Quality Control and Analytical Development Manager

Amylyx has an audacious mission to usher in a new era for treating diseases with high unmet needs. Where others see challenges, we see opportunities that we pursue with urgency, rigorous science, and unwavering commitment to the communities we serve. We are a clinical-stage company currently focused on post-bariatric hypoglycemia (PBH), Wolfram syndrome, and amyotrophic lateral sclerosis (ALS).

Our mission is powered by our people. Our core values – be audacious, be curious, be authentic, be engaged, and be accountable – creating a culture of caring. Amylyx has assembled an experienced team ready to take action because the communities we serve have no time to wait. If you share our passion and are determined to tackle some of medicine’s toughest problems, we encourage you to read the opportunity below and apply.

The Opportunity

The Quality Operations team is expanding and looking to hire a Manager of QC/AD, reporting to the Senior Director of QC/AD. This individual will be responsible for managing analytical development activities to support the Amylyx pipeline products including synthetic peptides, antisense oligonucleotides and small molecules. This individual will support phase appropriate analytical development, qualification/validation and oversight of GMP release and stability testing. The ideal candidate will be a motivated, self-starter, well versed in the GMPs, willing to actively collaborate cross functionally and excited about the potential to deliver therapies to patients in need.

Responsibilities

• Plan, coordinate and manage routine release testing and applicable stability programs at external CMOs and CTLs.
• Manage the technology transfer of method development, qualification and validation activities to support product characterization, release and stability across multiple programs.
• Technical review and trend analysis of in process, release and stability data across active pharmaceutical ingredients (API), drug substance (DS) and drug product (DP).
• Drive all analytical investigations of OOS, deviations, change controls, CAPAs, temperature excursions and troubleshooting with CMO/CTLs.
• Support QC GMP systems by maintaining reference standard, critical reagent and method performance programs.
• Author, review and approve documentation including technical reports, SOPs, test methods, specifications and CMC sections of regulatory filings.
• Collaborate cross functionally with teams including Preclinical R&D, External Manufacturing, Regulatory and Quality leadership to develop strategies and deliver on key objectives.

Requirements

• BA/BS, MS or PhD in chemistry, biochemistry or related discipline