Vacature GMP Documentation Innovation Specialist

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Equal Employment Opportunity Posters and GINA Supplement.

GMP Documentation Innovation Specialist

• Job Title GMP Documentation Innovation Specialist
• Function Quality
• Sub Function Quality Documentation
• Location Leiden, South Holland, Netherlands
• Date Posted Jan 08 2024
• Requisition Number 2406160596W

Description

GMP Documentation Innovation Specialist
Description
We are actively seeking a dedicated individual to join our team as a Process Innovation Specialist. In this role, you will play a crucial part in supporting the digital transformation and process optimization initiatives of our GMP Document Management team.
The candidate should be a good communicator with accompanied collaboration and influencing skills, a hard-working change agent, who should constantly maintain connection with internal partners to stay apace with customer needs.
You will be based at the campus in Leiden, The Netherlands.
GMP Document Management department
The GMP documentation management team is a part of the Quality department and is responsible for crafting and delivering training programs that ensure employees and contractors are knowledgeable about Good Manufacturing Practices (GMP) regulations.
Most of the activities within the department focuses on supporting the site in developing, maintaining of GxP documentation processes which support the GxP manufacturing, development and laboratory processes. Using a validated electronic documentation management system, the GMP documentation team processes all documentation creation, adjustment and archiving requests from departments for the entire Leiden biologics site.
The responsibilities & the impact You will have:
• See opportunities for digitalization and process improvement within the Document Management function and collaborate with cross-functional teams to implement innovative solutions.
• Analyze existing workflows, systems, and processes, and recommend improvements to streamline operations, increase efficiency, and ensure compliance with regulatory requirements.
• Collaborate closely with customers, including subject matter experts, trainers, and document controllers, to understand their needs, gather requirements, and translate them into practical digitalization solutions.
• Support the creation and maintenance of standard operating procedures (SOPs) and work instructions related to digital processes within the Document Management function.
• Supervise and analyze key performance indicators to assess the effectiveness and efficiency of implemented digitalization initiatives and recommend further improvements.
• Stay up to date with industry trends and advancements in digitalization and process improvement strategies to continuously improve the Document Management processes.

Who you are:
• Bachelor's degree or equivalent experience in a relevant field such as Life Sciences, Information Technology, or Business Administration.
• Preferred to have experience in digitalization, process improvement, or related roles within the pharmaceutical industry or similar highly regulated environments.
• Understanding of Training and Document Management processes, systems, and regulations, including GxP, FDA, and other industry standards.
• Proficient in applying digital tools, software, and platforms to enhance training delivery, document creation, management, and tracking processes.
• Analytical skills with the ability to identify bottlenecks, inefficiencies, and opportunities for improvement.
• Interest in developing project management capabilities, including the ability to lead cross-functional teams and motivate change.
• Communication and social skills, with the ability to collaborate optimally with customers at all levels of the organization.
• Diligent approach with a passion for delivering high-quality results while ensuring compliance and accuracy.
This is what awaits You at J&J
If you want to leave your personal mark and be valued for who you are, Johnson & Johnson offers an unusual experience to professionals. We provide you an environment to fulfil your career aspirations as well as promoting your physical and mental wellbeing. You will receive a competitive compensation and benefits package as well as benefits that can be tailored to what is valuable to you throughout different stages of your life. You'll have an opportunity to work for a global market leader working in a dynamic and inspiring working environment with many opportunities to work on exciting projects and assignments. Examples of some of the benefits offered are:
• Flexible working arrangements with J&J Flex, enabling you to work from home.
• 36 holidays. Based on full-time employment and 20 statutory holidays + 16 non-statutory holidays.
• Global Parenteral Leave policy offering 12 weeks of leave (birth/parenteral, adoption/foster care and parenteral) at 100% pay to parents.
• and more
For more than 130 years, diversity, equity & inclusion (DEI) are in our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo. We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values perspectives and life experiences. That is why we in The Netherlands are working to create an inclusive environment where a diverse group of backgrounds, perspectives and experiences are valued and each and every one feels that they belong and can reach their potential. No matter who they are. Diversity, Equity & Inclusion at Johnson & Johnson means "You
Join the team today and make a significant impact on our Training and Document Management processes! Together, we will drive digital transformation, streamline processes, and contribute to the success of our mission to deliver innovative pharmaceutical solutions.

We invite you to join our Global Talent Hub, where we keep in touch with people around the world who share our passions for bold innovations and are inspired by our mission of changing the trajectory of human health.

Functie:	gmp documentation innovation specialist
Startdatum:	13-01-2024
Ervaring:	Ervaren
Educatielevel:	HBO
Contracttype:	Vast
Salaris:	onbekend – onbekend
Uren per week:	1 – 40

Heb je interesse in deze vacature en wil je graag op deze functie solliciteren? Neem dan contact op met Johnson & Johnson via onbekend of onbekend. Of bezoek hun website onbekend.