Project Role :Quality Engineer


Project Role Description :Enables full stack solutions through multi-disciplinary team planning and ecosystem integration to accelerate delivery and drive quality across the application lifecycle. Performs continuous testing for security, API, and regression suite. Creates automation strategy, automated scripts and supports data and environment configuration. Participates in code reviews, monitors, and reports defects to support continuous improvement activities for the end-to-end testing process.
Must have skills :Test Management

Good to have skills :NA
Minimum 3 year(s) of experience is required

Educational Qualification :15 years full time education

As IT Quality & Compliance Manager
You develop and apply common quality standards along our
System Development Life Cycle, based on existing concepts
and knowhow, in order to secure and strengthen confidence in
our IT Product Portfolios.
You keep up to date with regulations and closely collaborate
with our globally distributed units (Information Security, Data
Protection, QSHE and Pharma & Healthcare), so that you can
streamline how teams can best meet the higher requirements
from customers and regulated industries.
You explore issues and challenges pertaining to quality and
compliance in the IT Product Portfolios, and provide support,
advice and coaching to help our Business Units/Operation
and Product Leads raising their level of quality and compli
ance.
You position yourself as a competent contact for all questions
concerning our quality standards and practices, and assist in
customer meetings and audits
You launch and lead internal awareness and training pro
grams for our quality standards.
Provide support and mentoring for development team mem
bers working in the area of quality management or compli
ance.
You are a competent advisor in all matters relating to process
documentation.
You actively support in building up and developing Center of
Excellence on topics such as CSV to gain and disseminate
acquired knowledge, skills and competences within KN.
(Pharma only) You take an active part in carrying out GxP
impact assessments and - where required - lead and carry out
Validation processes.


Practical experience in applying IT quality management effec
tively throughout a System Development Life Cycle.
Working with Management Systems, ideally for Quality and
Information Security, including handling of audits, documenta
tion requirements and compliance reporting (e.g. ISO 9001,
ISO 90003:2018 or ISO 27001).
Good understanding of complex enterprise software solu

tions, both self-developed and commercial off-the-shelf, with
a strong focus on quality, information security and data pro
tection.
Experience in auditing of IT processes.
Ability to communicate complex context on different levels of
management.
Ability to teach and train people.
Willingness to learn from each other and to share knowledge
and experience, in order to effectively improve the quality lev
el of the organization.
(Pharma only) Knowledge of existing regulation in Pharma
ceutical industry (FDA 21 CFR part 11 and 820, EU GMP An
nex 11)
(Pharma only) Experience in Computerized System Validation
methodologies and process, preferably based on GAMP5
framework.

Qualification
15 years full time education