Manager, Quality Control and Analytical Development

Amylyx Pharmaceuticals•Cambridge, MA

2d•$125,000 - $141,000•Remote

About The Position

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.

Requirements

BA/BS, MS or PhD in chemistry, biochemistry or related discipline
5+ years of experience working in the biotech and/or pharmaceutical industry with at least 3 years in Quality Control/Analytical Development
Technical knowledge of analytical methods for peptides and/or oligonucleotide products including HPLC/UPLC, LC-MS, GC
Ability to analyze, trend, interpret, organize and present data (experience with JMP and/or other statistical software preferred)
Demonstrated knowledge of cGMP/ICH/FDA/EU/PMDA regulations
Highly collaborative team player with strong communication skills
Ability to prioritize responsibilities and multi-task in a fast-paced environment with changing priorities

Nice To Haves

Experience managing external GMP QC/AD teams at manufacturing and testing partners is preferred
Background in sterile drug product and environmental monitoring investigations experience is a plus

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.