Find jobs
Pricing
Sign in
FIND JOBSPRICINGSIGN INSIGN UP
← Back
Pharmathen

Product Quality Lifecycle Supervisor

LocationMunicipality of Pallini, Attica, Greece
Work modeon-site
Typefull-time
DepartmentManagement
Company size1,001–5,000 people
First seen1w ago
Last seen3d ago
About the company
For almost six decades, Pharmathen has remained committed to its vision of improving patients’ lives through innovation and expanding access to complex pharmaceutical therapies.
Today, Pharmathen’s capabilities extend across a broad range of specialized dosage forms, including sustained-release products, long-acting injectables, and oral solid dosage forms, while its portfolio includes more than 100 commercial products available internationally through a strong network of partners.
These activities are supported by a robust Research & Development and Manufacturing ecosystem, with three facilities in Greece.
The driving force behind Pharmathen is its people. With more than 1,600 employees representing 27 nationalities, the company fosters a multicultural workplace where women account for 53% of the workforce and 40% of the Senior Leadership Team.
Grounded in its shared values of integrity, quality, innovation, leadership and performance, and guided by strong business ethics and a commitment to its vision, Pharmathen remains dedicated to its founding mission: improving patients’ lives.
About the role
Pharmathen offers a great opportunity for career development and is seeking to recruit a Product Quality Lifecycle Supervisor to join our Corporate Quality Management team at our Pallini premises**.**
The Product Quality Lifecycle Supervisor is responsible for ensuring that all products meet the company’s quality standards and specifications.
More particularly:
What you’ll do:
•
Collaborate with the quality control team to ensure that all products are tested and meet established quality standards before release
•
Implement and monitors inspection and testing processes to identify and address any deviations from product specifications
•
Lead investigations into product defects, determine root causes, and implement corrective actions to prevent recurrence
•
Identify opportunities for improving product quality and lead initiatives to enhance production processes and reduce defects
•
Ensure all products comply with cGMPs, relevant industry standards and regulatory requirements, to support product release
•
Maintain detailed records of quality control activities and prepare reports on product quality performance for management review
•
Work closely with production, R&D, and supply chain teams to ensure quality standards are integrated throughout the product development and manufacturing processes
•
Provide training to staff on quality standards, and industry best practices
•
Follow Company’s Quality Policy and comply with current operational standards and legislative requirements
•
Ownership of activities related with Process Validation, Cleaning Validation, OOS/OOT investigations, various statistical evaluations, various studies, APQR and stability oversight
•
Active participation in SOPs and Master Records preparation/review, Deviation handling, Complaint management, Document Management, Training system, Audit management including Self Inspection, Risk Management, Escalation process, KPIs monitoring, Change Management, CAPAS, Aseptic process Simulation, utilities/environmental monitoring, as well as other Quality Management System policies and site quality operations oversight and Data Integrity Campaign, as well as various transfer and engineering projects
Requirements
The ideal candidate should have:
•
Educational background in Chemical Engineering, Chemistry, Biological or Pharmaceutical sciences
•
Minimum of 5 years of experience in product quality management
Job-Specific Skills:
•
Excellent communication in English language (writing & speaking)
•
Computer literacy
•
Ability to prioritize tasks and meet deadlines
•
Exceptional communication skills, strong project management skills
•
Broad knowledge and extensive experience on pharmaceutical quality systems Extensive knowledge of European GMPs in order to be able to ensure compliance with national and European standards and legislation
•
Effective problem solver
•
Strong initiative and creativity skills
Benefits
What you’ll gain:
•
Involvement in a high-caliber, team-oriented and dynamic atmosphere
•
Exposure to challenging business issues and practices
•
Great opportunity to leverage and develop your business knowledge and skills
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.
Pharmathen is an equal opportunity employer. We welcome applications regardless of gender, race, age, religion, sexual orientation, and national origin.
More roles at Pharmathen
CSV Analyst (Rodopi)Raw Materials AnalystProduction Process SpecialistResearch ScientistQuality Assurance Senior Engineer
Seekless
Product
Find jobsCompaniesPricing
Legal
PrivacyTermsCookies
© 2026 SEEKLESS, INC. ALL RIGHTS RESERVED.BUILT WITH CARE