Chemical Process Engineer

Cincinnati, OH

Posted: 01/31/2020 Job Number: JN -012020-11370

Job Description

Chemical Process Engineer

SRG offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services. SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to rapidly and precisely match professionals to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.

Title: Chemical Process Engineer
Location: Cincinnati, Ohio
Industry: Pharmaceutical
Salary: $25.00-$28.00 paid weekly with benefits options
Employment Type: Contract- 1 year (Could be extended)

Prepare process validation and performance qualification protocols, reports and analyze data. Monitor validation and performance qualification processes to ensure strict accordance with documentation. Utilize knowledge in the areas of formulation development and process optimization using pharmaceutical processes such as wet granulation (high shear and fluid bed), pellet processes, direct compression (v-blenders and container blending systems), tablet compression, encapsulation, tablet coating, etc.

  • Coordinate validation activities to meet critical project deadlines and product launch dates.
  • Prepare, review and/or approve written documents to support technical projects, regulatory submissions and validation projects.
  • Assist with the integration of new companies and/or products resulting from acquisition, merger, or licensing agreements.
  • Execute process validation batches (including, site transfers, launch, alternate equipment, alternate vendor, etc.)
  • Maintain and monitor facility cleaning validation program for approved products and cleaning verification for unapproved products.
  • Prepare, review, approve SOP s, APR s Change Controls, CAPA s, IR s, DR s, MBMR s and create Oracle recipes.
  • Review work orders in data stream, review and approve equipment periodic reviews, review and approve equipment qualification protocols & reports.

  • Required Associate Degree required, Bachelor s Degree preferred.
  • 3-5 years pharmaceutical validation preferred.
  • Minimum 1-3 years Pharmaceutical Manufacturing or Validation.
  • Must be willing to travel up to 10% of the time.
  • Proficient use of specified computer software (Oracle).
  • Apply working knowledge of regulatory requirements (SOPs) and other related disciplines.
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