Job Description:

Airbus Defence and Space is looking for a IT- SAP/ERP Finance & Controlling senior specialist to reinforce its internal SAP team.

Your tasks and responsibilities :

This position contributes to the service delivery by the ERP Delivery Center covering all our AD ERP platforms including French national one.
 

Inside the scope of this functional domain your will have to manage project, enhancement and also support, bug fixing on SAP modules FI (AA, GL, AP, AR, TR) & CO including PS controlling and CATS. Fiori skills is a plus.

You will join an international group of around 45 SAP Functional Experts with around 15 SAP FICO Experts.

•Provide support on the SAP systems of AD (including new solution S4 hana), implement enhancements & projects on this system taking into account the guidelines of Airbus Defence & Space to manage them.

Integrate the SAP FICO team with an open mindset to ensure an excellent team work inside the DIGITAL organization and with the business (key) users.

•Support the team in all the new requirements they have coming from the key users. Understand their needs and propose solutions to their issues/requirements.

•Proven functional skills in ERP Finance (configuration, integration aspects in AA, GL, AP, AR and TR, CO modules).

•Role management in SAP assuring the segregation of duties at Finance level.

•Create the functional design and support the ERP developer at functional level to develop/modify the ABAP code to be adjusted to the new requirements.

Your profile :

This position is opened for senior and confirmed on SAP FICO domain.

Resource allocation complying with desired skills and qualifications.

The candidate has to be fully customer and delivery oriented.

English on negotiation level.

French national eyes only system implies national restriction and security inquires.

Your benefits :

•Attractive salary including holiday pay, Christmas bonus and profit sharing

•30 days holidays and extra days-off for special occasions

•Excellent upskilling opportunities and great development prospects

•Special benefits: employer-funded pension, employee stock options, discounted car leasing, special conditions for insurances, public transport subsidy, discounts at local businesses

•On-site-facilities: canteen and cafeteria, laundry services, fitness center

#LI-JR1

This job requires an awareness of any potential compliance risks and a commitment to act with integrity, as the foundation for the Company’s success, reputation and sustainable growth.

Company:

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By submitting your CV or application you are consenting to Airbus using and storing information about you for monitoring purposes relating to your application or future employment. This information will only be used by Airbus.
Airbus is committed to achieving workforce diversity and creating an inclusive working environment. We welcome all applications irrespective of social and cultural background, age, gender, disability, sexual orientation or religious belief.

Airbus is, and always has been, committed to equal opportunities for all. As such, we will never ask for any type of monetary exchange in the frame of a recruitment process. Any impersonation of Airbus to do so should be reported to emsom@airbus.com.

At Airbus, we support you to work, connect and collaborate more easily and flexibly. Wherever possible, we foster flexible working arrangements to stimulate innovative thinking.

Just-Evotec Biologics is seeking a highly motivated Senior Process Engineer Downstream - New Product Introduction (NPI) to join a fast-paced, collaborative, and multidisciplinary team to lead activities related to the introduction of new products to the J.POD Toulouse biotherapeutics manufacturing facility. The role will provide cross-functional leadership for all phases of Just-Evotec’s NPI process – stretching from project initiation through process validation and registration activities. 

The role will require close collaboration with all functional areas of the J.POD Toulouse team – including Product and Process Design, Process Engineering, Process Automation, Facilities Engineering, Quality Controls, Quality Assurance, Supply Chain, Manufacturing, Digital and EHS. The role will participate in client facing meetings to discuss topics related to NPI activities. The role will also collaborate with Just-Evotec Global MSAT, Client Program Managers, Global Supply Chain for client projects and continuous improvement efforts.

Responsibilities

• Reporting to the MSAT-NPI manager
• Lead Downstream stakeholders NPI process at J.POD Toulouse to support the start and rapid scale-up of commercial GMP manufacturing activities.
• Partner with Product and Process Design to coordinate successful efficient scale-up and transfer operations and to ensure the successful integration of process knowledge into manufacturing operations.
• Partner with supply chain to support Downstream Bill of Material development and demand planning for new products.
• Partner with Engineering and Digital disciplines to conduct facility fit assessments and plans to support system updates needed for new product introduction.
• Partner with Manufacturing to develop high-quality batch records, robust processes and innovative technology solutions for new product introduction.
• Partner with Quality, CQV and Global MSAT to develop and implement process validation and comparability study activities leading to successful product registration.
• Acting as a subject matter expert for regulatory and client inspection audits.
• Utilize the team’s technical skills and process knowledge to participate and/or lead investigations related to Downstream NPI activities. Collaborate with impacted groups to develop and execute effective CAPA.
• Apply Operational Excellence principles to lead continuous improvement in NPI activities.

Requirements:

• Ph.D. (or Masters) degree in relevant field or related program with 10+ (15+) years of pharmaceutical/biotech validation experience including a minimum of 3-5 years of experience leading a New Product Introduction program for biopharmaceutical products (Technology Transfer).
• Extensive knowledge and experience with late-stage clinical and commercial biologics drug substance manufacturing programs, including project leadership roles in process validation, PPQ, and commercial manufacturing.
• Proven record of accomplishment and self-directed leadership in GMP pharmaceutical or biotechnology is required.
• Technical mastery of cell culture, purification, and solution preparation operations using disposable-based manufacturing technologies
• Demonstrated leadership capabilities to build and mentor high-performing teams, drive change, and influence internal and external stakeholders
• Extensive knowledge of US FDA CFRs and European EMA, including ICH guidelines, as they relate to drug substance biological manufacturing
• Good interpersonal, team, and collaborative skills are required.
• Excellent verbal and written communication skills in French and English; ability to interface with all levels of the organization

Additional Preferred Qualifications:

• Experience in audits and inspections by health authorities, clients and other external auditors as a presenter or audit support staff.
• Experience in leading risk assessment and risk management for pharmaceutical products and processes.  Experience in applying principles of Quality by Design.
• Experience in developing submission packages for pharmaceutical product registration  
• Experience in client relations and communications.
• Demonstrated success in leading multi-disciplinary teams that span multiple organizations
• Entrepreneurial drive to achieve business objectives.

FR : Dans le cadre de sa politique Diversité, Evotec étudie, à compétences égales, toutes les candidatures dont celles des personnes en situation de handicap.

ENG : In the frame of our Diversity policy, Evotec considers, with equal competences, all applications including people with disabilities.