Job Description
We are investing in ourselves to change the way our company develops and harnesses the power of Artificial Intelligence. If you are eager to spearhead groundbreaking technologies that will make a meaningful impact on people's lives within a world-renowned pharmaceutical company, then look no further, we have the perfect role for you!
The Software Engineer will redefine what is possible and unleash the potential of Artificial Intelligence in applications. Reporting to the Director of Engineering in HyperAutomation & AI within our Chief Technology Office, this position is responsible for designing, building, and integrating AI into production systems to ensure seamless operation for our company. The ideal candidate is a tenacious problem solver with the keen ability to move with urgency to create sustainable solutions.
Join our team as we pioneer innovative solutions that redefine the boundaries of pharmaceutical advancements on a global scale.
Key Responsibilities
- Software development on backend and frontend (Python, SQL, REST, JavaScript, TypeScript / node.js + React framework)
- Write efficient and maintainable code following best practices in software engineering.
- Working with DevSecOps tools for deploying and versioning code.
- Deploy solutions on the cloud with CI/CD integration.
- Deliver enterprise AI projects, products, and platforms with a focus on scalability and reusability.
- Work on technical pilots and feasibility studies of new opportunities to create value and transitioning successful pilots to scalable production implementations.
- Develop integrations with other applications and services.
- Develop unit tests of the application both positive and negative cases.
- Application release and second level support
- Stay up to date with the latest advancements in software engineering technologies.
- Participate in Agile ceremonies with the team to execute on prioritized projects and features.
- Work closely with cross-functional teams, including product managers, data scientists, and software engineers, to understand requirements and deliver AI-driven solutions.
Requirements
- 4+ years hands-on coding and software design experience building robust and scalable software using Python, SQL, REST, JavaScript, TypeScript / node.js + React framework.
- Experience in building data intensive applications in a modern technology stack Cloud services (AWS, Azure), data pipelines, SQL/No-SQL databases (graph databases is a plus)
- Experience in designing, architecting, and maintaining applications.
- Experience building and consuming web-based APIs.
- Experience with CI/CD environments and test-driven development leveraging a Version Control system.
- Excellent collaboration and communication skills for working with cross-functional teams.
- Experienced with developing unit testing and different testing strategies such as performance testing Job Description
Are you a motivated professional with a keen interest in regulatory affairs within the innovative pharmaceutical industry? We are currently seeking a dedicated
Regulatory Affairs Specialist to join our team. In this role, you will play a vital part in ensuring our medicines meet the highest regulatory standards, allowing us to deliver safe and effective medicines to our patients.
Position Type Fixed-term Contract until end April 2026
Key Responsibilities
- Marketing Authorization Applications Under the guidance of the Country Lead/Senior Specialist, prepare and submit new Marketing Authorization applications to local authorities, ensuring timely follow-up and compliance with regulatory requirements.
- Maintenance of Products Ensure that all authorized products are maintained by submitting timely variations, renewal applications, and supplemental marketing authorizations.
- Labeling and Artwork Management Oversee the quality of labeling translations and manage artwork processes for assigned products, ensuring adherence to industry standards.
- Regulatory Intelligence Stay updated on relevant EU and local regulations and guidelines while collecting and sharing pertinent regulatory information with relevant teams.
- Relationship Management Foster positive relationships with internal teams and external regulatory authorities, ensuring effective communication and collaboration.
Major Activities
- Perform timely submissions and maintain tracking of new Marketing Authorization applications in cooperation with various departments.
- Ensure compliance by preparing and maintaining regulatory documents such as the Summary of Product Characteristics and Patient Package Inserts.
- Prepare and manage artwork documentation, conducting thorough reviews to ensure accuracy and compliance.
- Participate in cross-functional activities to address regulatory challenges while providing strategic advice during product launches.
Qualifications
- Education Minimum B.Sc. in Pharmacy.
- Experience Approximately 2 years of experience in the pharmaceutical industry, particularly in regulatory, medical, or laboratory roles.
- Skills Strong verbal and written communication skills in both the local language and English, with excellent organizational and planning abilities. Attention to detail and flexibility are essential to manage high-pressure situations effectively.
- Technical Proficiency Proficient in PC applications, including word processing, spreadsheets, and databases.
Why Join Us?
- Contribute to Innovation Be part of a dedicated team that impacts patient health through effective regulatory compliance and product management.
- Professional Development Enhance your skills and experience in a supportive and collaborative work environment.
- Work-Life Balance Enjoy a role that offers a balance between independent and collaborative work.
Application Process
If you are ready to make a difference in the pharmaceutical sector and meet the qualifications outlined above, we invite you to apply. Please submit your resume and a cover letter detailing your relevant experience.
Application Deadline 15th of January 2025
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
Project Temps (Fixed Term)
Relocation
No relocation
VISA Sponsorship
No
Travel Requirements
25%
Flexible Work Arrangements
Hybrid
Shift
Not Indicated
Valid Driving License
No
Hazardous Material(s)
n/a
Job Posting End Date
01/16/2025
- 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 R327914
