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Remote Scientist Process Chemistry Jobs (NOW HIRING)

Enliven Therapeutics

Director, Process Chemistry

$190K - $238K/yr

Remote Department: CMC Company Overview Enliven Therapeutics is a clinical-stage biopharmaceutical ... MS or PhD in Organic Chemistry, Chemistry, Chemical Engineering, or a related scientific discipline ...

DataAnnotation

$40/hr

A technology firm specializing in AI is seeking a Research Scientist (Chemistry) to evaluate AI chatbots' responses to complex chemistry questions. This remote position requires a solid knowledge of ...

MedSchoolCoach

Research Mentor (Remote)

Boston, MA · Remote

$75 - $100/hr

... process. We are seeking dedicated PhD mentors to provide one-on-one support to students as they ... Medical/Biological Sciences Physics, Chemistry Computer Science, AI Environmental Sciences ...

Mercor

STEM Expert - Fully Remote

New York, NY · Remote

$70 - $100/hr

... Chemistry , Biology , Mathematics , Statistics , Computer Science , Electrical Engineering ... Application Process (Takes 20-30 mins to complete) * Upload resume * AI interview based on your ...

Mercor

STEM Expert - Fully Remote

New York, NY · Remote

$70 - $100/hr

... Chemistry , Biology , Mathematics , Statistics , Computer Science , Electrical Engineering ... Application Process (Takes 20-30 mins to complete) * Upload resume * AI interview based on your ...

Learner Education

Online Organic Chemistry Tutor

Tampa, FL · On-site +1

$25/hr

Remote Hours: Set Your Own Schedule Pay: $25.00/hr About Learner Education Learner Education is on ... Tutors who can also support additional Science subjects such as Chemistry, Biology, or general high ...

Learner Education

Online Organic Chemistry Tutor

Tampa, FL · Remote

$25/hr

Remote Hours: Set Your Own Schedule Pay: $25.00/hr About Learner Education Learner Education is on ... Tutors who can also support additional Science subjects such as Chemistry, Biology, or general high ...

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Remote Scientist Process Chemistry information

What are the key skills and qualifications needed to thrive as a Remote Scientist in Process Chemistry, and why are they important?

To thrive as a Remote Scientist in Process Chemistry, you need a strong background in synthetic organic chemistry, analytical techniques, and typically a Ph.D. in chemistry or related field. Familiarity with chemical process modeling software, laboratory information management systems (LIMS), and data analysis tools is often required. Excellent problem-solving, time management, and clear communication are vital soft skills for collaborating virtually and driving projects forward. These competencies ensure efficient process development, innovation, and effective teamwork in a remote research environment.

What are some common challenges faced by Remote Scientist Process Chemists, and how can they be addressed?

Remote Scientist Process Chemists often encounter challenges related to communication and collaboration due to the lack of in-person interactions with lab teams and project stakeholders. To address these, effective use of digital collaboration tools, clear documentation, and regular virtual meetings are essential. Additionally, ensuring access to real-time data and remote monitoring systems can help streamline experimental progress and troubleshooting. Staying proactive in building relationships with colleagues and seeking feedback also enhances teamwork and contributes to project success.

What is a Remote Scientist in Process Chemistry?

A Remote Scientist in Process Chemistry is a professional who works primarily from a remote location to develop, optimize, and scale up chemical processes for manufacturing pharmaceuticals or other chemicals. Their responsibilities include designing experiments, analyzing data, and collaborating with teams to improve the efficiency, safety, and sustainability of chemical processes. This role often requires expertise in organic chemistry, strong problem-solving skills, and experience with laboratory and computational tools. Communication and collaboration with onsite teams are essential, as much of the work is coordinated virtually.

What is the difference between Remote Scientist Process Chemistry vs Remote Scientist Analytical Chemistry?

AspectRemote Scientist Process ChemistryRemote Scientist Analytical Chemistry
Required CredentialsBachelor's or Master's in Chemistry or Chemical Engineering; relevant experience in process developmentBachelor's or Master's in Chemistry; experience in analytical techniques and instrumentation
Work EnvironmentLaboratory, manufacturing, or R&D settings with process focusLaboratory or R&D with emphasis on testing and analysis
Employer & Industry UsagePharmaceutical, chemical manufacturing, biotechPharmaceutical, environmental, food testing labs
Common Search & ComparisonYesYes

Remote Scientist Process Chemistry and Remote Scientist Analytical Chemistry share similar educational backgrounds and work environments. The key difference lies in their focus: process chemistry involves developing and optimizing manufacturing processes, while analytical chemistry emphasizes testing, analysis, and quality control. Both roles are vital in the pharmaceutical and chemical industries, but they serve distinct functions within R&D and production.

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What cities are hiring for Remote Scientist Process Chemistry jobs? Cities with the most Remote Scientist Process Chemistry job openings:
What are the most commonly searched types of Scientist Process Chemistry jobs? The most popular types of Scientist Process Chemistry jobs are:
What states have the most Remote Scientist Process Chemistry jobs? States with the most job openings for Remote Scientist Process Chemistry jobs include:
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Remote Scientist Process Chemistry jobs near you
Infographic showing various Remote Scientist Process Chemistry job openings in the United States as of May 2026, with employment types broken down into 20% Full Time, and 80% Contract. Highlights an 69% Physical, and 31% Remote job distribution.
Director, Process Chemistry

Director, Process Chemistry

Enliven Therapeutics

Remote

$190K - $238K/yr

Full-time

Posted 17 days ago

Job description

Job Type
Full-time
Description
Position Title: Director, Process Chemistry
Job Status: Exempt, Full Time
Location: Remote
Department: CMC
Company Overview
Enliven Therapeutics is a clinical-stage biopharmaceutical company focused on the discovery and development of small molecule inhibitors to help people with cancer not only live longer but live better. The Company aims to address existing and emerging unmet needs with a precision oncology approach that improves survival and enhances overall well-being. Its discovery process combines deep insights in clinically validated biological targets and differentiated chemistry with the goal of designing therapies for unmet needs.
Summary
Enliven is seeking a Process Chemistry Lead to serve as the drug substance/API subject matter expert, defining and executing phase-appropriate CMC strategy to advance product candidates through late-stage development, pivotal trials, and potential commercial launch. Establish and maintain the API control strategy, including specifications and process controls, ensuring they are locked for pivotal studies and regulatory submission. Review and approve technical reports and GMP documentation such as batch records, protocols, campaign reports, specifications, and regulatory filing content. Oversee drug substance scheduling and manufacturing campaigns, ensure cGMP compliance and inspection readiness, and represent drug substance/API priorities on core cross-functional teams. Partner closely with CMOs and internal teams across Quality, Supply Chain, Regulatory CMC, Formulation, and Analytical Development to drive operational excellence and timely release of drug substance for clinical use.
Responsibilities:
  • Oversee late-stage drug substance/API development and manufacturing activities to support pivotal studies, regulatory submission, and commercial launch readiness
  • Help define and execute phase-appropriate API strategy for late-stage development, ensuring alignment with program milestones and submission goals
  • Ensure process design and control strategy are sufficiently established to support pivotal trials, registration, and commercial manufacturing readiness
  • Oversee external CDMO/CMO activities for late-stage API manufacturing, process performance, and supply continuity
  • Lead technology transfer activities between manufacturing sites to support scale-up, validation, and long-term commercial supply
  • Drive process characterization, CPP identification, validation planning, and PPQ readiness/execution for late-stage programs
  • Establish, maintain, and refine API control strategy, specifications, and supporting documentation for regulatory submission and commercial readiness
  • Oversee drug substance manufacturing campaigns, scheduling, site readiness, and operational execution to ensure timely supply for clinical and registration-enabling activities
  • Author, review, and approve technical reports and GMP documentation, including batch records, protocols, specifications, campaign reports, and regulatory CMC submission content
  • Partner closely with Quality, Regulatory CMC, Supply Chain, Analytical, Formulation, Legal, and external manufacturers to ensure cGMP compliance, inspection readiness, and successful health authority interactions
  • Help represent CMC/DS/API needs to core development team

Requirements
  • MS or PhD in Organic Chemistry, Chemistry, Chemical Engineering, or a related scientific discipline
  • 10+ years of relevant experience in the pharmaceutical or biotechnology industry, including significant hands-on experience in small molecule drug substance/API development and commercialization
  • Strong late-stage development experience supporting Phase 3 programs through NDA/BLA or equivalent regulatory submission
  • Deep technical expertise in small molecule API process chemistry, development, and scale-up
  • Demonstrated experience leading drug substance manufacturing activities in support of late-stage development and commercial readiness
  • Experience with process performance qualification, process validation, and commercial launch preparation
  • Deep understanding of impurity control strategies, including ICH Q3A/Q3B and ICH M7
  • Strong working knowledge of cGMP requirements and global regulatory expectations, including ICH Q7, Q11, and Q2
  • Experience authoring, reviewing, or contributing to Module 3 and other CMC documentation for regulatory submissions
  • Proven readiness to support regulatory inspections, ensure reliable API supply, and deliver successful outcomes across PPQ, submission, and commercial manufacturing

The annual salary range Enliven reasonably and in good faith expects to pay for this position at the time of this posting is $190,000 - $238,000. The actual salary offered will be determined based on factors such as experience, qualifications, skills and expertise, geographic location, and other job-related factors permitted by law. Benefits are included and other incentives such as bonus and equity may be provided. This range is subject to change based on business needs, job scope changes, market conditions, and individual qualifications. Employees and applicants may request the pay range for their position or for a position to which they are applying.
Enliven Therapeutics is proud to be an equal opportunity employer. All employment offers are contingent upon the applicant successfully completing a background screen.
Notice to agencies: Our in-house Talent Acquisition Team manages all employment opportunities at Enliven. Agencies and independent recruiters must be approved as a vendor by our HR team. To protect the interests of all parties, Enliven will not accept unsolicited resumes, profiles, or biographies. Any unsolicited submissions will be considered referrals and become the property of Enliven. Contacting hiring managers, executives, or any member of the HR team will not influence vendor approval and is strongly discouraged. Repeated outreach may impact future consideration.

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