Manufacturing Operator

Description

Are you looking for an opportunity to develop your manufacturing skills within a growing international pharmaceutical company? At ALK, our mission is to improve the lives of people living with allergies, and we are seeking a committed and proactive Manufacturing Operator to join our Manufacturing Department. In this role, you will join the team responsible for bulk formulation and manufacturing activities. This is an ideal position for a solution-oriented individual who enjoys working on the production floor, promotes excellence in Good Manufacturing Practice (GMP), drives continuous improvement, and thrives in a team environment. **KEY RESPONSIBILITIES** Execute manufacturing operations for products and intermediate solutions in accordance with established procedures, ensuring compliance with Good Manufacturing Practice (GMP) regulations, quality, safety, and documentation requirements, and contributing to the proper execution of production activities. **Manufacturing Operations** * Perform extraction, purification, and processing of materials via centrifugation, filtration, ultrafiltration/diafiltration, and/or chromatography, followed by sterile filtration. * Manufacture diluents for subsequent sterilization by filtration or dry heat. * Carry out concentration and dilution adjustment operations for non-sterile products. * Handle and control raw materials, auxiliary materials, and excipients required for manufacturing. * Manage and segregate waste generated during the production process according to established procedures. * Collect product samples in accordance with manufacturing instructions. * Perform in-process controls (IPCs) following manufacturing instructions and Standard Operating Procedures (SOPs). **Documentation and Compliance** * Complete manufacturing documentation, batch records, and logbooks, ensuring accuracy, integrity, and regulatory compliance. * Follow current work procedures and associated process documentation. * Prepare manufacturing lines and perform line clearance activities in accordance with established procedures. * Carry out equipment and facility cleaning in accordance with applicable SOPs. * Comply with gowning and access procedures for classified areas. * Ensure adherence to established material and personnel flow patterns to prevent contamination. **Communication and Continuous Improvement** * Report any incidents, deviations, or anomalies detected during the production process to the relevant supervisor. * Participate in investigations related to deviations, incidents, or corrective actions when required. * Propose and actively collaborate on continuous improvement initiatives within the department. * Maintain a proactive attitude toward quality, safety, and productivity. **REQUIRED EXPERIENCE** * Minimum 3 years’ prior experience in GMP environments or regulated industries (pharmaceutical, biotechnology, chemical, veterinary, or related fields). * Experience in manufacturing operations, material preparation, filtration, equipment cleaning, and completion of production documentation. **REQUIRED EDUCATION** * Technical/scientific education will be valued (e.g., Higher Vocational Training Cycle in Pharmaceutical, Biotechnological and Related Product Manufacturing; Laboratory Analysis and Quality Control; or equivalent). **KNOWLEDGE** * Basic knowledge of Good Manufacturing Practice (GMP) and Good Documentation Practice (GDP). * Knowledge of and ability to apply Standard Operating Procedures (SOPs). * Basic understanding of manufacturing equipment and process unit operations. **COMPETENCIES** * Ability to work effectively in a team. * Orientation toward quality and regulatory compliance. * Attention to detail and documentary rigor. * Responsibility and commitment. * Positive and proactive attitude. * Communication skills and ability to report incidents. * Flexibility to adapt to varying tasks and priorities. * Organizational skills and discipline in task execution. **PRACTICAL DETAILS** * Location: ALK Manufacturing Plant in Madrid (C/ Miguel Fleta, 19\). * Reporting line: Manufacturing Manager. * Working hours: Fixed morning shift (07:20–15:15). Back to job listings Print Submit application ### **Share on:** ### **Autonomous Community:** * Community of Madrid ### **Job Type:** Permanent Contract ### **Working Hours:** Full-time ### **Work Days:** Day ### **Application Deadline:** 12/09/2026 ### **Start Date:** 13/08/2026 ### **Province:** Madrid ### **Website:** www.alk.net ### **Office Address:** Calle Miguel Fleta 19, 28037 Madrid ### **Office Location:** \+ Leaflet \| © OpenStreetMap contributors, © OpenStreetMap UA contributors