Senior Director, Quality Control

Scorpion Therapeutics; United States; Remote; USD 216,000 - 270,000; Full time

Job summary

A leading company in genetic medicine is seeking a Senior Director for Quality Control Testing. This role involves overseeing a large team, ensuring compliance with regulatory standards, and providing technical leadership in gene therapy product testing. The ideal candidate will have extensive experience in the pharmaceutical industry, particularly in managing analytical testing laboratories. Join a mission-driven team dedicated to advancing innovative therapies for patients.

Benefits

Comprehensive benefits

Work-life resources

Qualifications

• 20 years in pharmaceutical-biologics industry required.
• 15 years managing cGMP analytical testing laboratories.
• Strong technical understanding of molecular virology.

Responsibilities

• Lead internal Quality Control Testing group of 50 analysts.
• Ensure timely completion of lot release and stability testing.
• Provide technical leadership and guidance to analytical testing groups.

Skills

Data Analysis

Statistical analysis

Project Management

Communication

Education

PhD in Biochemistry

MS in Molecular Biology

Tools

PCR

Chromatography

ELISA

Job description

If you're aiming for a job like this, you need an edge.

JobsAI gives you that edge—by helping you upgrade your resume, analyze hiring managers’ LinkedIn profiles, and prepare with a built-in interview coach.

This is the smarter, faster way to compete in today’s job market.

Check out JobsAI

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:

• Physical and Emotional Wellness
• Financial Wellness
• 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 Senior Director charged with overseeing all internal Quality Control Testing will lead a group of high-functioning QC analysts comprising approximately 50 individuals organized under 3-5 direct reports. The ideal candidate will be highly skilled in managing an integrated testing schedule that supports both a high-throughput late-phase, commercial manufacturing supply chain as well as a dynamic early phase clinical pipeline. The successful candidate will foster a collaborative environment and play a key role in executing the strategy that ensures a continuous global supply of Sarepta’s AAV gene therapies for neuromuscular disorders. The candidate will excel in a team-based environment, working closely with Sarepta’s Manufacturing, Quality Assurance, and Regulatory Affairs departments. Additionally, the Senior Director will possess superior technical, problem solving, and mentoring skills that facilitate team and individual development.

The Opportunity to Make a Difference

• Providing technical leadership and guidance to the internal analytical testing groups.
• Ensuring the successful and timely completion of all lot release and stability testing to support all Corporate and Tech Op’s business commitments and goals.
• Evaluating, reviewing, and approving assay development and qualification reports to ensure smooth and efficient transfer of analytical test methods to the Quality Control group.
• Building and managing an appropriate qualification/requalification program to ensure all analysts executing QC testing are fully trained and current on all aspects of their assigned analytical testing areas.
• Generating and managing monthly and quarterly metrics (KPIs) to track QC analytical testing performance.
• Authoring IND, BLA, NDA, and IMPD sections pertaining to drug product lot release testing for submission to regulatory agencies.
• Provide subject matter expertise when engaging in various discussions with external regulatory agencies such as FDA, EMA, and PDMA.
• Additionally, proposed expansions to corporate capabilities will require knowledge and experience with Quality Control Microbiology (EM/PM and utilities monitoring) and Quality Control Raw Materials Testing.

More About You

A PhD (or MS with appropriate experience) in Biochemistry, Molecular Biology, or Molecular Virology with twenty years of experience in the pharmaceutical-biologics industry is required. Additionally, we are looking for an individual with at least fifteen years of experience managing/directing cGMP analytical testing laboratories with a minimum of five to eight years of experience testing and releasing Gene Therapy products (AAV or similar products). Experience testing and releasing cell therapy products will be considered as appropriate. A strong technical understanding of molecular virology is required. Strong technical knowledge in all areas of AAV testing is a must. Areas of expertise must include:

• Data Analysis:
  • Data trending and reporting
  • Statistical analysis (Strong statistical skills are a must)
• General Laboratory – Chemistry Testing:
  • pH
  • Osmolality
  • Visual Inspection
  • Gravimetric and Volumetric analyses
• Particle Analysis:
  • Visible and Sub-visible
  • Aggregate analyses: SEC and DLS (Dynamic Light Scattering)
• Cell Culture and Bioassay Testing:
  • Aseptic sample handling and aliquoting techniques
  • Mammalian Cell Culture
  • Relative Potency Assays (PLA, 4PL/5PL)
  • Tissue Culture Infectivity Assays -50% (TCID50)
  • ELISA and other Protein Binding assays
• Nucleic Acid Testing:
  • Polymerase Chain Reaction: ddPCR, dPCR, qPCR, RT-qPCR
  • Sequencing: Sanger Sequencing and NGS
• Plasmid Manufacturing:
  • Molecular Cloning and Restriction Digestion analysis
• Separation Sciences:
  • Chromatography (LC, LC-MS)
  • Analytical Ultra Centrifugation (AUC)
  • Gel Separation Sciences (SDS-PAGE, CE-SDS)

Experience planning and managing budgets in excess of $50 million/year. Strong written and oral communication skills are a must. Proven ability to manage projects and work with cross-functional teams comprised of internal and/or external contacts, including CTLs.

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.

This position requires work on site at one of Sarepta’s facilities in the United States.

The targeted salary range for this position is $216,000 - $270,000 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.