of Quality Control Standards</li> <li>Supervise of Control of Audit trail</li> </ul><p> </p><p><strong>The ideal candidate should have:</strong></p><ul> <li>Minimum a BSc Degree in Chemistry or relevant field</li> <li>At least 2 years of experience in pharmaceutical product analysis</li> <li>Experience in a GMP or GLP environment </li> </ul><p> </p><p><strong>Job-Specific Skills: </strong></p><ul> <li>Excellent communication in English language (writing &amp; speaking)</li> <li>Competent in laboratory instrumentation (e.g., HPLC, GC, dissolution)</li> <li>Strong problem solving skills</li> <li>Excellent verbal and written communication skills</li> <li>Computer literacy</li> <li>Able to work in rotating shifts</li> </ul><p><strong>Benefits</strong></p><p><strong>What you'll gain:</strong></p><ul> <li>Involvement in a high-caliber, team-oriented and dynamic atmosphere</li> <li>Exposure to challenging business issues and practices</li> <li>Great opportunity to leverage and develop your business knowledge and skills</li> </ul><p> </p><p><strong>Join our team and experience the unique Pharmathen’s culture that gives you the opportunity to innovate, to make decisions, to achieve your own potential and to chart your own career. </strong></p><p><strong>Pharmathen is an equal opportunity employer. We welcome applications regardless of gender, race, age, religion, sexual orientation, and national origin.</strong></p>