Subject Matter Expert

Subject Matter Expert (SME) - Mathematics or Chemistry

Location

United States , Remote

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

Advanced knowledge in Mathematics or Chemistry
MS or PhD REQUIRED in Mathematics or Chemistry
Experience with high-level problem solving and technical writing
Prior experience with AI training, data annotation, or model evaluation preferred
Familiarity with platforms such as Scale, Outlier, Surge, or similar is a plus
Ability to work independently with minimal training (“plug and play”)
Strong attention to detail and structured analytical thinking
Teaching, research, or experience creating problem sets is a plus

Job Responsibility

Create advanced math or chemistry problems and detailed solutions
Write clear, step-by-step explanations of complex concepts
Review AI-generated responses for accuracy and reasoning quality
Identify logical, conceptual, or calculation errors
Score and provide structured feedback on technical content
Rewrite or improve incorrect or incomplete AI answers
Ensure content meets academic rigor and quality standards
Review other contributors’ work and support overall quality control

What we offer

medical
vision
dental
life and disability insurance
401(k) plan

Senior Scientist, Research

The Senior Scientist, Research, with limited guidance from more experienced scie...

Location

United States , Madison

Salary:

109000.00 - 185000.00 USD / Year

Exact Sciences

Expiration Date

Until further notice

Requirements

Ph.D. in life sciences, medical technology, clinical laboratory science, chemical/physical/biological science, or field related to the essential duties of the position
or Master’s degree in life sciences, medical technology, clinical laboratory science, chemical/physical/biological science, or field related to the essential duties of the position and 4 years of related experience in lieu of a Ph.D.
or Bachelor’s degree in life sciences, medical technology, clinical laboratory science, chemical/physical/biological science, or field related to the essential duties of the position and 6 years of related experience in lieu of Ph.D.
3+ years of industry or academia experience in biology and/or chemistry
2+ years of experience in medical device/IVD, biotech, life science, or pharmaceutical industry
Demonstrated proficiency in molecular biology and/or biochemical techniques
Demonstrated proficiency in the principles of molecular biology, biochemistry, next-generation sequencing (NGS), genomics, and/or protein research
Working knowledge of statistical and mathematical methods in biology/genetics
including, but not limited to, statistical software, such as JMP
Strong understanding of GMP, ISO, and Quality Systems

Job Responsibility

Provide leadership to a team of junior research associates and scientists
Independently develop, plan, and conduct advanced research experiments, identify problems and discrepancies, analyze results, and identify and address trends in study data
Analyze research/experimental data, interpret the results, and provide insights into the next steps
Utilize and apply methods or technologies effectively and provide ideas for new techniques, when appropriate
Provide technical input and develop research plans, experimental outlines, and design
Prepare and provide information and data for scientific abstracts, industry conferences, project meetings, or publication
Generate, document, and communicate development plans for critical aspects of a project
Prepare and approve detailed technical procedures, protocols, and reports
Evaluate impact of nonconforming data to product or process
Maintain lab notebook in a clear, complete, and consistent manner, following all legal, ISO, and QSR requirements

What we offer

paid time off (including days for vacation, holidays, volunteering, and personal time)
paid leave for parents and caregivers
a retirement savings plan
wellness support
health benefits including medical, prescription drug, dental, and vision coverage
bonus eligible

Fulltime

Process Development Scientist

The Process Development Scientist at Amgen leads in the design, development, and...

Location

Singapore , Tuas

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree OR Master’s degree and 2 years of directly related experience OR Bachelor’s degree and 4 years of directly related experience OR Diploma and 8 years of directly related experience
Strong knowledge of technologies and emerging scientific and regulatory directions for API processing is required
At least 6 years of relevant work experience in the commercial manufacturing environment within the biopharmaceutical industry is preferred
At least 4 years experience with regulated environments (i.e. cGMP) is preferred
Extensive knowledge of the manufacturing practices, regulatory requirements, scientific properties and risks associated with synthetic processing
Knowledge of different synthetic API processing platforms (i.e. reaction, concentration, crystallization, isolation, drying)
Experience in the development and qualification of methods used in release, in-process, and stability testing to analyze or to characterize synthetic molecule and product variants, and process-related impurities (e.g., HPLC, UPLC, mass spectrometry)
Setting up and running synthetic molecule laboratory-based experiment
Experience collaborating with experience networking and building solid working relationships across departments, with diverse and remote staff and with external collaborators
Team leadership, management, and facilitation skills

Job Responsibility

Lead in the design, development, and optimization of manufacturing processes
Apply scientific expertise to increase efficiency, improve product quality, and address manufacturing challenges, while maintaining adherence to regulatory standards
Be a Synthetic Chemistry subject matter expert
Provide scientific and technical direction to support commercial production of chemical synthetic drug substance
Support new product introduction, troubleshooting and improvement of existing and new API (synthetic molecule) processes
Assess initiatives associated to process improvements and optimizations
Develop and prepare laboratory-based experiments to support small scale model interrogation, investigations, and process improvements
Plan detailed procedures for defined projects, including timelines, milestones, methodological approaches, expected results and necessary resources
Support and/or lead cross-functional teams of experienced scientists and engineers through project challenges and implement advance scientific experiments
Support and/or lead process, process safety and material risk assessment performed on-site

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Senior Scientist, Early Formulation Science and Drug Delivery, Drug Product Design

This position will be reporting into the Early Formulation Science and Drug Deli...

Location

United States , La Jolla

Salary:

90900.00 - 151500.00 USD / Year

Pfizer

Expiration Date

Until further notice

Requirements

Recent PhD with 0-3 year post-doctoral experience, MS with 7+ years experience, or BS with 8+ years experience in Chemistry, Chemical Engineering, Physical Chemistry, Physics, Physical Organic Chemistry, Pharmaceutics, or Pharmaceutical Sciences
Experience working independently and collaboratively in a laboratory environment

Job Responsibility

Evaluate the physicochemical properties of potential small molecule drug candidates to inform a drug product formulation strategy and developability risk assessment
Design and develop fit for purpose and diagnostic traditional and enabled formulations for preclinical studies
Design, execute, and interpret the results of polymorph and salt screens for potential drug candidates related to stability, manufacturability, and bio-performance
Apply first principles understanding of thermodynamics and kinetic processes to dissolution and precipitation of drugs in biorelevant conditions and physical and chemical stability in the solid state
Work in cross-disciplinary teams and partner with subject matter experts in Medicinal Chemistry, Pharmacokinetics & Drug Metabolism, and Clinical Pharmacology departments to influence candidate selection and progression
Develop strategic collaborations with academic and industrial researchers for addressing gaps in fundamental or applied science related to the pharmaceutical sciences
Conduct novel research and present significant findings via internal and external presentations or publications

What we offer

401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution
paid vacation, holiday and personal days
paid caregiver/parental and medical leave
health benefits to include medical, prescription drug, dental and vision coverage
participation in Pfizer’s Global Performance Plan with a bonus target of 12.5% of the base salary
eligibility to participate in our share based long term incentive program
Relocation support available

Fulltime

Director of Quality Assurance, Clinical

Responsible for leading in the development, implementation and maintenance of QA...

Location

United States , Berkeley

Salary:

220000.00 - 235000.00 USD / Year

Caribou Biosciences

Expiration Date

Until further notice

Requirements

Undergraduate or graduate degree(s) in Biological Sciences, Chemistry, or related Science discipline
At least 15 years of experience in clinical quality assurance (GCP, GLP and PV) in cell & gene therapy/biotechnology and/or pharmaceutical industry
Experience working in biologics is strongly preferred
Subject Matter Expert (SME) working knowledge on current interpretation/implementation of United States Code of Federal Regulations, ICH Guidelines and other local government regulatory requirements governing clinical research
Proven track record in developing and implementing quality systems and processes in a clinical setting
Expertise in creating and executing audit plans outlining all service providers (vendor) audits, clinical investigator site audits, CSV audits and process audits
Advanced knowledge of Quality Assurance principles, concepts, industry practices, and standards
Prior GLP experience with quality oversight and auditing studies/vendors (preferred)
Excellent verbal and written communication skills
Ability to lead cross-functional teams and independently prioritize work

Job Responsibility

Compliance Oversight: Ensure that all clinical trial activities comply with guidelines and international regulations (e.g., ICH-GCP and ICH-PV), and applicable laws
Documentation Review: Conduct thorough reviews of study-related documentation, including protocols, investigator brochures, informed consent forms, and CSRs, to verify compliance with GCP requirements
Provide Clinical Quality Assurance (GCP) strategic and technical leadership and Subject Matter Expertise (SME) to clinical study teams
Partner with the teams to effect appropriate and timely documentation of quality event management, including CAPA plans in support of product pipeline
Plan and oversee activities in support of regulatory submissions and inspections
Lead GCP Inspection Readiness efforts, ensure implementation and prepare internal and external teams for Pre-Approval Inspections (PAI)
Implement, monitor, and promote best practices of all Quality Assurance Systems to ensure compliance with relevant FDA, EU and ROW regulations/directives/requirements and ICH guidelines
Quality Management System (QMS): Maintain and enhance Caribou’s QMS by implementing processes and procedures that ensure consistent adherence to GCP, GLP and PV standards throughout the clinical trial lifecycle
Develop and implement the appropriate suite of Standard Operating Procedures (SOPs), quality manuals, policies, and other related quality documents
Ensure that these systems are effectively communicated, understood, and followed by relevant stakeholders

What we offer

Comprehensive compensation package, which includes competitive salary, bonus, and equity for all employees
Generous paid vacation time, in addition to company-observed holidays
Excellent medical, dental, and vision insurance
401(k) retirement savings plan, which includes matching employer contributions
Employee stock purchase plan (ESPP)
Tuition reimbursement program

Fulltime

We are hiring 10 Subject Matter Experts (5 in Mathematics, 5 in Chemistry) to su...

Location

United States

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

Must have a Masters Degree or PhD in Mathmatics or Chemistry
Experience with AI training, model evaluation, or technical reviewing
Data annotation experience preferred
Strong analytical writing skills
Teaching or grading experience is a plus
Ability to work independently with minimal onboarding

Job Responsibility

Write complex math or chemistry problems and detailed solutions
Produce clear, step-by-step reasoning
Review AI-generated answers for correctness and logical soundness
Identify subtle conceptual or reasoning errors
Rewrite and improve flawed responses
Provide structured feedback and quality control

What we offer

medical, vision, dental, and life and disability insurance
eligible to enroll in our company 401(k) plan

Research Engineer: Machine Learning for Computational Drug Discovery and Genomic Data Analysis

This is an opportunity to play a key role in the Accenture Labs BioInnovation te...

Location

Ireland , Dublin

Salary:

Not provided

Accenture

Expiration Date

Until further notice

Requirements

Design and implement AI research prototypes for the life sciences, including genomic medicine and computational chemistry
Collaborate with research scientists and engineers and turn experimental methods and their output into full-fledged prototypes to showcase the impact of our research
Develop and implement machine learning models for de novo molecule generation, property prediction
Design and optimize deep learning architectures (e.g., graph machine learning, transformers) for molecular optimization
Design and implements prototypes to learn insights from multi-omics data (e.g. genomics, transcriptomics, proteomics)
Build data ingestion pipelines to process and analyze large-scale biochemical and multi-omics datasets (e.g., SMILES, PDB, proteomics, genomics, clinical records)
Collaborate with subject matter experts to integrate domain knowledge into our AI models and interpret results
Stay on top of the latest advancements in AI/machine learning, AI for drug discovery, computational chemistry
Write clean, well-documented code

Fulltime

Senior Scientist-Biocompatibility and E&Ls

Lucideon M+P is expanding our advanced chemistry and biocompatibility capabiliti...

Location

United States , Greenville

Salary:

70000.00 - 100000.00 GBP / Year

360 Resourcing Solutions

Expiration Date

Until further notice

Requirements

A degree in Chemistry, Biochemistry, Materials Science, or a related field
Experience in Extractables & Leachables (E&L), ISO 10993, or medical device analytical chemistry
Hands-on expertise with mass spectrometry and trace-level analysis
Strong communication skills and experience supporting client-facing scientific engagements
Experience leading technical programs or mentoring scientific staff

Job Responsibility

Lead and expand Extractables & Leachables (E&L) and ISO 10993 biocompatibility chemistry services
Design, execute, and oversee advanced analytical chemistry studies, including mass spectrometry and advanced chemistry workflows (e.g., LC-MS, GC-MS, ICP-MS, IC)
Prepare and support regulatory submissions (FDA, ISO) with high-quality data packages
Develop new testing methodologies, protocols, and service offerings aligned with industry needs
Serve as a subject matter expert at technical conferences, standards committees, and working groups
Engage with clients to understand challenges, design study strategies, and support product development
Manage scientific projects, timelines, deliverables, and mentor technical staff

What we offer

Healthcare benefits including medical, dental, and prescription coverage
401(k) with company matching
Tuition assistance, disability insurance, and life insurance
Generous paid time off

Subject Matter Expert - Chemistry

Khan Academy

Location:
India

Category:
Education

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
December 09, 2025

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