Merck KGaA
From Merck KGaA's careers page
Status: listed on the employer's own careers page when we last checked (daily). Confirm on their site before applying.
Work Your Magic with us!
Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That`s why we are always looking for curious minds that see themselves imagining the unimageable with us
Support the Mechanical Engineering team in delivering high-quality engineering outputs for standard products and the quality system.
Contribute to engineering change control processes, ensuring updates are accurately documented and implemented.
Maintain and update component databases to support data accuracy, traceability, and efficient engineering workflows.
Support the standardization of mechanical subassemblies across products and engineering projects.
Ensure mechanical designs, specifications, and related documentation are complete, accurate, and compliant with applicable requirements.
Collaborate with local and global teams, applying technical rigor and attention to detail throughout the engineering lifecycle.
You hold a bachelor’s degree in mechanical engineering or equivalent and bring a minimum of eight years of hands-on experience in two dimensional and three-dimensional modeling, sub assembly design, and technical drafting.
You have solid knowledge of Geometric Dimensioning and Tolerancing principles and are confident applying them in a manufacturing or engineering context.
You are proficient in engineering design software such as AutoCAD and Creo Parametric and are comfortable working with piping design tools and standard office productivity applications.
You have practical experience with engineering change control processes, including the preparation and modification of purchase specifications and the tracking of change responsibilities across cross functional teams.
You are familiar with engineering lifecycle management principles and have experience maintaining technical documentation in line with Standard Operating Procedures and ISO standards.
You work effectively both independently and as part of a team, communicate clearly in English, and adapt readily to shifting priorities and timelines.
Experience in the biopharmaceutical or life science industry, knowledge of quality tools, familiarity with international standards such as ISO 9001, or exposure to pressure vessel design and piping or skid modeling are considered a plus.
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging those impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of our diverse team
Scores your resume against this job the way resume scanners do: the job's hard and soft skills, searchability, recruiter tips and formatting.
Create a free account to see your score. Your resume stays in this browser until then, and we never store it.
Already a member? Sign in