Subject Matter Expert

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

Technical Quality Lead

We’re looking for a proactive and highly skilled Technical Quality Lead to manag...

Location

United Kingdom , Wallasey

Salary:

44000.00 - 50000.00 GBP / Year

360 Resourcing Solutions

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Chemistry, with working knowledge of quality management
Strong organic chemistry knowledge and analytical capability, with a logical and structured approach to decision making
Working HPLC knowledge
High attention to detail and a natural curiosity for problem solving
Strong leadership qualities — responsible, reliable, flexible, and with a strong work ethic
Confident communication style, able to question, challenge, and influence change
Highly motivated and analytical, with the ability to work under challenging time constraints
Passion for continuous improvement and enhancing existing processes

Job Responsibility

Leading the Manufacturing QC Lab team to deliver timely routine testing, product release documentation, technical investigations, action plan implementation and process optimisation
Managing the site lab, lab staff, and technical service contracts to ensure smooth, in-budget operation and support for on-time-in-full delivery of final products
Carrying out laboratory testing and driving continuous improvement initiatives
Acting as the on-site subject matter expert in manufacturing process chemistry
Providing customer-facing technical support and partnering with commercial colleagues where needed to ensure business continuity
Developing a strong quality culture within Operations by partnering closely with the Production Operations Manager
Overseeing all site technical contracts and ensuring delivery against KPIs
Identifying opportunities within processes and customer-specific procedures, and helping to develop innovative, practical solutions

What we offer

Share Options
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Income P

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

Biologics Analytical Principal Scientist

As a Principal Scientist in Physicochemical Analysis, you will independently lea...

Location

China , 苏州市

Salary:

300000.00 - 600000.00 CNY / Year

Randstad

Expiration Date

June 28, 2026

Requirements

A Master’s degree in Analytical Chemistry, Pharmaceutical Sciences or a related field is required, with a strong technical foundation in physicochemical analysis
Profound expertise in key analytical techniques including HPLC, UPLC, LC-MS, CE and cIEF for biologics and ADC characterization is highly essential
The candidate should have 8+ years of progressive CMC experience in biopharmaceutical companies, with a proven record in method development, regulatory compliance and project leadership

Job Responsibility

Design and perform analytical support to biologics development from early to late stage
Analytical method development, transfer and troubleshooting for product quality control and stability study
Draft protocol/report and execute study to support IND/NDA filings
Participate in projects as ARD subject matter expert and provide professional guidance whenever needed

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

Sr Scientist

We are seeking a motivated Senior Scientist in mass spectrometry-based proteomic...

Location

United States , Thousand Oaks

Salary:

127121.75 - 171988.25 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree (PhD, PharmD, or MD) with relevant experience
Master's degree and 4 years of directly related experience
Bachelor's degree and 6 years of directly related experience
Doctorate degree in proteomics, chemoproteomics, biochemistry, chemistry, or a related discipline
Strong track record in developing mass spectrometry-based proteomics assays, operating advanced platforms (e.g., Orbitrap Astral), and analyzing proteomics data
Experience with sample preparation miniaturization and automation platforms
3+ years of experience in the biotech or pharmaceutical industry
Demonstrated innovation in assay, method, or platform development
Strong quantitative and computational expertise in high-dimensional proteomics data analysis
Ability to work effectively in a highly integrated, collaborative team environment, with excellent organizational, verbal, and written communication skills, and a proven track record of producing reliable and reproducible results

Job Responsibility

Deliver critical insights to support target identification and drug discovery, while advancing innovative proteomics platform technologies
Contribute to both pipeline advancement and screening platform innovation by developing and implementing cutting-edge, high-throughput proteomics approaches
Execute automated sample preparation and mass spectrometry analyses across a range of assays
Design, optimize, and continuously enhance next-generation screening workflows and analytical platforms
Collaborate closely with chemistry, biology, and disease area teams as a technical and scientific subject matter expert, contributing to data-driven decision-making
Perform data analysis and generate insights into mechanism of action, target engagement, and selectivity using proteomics approaches
Present research findings at internal and external meetings and effectively communicate plans, results, and analyses to cross-functional teams
Maintain accurate and organized documentation of experiments, protocols, and analyses

What we offer

Health and welfare plans for staff and eligible dependents
Financial plans with opportunities to save towards retirement or other goals
Work/life balance
Career development opportunities
Retirement and Savings Plan with generous company contributions
Group medical, dental and vision coverage
Life and disability insurance
Flexible spending accounts
Discretionary annual bonus program
Stock-based long-term incentives

Fulltime

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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