Quality Control Analyst

Overview

The Quality Control Analyst I in support of QC Raw Materials/Sample Management (QC‑RMSM) plays a crucial role in sample management operations for our internal and external GMP laboratories. The role ensures high standards of quality and compliance are met in support of early‑stage development through commercial Alnylam programs. The Analyst will assist in the qualification, management, and inventory control of required reference materials and the raw material program.

This position is onsite and will be primarily located in Norton, MA, with occasional responsibilities at a secondary location in Cambridge, MA or off‑shift as required by business need.

• Assist in the qualification and requalification of primary, secondary and working reference standards as well as critical reagents.
• Engage in collection, analysis and review of QC data to ensure data availability.
• Maintain up‑to‑date training records, adhere to the testing schedule, and ensure timely completion of all assignments to support seamless operation of QC activities and uphold the department’s commitment to meeting project timelines and quality metrics.
• Accurately document all results in laboratory notebooks, LIMS, or other controlled systems in compliance with GMP standards; may qualify as a data reviewer to ensure timely and efficient data availability.
• Participate in raw material program, including inspection of incoming raw materials.
• Collaborate cross‑functionally with other functions including Quality Control, Quality Assurance, and CMC to ensure reference material availability and timelines.
• Contribute to revision and updating of controlled documents, including SOPs, work instructions, and test methods, to ensure continuous improvement and compliance with ALNY requirements.
• Participate in inspection readiness activities and support onsite audits and inspections as needed.

• B.S. in chemistry, biology, or biochemistry, or related scientific field; A.S., biotech certificate or equivalent considered.
• 0‑4 years of experience in a regulated laboratory setting within the pharmaceutical/biotech industry, or equivalent experience with reference material lifecycle.
• Ability to work under direction, with attention to detail and strong organizational skills, in an environment where priorities shift.
• Good communication and teamwork abilities, capable of working effectively in a collaborative environment.
• Knowledge of LIMS and Microsoft Suite of Applications is helpful.

U.S. Pay Range: $61,500.00 - $83,300.00. Base pay will be determined based on experience, skills, and education. The role is eligible for an annual short‑term incentive award (e.g., bonus or sales incentive) and an annual long‑term incentive award (e.g., equity).

Alnylam’s robust total rewards package includes medical, dental, and vision coverage; life and disability insurance; lifestyle reimbursement program; flexible spending and health savings accounts; 401(k) with company match; paid time off, wellness days, holidays, and recharge breaks; generous family resources and leave.

For more information on benefits, visit

At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. Qualified applicants will receive consideration for employment without regard to sex, gender, sexual orientation, race, color, ethnicity, national origin, ancestry, citizenship, religion, creed, physical or mental disability, pregnancy status or related conditions, genetic information, veteran or military status, marital or familial status, political affiliation, age, or any other factor protected by federal, state, or local law.

Alnylam is an E-Verify Employer.