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Manufacturing Technician 4 - Rotating Shift

 

Work Your Magic with us! Start your next chapter and join EMD Serono.

 

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 unimaginable with us.  

 

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

 

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. 

 

Your Role:

The Manufacturing Technician 4 at our St. Louis Cherokee site  is a key role within our GMP Manufacturing. Expectations is to ensure “Compliance “and “Readiness” within our GMP Operations teams, enabling high manufacturing success. Standard operations involve facility preparations, on-the-floor formulations, automated/manual ultrafiltration, and chromatography. Job duties include:

  • Rotating schedule Monday- Friday (1st, 2nd and 3rd shift (including evenings and nights). This role will eventually be rolled into a 24/7 schedule  
  • Evaluate products according to established protocols and perform operations in support of the group and department. 
  • Safely perform operations to meet quality expectations.  Safely and properly dispose cleaning and process waste per approved procedures.
  • Maintain required training to perform tasks/assignments.
  • Perform routine processes and unit operations. Buffer formulation, ultrafiltration, and chromatography are standard.
  • Clean equipment and working areas during and after operations.
  • Support functions of the facility (e.g., maintain equipment, prepare reagents, and restock supplies, waste disposal).
  • Communicate the status of operations and convey concerns to the supervisor.
  • Provide complete and accurate records consistent with quality guidelines.  Utilize quality approved operating procedures and document activities with adherence to GDP standards.
  • Ensure all applicable logbooks are completed as required by current procedures.
  • Interact with other departments as needed and performs procedures independently and part of a team.
  • Improve processes through application of experience and principles, in compliance with change control. 
  • Develop and assist in the implementation of process improvement, safety, quality, and 6S.
  • Take action to resolve unsafe conditions. 

 

Physical Attributes  

  • Stand for extended periods of time.   
  • Lift, push, and or pull up to 50lbs.  
  • Wear mask, safety shoes, gloves, Tyvek suits, respirator, and related personal protective equipment 

 

Who You Are

 

Minimum Qualifications

  • High school diploma or GED. 
  • 6 + months of experience working in a cGMP environment

 

Preferred Qualifications

  • cGMP experience
  • Prior experience in an API manufacturing environment
  • Strong mechanical aptitude
  • Demonstrated process improvement experience.
  • Familiarity with FDA, EMA, and other regulatory standards
  • Demonstrated knowledge and experience in various computer skills, including Windows (Word, Excel, PowerPoint, etc.

RSREMD


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 that impacts millions and empowers everyone to work their magic and champion human progress!
 
Apply now and become a part of our diverse team!

 

If you would like to know more about what diversity, equity, and inclusion means to us, please visit https://www.emdgroup.com/en/company/press-positions.html

 

Job Requisition ID:  286296
Location:  St. Louis
Career Level:  C - Professional (1-3 years)
Working time model:  Full-time

North America Disclosure
The Company is committed to accessibility in its workplaces, including during the job application process. Applicants who may require accommodation during the application process should speak with our Candidate Services team at 844-655-6466 from 8:00am to 5:30pm ET Monday through Friday. If you are a resident of a Connecticut or Colorado, you are eligible to receive additional information about the compensation and benefits, which we will provide upon request.  You may contact 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday, for assistance.

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