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Alnylam Pharmaceuticals

Develops RNAi-based therapies for genetic diseases

Quality Assurance Associate - GxP Audits & Inspection Excellence

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeCambridge, MA, USA$60.4k - $81.7k

About the Job

Requirements

  • A bachelor's degree in Life Sciences or a related field, or equivalent quality assurance experience.
  • One to three years of experience in a regulated pharmaceutical, biotechnology, or medical device environment.
  • Strong organizational and time-management skills.
  • Accountability and reliability in completing assigned responsibilities.
  • Attention to detail and documentation practices.
  • Working knowledge of GxP regulations and Quality Systems.
  • Ability to work collaboratively in a cross-functional environment.
  • Willingness to learn and develop within the Quality function.

Responsibilities

  • Support execution of GxP audit and inspection processes in alignment with enterprise processes.
  • Support audit and inspection lifecycle activities, including resourcing, coordination, facilitating preparation and debrief meetings, organizing documentation, updating trackers, and reporting status.
  • Support preparation of audit and inspection materials, dashboards, and readiness documentation.
  • Participate in regulatory inspections in assigned support roles, including document quality control, scribing, and other applicable activities.
  • Maintain and review audit and inspection records to ensure histories, timelines, commitments, and related information are complete, accurate, consistent, and compliant with standard operating procedures.
  • Support tracking of inspection commitments and corrective and preventive actions in collaboration with cross-functional colleagues.
  • Support user access, data entry, and routine administration of audit and inspection systems.
  • Provide administrative and operational support for other Quality Management System activities, including deviations, corrective and preventive actions, change controls, and related quality records.
  • Support process improvement activities, including developing and updating audit and inspection templates and tools.
  • Use established procedures, available information, and sound judgment to make routine decisions within assigned responsibilities and determine when matters should be escalated.

Desired Qualifications

  • Experience working in Quality Management System or quality databases.

About the Company

Alnylam Pharmaceuticals

Develops RNAi-based therapies for genetic diseases

Alnylam Pharmaceuticals develops RNA interference (RNAi) therapeutics to silence disease-causing genes, aiming to treat rare genetic disorders. Its products work by using RNA molecules that block gene expression, reducing the impact of specific genetic diseases. The company differentiates itself by concentrating on RNAi-based drugs for rare diseases and by building a pipeline through large clinical programs and strategic partnerships, such as commercialization deals in the Gulf States and collaborations with investors. Revenue comes from approved drug sales, licensing agreements, strategic collaborations, and related services like genetic testing and counseling. The company’s goal is to advance and commercialize RNAi therapies to improve outcomes for patients with genetic disorders, expanding its portfolio through partnerships and investments.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Cambridge, MA
Founded
2002

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