Quality Control Analyst - Chemist

• University degree in Chemistry, Higher Vocational Training (CFGS) in Analysis and Control, with experience in chemical analysis laboratories, or similar.
• Intermediate level of English.
• Minimum of 1 year of experience as a laboratory analyst, preferably in a pharmaceutical, chemical, or regulated environment.
• Practical knowledge of analytical techniques and routine handling of laboratory instrumentation (experience in HPLC or other chromatographic, spectroscopic, etc., techniques will be valued).
• Experience or knowledge in LIMS, data integrity, or validations (valuable).
• Familiarity with GMP environments and working under standardized procedures.
• Valuable competencies and skills
• High learning capacity and motivation for continuous technical development.
• Good interpersonal skills, effective communication, and a collaborative attitude.
• Capacity for organization, rigor, attention to detail, and quality orientation.
• Proactivity, responsibility, and a continuous improvement mindset.
• Capacity to adapt to changes in priorities and work in a team.

B. Braun Medical is looking to hire a Chemical Quality Control Laboratory Analyst for its Rubí center, joining the Pharma Quality Control Labs area and reporting to the Chemical Quality Control Management, working a 4th shift, from Wednesday to Sunday in the afternoon shift with the possibility of having 2 out of every 5 weekends off, subject to prior agreement.

The selected person will join a highly regulated, dynamic, and collaborative environment, with opportunities for technical development and continuous learning.

• Execute the analytical tests necessary for the approval or rejection of raw materials, in-process product, finished product, and stability studies, guaranteeing compliance with procedures and deadlines.
• Perform sampling, reception, identification, registration, and filing of samples, reagents, and materials.
• Prepare, record, and review analytical data, certificates of analysis, calibrations, and associated controls.
• Use and verify the laboratory's analytical instrumentation, ensuring its correct operation.
• Collaborate in the investigation of incidents, out-of-specification (OOS) results, and other quality events.
• Participate in validations and transfers of analytical methods, under the supervision of technical personnel.
• Ensure compliance with GMP principles and Data Integrity in all analytical activity.
• Contribute to the preparation and updating of area documentation (SOPs, records, reports, etc.).
• Coordinate effectively with other departments (Manufacturing, QA, R&D, among others).
• Actively participate in continuous improvement activities and laboratory optimization initiatives.
• Collaborate in internal training activities, both by receiving it and by transmitting knowledge when necessary.
• Ensure compliance with safety, occupational risk prevention, and environmental regulations.