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68 Summit Summit Software Engineer Jobs Hiring Near You

Summit Utilities Inc

Data Engineer II

Fayetteville, AR · On-site

$98.40K - $118.10K/yr

Summit was also recently named one of Forbes 2023 America's Best Small Employers. Summit is a ... software development, or ETL/integration roles preferred * Proven experience designing and ...

Summit Utilities Inc

Data Engineer II

Fort Smith, AR · On-site

$110.20K - $132.40K/yr

Summit was also recently named one of Forbes 2023 America's Best Small Employers. Summit is a ... software development, or ETL/integration roles preferred * Proven experience designing and ...

Summit Human Capital

Remote Cloud Data Engineer

Richmond, VA · Remote

$113.60K - $136.40K/yr

Summit Human Capital is seeking a highly motivated Cloud Data Engineer with software engineering and data manipulation expertise. The ideal candidate will meet the following criteria: Requirements:

Summit Human Capital

Remote Cloud Data Engineer

Richmond, VA · Remote

$113.60K - $136.40K/yr

Summit Human Capital is seeking a highly motivated Cloud Data Engineer with software engineering and data manipulation expertise. The ideal candidate will meet the following criteria: Requirements:

SynergisticIT

Junior Software Engineer

Dallas, TX

Currently, We are looking for entry-level software programmers, Java Full stack developers, Python ... Summit (Florida) Oracle CloudWorld Event (OCW) Las Vegas 2022 | SynergisticIT - YouTube ...

SynergisticIT

Junior Software Engineer

Magna, UT

Currently, We are looking for entry-level software programmers, Java Full stack developers, Python ... Summit (Florida) Oracle CloudWorld Event (OCW) Las Vegas 2022 | SynergisticIT - YouTube ...

SynergisticIT

Junior Software Engineer

Washington, DC · On-site

Currently, We are looking for entry-level software programmers, Java Full stack developers, Python ... Summit (Florida) Oracle CloudWorld Event (OCW) Las Vegas 2022 | SynergisticIT - YouTube ...

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What is it like to work at Summit?

Summit is a company that values collaboration and innovation, fostering a dynamic and supportive work environment where employees can share ideas and expertise.

The company's structure is designed to encourage teamwork and open communication, with a flat organizational hierarchy and regular cross-functional meetings. Summit's mission is to develop cutting-edge technologies that drive positive change, and employees are encouraged to contribute to this mission through various projects and initiatives.

Working at Summit may appeal to candidates who are passionate about technology and social impact, as the company offers opportunities for professional growth, skill development, and collaboration with a diverse and talented team.
What are the most popular jobs at Summit?
What are the most popular categories at Summit?
Infographic showing various Summit Software Engineer job openings at Summit in the United States as of May 2026, with employment types broken down into 87% Full Time, and 13% Part Time. Highlights an 97% Physical, and 3% Remote job distribution.

Senior Principal Engineer/Associate Director, Drug Product MSAT

Summit Therapeutics

Princeton, NJ • On-site

Full-time

Posted yesterday

Job description

About Summit:
Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life, increasing potential duration of life, and resolving serious unmet medical needs. At Summit, we believe in building a team of world class professionals who are passionate about this mission, and it is our people who drive this mission to reality. Summit's core values include integrity, passion for excellence, purposeful urgency, collaboration, and our commitment to people. Our employees are truly the heart and soul of our culture, and they are invaluable in shaping our journey toward excellence.
Summit's team is inspired to touch and help change lives through Summit's clinical studies in the field of oncology. Summit has multiple global Phase 3 clinical studies, including:
Non-small Cell Lung Cancer (NSCLC)
  • HARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI.
  • HARMONi-3: Phase 3 clinical study which is intended to evaluate ivonescimab combined with chemotherapy compared to pembrolizumab combined with chemotherapy in patients with first-line metastatic NSCLC.
  • HARMONi-7: Phase 3 clinical study which is intended to evaluate ivonescimab monotherapy compared to pembrolizumab monotherapy in patients with first-line metastatic NSCLC.

Colorectal Cancer (CRC)
  • HARMONi-GI3: Phase 3 clinical study intended to evaluate ivonescimab in combination with chemotherapy compared with bevacizumab plus chemotherapy.

Ivonescimab is an investigational therapy not presently approved by any regulatory authority other than China's National Medical Products Administration (NMPA). Summit is headquartered in Miami, Florida, and has additional offices in California, New Jersey, the UK, and Ireland.
Overview of Role:
We are seeking a highly experienced and strategic Senior Principal Engineer/Associate Director of MSAT - Drug Product to join the CMC team and be a key contributor to ongoing process development, technology transfer, process validation, BLA/MAA/IND/IMPD authoring and readiness, and agency interaction activities, in preparation for commercialization and incremental clinical/commercial batch production of our main asset. This role will focus on leading DP Tech transfer(s), authoring technical reports and on providing content to the CMC chapters of regulatory submitted documents, ensuring all required data integrity and technical compliance standards are met. The ideal candidate will bring significant experience in biologics manufacturing, sterile drug product operations, and regulatory expectations.
Role and Responsibilities:
  • Provide technical expertise for phase-appropriate drug product process development, characterization, validation, and technology transfer for sterile drug product (DP).
  • Assess and manage process risks arising from manufacturing or process changes.
  • Serve as a primary or supporting technical interface with external CDMOs and internal manufacturing teams.
  • Lead or significantly contribute to implementation of process, product, and site changes across the product lifecycle.
  • Support and guide execution of clinical and commercial batch manufacturing activities to meet development and supply timelines.
  • Assist in the authorship, data verification, update, and/or review of regulatory filings.
  • Provide technical feedback during regulatory agency inquiries.
  • Lead PPQ execution and manufacturing oversight in alignment with GMP and quality system requirements through person in plant.
  • Collaborate closely with Regulatory, Quality, Supply Chain, and other CMC functions to ensure integrated planning and execution.
  • Ensure GMP compliance across all assigned activities.
  • Support audits, inspections, and continuous improvement initiatives.
  • Manage process deviation investigations and change controls.
  • Travel as needed to support technology transfer, process scale-up, and collaboration with external partners.
  • All other duties as assigned

Experience, Education and Specialized Knowledge and Skills:
  • Bachelor's degree in chemical engineering, biotechnology, pharmaceutical science, or a related field required. Advanced degree (Masters or PhD) preferred.
  • Minimum of 10+ years of relevant experience within the life sciences industry
  • Demonstrated experience in process development, MSAT (Manufacturing Science and Technology), and/or manufacturing with a focus on sterile drug product and late-phase development (preferably mAbs) is essential.
  • Experience with technology transfer across different systems, scales, and sites is highly valued
  • Experience in late-stage process development, characterization and validation is highly valued
  • IND/IMPD and BLA/MAA Module 3 authorship experience and Continuous Process Verification planning and execution highly preferred
  • Data Analytics experience including JMP and other data organization (AI-based or not) platforms a strong plus
  • Strong communication, management, and interpersonal skills to effectively influence across the organization and with CDMOs/CMOs.
  • Excellent attention to detail and organizational skills, with a focus on quality and technical excellence.
  • Good information management and data organization skills
  • Exceptional interpersonal skills with the ability to work individually, within a multi-disciplinary team, as well as with external partners and regulators.
  • A track record of working under pressure and delivering high-quality results to tight deadlines.

This is the pay for this position
Pay Transparency
$180,000-$195,000 USD
Actual compensation packages are based on several factors that are unique to each candidate, including but not limited to skill set, depth of experience, certifications, and specific work location. This may be different in other locations due to differences in the cost of labor. The total compensation package for this position may also include bonus, stock, benefits and/or other applicable variable compensation.
Summit does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact Summit's Talent Acquisition team at recruiting@smmttx.com to obtain prior written authorization before referring any candidates to Summit.
Summit Therapeutics Inc. is an Equal Opportunity Employer and takes pride in creating and maintaining diverse environment. We do not discriminate in recruitment, hiring, training or promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.

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