Drug Product Lab Head

• Ensure and plan the chemical analysis of semi‑finished, finished, and stability products, in accordance with GMP and internal procedures.
• Approve and close the analytical results of semi‑finished, finished, and stability products in the corresponding computer system.
• Collaborate with the Quality Control Manager by providing the specialized laboratory support needed to implement programs aimed at improving processes and products.
• Coordinate, allocate, and control the human, material, and supply resources of the quality control laboratory.
• Review, evaluate, and follow up on Out-of-Specification (OOS) result reports.
• Manage and participate in internal audits aimed at continuous improvement of the area and regulatory compliance applicable to the company. Likewise, manage the closure of corrective and preventive actions (CAPAs) generated in the area.
• Collaborate with the Quality Control Manager to finalize the investment plans for the area.
• Manage the ongoing execution, supervision, and promotion of occupational health and safety and environmental actions within the operation, such as: reviewing EHS Management System documentation, leading investigations of occupational and environmental incidents occurring in the area, analyzing detected non‑conformities, and establishing improvement actions, while leading EHS activities in the area and complying with legal requirements.
• Strictly comply with ALCOA+ principles in all documentation processes associated with the role, and with Good Manufacturing Practices and GxP at all stages in which the area operates, reporting any deviation or anomaly related to legal regulations and internal procedures through the quality system.
• Manage the team comprehensively in a safe and motivating environment aligned with the ambition of being a great place to work. This includes close performance management, ensuring that team members have appropriate objectives aligned with the company strategy, supporting their performance and personal development plans (PDP) through feedback, coaching, and frequent one‑on‑one meetings; leading by example with corporate values and a culture of continuous improvement, balancing business results with the development, engagement, and experience of team members.

What you'll bring to the table
To make the most of this role and truly thrive, you should have:

• Degree in Chemistry, Pharmacy, or a related field.
• 3 to 5 years of experience in the pharmaceutical industry, leading teams.
• Experience in areas such as Quality Assurance or physicochemical analysis laboratories.
• Advanced English.
• Knowledge of local and international GMP / GLP regulations.
• Experience with operational excellence tools.
• Intermediate Microsoft Office skills.