Subject Matter Expert - Chemistry Job at Khan Academy

New

Business Development Associate

Life changing therapies. Global impact. Bridge to thousands of biopharma compani...

Location

United States , Bedford

Salary:

Not provided

PCI Pharma Services

Expiration Date

March 02, 2026

Requirements

Strong interpersonal, communication, and organization skills
Outstanding attention to detail
Proficiency with MS Office suite applications
Drug product development and manufacturing experience
Ability to write highly technical proposals
Strong business acumen and problem-solving skills
Excellent planning and organizational skills
Ability to work in a fast-paced, cross-functional team
Superior verbal and written communication skills with both internal and external customers
Bachelor’s Degree or higher in Pharmaceutical Sciences, Chemistry, or closely related field

Job Responsibility

Responsible for writing high-quality proposals for including but not limited to Early-Stage Development
Interact with Business Development (BD) team and external customers on Requests for Proposals (RFPs)
Leads and/or supports meetings with internal departments and external clients to discuss expectations associated with Proposals, revisions to proposals, and Change Orders
Coordinates with Business Development and/or Project Management to schedule Subject Matter Expert (SME) meetings for RFQ reviews
Responsible for working with key stakeholders to clearly define project scope, strategy, resource requirements, timelines, deliverables, and pricing
Prepare detailed project proposals, including supporting materials such as cost workbooks and high-level Gantt charts
Participates in peer review of proposals to support the Business Operations team
Participates in the development and implementation of new approaches, procedures, and processes to optimize and harmonize business processes across business segments
Acquires and maintains an in-depth knowledge of the organization’s areas of expertise and services for appropriate cross-sell opportunities to existing clients
Collaborates with Subject Matter Experts (SME) to gather supporting information to be captured within Proposals

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

New

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

Principal Scientist – Synthetic Separations

Amgen is seeking a highly motivated Senior Principal Scientist for their Discove...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Ph.D. in Chemistry, Analytical Chemistry, or related field with 8+ years of relevant experience, or M.S. with 12+ years of relevant experience in analytical or discovery chemistry within the biopharmaceutical industry
PhD in Analytical Chemistry or a related discipline with 8+ years of relevant industry experience in chromatographic analysis and/or purification of small molecules within a pharmaceutical R&D environment
Minimum of 5 years in a leadership or people management role
Develop, optimize, and implement analytical methods (LC, LC/MS, GC, SFC, NMR, HRMS, and related techniques) for purity assessment, structural confirmation, quantitative analysis, and reaction monitoring of synthetic compounds
Develop, optimize, and implement analytical methods (LC, LC/MS, GC, SFC, NMR, etc.) for purity assessment, structural confirmation, and reaction monitoring of synthetic compounds
Design, qualify, and maintain high-throughput or automated analytical workflows to support medicinal chemistry cycles
Collaborate with cross-functionally digital and automation groups to enable data-driven analytics and AI-supported structure prediction
Drive continuous improvement in analytical workflows and laboratory efficiency through process automation and robotics
Excellent written and verbal communication skills
Prepare concise, high-quality reports and presentations for internal review and external disclosure

Job Responsibility

Lead analytical strategy and execution for drug discovery-stage projects, enabling medicinal chemistry and early candidate selection through deep expertise in analytical and separation sciences
Bridge synthetic and analytical chemistry, ensuring rapid, reliable characterization of novel compounds and intermediates that drive Amgen’s small molecule discovery pipeline
Lead and manage the Synthetic Separations group, providing strategic direction, technical leadership, and mentorship to staff while prioritizing workloads, optimizing team performance, and serving as both a people manager and subject matter expert in synthetic separations
Design and qualify automated workflows enabling rapid turnaround and consistent data quality for purification and analysis of diverse compound libraries
Utilization of a diverse set of instruments and technologies, such as (but not limited to) HPLC, SFC, MS, mass-directed purification, and preparative-scale SFC and LC is necessary
Lead library purification efforts across multiple scales, ranging from microgram-level purification of screening compounds to hundreds of milligrams for advanced characterization
Assist in research efforts directed at improving process efficiencies, expanding the range of assays and applications, building state-of-the-art analytical capabilities, and improving technologies and infrastructure

New

Quality Assurance Coordinator

This position is responsible for ensuring all required analyses are performed as...

Location

Canada , Chatham, Ontario

Salary:

Not provided

Greenfield Global

Expiration Date

Until further notice

Requirements

Completion of post-secondary education with a Bachelor of Science in Chemistry, degree in Chemical Laboratory Technology, or other related discipline
Three to five years of relevant work experience
Knowledge of GMP, HACCP, FSMA, FEMAS, ISCC and ISO standards and experience with risk-based methodology
Competent person who is knowledgeable of the Occupational Health & Safety Act and regulations
Resourceful and practical, with demonstrated problem solving and decision-making capabilities
Strong organizational skills paired with an ability to manage multiple priorities with competing demands and attention to detail
Focused individual who works to achieve department objectives while maintaining safety standards

Job Responsibility

Comply with and support the fulfillment of all company environmental, health and safety, quality policies and regulatory requirements
Support department objectives and lead continuous improvement initiatives
foster collaboration within team members to achieve desired results in a manner aligned to our core values and principles
Coach, mentor, support and develop team members providing timely and constructive feedback
Maintain QA team schedule
Coordinate daily activities involving the lab in collaboration with other departments
Accountable for Quality related Management Systems (ISO, FMSA, etc.) implementation, training, compliance, maintenance and internal and external audits
Maintain product specifications, customer documentation, audits and customer communication resolution
Responsible for tracking audit results, customer communication, investigation and corrective actions
Oversees sensory program at the Chatham facility

What we offer

Formal and informal training opportunities
Comprehensive health and dental benefits
Income protection: short- and long-term disability coverage, life insurance, paid personal sick time
Vacation time exceeding industry standards
Company funded retirement savings program with individual contribution opportunities
Meaningful and challenging work
Curated intentional culture focused on growth and development, engagement, and communication

Fulltime

New

Manager, Regulatory Product Compliance, Pif & Registration

At Coty, you’ll get to work in a passionate team of experts, with the freedom to...

Location

Monaco , Monaco

Salary:

Not provided

Coty Inc.

Expiration Date

Until further notice

Requirements

Minimum 5 years of regulatory experience in a similar regulatory compliance role, ideally in skincare
Minimum 7-10 years of cosmetic industry experience
Master the European cosmetic regulation and requirements for product registration in various countries, including China
Fluent in English and French
Bachelor or Master in cosmetics or other sciences (Biology, Pharmacy, chemistry…)
Self-starter, you like to learn about new area and develop your expertise
Proficiency with MS-Office and high command of IT in general
Quick learner of new software and systems and good ability to present and train others

Job Responsibility

Manage the regulatory aspects of skincare, sun and bodycare products developed in Monaco
Guide different stakeholders to develop products in compliance with the regulations of the desired country and approve all aspects of the products (formulas, raw materials, formulas, labeling, packaging, communication…)
Review, approve and/or issue technical documents to ensure complete and accurate Product Information Files (PIFs) and registration dossiers
Act as the Subject Matter Expert on PIF requirements, train and guide other team members as applicable
Lead your project to ensure it meets the overall timelines, interact with multiple functions on site or other Coty locations, enable resolutions of challenges related to product registration
Follow-up with other internal functions (Product Development, Artwork planners, Initiative leaders, packaging, MD…) as to resolve questions related to the documentation

What we offer

A salary that matches your knowledge and experience
A very good health care cover and social benefits
Omniworking flexible arrangements

IT Solutions Delivery Lead, R&D Operations

The IT Solutions Delivery Lead, R&D Operations role is critical to ensuring succ...

Location

United States , San Rafael

Salary:

112000.00 - 154000.00 USD / Year

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

Bachelor of Science or greater in Computer Science, Business Administration, Information Technology, Biology, Chemistry or a related technical field or significant experience in supporting research systems in the pharmaceutical industry
Minimum of 5 years’ experience in technical or business analyst role with a focus on R&D functional systems and/or Information Technology
Experience in computer database management, programming, or software development familiar with developing Power Apps and Power Automate
Experience with Pharma/BioTech R&D systems such as SAS 9.4, SAS Viya, R-Studio, Phoenix WinNonLin, PumasAI, etc.
Data analysis expertise familiar with database technologies such as SQL, Oracle, Excel, Power BI, etc.
Delivering mid-to-large size projects with teams of 5 to 15 members on time and within budget
Have a general knowledge of the underlying scientific principles applied to the development and manufacture of biopharmaceuticals

Job Responsibility

System Ownership: Technical ownership of SAS 9.4, SAS Viya, R-Studio, Phoenix WinNonLin, PumasAI, etc.
Lifecycle Management of applications
Financial responsibility of all system operational expenses
Manage Software Vendors to ensure SLAs are met
Manage Licensing including budgeting and growth forecasting
Facilitate Application Steering Committees
Participate in change control boards and design review committees
Bridge the gap between business needs and technology constraints
Project Delivery: Support new application and system deployment projects
Participate as subject matter expert (and in some cases lead) projects

What we offer

Discretionary annual bonus
Discretionary stock-based long-term incentives
Paid time off
Company-sponsored medical, dental, vision, and life insurance plans

Fulltime

Manager Quality Control - HPLC Labs

Lead the HPLC Labs during the 2nd shift —ensuring compliant, accurate testing an...

Location

United States , Juncos

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree
OR Master’s degree and 3 years of Manufacturing Support, Quality Control and/or Laboratory experience
OR Bachelor’s degree and 5 years of Manufacturing Support, Quality Control and/or Laboratory experience
OR Associate’s degree and 10 years of Manufacturing Support, Quality Control and/or Laboratory experience
OR High school diploma / GED and 12 years of Manufacturing Support, Quality Control and/or Laboratory experience
Experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation of resources
Educational background in Life Sciences, Chemistry, Biochemistry, or related fields
Experience in Quality and/or Biochemistry Laboratory operations within a GMP environment, preferably in HPLC testing
Strong knowledge of analytical techniques such as HPLC
Familiarity with laboratory systems such as LIMS, LMES, CIMS, and Empower for HPLC data management

Job Responsibility

Lead and develop a successful QC team, fostering a culture of safety, compliance, and continuous improvement
Oversee daily QC operations to ensure timely, accurate, and reliable testing aligned with production schedules
Serve as the QC subject matter expert during audits and inspections, ensuring inspection readiness
Provide technical guidance and troubleshooting support for complex assays and testing issues
Drive training initiatives and ensure team members are appropriately cross-trained for operational flexibility
Monitor assay results and documentation to ensure compliance with cGMP, SOPs, and regulatory standards
Communicate clear expectations on safety, quality, and compliance, addressing discrepancies promptly
Organize and prioritize team tasks based on impact and deadlines, adjusting as needed to meet changing requirements
Use data and dashboards to monitor QC performance metrics, identify trends, and implement improvements
Collaborate with cross-functional stakeholders to align QC activities with broader site and organizational goals

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental & vision coverage, and life & disability insurance
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans and an annual site shutdown
Flexible work models where possible

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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Subject Matter Expert - Chemistry

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Location:India

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Job Description:

Job Responsibility:

Requirements:

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