QC Compliance Officer

3 days ago

Pallini, Attica, Greece Pharmathen Full time €30,000 - €60,000 per year

Description
Founded 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 Compliance Officer
to join our
Quality Control
team in our
Pallini premises
.

As a
QC Compliance Officer
, the ideal candidate will lead laboratory investigations and/or resolution of Deviations, OOS, OOT results and will be responsible for ensuring GMP Compliance within Quality Control.

Requirements
More particularly:

What You Will Do

  • Analyze and investigate all Deviations, OOS and OOT incidents related to Quality Control
  • Ensure GMP compliance within the Analytical Laboratory
  • Apply regulatory requirements (EU/US) to Quality Control operations
  • Draft and revise Quality Control Standard Operating Procedures (SOPs)
  • Apply statistical control to analytical results and identify potential trends
  • Oversee the implementation and assurance of Quality Control standards
  • Supervise the monitoring and control of audit trails

The Ideal Candidate Should Have

  • Minimum a BSc Degree in Chemistry or relevant field
  • At least 2 years of experience within a pharmaceutical environment/Quality control
  • Experience in a GMP or GLP environment

Job-Specific Skills

  • Excellent communication in English language (writing & speaking)
  • Competent in laboratory instrumentation (e.g., HPLC, GC, dissolution)
  • Strong problem solving skills
  • Excellent verbal and written communication skills
  • Computer literacy

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.

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