Senior Manager, Process Development and Manufacturing

Assembly Biosciences, Inc.

• $199K — $203K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Ph.D. with 3+ years, MS with 6+ years, or BS with 8+ years in small molecule drug substance development.
  • Strong technical skills in process chemistry and drug substance manufacturing equipment.
  • Knowledge of global pharmaceutical regulatory requirements (cGMP, ICH, USP).
  • Experience with CROs/CMOs for drug substance development and manufacturing.
  • Effective communicator with strong collaboration and time-management skills.
  • Self-motivated and adaptable in a fast-paced environment.

Responsibilities

  • Support drug substance development and manufacturing at CMOs for timely delivery.
  • Collaborate with CMOs to design and implement chemical synthesis processes.
  • Facilitate technical transfer of processes between sites as needed.
  • Contribute to synthetic route design and control strategy implementation.
  • Ensure seamless transitions between drug substance and drug product programs.
  • Provide technical support for CMO compliance with cGMPs.
  • Review and approve batch records, deviations, and technical reports.
  • Design and execute experiments for process optimization and validation.
  • Summarize process development results and analytical data from CROs/CMOs.
  • Support authoring drug substance sections in regulatory submissions.

Benefits

  • Hybrid work model with flexibility in location.
  • Opportunity to work in a dynamic team culture.
  • Engagement in cutting-edge drug development processes.
  • Collaboration with industry-leading CMOs and CROs.
  • Professional growth opportunities in a fast-paced environment.
Full Job Description
POSITION SUMMARY

Position Title: Senior Manager, Process Development and Manufacturing

Reports to: Executive Director, Process Development and Manufacturing

Status: Regular, Full-time, Exempt

Location: South San Francisco, CA/Hybrid

Summary: The Senior Manager of Process Development and Manufacturing will be responsible for supporting process chemistry activities for Assembly Biosciences' small molecule compounds, including development of drug substance manufacturing routes, process scale-up, technology transfers and CMO coordination.

Specific responsibilities include, but are not limited to:
  • Supporting drug substance development and manufacturing activities at CMOs to ensure timely delivery of drug substance meeting quality standards.
  • Collaborating with CMOs to design, develop, and implement robust chemical synthesis processes for starting materials, intermediates, and APIs.
  • Supporting technical transfer of starting material, intermediates, and API processes between sites as needed.
  • Contributing to phase-appropriate synthetic route design and control strategy implementation (including fate and purge studies and mutagenic impurity evaluation) for starting materials, intermediates, and APIs across early- and late-stage programs.
  • Collaborating cross-functionally to ensure seamless transitions between drug substance and drug product programs and CMOs.
  • Providing technical support in ensuring that CMO manufacturing facilities are compliant with cGMPs.
  • Providing technical review and approval of batch records, deviations, investigations, and technical reports.
  • Designing and executing experiments for process robustness, optimization, scale-up, transfer, and validation.
  • Reviewing and summarizing process development results and analytical data from CROs/CMOs.
  • Supporting authoring and reviewing drug substance sections in regulatory submissions, including technical justifications for regulatory questions.
  • Functioning as a highly effective communicator, discussion leader, and team player in a dynamic team culture.


This job description outlines the primary duties and responsibilities of the role; however, it is not intended to be all-inclusive. The scope of responsibilities may be modified, expanded, or adjusted at the discretion of the organization to meet evolving business needs.

Qualifications Include:
  • Ph.D. with 3+ years, MS with 6+ years, or BS with 8+ years of small molecule drug substance development experience in the pharmaceutical or biotech industry.
  • Strong technical skills and hands-on experience in process chemistry, including in-depth knowledge of drug substance manufacturing equipment.
  • Knowledge of global pharmaceutical regulatory requirements (e.g., cGMP, ICH, USP).
  • Experience working with CROs/CMOs for drug substance development, manufacturing, and testing.
  • Effective communicator with strong interpersonal, collaboration, and time-management skills.
  • Self-motivated and adaptable in a fast-paced environment, able to manage multiple projects and shifting


Pay Range: $199,400 - $203,700 annualized

The stated pay range for this position reflects the San Francisco Bay Area job market. Assembly Bio establishes pay ranges based on geographic work locations. Additional factors such as academic credentials and relevant experience will influence the actual salary offered.

Information for Recruitment Agencies

Assembly Bio does not accept from recruiters/agencies any unsolicited resumes, or any candidate information including blinded resumes and will not be responsible for any fees related to resumes or candidate information that is unsolicited. Please do not contact hiring managers or Assembly Bio employees directly with any information related to a resume or a candidate. We handle all recruiting through our internal Human Resources team, and we will reach out to you directly should we wish to engage in a search. Your willingness to comply with this will significantly impact any decision we may make about doing business with you.

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