Manufacturing jobs in Spain

To plan, schedule, organize, manage and control the production and engineering activities of bulk drug substances in Production Building to achieve targeted production levels cost effectively, efficiently and reliably, within the framework of current Good Manufacturing practices (cGMP), quality, safety, occupational hygiene, responsible environmental protection and in cognizance of the dynamic business environment.

• Focus on the routine manufacture activities to ensure that production of bulk drug substances meets stipulated quality, time and cost specifications and in full compliance with the relevant internal and external requirements, regulations and standards.
• Manage a group of professionals e.g. Manufacturing Engineer/Chemist etc. to trouble shoot all process, manufacturing and customer related issue and implement remedial actions to minimize impact to production.
• Monitor and ensure compliance by section’s staff with the various operating procedures, documentation, GMP, safety, occupational hygiene, environmental and regulatory requirements.
• Develop, review and approve all relevant manufacturing documents in accordance to site procedures.
• Support the generation of the capital expenditure (CAPEX) proposal list for budgeting. Work closely with the Technical Operations Team to establish windows for New Production Introduction (NPI) and capital projects implementation.
• Generate operating budget for own section and manage expenditure to ensure achievement of operational targets and drive cost reduction initiatives.
• Ensure information related to routine production activities are actively tracked & captured for consolidation at the departmental level & submitted to management for decision. Perform various tier reviews and ensure visuals for various metrics are updated.
• Manage, develop, and motivate staff to help realize their maximum potential so as to contribute towards achieving the objectives of the department.
• Fulfill the role of Value Stream Embedded GSK Production System (GPS) Practitioner to drive reduction in accidents, defects and waste including continuous improvement within the Value Stream.

• A degree in Chemistry or Chemical Engineering or any relevant field.
• At least 5-8 years of relevant experience in the pharmaceutical, chemical or petrol chemical industry.
• Good commissioning and operational experience in pharmaceuticals plants.
• Very good knowledge of product, production processes and the plant.
• Good engineering maintenance knowledge.
• Good statistical knowledge.
• Good troubleshooting skills.
• Good knowledge of GMP, safety, hygiene and environment regulations.
• Good knowledge of NDA registration procedures.
• Good project management skills.
• Good presentation skills.
• Good communication skills.
• Good management skills.
• Good interaction skill with other department stakeholders.
• Good understanding of the business processes and MERPS.
• Good knowledge in LeanSigma principles and application.

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Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

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