Scientist II

  • Permanent
  • Anywhere

Website Actalent


Company : Actalent

Country: United States

Location : St. Louis, Missouri

Post: Sat, 11 Sep 2021 05:10:19 GMT

Expires: Mon, 11 Oct 2021 23:59:59 GMT

Apply Job : Apply Online

—————————— Job Description ——————————


Scientist II, Upstream Process Development Position Summary: Provides moderately complex analyses in a biology environment within defined procedures and practices. Participates in the development of scalable processes with improved product yield and reduced costs in a biologics environment. Supports internal development and/or manufacturing operations. May research and implement new methods and technologies to enhance operations. Makes detailed observations and reviews, documents, and communicates test results; recommends solutions. Maintains lab equipment. Typically assigned to a specific discipline, such as analytical, cell culture, process validation, or purification. Key Responsibilities: Assists with the design of experimental plans based on the defined deliverables. Conducts semi-routine and moderately complex tasks and sample analyses to support process development. Works with Process Development and Manufacture groups to troubleshoot process challenges. May function as a process subject matter expert in a cGMP environment. Records results in notebook accurately, clearly, and regularly. Assists with preparing protocols, reports, and test methods. Maintains and ensures a safe laboratory environment and work practices. Helps to maintain laboratory and order common supplies. Executes, records, and evaluates experimental data appropriately, including the writing and revising of process development reports and technology transfer protocols as needed. Cell Culture: Develops mammalian cell culture processes to support the production and manufacturing of recombinant proteins (including mAbs) under varying levels of direction, including, but not limited to cell culture scale-up, media development, harvest (recovery) process development, process range finding, and statistical analysis of data. Performs media optimization, bioreactor process development, and cell culture clarification.


Cell Culture, cGMP, upstream process, biochemistry, purification, process validation, glp, protein purification, protein expression, protein assays, biology, assay development, gmp, chemistry


Cell Culture,cGMP,upstream process,biochemistry,purification,process validation,glp,protein purification,protein expression,protein assays


Minimum Requirements/Qualifications: Bachelor’s degree in biology, chemistry, biochemistry, chemical engineering, or a related field. With a Bachelors degree, minimum of 2 years of experience related to pharmaceutical manufacturing, process, development, or academic laboratory. Relevant industry experience preferred. With a Master’s degree, no experience is required; related industry experience is preferred. Experience using advanced statistical software packages and experience with design of experiments (DoE) software (i.e. MiniTab, JMP) preferred. Other Job Requirements: Adhere to OHS policies and procedures and ensure a safe and healthy workplace environment Applied knowledge from the experience of applying the principles, concepts, and practices of the discipline. Working knowledge of GMP/GLP regulations in cGMP/cGLP manufacturing environment preferred. Solid lab skills. Good problem solving and critical thinking skills. Good writing, communication, and presentation skills. Good MS Excel, PowerPoint, and Word skills. Excellent organization and planning skills. Strong attention to detail and ability to adhere to standards procedures. Ability to design and execute tasks and studies based on the deliverables. Ability to analyze and summarize moderately complex scientific data. Ability to properly document work and write reports. Ability to function in a rapidly changing environment. Strong attention to detail and ability to adhere to standards procedures. Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations. Ability to make decisions that require choosing between limited alternatives to resolve problems of moderate complexity.


Entry Level ABOUT ACTALENT: Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. Were supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

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