QC Associate

  • Permanent
  • Anywhere

Website Actalent


Company : Actalent

Country: United States

Location : Danbury, Connecticut

Post: Sun, 19 Sep 2021 05:15:49 GMT

Expires: Tue, 19 Oct 2021 23:59:59 GMT

Apply Job : Apply Online

—————————— Job Description ——————————


Position Summary: Provides general support to maintain quality control systems within the company. Ensures that performance and products conform to established company and regulatory standards. Analyzes chemical, biological or microbiological products, raw materials, in process materials, or stability samples in support of the companys quality program. Interprets and evaluates the analyses in terms of accuracy and precision and recommends corrective action where necessary. Performs qualitative tests or quantitative assays on samples using techniques that vary from use of standard analytical equipment to highly modern and automated instrumentation. Responsibilities: Conduct routine and non-routine analysis of raw materials, in process, and finished formulations according to standard operating procedures. Perform microbiological and/or chemical analyses of product to ensure stability. Compile data for documentation of test procedures that may include microbiological and/or chemical assays, stability program testing and formulation studies. Calibrate and maintain lab equipment. Participate in the preparation of investigations, summaries and reports. May assist in developing testing methods. Review data obtained for compliance to specifications and report abnormalities. Revise and update standard operating procedures as needed. May perform special projects on analytical and instrument problem solving. Applies knowledge of good manufacturing practices, good laboratory practices and good record keeping practices on a daily basis. Follows written test methods and protocols. Process data, report data and prepare tables and graphs for the completed testing. Identify problems, e.g. out of trend data. Professional interactions are primarily within the QC organization


hplc, wet chemistry, Quality control


hplc,wet chemistry,Quality control


BS Degree in a scientific discipline with 0-2 years related experience or an equivalent combination of training and experience At least 1 year experience in a laboratory setting, preferably in pharma 1 years experience in quality control systems Good written communication skills Understanding of GMPs and regulatory guidelines as they relate to the pharmaceutical products preferred Good interpersonal skills Access, Excel, Word and Power Point skills


Intermediate 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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