# Production Process Specialist

**Company:** [Pharmathen](null/companies/ukom1cGutkhsccg8YJU6j6.md)
**Location:** Sapes, Greece
**Workplace:** on site
**Employment type:** Full-time
**Department:** Industrial & Supply Chain

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## 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 **Production Process Specialist** to join our team at our Sapes premises

## Requirements

**More particularly:**

**What you’ll do:**

-   Enhance GMP compliance and Data Integrity and Safety culture in production department
-   Take part in preparation and review of the Production department’s SOPs, process TDRs and other controlled documents of the Quality System
-   Participate and oversight the upscaling, trial and process validation and launch batches’ manufacturing in collaboration with MS&T dpt
-   Oversight, evaluate and interpret of production processes in respect of optimization
-   Handling of Electronic Quality Management System (EQMS) in respect of Production department Quality Records as “Change Control”, “Deviation Management”, “CAPA Management”, “OOS Management” and Training records
-   Participate in Operational Excellence projects and optimization of manufacturing processes

**Minimum Qualifications:**

-   Minimum an BSc Degree in Chemical Engineering, Chemistry, Pharmacy or relevant field
-   At least 3 years of experience in a pharmaceutical industry

**Job-Specific Skills:**

-   Excellent communication in English language (writing & speaking)
-   Excellent knowledge of MS Office
-   Good Technical Writing ability

## 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.**