Alnylam Pharmaceuticals

Associate Director, Early Development Quality Lead, R&D QA

Alnylam Pharmaceuticals$164K — $222K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Master's degree in life sciences or equivalent experience preferred
  • Minimum 8 years of relevant bioanalytical and toxicology experience
  • Experience with GLPs, GCPs, and GCLPs is essential
  • Familiarity with modern biomarker assays like PCR, ELISA, and FISH preferred
  • Proficiency in risk-based thinking and quality assurance practices

Responsibilities

  • Set strategic quality oversight for internal and outsourced laboratory activities
  • Establish and maintain quality oversight of external laboratories
  • Collaborate with clinical teams to integrate quality into lab selection and management
  • Ensure compliance of biomarker development work with regulatory standards
  • Implement a risk-based vendor oversight and audit program globally
  • Manage nonclinical and clinical lab quality issues related to outsourcing
  • Serve as the Quality escalation point for CRO/vendor issues

Benefits

  • Comprehensive medical, dental, and vision coverage
  • Life and disability insurance
  • Flexible spending and health savings accounts
  • 401(k) with generous company match
  • Paid time off and wellness days
  • Generous family resources and leave
  • Company-wide recharge breaks
Full Job Description
Associate Director, Early Development Quality Lead, R&D QA

Overview

The Early Development Quality Lead is responsible for the strategic quality oversight of internal and external (outsourced) activities in support of nonclinical studies (GLP and non-GLP), IND enabling work, as well as the utilization of Biomarkers within development programs (preclinical and clinical).

This role will partner with Alnylam colleagues within Early Development, Bioanalytical, Nonclinical Writing, Research, and Clinical Research to provide quality support and oversight and ensure the identification, mitigation, and escalation of emerging quality risks and concerns.

This position will be located within the US and can be hybrid, onsite, or remote.

Key Responsibilities
  • Sets the strategic quality oversight direction for internal and outsourced laboratory activities supporting nonclinical studies (GLP and non-GLP), including toxicology, bioanalytical and biomarker data that supports IND submissions.
  • Establish and maintain quality oversight of external laboratories including Test Facilities, Test Sites, and Clinical Laboratories by implementing governance framework and ongoing performance monitoring.
  • Collaborate with nonclinical and clinical teams (in partnership with GCP Program Leads) to integrate quality considerations into the selection, contracting, and management of external labs.
  • Ensure internally developed and outsourced biomarker development / analytical work complies with internal quality system requirements and external regulatory standards including GCP, GLP, ICH, and OECD.
  • Refine and continuously implement robust, risk-based vendor oversight and audit program globally for nonclinical work. Lead the risk assessment and audit strategy for external laboratories and ensure planned audits are executed in alignment with the GCP/GLP yearly audit program.
  • Support the management of nonclinical and clinical lab focused quality issues arising from outsourced activities, including quality events, significant quality issues, and CAPA oversight.
  • Serves as the Quality escalation point for CRO/vendor quality issues and leads quality governance activities to ensure appropriate identification, issue escalation and the mitigation of emerging compliance risks.
  • Provides quality strategic direction for the functional evaluation of CRO or key vendor processes or process improvement opportunities.
  • Drive the strategic identification and implementation of process improvement opportunities within Alnylam's QMS, in support of early development and research.
  • Partners with Legal/Procurement for appropriate oversight language in contractual agreements and ensure compliance

Qualifications
  • Educated preferably in life sciences (technology, biological science, pharmacy or other health related discipline preferred) or equivalent qualification or work experience. Master's degree in a science, technology or industry related discipline, preferred.
  • Minimum of 8 years of relevant experience, inclusive of bioanalytical and toxicology subject matter, as it relates to GLPs, GCPs and GCLPs.
  • Direct experience in the field of assay development and validation and familiarity with modern biomarker-based assays (e.g., PCR, ELISA, FISH) is preferred.
  • Prior experience in risk-based thinking, quality assurance, auditing, managing quality issues/escalations, or other relevant QMS elements.
  • Prior expertise in global GLP, GCP, GCLP regulations and guidance across regulatory bodies such as FDA, PMDA, European Union, MHRA, etc.

#LI-AB1 #LI-Virtual

U.S. Pay Range

$164,500.00 - $222,500.00

The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on a number of factors including, but not limited to, relevant experience, skills, and education. This 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 is designed to support your overall health and well-being. We offer comprehensive benefits including medical, dental, and vision coverage, life and disability insurance, a lifestyle reimbursement program, flexible spending and health savings accounts and a 401(k)with a generous company match. Eligible employees enjoy paid time off, wellness days, holidays, and two company-wide recharge breaks. We also offer generous family resources and leave. Our commitment to your well-being reflects our belief that caring for our people fuels the impact we create together.

Learn more about these and additional benefits offered by Alnylam by visiting the Benefits section of the Careers website: https://www.alnylam.com/careers

About Alnylam Pharmaceuticals

Alnylam Pharmaceuticals is a biotechnology company that focuses on RNA interference (RNAi) therapeutics. The company's products are designed to silence specific genes that cause diseases. Alnylam's pipeline includes products for the treatment of genetic, cardio-metabolic, and hepatic infectious diseases. The company was founded in 2002 and is headquartered in Cambridge, Massachusetts.
Learn more about Alnylam Pharmaceuticals
Size
1,665 employees
Market Cap
$28.7 billion
Industry
Net Income
-$858.2 million
Founded
2002
5 Year Trend
+78.1%
Revenue
$492.8 million
NASDAQ

Similar Jobs

More Jobs at Alnylam Pharmaceuticals

More Pharmaceuticals & Biotech Jobs

Find similar Associate Director, Early Development Quality Lead, R&D QA jobs: