# CSV Analyst (Rodopi)

> Pharmathen · Sapes, Greece (Hybrid) · — · Posted 2026-09-16

**Workplace:** hybrid

**Department:** Business Applications & Systems Validation

## 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 **CSV Analyst** to join our **Business Applications & Systems Validation** team at our **Sapes** premises**.**

The **CSV Analyst** ensures that computer systems and their use comply with the regulatory requirements (including guidelines and current practice).

**More particularly:**

**What you’ll do:**

-   Participate in generation & execution of various GMP related documents and protocols, including several of the following: URS, FS/ DS, IQ, OQ & PQ
-   Participate in the creation, revision and implementation of IT related policies or procedures
-   Assist in the audit, review, development and implementation of computerized systems to ensure they meet required standards of quality and compliance
-   Assist with queries regarding computer systems operation, development and validation during regulatory and due diligence inspections
-   Collaborate with other departments to monitor compliance with standards/ regulations which dictate the operation of the company’s IT systems
-   Communicate with external parties (customers, suppliers) to ensure appropriate level of support
-   Manage and support the core project team/ users on a day-to- day basis.

## Requirements

**Minimum Qualifications:**

-   BSc n Electrical Engineering, Computer Science or relevant field

**Minimum Experience:**

-   Minimum 2 years’ experience in a similar role
-   Basic knowledge of Computerized Systems Validation—Legislation

**Job-Specific Skills:**

-   Preparation of Validation/ Verification Protocols (URS, FS, DS documents)
-   Preparation of automated/ manual testing scripts (IQ/ OQ/ PQ Documents)
-   Participation in SAT (Site Acceptance Test)/ UAT (User Acceptance Test) Activities
-   Good Documentation Practices
-   Risk Management Methodology for Validation
-   IT- QA Audits for leveraging software supplier
-   Deviation Investigation
-   Change Control Management

## Benefits

**What you will 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/ scientific 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](https://apply.workable.com/pharmathen/j/A5F26F6645/apply)

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