QC Senior Analyst

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 looking for a dynamic and skilled individual to join our team as a Senior Analyst QC System Support

The role's main accountabilities will be the following:

• Review and approve analytical results of finished products, raw materials, packaging materials, semi-finished products and stability studies, and report findings to the Laboratory Supervisor
• Coordinate daily scheduling and execution of analysts' tasks in alignment with the Laboratory Supervisor and production priorities
• Issue Certificates of Analysis, specifications, analytical methods and related documentation in compliance with GMP requirements
• Record, code and investigate OOS/OOT results; participate in laboratory investigations and perform annual statistical reviews of laboratory deviations
• Initiate and support Change Controls, Deviations and CAPAs in coordination with the QC Manager; apply spreadsheet validation procedures
• Oversee equipment qualification activities, maintenance logs and calibration records; ensure compliance with all applicable laboratory SOPs and protocols
• Monitor and release critical materials; manage reagents, reference standards and retain samples, including electronic record-keeping
• Author and revise laboratory instructions (SOPs) for the physicochemical sterile products laboratory; support continuous improvement initiatives and monitor evolving regulatory requirements
• Train, support and mentor junior analysts in day-to-day laboratory operations

Requirements

• BSc in Chemistry or other relevant discipline. Postgraduate degree will be considered as a plus.
• At least 2 years of experience in quality control within the pharmaceutical sector
• Hands-on laboratory experience in a GLP/GMP environment is strongly desired
• Solid understanding of physicochemical analytical techniques and GMP documentation practices
• Detail-oriented and highly organized, with the ability to manage multiple tasks within strict timelines, working both independently and collaboratively

Benefits

• Competitive Compensation
• Private Health Insurance
• Career Development Opportunities
• Work-Life Balance
• Company Bus
• Innovative Work Environment
• Community Engagement
• Recognition and Rewards

Why Join Us

At RAFARM, you'll be part of a passionate team dedicated to making a positive impact on global health. You’ll grow your career in a dynamic and innovative environment where your contributions matter.

After the collection and evaluation of all CV's, 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.