JOB TITLE: CONSULTANT - SAP QCS

CAREER LEVEL: C3

Leverage technology to impact patients and ultimately save lives

Do you have expertise in, and passion for, information technology? Would you like to apply your expertise to impact the IT strategy in a company that follows the science and turns ideas into life changing medicines? If so, AstraZeneca might be the one for you!

ABOUT ASTRAZENECA

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that

focuses on the discovery, development and commercialisation of prescription medicines for some of the world’s most serious disease. But we’re more than one of the world’s leading pharmaceutical companies. At AstraZeneca we’re dedicated to being a Great Place to Work.

ABOUT OUR IT TEAM

It’s a dynamic and results-oriented environment to work in – but that’s why we like it. There are countless opportunities to learn and grow, whether that’s exploring new technologies in hackathons, or redefining the roles and work of colleagues, forever. Shape your own path, with support all the way. Diverse minds that work cross- functionally and broadly together.

ABOUT THE ROLE

• As a QCS consultant, will be responsible to ensure compliance to Computer System Validation principles & practices in SAP portfolio.
• Responsible for completing all tasks assigned by team lead and project manager.
• Responsible for interacting and guiding functional and technical team members on Computer Validation principles & practices.
• Responsible to ensure all deliverables by the functional and technical teams are as per process documents and any non-compliance is identified and reported within required timeframe.
• Exposure to Computer System Validation activities.
• Ability to perform quality reviews for design documents.
• Experience of reviewing testing document from quality assurance perspective.
• Ability to define and maintain SOPs and quality standards.
• Exposure to compliance issue management and root cause analysis.
• Knowledge of documentation standards and methodology.
• In-depth Knowledge of Pharma GXP regulatory guidelines.
• Understanding of ITIL processes and Application life cycle management.
• Ability to work in large and diverse teams.
• Excellent communication and interpersonal skills.
• Well versed in English. Excellent spoken and written skills.
• Willingness to work in shifts.

ESSENTIAL SKILLS REQUIRED

• Experience of Quality approver role as part of change advisory board.
• Supported Wide-ranging regulatory audits.
• Knowledge on IS/IT S404 SOx and FCF controls.
• Exposure to Run SAP (Solution Manager) methodologies.
• Self-motivated, quick learner and admirable team player.
• Zeal to improve analytical and validation skills.
• Experience working in a globally distributed team.
• Proactive approach to problem solving.

WHY JOIN US ?

We’re a network of entrepreneurial self-starters who give to something far bigger. We enable AstraZeneca to perform at its peak by delivering extraordinary technology and data solutions.

We’re not afraid to take ownership and run with it. Empowered with unrivalled freedom. Put simply, it’s because we make a significant impact. Everything we do matters.

SO, WHAT’S NEXT?

Are you already envisioning yourself joining our team? Good, because we’d love to hear from you! Click the link to apply and we’ll be in touch as soon as we can.

WHERE CAN I FIND OUT MORE?

Our Social Media, Follow AstraZeneca on LinkedIn https://www.linkedin.com/company/1603/

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status.

Date Posted

19-May-2021

Closing Date

22-Jun-2021

AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.