Job Description

Quality Control Chemist
Job Number: 21-04133
 
Be part of a company that delivers life-changing healthcare solutions. Eclaro is looking for a Quality Control Chemist for our client in Andover, MA. 
 
Eclaro’s client is among the world’s largest pharmaceutical companies, trusted by billions to provide superior, cutting-edge, and inexpensive medicine that improves health and well-being. If you’re up to the challenge, then take a chance at this rewarding opportunity!
 
Position Overview:
  • The qualified candidate will provide support for analytical laboratory testing in a cGMP quality control analytical (QCA) laboratory.
  • This includes analytical testing supporting of Drug substance release and stability testing.
  • Provides analytical support to client groups.
  • Analytical research and development activities will include literature searches, analytical method development, test procedure writing, analytical method validation, and method transfer.
  • Analyzes early-stage prototypes, lab samples, pilot plant samples, production samples, stability samples and competitor samples.
  • Possesses extensive knowledge of various laboratory instruments like HPLC, GC, AA, Dissolution, IC, etc.
 
Responsibilities:
  • Perform and Support analytical lab testing: execute testing, review data and documents for compliance and accuracy.
  • Support laboratory investigations
  • Support assay troubleshooting and look for CI opportunities/method improvements.
  • Identify technical issues, atypical or out-of-specifications test results, instrument malfunctions and methodology problems and participates in the investigation to resolve and correct.
  • Maintain all related data and records in compliance with cGMPs and quality procedures
  • Perform laboratory support functions and maintain work area in compliance with cGMP and quality procedures.
  • Collaborate with site functional areas and customers to support site goals and objectives and transfer timelines.
  • Meet all timelines and deliverables in support of Andover manufacturing.
 
Qualifications:
  • Extensive knowledge and practical application of relevant analytical techniques (analytical testing and troubleshooting)
  • Expertise in performing HPLC, UV Spectrophotometry, agarose gel electrophoresis. Knowledge in ELISA.
  • Experienced in cGMP, regulatory guidance and audits
  • Proficiency with computer systems (Microsoft Office applications, LIMS, etc.).
  • Excellent communication skills both oral and written.
  • Strong understanding of continuous improvement tools and skills preferred (standard work, visual management, DMAIC)
  • Relevant Experience:
    • Relevant Experience with Scope of Work and Company
    • Must be cGMP Technical Environment
    • With one or more of the following:
      • HPLC
      • UV Spectrophotometry
      • Gel - Electrophoresis
    • NOT – School, Lab or Research:
      • Must be Method Transfer Work
 
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:
Maria Castañeda
maria.castaneda@eclaro.com
6463571235
Maria Castañeda | 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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