Production Operator (Temporary)

Description

Job Summary: Centrient Pharmaceuticals is seeking technical professionals to support the manufacturing process of basic pharmaceutical products in its Operations department. Key Responsibilities: 1. Coordinate production tasks in accordance with current standards and SOPs. 2. Perform and document assigned operations and monitor processes. 3. Report deviations and propose corrective actions to the supervisor. Centrient Pharmaceuticals is the leading manufacturer of beta-lactam antibiotics and a supplier of next-generation statins and antifungals. We produce and sell intermediates, active pharmaceutical ingredients (APIs), and finished dosage forms. We are proud to be at the heart of modern healthcare as manufacturers of life-saving essential medicines. With our commitment to quality, reliability, and sustainability at the core of everything we do, our more than 2\.200 employees continuously work to meet our customers’ needs. We strive for a sustainable future by actively participating in the fight against antimicrobial resistance. Founded 150 years ago as "Nederlandsche Gist\- en Spiritusfabriek", our company was formerly known as Gist Brocades. Headquartered in Rotterdam (the Netherlands), we operate production facilities and sales offices in China, India, the Netherlands, Spain, the United States, and Mexico. Centrient Pharmaceuticals is wholly owned by Bain Capital Private Equity, one of the world’s leading private investment firms. Centrient Pharmaceuticals seeks to hire technical professionals to support the manufacturing process of basic pharmaceutical products in its Operations department at our Santa Perpètua de Mogoda plant. **Main Functions and Responsibilities** Perform and coordinate production tasks within respective units during the assigned shift, in compliance with established standards and current SOPs, aiming to achieve targeted production volumes within defined yields and correct quality, while adhering to SHE and GMP requirements. * Perform and document operations assigned by your supervisor. * Complete all documentation in accordance with GMP standards. * Maintain tools in optimal condition. * Monitor and control processes. * Report process deviations and propose corrective actions to the supervisor. * Serve as the first-response team upon detection of any incident requiring immediate action. * Maintain order and cleanliness across all production areas. * Comply with and ensure adherence to established procedures in all areas. * Complete all documentation related to performed production processes. **Requirements** * Vocational training (Intermediate Level) specializing in Chemistry. * Minimum 2 years of experience in Industrial Chemical or Pharmaceutical Production departments. * Availability to work weekends, holidays, and nights: rotating shifts. * Proficiency in Microsoft Office (user level). * Basic English language skills. * Personal vehicle for commuting to the workplace. **Application Procedure** Please submit your application via the "apply" button and upload your CV. Only applications accompanied by a CV will be considered. For detailed information about the position and the selection process, please contact us at hresp@centrient.com. We invite you to visit our website www.centrient.com for further information about our company. Reference checks are part of Centrient’s hiring and selection process. We will contact you when reference verification is required.