Site IT Lead (all genders)

AGC Biologics; Heidelberg; Vor Ort; EUR 70.000 - 90.000; Vollzeit

Zusammenfassung

A leading biopharmaceutical company in Heidelberg is seeking a Site IT Lead to manage IT projects and ensure compliance with industry regulations like GMP. The ideal candidate should have a Masters degree in computer science, 8 years of IT experience in the pharmaceutical manufacturing industry, and strong communication skills in German and English. This role offers a competitive compensation package and a collaborative work environment.

Leistungen

Modern working environment

Flexible working hours

Annual bonus programme

Qualifikationen

• 8 years of IT experience in pharmaceutical manufacturing.
• Broad understanding of user support and help desk methodologies.
• Experience with laboratory production and operational technology systems.

Aufgaben

• Manage IT projects supporting critical manufacturing and quality control systems.
• Ensure compliance with industry regulations like GMP.
• Support validation and qualification of IT systems.

Kenntnisse

IT experience

Understanding of systems operations

Analytical and problem-solving skills

Interpersonal skills

Communication skills in German and English

Ausbildung

Masters degree in computer science or equivalent work experience

Tools

Microsoft 365

ServiceNow

Jobbeschreibung

Overview

Our purpose is to bring hope to life by enabling life-changing therapies for patients around the globe creating a healthier and happier tomorrow. Our mission is to work side by side with our customers in order to improve patients lives by bringing new biopharmaceuticals to market.

Job Summary

The Site IT Lead for our Heidelberg site acts as the subject matter expert and single point of contact to the plant business leadership team regarding any topic as it pertains to information technology. The Site IT Lead understands the business requirements and technology needs for API (Active Pharmaceutical Ingredient) & Biotechnological Manufacturing and is responsible for managing IT projects supporting critical manufacturing and quality control systems and ensuring compliance with industry regulations like GMP (Good Manufacturing Practice). In this role you will be part of the Global IT Leadership Team reporting to the Sr. Director IT Manufacturing.

Responsibilities

• Maintain close relationships with Heidelberg site leadership team and other business partners to understand site technology needs and support requirements across the site.
• Ensure site IT infrastructure lifecycle management and align to capacity growth proactively with accurate forecasts.
• Planning implementation and management of local IT projects as well as leading and participating in global projects (e.g. LIMS ERP IT infrastructure projects).
• Support validation and qualification of IT systems in compliance with GMP requirements.
• Work closely with manufacturing operations technology and quality to maintain and manage a compliant GxP environments. Review multiple team group or service deliverables to ensure quality (design walk-through test results etc.) and adherence to processes standards and regulatory requirements. Participate in all internal and external audits and provide services in a timely manner.
• Participate on the global IT leadership team as a strategic partner in developing a world-class global IT organization.
• Communicate IT strategies and roadmaps to site leadership and local needs to global IT.
• Build and maintain a close working relationship with the internal peers and the larger IT organization to provide services around networks hosting process control monitoring and IT security.
• Manage our external partner for IT services and vendor relationships.
• Responsible for managing the local escalation process of problems to appropriate support personnel. Evaluate business needs and alignment of work environment for possible process improvements and implement accordingly.
• Maintenance of ITIL methodologies (incident problem change configuration release capacity-management) in the ITSM platform ServiceNow.

Qualifications

• Masters degree in computer science management information systems or equivalent work experience.
• 8 years of IT experience preferably experience in (pharmaceutical) manufactory industry at least a mid-size plant required.
• Broad understanding of systems operations systems management user support and help desk methodologies.
• Experience with laboratory production and utility systems (operational technology systems).
• Very good knowledge of Microsoft eco-system (O365 Hyper-V).
• Experience in analysis implementation and evaluation of IT systems and their specifications.
• GxP experience is required.
• Sound administration and interpersonal skills. Must be able to interact in a team environment.
• Strong analytical and problem-solving skills.
• Strong verbal and written communication skills in German and English language.

We Offer

• A modern working environment with exciting tasks in a future-oriented industry
• Experienced colleagues support you during the induction
• Working in an intercultural and international team with short communication channels across national borders
• A corporate culture characterized by openness and appreciation
• Regular company events
• Capital-forming benefits
• Jobticket
• Employer allowance for lunch with Lunch-It
• JobRad (bike leasing)
• Flexible working hours through a modern time recording system
• Free drinks (water soft drinks tea coffee) and fruits
• Annual bonus programme

Application

If you are interested in this role we look forward to receiving your application via our recruitment portal.

AGC Biologics GmbH

Czernyring 22

69115 Heidelberg

Phone : 06221 / 9026-0

Our culture at AGC Biologics is defined by the six core values : Knowledge Trust Quality Ingenuity Accountability and Teamwork. Our core values stem from our team members and are embedded into our DNA. They provide a common language and understanding of how we as an organization are connected across three continents. Our core values serve as a compass and reminder of how we achieve our purpose of bringing hope to life for patients around the globe.

AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners every step of the way. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins plasmid DNA (pDNA) messenger RNA (mRNA) viral vectors and genetically engineered cells. Our global network spans the U.S. Europe and Asia with cGMP-compliant facilities in Seattle Washington; Boulder and Longmont Colorado; Copenhagen Denmark; Heidelberg Germany; Milan Italy; and Chiba Japan. We currently employ more than 2500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients most complex challenges including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more visit . W ant to keep posted about our growth and learn more about our company Follow us on LinkedIn and give us a quick Like on Facebook!

AGC Biologics offers a highly competitive compensation package and a friendly collaborative culture that values personal initiative and professional achievement. AGC Biologics is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age ancestry color family or medical care leave gender identity or expression genetic information marital status medical condition national origin physical or mental disability political affiliation protected veteran status race religion sexual orientation or any other characteristic protected by applicable laws regulations and ordinances.

Key Skills

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Employment Type : Full-Time

Experience : years

Vacancy : 1