Quality Control Analyst I

Alnylam Pharmaceuticals•Norton, MA

6d•$61,500 - $83,300•Onsite

About The Position

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. This role ensures high standards of quality and compliance are met in support of early-stage development through commercial Alnylam programs. The QC-RMSM Analyst I will assist and participate in the qualification, management, and inventory control of required reference materials as well as the Raw Material program. This position is onsite and will be primarily located in Norton, MA. There may occasionally be responsibilities at a secondary location in Cambridge, MA or off-shift as required by business need.

Requirements

B.S. in chemistry, biology, or biochemistry, or related scientific field; Associates Degree, Biotech Certificate, or equivalent considered
Pharmaceutical/Biotech industry experience with 0-4 years in a regulated laboratory setting, Quality Control, or equivalent relevant 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

Nice To Haves

Knowledge of LIMS and Microsoft Suite of Applications is helpful

Responsibilities

Assist in the qualification and requalification of primary, secondary and working reference standards as well as critical reagents
Engage in the collection, analysis, and review of QC data to ensure availability of data
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 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 organizational functions including those in Quality Control, Quality Assurance, and CMC to ensure reference material availability and timelines.
Contribute to the 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 as well as supporting onsite audits and inspections, as needed.