Chemical Lab Reviewer

Chemical Lab Reviewer

Pharmathen · Municipality of Pallini, Greece · Full-time · Posted 2026-10-16

Workplace: on_site

Department: QC Pallini Plant

Description

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.

Pharmathen offers a great opportunity for career development and is seeking to recruit a Chemical Lab Reviewer to join our Quality Control team in our Pallini premises.

As a Chemical Lab Reviewer, the ideal candidate will be responsible for conducting packaging materials’ quality control testing adhering to standard operating procedures and under GMPs.

Requirements

More particularly:

What you will do:

• Support complaint investigations, continuous improvement activities, and non-standard testing protocols
• Complete and maintains the required quality records and/or documents as directed by the departmental standard operating procedures and perform all required QC review activities
• Review Batch/Fill Cards for proper compliance with established specifications
• Maintain the batch record including the analytical directives and other documents for their review
• Cross checks data against ERP system as well as master records and other QC databases (LIMS)
• Follow all QMS SOPs including Change Controls, Deviations, OOS, OOT and other quality-related processes

The ideal candidate should have:

Minimum Qualifications / Ελάχιστα προσόντα:

• BSc Degree in Chemistry or relevant field is

• MSc Degree in Analytical Chemistry is highly preferred

Minimum Experience / Ελάχιστη εργασιακή εμπειρία:

• 2 years of experience in pharmaceutical product analysis

Job-Specific Skills / Δεξιότητες συνδεδεμένες με τη συγκεκριμένη εργασία:

• Excellent communication in English language (writing & speaking)

• Competent in laboratory instrumentation (e.g., HPLC, GC, dissolution)

• Strong problem-solving skills

• GMP/GLP and biopharmaceuticals experience preferred

• Good skills of MS Office

• Comfortable & flexible with working in shifts/daytime

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.

Apply

Apply at Pharmathen

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