Entrada Therapeutics

Entrada Therapeutics

Associate Director, Drug Product Development & Manufacturing

Boston, MA · Director

Sponsorship not specified$44k-$601kDetected 44 days ago
ExcelGMPFDA RegulatoryCommunicationCollaborationOrganizational Skills

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odds of building a lasting career here

59Sponsors, lottery-bound
Cap-exempt (no lottery)0
Sponsors this role80
Entry-level history0
PERM / green-card track0
Lottery odds (Level IV)94
Fits your clock70

Sponsors, but it's cap-subject — you still face the weighted lottery (~61% per draw at Level IV). Good if you win; have a cap-exempt backup on your list.

Lottery odds assume a STEM candidate.

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About the role

  • The Associate Director, Drug Product Development & Manufacturing, is accountable for leading drug product manufacturing activities to support Entrada's clinical stage assets and novel pipeline programs.
  • This role ensures successful execution of clinical manufacturing operations for parenteral drug products and partners cross-functionally to deliver uninterrupted clinical supply.

Responsibilities

  • Lead drug product formulation, characterization, process development, technology transfer, scale-up, and manufacturing activities for early to late-stage pipeline programs.
  • Develop, author, review, and approve technical study protocols, reports, and documentation related to development and manufacturing.
  • Author/review related sections in regulatory filing documents (IND, IMPD, NDA, etc.).
  • Collaborate cross-functionally across a wide variety of teams, including Discovery, Chemistry, DS Development & Manufacturing, Analytical Development & Quality Control, Quality Assurance, Clinical Operations, and CRO/CDMOs.
  • Meaningful Work, Fair Rewards, and Real Support
  • We believe meaningful work deserves meaningful reward, and view compensation as one way to show appreciation for the collaboration, curiosity, and commitment that drive our mission forward.

Nice to have

  • Experience in parenteral drug product formulation development and manufacturing, with demonstrated ability to provide CDMO oversight.
  • Direct experience with intravitreal injections is a plus.
  • Strong knowledge of sterile manufacturing and fill-finish operations with demonstrated experience with batch records, deviations, change controls, and tech transfer.
  • Late-stage experience is a plus.

Compensation

  • $175,355 - $201,235 USD
  • The salary for this opportunity ranges from $175,000 - $201,000.

Benefits

  • At Entrada Therapeutics, we understand that compensation and total rewards are a major consideration when exploring a new opportunity.
  • When you join Entrada, you'll be part of a mission-driven team with access to comprehensive health, dental and vision coverage
  • life and disability insurance
  • At Entrada, our approach to compensation is grounded in transparency, equity, and performance, recognizing the unique contributions each person brings.

Company info

  • MS in a scientific related discipline with 8 + years of biotech or pharmaceutical experience preferred.
  • Experience in parenteral drug product formulation development and manufacturing, with demonstrated ability to provide CDMO oversight. Direct experience with intravitreal injections is a plus.
  • Strong knowledge of sterile manufacturing and fill-finish operations with demonstrated experience with batch records, deviations, change controls, and tech transfer. Late-stage experience is a plus.
  • Demonstrated ability to lead authoring and review of technical study protocols and reports, manufacturing documentation, and regulatory documents.
  • Knowledge of cGMP, ICH, FDA and EMA guidelines regarding sterile drug product development and manufacturing.
  • Excellent verbal and written communication skills.
  • Ability to stay highly organized while managing multiple programs in a fast-paced environment and working effectively across functions.
  • Desire to work in an innovative and collaborative environment.
  • Ability to travel (estimated 20% or as needed) to CDMOs for supporting manufacturing campaigns.
  • At Entrada, our passion for science, our devotion to patients and our values drives our behavior:
  • Tenacity - We are relentless and persistent in the pursuit of developing therapies for patients.
  • Creativity - We are creative problem solvers.
  • Collaboration - We are more than the sum of our parts.

Equal opportunity

  • Entrada Therapeutics is an equal opportunity employer.
  • Qualified candidates will receive consideration for employment without regard to race, color, religion, national origin, gender, sexual orientation, gender identity or expression, age, mental or physical disability, and genetic information, marital status, citizenship status, military status, protected veteran status or any other category protected by law.
  • Third Party Staffing Agencies
  • Entrada does not accept unsolicited resumes from any source other than directly from candidates.

Visa & Work Authorization

  • rientation, gender identity or expression, age, mental or physical disability, and genetic information, marital status, citizenship status, military status, protected veteran status or any other category protected by law
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This listing is sourced directly from Entrada Therapeutics's careers page and normalized into a canonical job model.