QA Batch Review Officer at RAFARM

Paiania, Attica, Greece -

Full Time

Start Date

Immediate

Expiry Date

25 Dec, 25

Salary

0.0

Posted On

26 Sep, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Assurance, Batch Documentation, GMP Standards, Corrective Actions, Communication Skills, Interpersonal Skills, Detail-Oriented, MS Office, Pharmaceutical Manufacturing, Collaboration, Continuous Improvement, Regulatory Compliance, Health Authority Inspections, Teamwork, Self-Motivated, Adaptability

Industry

Pharmaceutical Manufacturing

Description

QA Batch Review Officer (Ref: QABR_0925) About the company RAFARM is an innovation-driven, dynamically growing pharmaceutical company and a well-established European manufacturer with an outward-looking orientation that invests 13% of net turnover in Research and Development. We introduce high technology in our state-of-the-art sterile manufacturing plant and create new production lines with cutting-edge technology and robotic equipment. RAFARM is a place where our people evolve and are full of passion and interests. We are a dynamic team that empowers talent, embraces diversity, and accelerates development. About the role We are seeking a meticulous and proactive QA Batch Review Officer to join our Quality Assurance department. This role is integral to ensuring that batch documentation complies with all quality standards and regulatory requirements for pharmaceutical manufacturing. The successful candidate will review batch records, coordinate with internal departments, and support compliance activities to maintain product integrity and ensure timely product release. The role main accountabilities will be the following: Review batch manufacturing records and related documentation to ensure compliance with GMP standards and company procedures. Identify and address deviations or inconsistencies in batch records, ensuring appropriate corrective actions are taken. Collaborate with Production, Quality Control, and other relevant departments to obtain necessary documentation and resolve any discrepancies. Maintain batch documentation records in a systematic and traceable manner & handle batch records archive. Coordinate with the quality team to support batch release activities and ensure timely communication of any issues that could delay product release. Participate in internal audits, contribute to continuous improvement initiatives in batch documentation, and review processes. Support CAPA (Corrective and Preventive Actions) processes, including follow-up to ensure timely implementation. Assist in preparation for Health Authority inspections and customer audits, providing necessary batch documentation and information. Ensure documentation aligns with regulatory guidelines and internal quality systems. University degree in Chemistry, Chemical Engineering, Pharmacy, or a related scientific field. Minimum of 1 year of relevant experience in batch documentation review, Quality Assurance, or Quality Control within a pharmaceutical manufacturing environment. In-depth understanding of GMP regulations, batch record review practices, and pharmaceutical quality standards. Highly detail-oriented and capable of maintaining meticulous records. Proficient in English and experienced in MS Office applications. Excellent communication and interpersonal skills to collaborate effectively with multiple teams. Self-motivated, adaptable, and able to work both independently and as part of a team. Why Join Us Competitive Compensation Private Health Insurance Career Development Opportunities Work-Life Balance Company Bus Innovative Work Environment Community Engagement Recognition and Rewards At RAFARM, you will be part of a passionate team dedicated to making a positive impact on global health. You will grow your career in a dynamic and innovative environment where your contributions matter. After the collection and evaluation of all CVs, we will contact only those candidates who meet the requirements of the position to be filled in order to set an appointment for an interview. All applications are considered strictly confidential.

Responsibilities

The QA Batch Review Officer will review batch manufacturing records to ensure compliance with GMP standards and company procedures. They will also collaborate with various departments to resolve discrepancies and support batch release activities.