Why Sarepta? Why Now?
The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold leadership positions in Duchenne muscular dystrophy (DMD) and limb-girdle muscular dystrophies (LGMDs), and we currently have more than 40 programs in various stages of development in gene therapy, RNA and gene editing. In 2023, we launched our fourth therapy and the first ever gene therapy to treat Duchenne.
We’re looking for people who see unlimited potential in themselves and who are motivated by an unwavering commitment to patients.
What Sarepta Offers
At Sarepta, we care deeply about all the people in our community and believe in the importance of supporting them in all aspects of their lives. We aspire to maintain a culture that acknowledges people bring their whole selves to work, and we will strive to help everyone in our community integrate their work and personal lives while maintaining productivity. We are committed to offering a range of benefits and work-life resources designed to support people in the following areas:
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Physical and Emotional Wellness
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Financial Wellness
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Support for Caregivers
For a full list of our comprehensive benefits, see our website: https://www.sarepta.com/join-us
The Importance of the Role
The Manager, Gene Therapy Commercial Supply Operations, will be the person-in-plant supporting CMO-lead finished goods labeling, packaging, and logistics operations management for a new class of clinical and commercial Gene Therapy products. This position will work closely with the CMO to oversee and direct these specialized operations. This position will have responsibility for overseeing CMO activities related to operations, order management, inventory, and logistics. The Manager will work closely with Global Supply Chain, Logistics, Commercial Operations, Finance, Quality, and IT.
The Opportunity to Make a Difference
- This position is the person-in-plant in Philadelphia and is critical to ensure uninterrupted supply of new and novel gene therapy products.
- Prioritize CMO scheduling label/pack operations, order management, and logistics activities.
- Coordinate the scheduling of patient shipments. Track all shipments and triage any deviations from the plan or procedures.
- closely with CMO personnel to develop a deep understanding of capacity, procedures, and related processes.
- Direct oversight and responsibility for managing CMO-lead labeling, packaging, and logistics operations management.
- Ensuring the timely execution of CMO compliance of operational activities.
- Occasional travel may be required.
More about You
- 5+ yrs Pharmaceutical Packaging Operations and/or Pharmaceutical Packaging Project Management experience. B.A./B.S. required
- Strong understanding of Project Management fundamentals.
- Experience with Smartsheet or similar program preferred.
- Project or Production Scheduling experience preferred.
- Intermediate to advanced knowledge of Microsoft Excel preferred
- This role requires an understanding of pharmaceutical labeling and packaging operations, logistics, supply chain as well as financial and project management skills. Experience with contract manufacturing is desirable.
What Now?
We’re always looking for solution-oriented, critical thinkers.
So, if you’re comfortable with ambiguity and candor, relish challenging yourself, and place kindness and integrity at the forefront of how you approach your peers and work, then we encourage you to apply.
#LI-Hybrid
#LI-TR1
This position is hybrid, you will be expected to work on site at one of Sarepta’s facilities in the United States and/or attend Company-sponsored in-person events from time to time.
The targeted salary range for this position is $112,000 - $140,000 per year. Sarepta is making a good faith effort to be transparent and accurate around our hiring ranges. The salary offer is commensurate with Sarepta’s compensation philosophy and considers factors including, but not limited to, education, training, experience, external market conditions, criticality of role, and internal equity.
Candidates must be authorized to work in the U.S.
Sarepta Therapeutics offers a competitive compensation and benefit package.
Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e-Verify.
What We Do
Sarepta Therapeutics, headquartered in Cambridge, Massachusetts, is a global biotechnology company on an urgent mission: engineer precision genetic medicine for rare diseases that devastate lives and cut futures short. We hold leadership positions in Duchenne muscular dystrophy (DMD) and limb-girdle muscular dystrophies (LGMDs), and we currently have more than 40 programs in various stages of development. Our vast pipeline is driven by our multi-platform Precision Genetic Medicine Engine in gene therapy, RNA and gene editing.
For information on our Community Guidelines, please visit sarepta.com/community-guidelines.
We want to share a reminder with all job seekers and candidates regarding the persistence of recruiting fraud. Please read a message about recruiting fraud and steps you can take to protect yourself here: https://www.sarepta.com/recruiting-fraud