At a Glance
- Tasks: Lead external manufacturing strategy and partnerships for innovative clinical and commercial programmes.
- Company: Join Amylyx, a pioneering company transforming treatment for high unmet medical needs.
- Benefits: Competitive salary, remote work options, and a culture of care and accountability.
- Other info: Remote work available; travel to Cambridge, MA required several times a year.
- Why this job: Make a real impact in healthcare by tackling some of medicine's toughest challenges.
- Qualifications: 15+ years in pharma/biotech with strong leadership and CDMO management experience.
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 – create a culture of caring. Amylyx has assembled an experienced team ready to take action because the communities we serve have no time to wait.
The Senior Director, External Manufacturing is a critical leadership role responsible for shaping and executing the external manufacturing strategy across clinical and future commercial programs. This individual will lead a global network of CDMO partners supporting a diverse and growing portfolio spanning peptides, oligonucleotides, and small molecules. As Amylyx advances toward commercialization and expands its global manufacturing footprint, this role will be instrumental in ensuring supply continuity, operational readiness, and long-term scalability. The Senior Director will partner cross-functionally to enable successful product launches, manage increasing manufacturing complexity, and build the infrastructure needed to support future growth and global expansion.
Responsibilities
- Provide strategic leadership and oversight of external manufacturing across clinical development and commercial supply.
- Establish and govern CDMO partnerships to ensure strong performance, accountability, and alignment with program objectives.
- Define and execute manufacturing strategies to support technology transfer, scale-up, commercialization, and lifecycle management.
- Establish supplier performance metrics and business review process.
- Mentor and build a team of relationship owners responsible for leading the internal supplier relationship teams and serving as the supplier point of contact.
- Ensure supply continuity through proactive risk identification, mitigation planning, and issue escalation across external partners.
- Oversee technology transfer, manufacturing execution, and process performance across a global network of external sites.
- Support commercial launch readiness, including validation, supply planning, and inspection preparedness.
- Partner cross-functionally with Finance, Legal, CMC, Quality, and Supply Chain to drive aligned execution.
- Build scalable, robust external manufacturing infrastructure, operating models, and governance frameworks to support organizational growth.
Required Qualifications
- Bachelor’s degree in engineering, life sciences, or related field; advanced degree preferred.
- ~15+ years of experience in pharmaceutical or biotechnology manufacturing, including significant external manufacturing leadership.
- Proven track record managing CDMOs across clinical and commercial supply environments.
- Deep understanding of cGMP regulations, global manufacturing requirements, and regulatory expectations.
- Experience in manufacturing strategy, technology transfer, and commercialization activities.
- Demonstrated ability to lead in complex, multi-program environments and drive cross-functional alignment.
- Strong leadership, communication, and stakeholder management skills.
- Prior experience supporting commercial product launches, conducting RFPs, negotiating supply agreements, and managing high value budgets.
- Experience across multiple supply nodes (API, Drug Product, Packaging, Device).
- Ability to travel domestically and internationally ~10%.
Preferred Requirements
- Experience across multiple modalities (small molecule, peptide, oligonucleotide).
- A track record of process scale-up, validation and continuous improvement.
Work Location and Conditions
At Amylyx, we proudly support remote work opportunities within the United States. However, due to business considerations related to health insurance coverage and state tax regulations, we are unable to hire employees who reside and/or work in certain states. Currently, we are not considering applicants from Alaska, Arizona, Hawaii, Michigan, and Tennessee. Preference may be given to candidates residing within or near the geographic region they support.
You will be expected to travel to our corporate location in Cambridge, MA several times a year and attend other company-related events as necessary and requested. You must have access to work in a setting which enables meeting all requirements of the role (including privacy, reliable internet access, phone, ability to video conference, etc.) at your remote location.
Compensation
The pay range posted below represents our good faith estimate of compensation for this role, based on market data and internal benchmarks. The final offer may vary depending on a candidate’s experience, skills, and qualifications, as well as considerations of internal equity. Estimated Pay Range: $245,000 - $276,000 USD.
To stay connected with us, follow Amylyx Pharmaceuticals on LinkedIn.
Amylyx Pharmaceuticals is an Equal Opportunity Employer that does not discriminate on the basis of actual or perceived race, colour, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, pregnancy-related conditions, and lactation), gender identity or expression (including transgender status), sexual orientation, marital status, military service and veteran status, physical or mental disability, genetic information, or any other characteristic protected by applicable federal, state, or local laws and ordinances. Amylyx’s management team is dedicated to this policy with respect to recruitment, hiring, placement, promotion, transfer, training, compensation, benefits, employee activities, access to facilities and programs, and general treatment during employment. Accommodations are available for candidates who require them in our selection process. If you need an accommodation, please let your Amylyx Talent Acquisition contact know.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Senior Director, External Manufacturing in Cambridge employer: Amylyx Pharmaceuticals
At Amylyx, we are driven by our mission to transform the treatment landscape for diseases with high unmet needs, fostering a culture of audacity, curiosity, and accountability. As a Senior Director in External Manufacturing, you will be part of a dynamic team that values innovation and collaboration, offering ample opportunities for professional growth while working remotely within the United States. Our commitment to employee well-being and development, combined with the chance to make a meaningful impact in the lives of patients, makes Amylyx an exceptional employer.
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