Department Head Engineering(m/f/d)
The Site Lead Engineering is responsible to ensure an efficient Engineering Organization – in accordance with the company strategy and pharmaceutical-technical requirements (cGMP, Health, Safety, Environmental & Sustainability). This includes the areas of Sustainability, Facilities/Utilities, Capital Projects, Engineering Compliance, Automation and Production Engineering.
The position holder reports to the site manager and is a member of the Site Leadership Team (SLT) and is therefore decisively involved in the most important business and decision-making processes at the Marburg site.
The fulfillment of the employer´s duties regarding occupational safety, the prevention of occupational accidents and diseases as well as the implementation of necessary work-related health measures for Engineering Marburg.
Ensure an efficient Engineering organization
Ensure alignment of the Engineering organization with the company objectives. Ensure optimization of business processes within Engineering and in cooperation with cross-functional areas. Ensure adherence to service agreements and contracts for all relevant technical outsourcing services in terms of resources, quality and expenses.
Ensure cost planning (CAPEX) and project execution in accordance with relevant demand.
Review and assessment of projects from a technical perspective and contribution to approval processes within Marburg Capital Review Board (MCRB).
Ensure execution of investments by means of high-level project management in terms of resources and application of approved budget with regards to profitability, timelines and requirements.
Ensure the professional and harmonized implementation of Engineering tasks with best possible use of synergies.
Ensure that improvement opportunities within the area of Engineering core functions are identified, analyzed and implemented by use of synergies.
Ensure and survey general compliance and implementation of internal, legal and regulatory requirements in terms of cGMP, technical execution quality and pharmaceutical process engineering.
Consolidation of technical processes and functions to implement harmonized and site conform engineering processes, documents, and tools.
Support of global engineering organization and contribution to ensure harmonized engineering processes.
Ensure implementation of all EHSS guidelines within the Engineering organization.
Ensure adherence to site risk management process in accordance with Global Supply Chain Risk Management Written Standard (VQD-SOP-082388).
Bachelor or Master of Engineering degree in a relevant field
Extensive experience at a similar level in the pharmaceutical or related manufacturing & engineering industry.
Excellent knowledge of the legal framework including standards, regulations, etc.
Fluent in English and German
Confident, determined and courteous appearance towards all business partners internal and external.
We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme.
our Performance with Choice programme offers a hybrid working model, empowering you to find the optimal balance between remote and in-office work.
Discover more about our company wide benefits and life at GSK on our webpage Life at GSK | GSK
When applying for this role, please use the ‘cover letter’ of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.
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