Chemistry Development Scientist Job at MillenniumSoft Inc (Sparks)

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 I/II - Analytical Development (CMC)

The Senior Scientist will be responsible for managing analytical development, gu...

Location

United States , Brisbane

Salary:

150000.00 - 176000.00 USD / Year

Mammoth Biosciences

Expiration Date

Until further notice

Requirements

PhD in Analytical Chemistry, Pharmaceutical Sciences, Biochemistry, or related field with 3+ years of relevant industry experience
MS with 6 years of experience in a biotech/pharma setting
Scientist II: PhD + 5 years minimum experience or MS + 8 years minimum experience
Strong working knowledge of oligo/mRNA-LNP related analytical methods
Hands-on expertise with relevant analytical techniques for gene/cell therapies or complex biologics (e.g., HPLC, LC-MS, DLS, UV, ELISA, qPCR/ddPCR, particle/aggregate characterization, and/or enzymatic assays)
Strong understanding of ICH guidelines, phase-appropriate method validation, and regulatory expectations
Proven track record of guiding method qualification and validation in early phase settings
Experience managing analytical workflows at CDMO/CTLs
Excellent problem-solving, communication, and cross-functional collaboration skills
Ability to regularly work onsite at our Brisbane, CA location

Job Responsibility

Support analytical method development and implementation, both internally and via contract labs, to support the characterization, release testing, and stability of CRISPR-based drug substance and drug product
Establish internal capabilities for select analytical assays in R&D labs, including method qualification and troubleshooting for nucleases, guide RNAs, and delivery vehicles
Manage relationships with external testing labs (CTLs) and manufacturing partners (CDMOs) to ensure method development, validation, and transfer meet project timelines and regulatory expectations
Draft and review protocols, reports, and method qualification and validation documentation in compliance with ICH and relevant regulatory guidelines
Provide technical leadership on assay design and analytical strategy, ensuring methods are phase-appropriate, scalable, and tailored for novel CRISPR-based genetic medicines
Support preparation of CMC documentation for regulatory submissions (e.g., INDs)
Evaluate and implement emerging analytical technologies that align with ultracompact CRISPR platform and pipeline needs
Help build and mentor a small team as the company scales

What we offer

Company-paid health/vision/dental benefits
Unlimited vacation and generous sick time
Company-sponsored meals and snacks
Wellness, caregiver and ergonomics benefits
401(k) with company matching

Fulltime

Junior Research Scientist

The peptide chemistry unit is seeking a talented chemist with a background in sy...

Location

Italy , Pomezia

Salary:

Not provided

IRBM

Expiration Date

Until further notice

Requirements

Master of Science Degree (Laurea Magistrale) or PhD in Chemistry
Expertise in peptide chemistry for the synthesis of complex peptides, including peptide conjugates, macrocycles, and small proteins
Design and execution of synthetic routes and synthesis of non-natural or special amino acids and building blocks using organic chemistry techniques
Mastery of use of laboratory equipment with a preference for knowledge on the use of peptide synthesizers
Knowledge of common purification techniques (HPLC, IEX, GPC) and analytical techniques (UPLC/HPLC and mass spectrometry)
Knowledge in structure elucidations of organic molecules by NMR and MS
Outstanding organizational skills
Excellent communication skills, both verbal and written
Good knowledge of English is mandatory
Ability to productively work in teams

Job Responsibility

Develop and execute synthetic strategies towards complex molecules using state-of-the-art synthetic methodologies
Analyze and identify compounds using different purification and spectroscopic techniques
Present data and reports on project status at individual and group meetings
Conduct laboratory operations in a safe manner
Exhibit safety awareness and safe work practices
comply with all safety requirements according to Italian laws

Materials Scientist

If you’re interested in materials behaviour and want to get stuck into research ...

Location

United Kingdom , Aldermaston near Reading

Salary:

Not provided

AWE

Expiration Date

Until further notice

Requirements

Materials Science or Chemistry with a passion for materials development and/or analytical Chemistry
Natural Sciences (disciplines with a Chemistry, Physics, Materials focus)
Growth mindset
Curiosity
Innovation
Resilience
Teamwork
Must be a British Citizen

Job Responsibility

Undertaking material property research on warhead materials including metals, ceramics, inorganic salts, rubbers, foams, adhesives, high explosives and radioactive substances
Exploring safer ways to make materials
Putting theories to the test using advanced techniques like X-Ray CT and crystallography
Practicing coding skills
Working through data analysis and chemistry processes
Understanding how materials behave in complex systems
Collaborating with scientists, engineers and international partners

What we offer

£23,500 + BENEFITS
270 hours of annual leave
Nine-day fortnight (every other Friday off)

Fulltime

Research Scientist

The peptide chemistry unit is seeking a talented peptide chemist with a strong b...

Location

Italy , Pomezia

Salary:

Not provided

IRBM

Expiration Date

Until further notice

Requirements

Master of Science Degree (Laurea Magistrale) in Chemistry with 5 years of experience doing peptide chemistry in a pharmaceutical or biotech environment
PhD in Chemistry with one or more relevant postdoctoral experiences or with experience in a pharmaceutical or biotech environment
In/depth knowledge of peptide chemistry
Expertise in design and synthesis of complex peptides, including peptide conjugates, macrocycles, and small proteins
Mastery of use of laboratory equipment with a preference for knowledge on the use of peptide synthesizers
Design and execution of synthetic routes for the synthesis of amino acids and building blocks
Excellent knowledge of common purification techniques (HPLC, IEX, GPC) and analytical techniques (UPLC/HPLC and mass spectrometry)
Knowledge in structure elucidations of organic molecules by NMR and MS
Outstanding organizational skills
Excellent communication skills, both verbal and written

Job Responsibility

Develop and execute synthetic strategies towards complex molecules using state-of-the-art synthetic methodologies
Analyze and identify compounds using different purification and spectroscopic techniques
Contribute to the design of peptides with improved potency and physiochemical properties to advance programs according to scientific strategies and goals within a project team setting
Present data and reports on project status at internal and external meetings
Conduct laboratory operations in a safe manner
Exhibit safety awareness and safe work practices
comply with all safety requirements according to Italian laws

Fulltime

Oncology clinical scientist intern

The Global Oncology Internship Program at Johnson & Johnson is a comprehensive l...

Location

Belgium , Beerse

Salary:

Not provided

Randstad

Expiration Date

January 25, 2026

Requirements

Legally/permanently authorized to work in Belgium with no required sponsorships
Must be currently enrolled in an accredited University or College program throughout the duration of the internship
Must not be graduating before, during, or after the start or end of the internship program
Currently enrolled in biology, cell/molecular biology, chemistry, pre-med, nursing program, public health, biochemistry, biomedical engineering, oncology, clinical pharmacology, clinical or translational research, computational biology, precision medicine, or similar areas of study
Undergraduate students with completion of a minimum of four semesters at program start or graduate students are eligible
Minimum cumulative GPA of 3.0
Students in good standing, working towards the completion of an undergraduate or graduate degrees
Graduate students must be pursuing a master’s, PharmD, Physician Assistant or PhD or other clinical related degrees
Self-motivated, future scientist leaders passionate about drug development and clinical research
Detailed oriented with good organizational skills

Job Responsibility

Gaining overall understanding of clinical research and drug development including but not limited to Good Clinical Practices (GCPs), International Conference of Harmony (ICH) guidelines, and Standard Operating Procedures (SOPs)
Attend “Bench to Bedside” Lecture Series to gain knowledge of the drug development process and clinical research
Assisting with management of trial activities including patient tracking through screening process, and eligibility/enrollment reviews
Assisting with document processing and management within the electronic master file (i.e., vTMF)
Participating in department and team meetings
Participating in cross-functional team and clinical team meetings
Developing study training materials/documents
Shadowing key clinical and or functional roles for learning/development opportunities
Observing Site Initiation Visit (SIV) Meetings (if applicable for assigned projects)
Supporting Clinical Team with study start up activities during trial set up, and other study tasks during conduct, and close out (depending on the stage of the trial)

What we offer

We offer an inclusive work culture that is open, innovative, and performance driven

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

Quantum Application Scientist

As a quantum application scientist, you will be responsible for research and dev...

Location

France , Paris

Salary:

Not provided

C12 Quantum Electronics

Expiration Date

Until further notice

Requirements

PhD in computer science, quantum computing, mathematics, engineering physics or related fields
5 years of research and/or industry experience in developing hybrid end-to-end solutions for quantum computing applications would be appreciated
Experience in applying quantum algorithms to practical problems in areas like optimization, simulation or machine learning
Passion for tackling big challenges
Self-motivated and able to work independently
Able to collaborate across diverse teams of expert engineers from various backgrounds (chemistry, experimental physics, mathematics, engineering …)
Good command of English (oral and written)

Job Responsibility

Develop impactful hybrid quantum algorithms and applications that promise commercial advantages in practice and scale
Collaborate with the software team to implement and develop optimized hybrid workflow of quantum algorithms for our quantum architecture
Collaborate closely with our business team and industrial partners to explore the potential of quantum computing for specific industries
Partner with our clients and strategic partners to define and solve problems of real-world interest, and to develop quantum algorithms tailored to their specific needs
Participate in scientific collaborations with academic and industrial partners
Present research findings in technical discussions and journal publications

What we offer

Flexible rhythm of remote work
Stock options for every employee (BSPCE/ESOP)
Two incredible office spaces in the heart of Paris (both next to the famous Panthéon!)
Sponsored trip to conferences around the world
A highly dynamic international team
Swile meal vouchers
Breakfast for all every Friday
Mental health support with moka.care
Training budgets/ Annual Learning & Development Allowance
Sabbatical leave (after 2 years in the company)

Fulltime

Chemistry Development Scientist

MillenniumSoft Inc

Location:
United States , Sparks

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
January 11, 2026

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