Job Description

Engineering - Bio Process Associate - 2nd Shift
Job Number: 21-14960
 
Be part of a company that delivers life-changing healthcare solutions. Eclaro is looking for an Engineering - Bio Process Associate - 2nd Shift for our client in Devens, MA. 
 
Eclaro’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all over the world. If you’re up to the challenge, then take a chance at this rewarding opportunity!
 
Position Overview:
  • The Bioprocess Associate assists in the execution of commercial manufacturing processes according to established electronic work instructions and production records for the manufacture of therapeutic proteins in accordance with current Good Manufacturing Practices (cGMPs).
 
Responsibilities:
  • Works on routine manufacturing assignments per written procedures that are moderately complex with minimal instructions, where ability to recognize deviation from accepted practice is required.
  • Adheres to Good Manufacturing Practices and standard operating procedures.
  • Weighs and checks raw materials.
  • Assembles, cleans and sterilizes process equipment, monitors processes.
  • Completes electronic work instructions and maintains clean room environment to comply with regulatory requirements.
  • Operates primary production equipment within the assigned functional area (i.e. bioreactors, chromatography skids, media or buffer preparation equipment etc.) as instructed.
  • Effectively uses in process automation systems (i.e. Delta V and Syncade Interactions, OSI/Pi Historian) and some supporting business systems (i.e. SAP. Trackwise, Maximo etc.) to maintain production records.
  • Revises and creates process documents with little to no instruction, assists with process related investigations.
  • Leads in maintaining material and components inventory level.
  • Assists with reviewing batch and exception reports associated with each manufacturing lot, in conjunction with supervisor and Quality representative.
  • Provide assistance for areas specific initiatives associated with work safety.
 
Qualifications:
  • High school diploma is required.
  • Knowledge of science generally attained through completion of a certificate program or Associates Degree in Biotechnology or a related field.
  • Prior experience with Good Manufacturing Practices (GMP) regulations and/or prior work experience in a clean room or highly regulated environment a plus.
  • Prior evidence of successful participation on work teams where combined contribution, collaboration, and results were expected.
  • Demonstrated proficiency in common computer tools such as word processing, spreadsheet and web based applications.
  • Previous work experience where attention to detail and personal accountability were critical to success.
  • Demonstrates good interpersonal skills, is attentive and approachable.
  • Maintains a professional and productive relationship with area management and co-workers.
 
If hired, you will enjoy the following Eclaro Benefits:
  • 401k Retirement Savings Plan administered by Merrill Lynch
  • Commuter Check Pretax Commuter Benefits
  • Eligibility to purchase Medical, Dental & Vision Insurance through Eclaro
 
If interested, you may contact:
Jane Bautista
froilyn.bautista@eclaro.com
2012858622
Jane Bautista | LinkedIn
 
Equal Opportunity Employer: Eclaro values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

Application Instructions

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