Job Description
At our company, we aspire to be the premier research-intensive biopharmaceutical company. We're at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We use the power of leading-edge science to save and improve lives around the world. Join our team and be part of a dynamic environment where your contributions will make a significant impact.
Responsibilities
- Partner with R&D scientists, product managers, and technical teams to analyze laboratory workflows and translate them into clear business and functional requirements.
- Act as a subject matter expert (SME) for laboratory systems supporting experimental design, data capture, and analysis.
- Follow agile product model ways of working to develop and maintain user stories, functional specifications, and process documentation aligned with product roadmaps and scientific needs.
- Support the implementation, configuration, and lifecycle management of laboratory systems and related R&D informatics platforms.
- Collaborate with vendors and internal engineering teams to evaluate enhancements, integrations, and system upgrades.
- Ensure laboratory data is captured, stored, and retrieved in a manner that supports scientific reproducibility and downstream analysis.
- Translate scientific and business needs into clear product requirements.
- Partner with Quality stakeholders to support system validation, change control, and User Acceptance Testing (UAT).
- Contribute to the creation and maintenance of SOPs and validation documentation.
- Serve as a primary point of contact for R&D users, gathering feedback and identifying opportunities for system and workflow improvements.
- Support user onboarding, training, and adoption of new features or platforms.
- Monitor system usage and user feedback to drive continuous improvement and maximize product value.
Qualifications
Required
- High School Diploma required.
- Minimum of 2 years of experience as an IT Product Analyst, Business Analyst, or similar role.
- Working knowledge of GxP regulations and their application to R&D IT systems.
- Strong ability to translate scientific workflows into technical and product requirements.
Preferred
- Academic or industry background within pharmaceutical, biotech, or life sciences R&D function.
- Familiarity with regulated SaaS platforms used in pharmaceutical R&D.
- Experience working in agile or product-centric IT organizations.
- Familiarity with regulatory expectations and requirements for laboratory information systems operating in pharmaceutical R&D environment.
What We Offer
- Exciting work in a great team, global projects, international environment
- Opportunity to learn and grow professionally within the company globally
- Hybrid working model, flexible role pattern
- Competitive salary & incentive pay
- Pension and health insurance contributions
- Internal reward system and referral scheme
- 5 weeks annual leave, 5 sick days, 15 days of certified sick leave paid above statutory requirements annually, 40 paid hours annually for volunteering activities, 12 weeks of parental contribution
- Cafeteria for tax free benefits according to your choice (meal vouchers, sport, culture, health, travel, etc.), Multisport Card
- Vodafone, Raiffeisen Bank, Foodora, and discount programmes
- Up-to-date laptop and iPhone
- Parking in the garage, showers, refreshments, massage chairs, library, music corner
Ready to take up the challenge? Apply now!
Know anybody who might be interested? Refer this job!
Required Skills
Agile Application Development, Agile Methodology, Asset Management, Benefits Management, Continuous Process Improvement, Functional Specifications, IT Project Lifecycle, Lab Equipment Maintenance, Laboratory Design, Laboratory Informatics, Laboratory Information Management System (LIMS), Laboratory Maintenance, Management System Development, Product Management, Product Roadmap, Requirements Management, Stakeholder Relationship Management, Strategic Planning, System Designs, Systems Thinking
Preferred Skills
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:
No relocation
VISA Sponsorship
No
Travel Requirements
10%
Flexible Work Arrangements
Hybrid
Shift
1st - Day
Valid Driving License
No
Hazardous Material(s)
n/a
Job Posting End Date
06/14/2026
- 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:R399494
