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Tech Ops and Quality Quality Control Analyst I
Job Location:
Job Location:
Norton, OH - USA
Hourly Salary:
USD 30 - 30
Hourly Salary:
Posted:
22 October 2026 (23 hours ago)
Posted:
Application Deadline:
19 January 2027
Application Deadline:
Vacancies:
1 Vacancy
Vacancies:
Job Summary
Overview
The Analyst I in Quality Control Operations will play a critical role in executing assays generating accurate and reliable data and supporting the general operations of the laboratory to ensure the quality and compliance of our products from development through to commercialization.
This position is onsite and will be primarily located in Norton MA. There may occasional responsibilities at a secondary location in Cambridge MA.
Key Responsibilities (including but not limited to):
Qualifications
The Analyst I in Quality Control Operations will play a critical role in executing assays generating accurate and reliable data and supporting the general operations of the laboratory to ensure the quality and compliance of our products from development through to commercialization.
This position is onsite and will be primarily located in Norton MA. There may occasional responsibilities at a secondary location in Cambridge MA.
Key Responsibilities (including but not limited to):
- Perform routine and non-routine analytical assays to support raw materials in-process samples product release and stability studies under supervision following established SOPs
- Maintain up-to-date training records adhere to the testing schedule and ensure the timely completion of all assignments to support the seamless operation of QC activities and uphold the departments commitment to meeting project timelines and quality metrics
- Assist in the maintenance of laboratory equipment and inventory including the preparation of reagents and samples to ensure smooth laboratory operations
- Accurately record experimental data and observations in compliance with GxP standards. Participate in the review of data commensurate with experience.
- Contribute to the revision and updating of controlled documents including SOPs work instructions and test methods to ensure continuous improvement and compliance with current industry standards and regulatory requirements
- Adhere to internal standards policies and SOPs as well as regulatory and industry standards (e.g. GMP GLP ICH guidelines) to maintain the highest levels of quality and compliance.
- Actively participate in continuous improvement efforts by identifying and suggesting enhancements to methods and laboratory processes particularly those related to efficiency and reliability.
- Collaborate with QC and cross-functional teams to ensure seamless quality control operations and to support the collective Alnylam goals
- Pursue ongoing training and development to deepen expertise in QC analytical techniques and regulatory compliance.
Qualifications
- Bachelors degree in Chemistry Biochemistry Pharmaceutical Sciences or a related field
- 0 to 2 years of experience in a GMP/GLP regulated laboratory environment with exposure to pharmaceutical or biotechnology industries preferred
- Understanding of analytical techniques and their application in raw materials in-process testing release and stability studies is preferred
- Strong documentation skills and attention to detail with an unwavering commitment to quality and compliance
- Basic awareness of regulatory guidelines relevant to pharmaceutical QC (GMP GLP ICH) is desirable
- Effective communication and teamwork skills with the ability to work collaboratively across functions
Required Experience:
IC
About Company
LanceSoft is a global workforce solutions company connecting businesses with top talent across industries and geographies.
