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Quality Control Chemist

Job in Norton, Bristol County, Massachusetts, 02766, USA
Listing for: Integrated Resources, Inc ( IRI )
Full Time position
Listed on 2026-01-04
Job specializations:
  • Quality Assurance - QA/QC
Salary/Wage Range or Industry Benchmark: 35 - 38 USD Hourly USD 35.00 38.00 HOUR
Job Description & How to Apply Below

Quality Control Analyst II

Job Title: Quality Control Analyst II

Location: Norton, MA

Duration: 12 Months+

Shift: First shift, Friday–Monday (4 × 10 hours), with initial Monday–Friday training.

Base Pay Range: $35.00/hr - $38.00/hr

Job Summary Overview: The Quality Control Operations (QCO) Analyst II Contractor supports maintaining high standards of quality and compliance from development through commercialization. The role includes performing routine and non‑routine testing, participating in data trending, investigations, and lab operations, and supporting method transfers, qualification/validation, verification, and implementation. This position enhances QC efficiency and effectiveness.

This is an on‑site role in Norton, MA, with occasional responsibilities at other Alnylam locations. Weekend coverage is required.

Key Responsibilities
  • Perform routine and non‑routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in‑process samples, product release, and stability studies following SOPs
  • Support weekend lab operations and maintain training records
  • Assist in lab equipment and inventory maintenance, including reagent and sample preparation
  • Review data timely and qualify as a data reviewer
  • Perform operational assignments (raw material processes, environmental monitoring, in‑process testing)
  • Contribute to updating controlled documents (SOPs, work instructions, test methods)
  • Follow internal policies, SOPs, and regulatory standards (GMP, GLP, ICH)
  • Participate in continuous improvement initiatives and cross‑functional collaboration
  • Support regulatory submissions, inspection readiness, and audits
Qualifications
  • B.S. in chemistry, biology, biochemistry, or related field
  • 4–8 years of pharmaceutical/biotech experience in GMP QC or equivalent
  • Experience in method transfer/implementation; understanding of method lifecycle management preferred
  • Strong technical writing, data analysis, problem‑solving, and organizational skills
  • Excellent communication and teamwork
  • Proficiency in Lab Ware LIMS, Excel, Word, and PowerPoint preferred
Seniority Level

Mid‑Senior level

Employment Type

Contract

Job Function

Other

Industries

Pharmaceutical Manufacturing and Biotechnology Research

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