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Analyst
Quality Control/cGMP/Compliance
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Location: Northborough, MA
Pay Rate: Contract: 34.53 to 44.64 $/hr
Salary: 71.82 to 92.85 K$/yr
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Position Type/ Job Duration: Contract 3 - 4 months
Education Required: BS 
Years Experience Required: 1

Industry:
Mfg
Job Posted: 10/4/2017
Should I worry about this date?
Apply Deadline: 10/25/2017 12:00:00 AM
Job #: 127920IP1
Job order status: Client is actively seeking candidates
Relocation available: Not Available


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A French multinational pharmaceutical company is currently seeking a Quality Control Analyst in Northborough, MA. This is a 3-month CONTRACT position, with the possibility of extension. No per diem available.

Responsibilities

  • Act as study director for validation of analytical methods and lab equipment. Author validation protocols / reports, test methods and records. Contribute scientific knowledge, analytical skills, and interpretation of data
  • Ensure a consistent style of QCRM documents to maintain quality and ease of review. Support analytical SOP method optimization, validation, transfer, and life cycle management. Support Out-of-Specification Investigations, CAPA events and Change Controls.
  • Support readiness for regulatory inspections and compliance audits. Assess routine compendial updates for impact to existing testing procedures. Support development of junior analysts through mentoring.
  • Practice safe work habits and adhere to Genzyme’s safety procedures and guidelines. Maintain proficiency training per assigned curricula.

Requirements

  • Bachelor’s degree in a related discipline
  • 5+ years of experience in cGMP laboratory environment with first-hand experience with compendial analysis of raw materials and a broad range of lab equipment.
  • Previous experience with lab control operations and quality systems
  • Preferred experience with chromatography data systems (Empower)

Benefits

  • Health Benefits
  • 401K
 
 
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Related Keywords quality control analyst, qc, cgmp, compliance, testing, test methods, scientific knowledge reports, lab equipment, compendial update, testing procedures, development, validation, sop, life cycle management, regulatory inspections
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