1

Director Metabolic Engineer Jobs (NOW HIRING)

Senior Engineering Manager

New York, NY · Remote

$225K - $262K/yr

... of hormonal, metabolic, and reproductive care. Allara provides ongoing support for hormonal ... direct contribution * Own a clear mission or product area, driving the roadmap and being ...

Senior Engineering Manager

New York, NY · On-site

$225K - $262K/yr

... of hormonal, metabolic, and reproductive care. Allara provides ongoing support for hormonal ... direct contribution * Own a clear mission or product area, driving the roadmap and being ...

next page

Showing results 1-20

Director Metabolic Engineer information

See salary details

$59.5K

$111.6K

$203K

How much do director metabolic engineer jobs pay per year?

As of Jun 9, 2026, the average yearly pay for director metabolic engineer in the United States is $111,632.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,500.00 and $132,500.00 per year, depending on experience, location, and employer.

What does a Director Metabolic Engineer do?

A Director Metabolic Engineer leads teams that design and optimize biological processes to improve the production of chemicals, fuels, or pharmaceuticals using microorganisms. They set research strategies, oversee project execution, and collaborate with cross-functional teams in areas like synthetic biology, fermentation, and process development. This role requires a deep understanding of metabolic pathways, leadership skills, and the ability to translate scientific advances into commercial applications. Directors in this field also manage budgets, mentor scientists, and ensure regulatory compliance.

What are the key skills and qualifications needed to thrive as a Director Metabolic Engineer, and why are they important?

To thrive as a Director Metabolic Engineer, you need advanced expertise in metabolic engineering, systems biology, and biochemical pathway optimization, typically supported by a PhD in a relevant field. Experience with computational modeling tools, laboratory automation platforms, and regulatory compliance, as well as familiarity with project management systems, is crucial. Leadership, strategic thinking, and strong communication skills help drive cross-functional teams and foster innovation. These skills are vital for successfully leading complex projects, advancing research objectives, and achieving organizational goals in biotechnology or pharmaceutical settings.

What are the typical team structures and collaborative dynamics for a Director Metabolic Engineer in a biotechnology company?

As a Director Metabolic Engineer, you will typically lead a multidisciplinary team of scientists, research associates, and engineers focused on strain development, pathway optimization, and process scale-up. Collaboration is key, as you’ll work closely with molecular biologists, fermentation experts, and downstream processing teams to ensure seamless project execution. You may also interact with executive leadership, regulatory affairs, and business development to align scientific goals with company strategy. Effective communication and project management skills are essential, as you’ll coordinate research timelines and foster a culture of innovation within your team.

What is the difference between Director Metabolic Engineer vs Senior Metabolic Engineer?

AspectDirector Metabolic EngineerSenior Metabolic Engineer
CredentialsAdvanced degrees (PhD preferred), extensive industry experienceMaster's or PhD, significant industry experience
Work EnvironmentLeadership roles, strategic planning, cross-functional teamsResearch-focused, project execution, technical development
Employer & Industry UsageBiotech, pharmaceutical, industrial biotech companiesResearch labs, biotech firms, R&D departments

The main difference between a Director Metabolic Engineer and a Senior Metabolic Engineer lies in their level of responsibility and focus. The Director typically oversees strategic initiatives and manages teams, while the Senior Engineer focuses on technical execution and project development. Both roles require strong expertise in metabolic engineering, but the director role emphasizes leadership and strategic planning.

More about Director Metabolic Engineer jobs
What cities are hiring for Director Metabolic Engineer jobs? Cities with the most Director Metabolic Engineer job openings:
What are the most commonly searched types of Metabolic Engineer jobs? The most popular types of Metabolic Engineer jobs are:
What states have the most Director Metabolic Engineer jobs? States with the most job openings for Director Metabolic Engineer jobs include:
What job categories do people searching Director Metabolic Engineer jobs look for? The top searched job categories for Director Metabolic Engineer jobs are:
Infographic showing various Director Metabolic Engineer job openings in the United States as of May 2026, with employment types broken down into 20% Full Time, 20% Part Time, 20% Temporary, and 40% Contract. Highlights an 76% Physical, 1% Hybrid, and 23% Remote job distribution, with an average salary of $111,632 per year, or $53.7 per hour.
Associate Director/Director, Statistical Programming

Associate Director/Director, Statistical Programming

Structure Therapeutics

South San Francisco, CA • On-site

$180K - $250K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 9 days ago


Job description

About Us:
Structure Therapeutics develops life-changing medicines for patients using advanced structure-based and computational drug discovery technology. The company's platform combines the latest advancements in visualization of molecular interactions, computational chemistry, and data integration to design orally available, superior small molecule medicines that overcome current limitations of biologic and peptide drugs. We are advancing a clinical-stage pipeline of differentiated treatments focused on chronic diseases with high unmet need, including cardiovascular, metabolic, and pulmonary conditions.
Structure Therapeutics is led by an experienced group of international drug innovators and financed by top-tier global life sciences investors. The company completed an initial public offering (IPO) in February 2023. With offices in California and Shanghai, Structure Therapeutics has the benefit of being at the center of life science innovation in both the US and China and capitalizing on the strengths of each geographic location.
POSITION SUMMARY
The position supports statistical programming for studies and regulatory submissions, ensuring high-quality, compliant deliverables aligned with CDISC standards and global regulatory requirements (e.g., FDA, EMA). The role maintains oversight of work performed by CROs, including review and verification of outputs to ensure accuracy and compliance; contributes to data review and cleaning; and advances internal programming capabilities through development of macros, processes, and automation to improve efficiency and consistency. Operating with a high degree of independence, they partner cross-functionally to ensure high-quality, timely delivery of statistical programming outputs.
Essential Duties and responsibilities
  • Provides statistical programming support to Structure's expanding portfolios
  • Support and perform statistical programming for clinical studies and regulatory submissions
  • Author and review SDRG, ADRG, and dataset specifications (SDTM and ADaM) to ensure compliance, traceability, and submission readiness
  • Develop, validate, and maintain CDISC-compliant datasets (SDTM and ADaM) and analysis outputs (TFLs) using SAS (and/or R)
  • Ensure timely delivery of high-quality, compliant deliverables aligned with CDISC standards and global regulatory requirements (e.g., FDA, EMA)
  • Maintain oversight of work performed by CROs, including review and verification of outputs to ensure accuracy, quality, and compliance
  • Perform hands-on programming for complex analyses, ad hoc requests, and critical deliverables as needed
  • Review study documents, including protocol, CRFs, SAP, DTS, and TFL shells
  • Contribute to data review and cleaning activities to support data integrity and analysis readiness
  • Collaborate cross-functionally with Biostatistics, Data Management, Clinical Development, and Regulatory teams
  • Develop and implement programming standards, macros, and automation to improve efficiency, consistency, and scalability
  • Review datasets, TFLs, and define.xml to ensure quality and adherence to standards and specifications
  • Support regulatory submissions, including preparation, validation, and response to health authority queries
  • Identify and drive process improvements and best practices in statistical programming
  • Operate with a high degree of independence to manage priorities and ensure timely, high-quality deliverables
  • Perform other duties and responsibilities as assigned

REQUIREMENTS
  • Bachelor's or master's degree, in Statistics, Mathematics or other related discipline and at least 9 years Pharmaceutical/Biotech programming experience
  • Excellent knowledge of CDISC submission requirements regarding SDTM, ADaM, Define.xml, Reviewers Guide and Validation Rules
  • Demonstrated experience authoring and reviewing SDRG, ADRG, and dataset specifications (SDTM/ADaM)
  • Ability to develop macros, utilities, and automation to improve programming efficiency
  • Expert level SAS programming and management background along with Solid knowledge and experience of SAS Programming language including SAS Base, SAS/Macros, SAS/Graph and SAS/Stat required
  • Experience overseeing CRO programming activities, including review and verification of deliverables
  • Strong interpersonal communication skills to collaborate with colleagues, stakeholders, and vendors effectively and clearly in small biotech setting

Preferred Experience
  • Experience with global submissions (NDA, MAA, JNDA)
  • Exposure to process improvement initiative and standardization efforts
  • Ability to work in a fast-paced, cross-functional environment

Travel
5% travel required
Structure Therapeutics Inc. is an Equal-Opportunity Employer.
Structure Therapeutics is committed to fair and equitable compensation practices, and we strive to provide employees with total compensation packages that are market competitive. For this role, the anticipated base pay range is $180,000-$250,000. The exact base pay offered for this role will depend on various factors, including but not limited to the candidate's geography, qualifications, skills, and experience.
At Structure, base pay is only one part of your total compensation package. The successful candidate will be eligible for an annual performance incentive bonus, new hire equity, and ongoing performance-based equity. Structure Therapeutics also offers various benefits offerings, including, but not limited to, medical, dental, and vision insurance, 401k match, unlimited PTO, and a number of paid holidays including winter shutdown.
Notice to Recruiters/Staffing Agencies
Recruiters and staffing agencies should not contact Structure Therapeutics through this page. All recruitment vendors (search firms, recruitment agencies, and staffing companies) are prohibited from contacting our hiring manager(s), executive team members, or employees.
We require that all recruiters and staffing agencies have a fully executed, formal written agreement on file.
Structure Therapeutics' receipt or acceptance of an unsolicited resume submitted by a vendor organization to this website or employee does not constitute an actual or implied contract between Structure Therapeutics and such organization and will be considered unsolicited and Structure Therapeutics will not be responsible for related fees.
Fraud Alert
To all candidates: your personal information and online safety are a top priority for us. At Structure Therapeutics, direct candidates to apply through our official career page at BambooHR.
Recruiters will always contact you using the domain of Structuretx.com. We will never request payments, ask for financial account information or sensitive information like social security numbers. If you are unsure if a message is from Structure Therapeutics, please email human resources.