Process Validation Engineer

About the Job

Location: Missouri
Start: May 26, 2021
End: November 5, 2021

This position is for an individual contributor to the Quality Operations Validation department.
The successful candidate will assist in the development of assembly and packaging validation protocols, performs testing and write validation reports for various equipment. Generate validation protocols using templates. Primary responsible for protocol execution of various types of basic processing equipment under the direction of Validation Manger.

Responsibilities:

  • Assists with development of assembly and packaging validation protocols, perform testing and write validation reports for various equipment. Generate validation protocols using templates. Primary responsible for protocol execution of various types of basic processing equipment under the direction of Validation Manger.
  • Issue data, memos and reports concerning above projects.
  • Help to determine process capability of new equipment through execution of approved protocols and assures defined parameters are incorporated into respective operating procedures and batch records.
  • Perform special projects as assigned by department manager.
  • Adhere to all company and GMP procedures, along with safety regulations within the plant.
  • Assist with validation activities performed by outside validation companies; assures that department and company policies are adhered to.
  • Assist with the Site Change Management Program to keep all finished products, equipment, processes and facilities in compliance with contemporary industry standards and regulatory filings.

Qualification Criteria:

  • BS in Chemistry, Biochemistry, Microbiology, Engineering, Pharmacy or related science and 5 plus years related experience and/or training; or equivalent combination of education and experience.
Industries: Pharmaceutical
Employment Type: Contract Other
Skills: Quality Validation
Location: Missouri

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