Job Description

QC Associate
JobDiva # 19-11010

Be part of a company that delivers life-changing healthcare solutions. Eclaro is looking for a QC Associate 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!
 
Postion Overview: This position will be responsible for performing activities within the Quality Control Sample Management Department including receipt, logistics, inventory, and disposal of various sample types in support of Quality Control testing in a GMP Quality Control Laboratory in accordance with local and global SOPs, regulatory guidelines, and EHS procedures.

Responsibilities:
  • Receive and aliquot Drug Product and Drug Substance release and stability samples
  • Perform inventory for sample types including test reserves, critical reagents, and regulatory retains
  • Prepare and ship samples to third parties for testing
  • Transcribe data into Sample Manager LIMS system in support of Drug Substance lot disposition
  • Prepare and ship stability samples to third party stability sites
  • Schedule and coordinate maintenance for controlled temperature units (CTUs), Pipettes, and Biosafety Cabinets (BSC).
  • Dispose of samples when authorized

Required Experience:
  • Experience with good documentation practices (GDP)
  • Experience working in a BSC
  • Experience in at least one of the computerized systems (Maximo, SMLIMS, Velquest LES, DCA, DeltaV, Trackwise)
  • Experience working in a GxP QC laboratory environment (2+ years)
  • Experience working with dry ice, biological waste, and sharps
  • Experience with and understanding of Data Integrity as it pertains to a GMP/GLP environment

Qualifications:
  • Experience with SMLIMS, LES, and/or Maximo
  • Experience in shipping temperature controlled materials to contract test labs (CTLs)
  • Regulatory or QA audit exposure in a GMP / GLP environment
  • Experience with or understanding of biologic / cell culture manufacturing process
  • Multitasking and attention to detail
  • Bachelor’s Degree in related field
  • Strong verbal and written communication skills
  • Ability to work independently and as part of a team

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:
Melrose Madrigal
Melrose.Madrigal@eclaro.com
6468495355
Melrose Madrigal | 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

Please click on the link below to apply for this position. A new window will open and direct you to apply at our corporate careers page. We look forward to hearing from you!

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