Our client is a well-established pharmaceutical company focused on research, development, and production of biological and small-molecule medicines. In addition to its own product lines, the company distributes licensed pharmaceuticals and hospital-use medicine.
Responsibilities
- Manage production documentation and processes, ensuring alignment with quality and operational standards across manufacturing lines.
- Develop and update production protocols in line with current regulations and company procedures.
- Oversee the execution of production activities, ensuring consistency and compliance with technical guidance and internal policies.
- Maintain compliance in the assigned area, including management of deviations, incidents, procedures, and related documentation.
- Ensure all personnel are properly trained and qualified to perform their production tasks.
- Review and approve production documentation to ensure accurate completion and timely closure.
- Participate in continuous improvement initiatives aimed at enhancing manufacturing efficiency and product quality.
- Monitor adherence to safety procedures and preventive measures within the production area.
- Coordinate material requests and ensure proper documentation and traceability of production processes.
Requirements
- Degree in Pharmacy, Chemical Engineering, Industrial Engineering, or a related scientific or technical discipline.
- 2–5 years of experience in pharmaceutical manufacturing or process operations.
- Good knowledge of GMP standards and production documentation practices.
- Strong organizational and analytical skills with attention to detail.
- Ability to collaborate effectively with cross-functional production and quality teams.
- Fluency in Spanish; English proficiency is an advantage.
What’s Offered
- Stable position within an innovative pharmaceutical environment.
- Competitive salary and benefits package.
- Opportunity for professional growth and involvement in process optimization projects.
If you are interested in this challenging position we are looking forward to receiving your comprehensive application for
ref.no. 108,831 preferably through our
ISG career portal or via email.
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