Senior Specialist Regulatory Information Management

Job Description

Join our innovative R&D IT team, where your expertise will play a crucial role in driving product discovery and compliance. As the vital link between IT and our Research & Development organization, you will ensure software quality and address evolving customer needs, all while fostering a culture of continuous improvement. If you are ready to make a significant impact in the pharmaceutical industry, we invite you to bring your skills and passion to our team as a

Senior Specialist Regulatory Information Management

Welcome in our team

Our R&D IT team brings state-of-art IT products & solutions for our business partners to enable discovery of new products and to accelerate time to market. We strive to be the trusted partner of Research & Development organization to drive innovation, reduce time to market, ensure compliance, and safeguard business continuity.

Purpose of the role

As a Senior Specialist Regulatory Information Management you will serve as the Veeva Vault expert, developing and supporting technology applications for Regulatory Information Management through close collaboration with stakeholders to create front-end and back-end solutions, ensuring software quality with unit testing, and partnering with scrum teams and vendors to address customer needs and identify risks. You will be the link between IT and the business.

Tasks and responsibilities include, but are not limited to:

• Designs, configures, and verifies software systems and integrations by configuring software programs subject to estimation, measurement, quality processes, appropriate documentation, and continuous improvement processes
• Enables and maintains software configuration management capability across heterogeneous technology environments, architectures, and platforms
• Designs, creates and adapts software configuration applications and interfaces
• Validates and tests integrated systems subject to organizational standards regarding security, reporting, observation, and control
• Includes specializations such as API Platform Engineer (not exhaustive)
• Representing the team in companywide Communities of Practice.

Your profile:

• Bachelor’s or master’s Degree, preferably computer science or IT
• Minimum of 5 years of experience in pharmaceutical industry Regulatory Information Management
• Experience with Animal Health is a preference
• In-depth knowledge and hands-on experience with RIM (Veeva Preferred), including system configuration, process optimization, and training delivery
• Proven track record of technical skills such as Document Management, Software Development Lifecycle (SDLC), Agile and Jira
• Strong Business Analysis skills, including project management
• Demonstrated success working independently with all levels of a matrix organization
• Strong written and oral communication skills in English and Dutch

What we offer

We welcome you to a truly global, dynamic and challenging environment with great opportunities for personal development.

• Competitive salary and a 3% year-end bonus;
• 35,5 days of leave;
• Attractive collective health care insurance package with considerable reduction rates;
• Solid Pension Plan;
• Incentive Plan;
• Travel allowance for commuting;
• Numerous training, coaching and e-learning modules for long term job opportunities and development.

Current Employees apply HERE

Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company.  No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:

Regular

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Hybrid

Shift:

Valid Driving License:

Hazardous Material(s):

Required Skills:

Data Engineering, Data Visualization, Design Applications, Software Configurations, Software Development, Software Development Life Cycle (SDLC), Solution Architecture, System Designs, Systems Integration, Testing

Preferred Skills:

Job Posting End Date:

12/5/2024

*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Requisition ID: R321855