QC Planner (Rodopi)

DescriptionFounded in 1969, Pharmathen has grown to become one of the largest, vertically integrated developers of complex drug delivery technologies and is among the top 50 pharmaceutical research companies in Europe.The company has one of the most extensive and advanced pipelines of long acting injectables (LAI), sustained release and ophthalmic formulations.Pharmathen’s highly diversified portfolio consists of over 90 commercialized products, 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.Pharmathen proudly employs more than 1,600 people from over 28 different nationalities, 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.Due to continuous growth and expansion, Pharmathen Pharmaceuticals offers a great opportunity for career development and is seeking to recruit a QC Planner to join our Quality Control team at our premises in Sapes, Northern Greece.As a QC Planner, the ideal candidate will be responsible for the efficient planning, scheduling, and coordination of laboratory testing activities to support production, release and stability testing. This role ensures that QC operations are aligned with manufacturing schedules and regulatory timelines while maximizing lab efficiency and resource utilization. The QC Planner acts as a key liaison between QC, production, QA, and supply chain teams.RequirementsMore particularly:What You Will DoDevelop and maintain short- and long-term testing schedules for QC laboratories, including raw material, in-process, finished product, and stability testingCoordinate with production planners to align QC testing with manufacturing and batch release and stability timelinesMonitor sample receipt, prioritization, and distribution to ensure testing deadlines are metTrack testing status, turnaround times (TAT), and backlog, escalating delays or issues as necessaryAllocate testing tasks based on analyst availability, workload balancing, and technical capabilityCollaborate with QC supervisors to ensure appropriate resource planning (personnel, equipment, reagents)Maintain and update planning tools, dashboards, and KPIs related to lab performance and schedulingCoordinate retests, investigations (OOS/OOT), and urgent testing requirements with relevant stakeholdersCommunicate regularly with QA, Regulatory Affairs, Production, and Supply Chain teams regarding testing status and timelinesParticipate in meetings and provide updates on testing progress, challenges, and metricsSupport continuous improvement initiatives to streamline QC planning, reduce bottlenecks, and enhance testing efficiency.The Ideal Candidate Should HaveMinimum a BSc Degree in Chemistry or relevant field3-5 years of experience in a pharmaceutical QC / stability lab environment Experience in a GMP or GLP environment Job-Specific SkillsExcellent communication in English language (writing & speaking)Strong knowledge of analytical techniques (HPLC, GC, UV, KF, dissolution, etc.)In-depth understanding of cGMPProficient in reviewing and troubleshooting analytical data and test methodsFamiliarity with LIMS, Empower, and other laboratory software systemsExcellent organizational, communication, and leadership skillsAbility to manage multiple priorities and work under pressureAble to work in rotating shiftsBenefitsWhat you'll gain:Involvement in a high-caliber, team-oriented and dynamic atmosphereExposure to challenging business issues and practicesGreat opportunity to leverage and develop your business knowledge and skillsJoin 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. Pharmathen is an equal opportunity employer. We welcome applications regardless of gender, race, age, religion, sexual orientation, and national origin.