Sr. Associate Production Scientist
MilliporeSigma

St. Louis, Missouri

This job has expired.


A career with MilliporeSigma is an ongoing journey of discovery: our 60,300 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Electronics. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others. MilliporeSigma is a business of Merck KGaA, Darmstadt, Germany.

Your Role:

At MilliporeSigma, theAssociate Production Scientist in the Functional Genomics Operations Group will manufacture made to order products Bacterial, DNA, RNA, and Viral formats for academic, pharmaceutical, and research centers.

  • Provide leading functional genomics technologies including RNA interference (shRNA) for gene silencing and cutting-edge systems for gene editing and gene knockout (CRISPR/Cas9, ZFN's).
  • Work cross-functionally with R&D, Marketing, Sales and Bioinformatics on development, transfer, and manufacturing of existing and new products.
  • Responsible for all Manufacturing, QC, Packaging and Shipping.
  • Manufacture products according to established protocols.
  • Provide technical support to others.
  • Perform operations in support of the group and department.
  • Organize, set up and execute production operations ensuring quality and quantity of product throughout the production process.
  • Communicate and document status of processes, products, and equipment.
  • Provide complete and accurate batch records at the conclusion of production operations consistent with quality guidelines including any deviations.
  • Write and modify production procedures consistent with quality guidelines.
  • Ensure all applicable logbooks have been filled out completely as required by current procedures.
  • Perform and interpret analytical evaluations of products and intermediates.
  • Perform necessary analytical tests and evaluate results during the process and at the completion of the run.
  • Ensure purity of starting material, intermediates and final products are consistent with history and product specifications.
  • Perform daily operations in a safe and orderly manner by following production procedures and safety policies at all time.
  • Take the necessary action to resolve any unsafe conditions.
  • Maintain good housekeeping in laboratory and working areas.
  • Conduct investigations and implement ideas for process improvements using existing technology and/or novel approaches.
  • Be a technical resource to others by training co-workers.
  • Supportnew product development and the transfer of new processes and products into operations.
  • Evaluate, justify, and implement new instrumentation providing accurate and concise documentation to facilitate the use of the new equipment by other personnel.

Who You Are:

Basic Qualifications:
  • Bachelor's Degree in Biology, Biochemistry, Biotechnology or related life science discipline
  • 3+ years in a laboratory or pharmaceutical production environment

Preferred Qualifications:
  • Mammalian cell culture experience
  • Virus Production and Concentration technique
  • Microscopy
  • Elisa assay
  • Colony Forming Unit & Selection assays in mammalian cell lines
  • Flowcytometry
  • DNA/RNA Purification
  • Primer design & PCR
  • Cloning
  • Electroporation/Nucleofection
  • Restriction digestion
  • Sanger & Next-Generation Sequencing
  • Experience with liquid handling systems/robotics (Biomek, Tecan),
  • 2D barcode scanners & tube pickers, UV/VIS & Fluorescent plate readers
  • Proficient in Microsoft Office Suite (Word, Excel, Access, Powerpoint)
  • Communication skills, oral and written
  • Organizational skills
  • Familiarity with LIMS, SAP, Trackwise and Mango systems
  • Troubleshooting skills
  • Knowledge of safe chemical handling methods
  • Knowledge of ISO quality standards

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. We believe that it drives excellence, innovation, and human progress. We care about our customers, patients, and our rich mix of people. This diversity strengthens our ability to lead in science and technology.
We are committed to creating access and opportunities for all and empower you to fulfil your ambitions. Our diverse businesses offer various career moves to seek new horizons.
Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to bring their curiosity to life!

Curious? Chat with one of our curious minds on our interactive Q&A platform and catch a glimpse of our people, values, and culture. You can also apply and find more information at https://jobs.vibrantm.com
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

If you are a resident of a NYC, 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.

The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

As an employee of the Company, you will be required to comply with all of the Company's COVID-19 safety protocols and policies. The organization has currently suspended enforcement of its COVID-19 Vaccination Policy, but that policy may be reinstated by the Company in its discretion.

Job Requisition ID: 240883

Location: St. Louis

Career Level: D - Professional (4-9 years)

Working time model: full-time


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