Analytical Chemistry Development Scientist 1 Job at MillenniumSoft Inc (Vernon Hills)

Senior Scientist, Analytical Projects - Device, Particle Size and XRPD

You will join Analytical Projects focused on device, particle size, and X-ray po...

Location

United States , Collegeville

Salary:

Not provided

GSK

Expiration Date

Until further notice

Requirements

Bachelor’s degree in analytical chemistry, materials science, pharmaceutical sciences, or related discipline plus minimum 3 years of relevant laboratory experience
or Master’s degree with minimum 1 year of relevant experience
Experience with analytical instrumentation and data collection, such as PSD, XPRD
Experience operating and maintaining laboratory instruments and performing method validation
Experience with data integrity, safety, and good laboratory practices

Job Responsibility

Develop and validate analytical methods for device characterization, particle sizing, and XRPD analysis
Plan and perform experiments, collect high-quality data, and interpret results to inform project decisions
Troubleshoot instrumentation and method challenges and propose practical, evidence-based solutions
Prepare clear technical reports, maintain accurate laboratory records, and present findings to project teams
Support root cause investigations and cross-functional projects to resolve technical issues
Mentor junior colleagues, share best practices, and contribute to continual improvement of lab workflows
Strong written and verbal communication skills for clear reporting and teamwork

What we offer

Competitive base salary
Annual bonus based on company performance
Flexible working options available for most roles
Learning and career development
Access to healthcare & wellbeing programmes
Employee recognition programmes

Fulltime

Process Development Principal Scientist

Location

United States , Thousand Oaks

Salary:

148363.00 - 171657.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

PHD degree or (foreign equivalent) in analytical chemistry, chemistry, or related field & 3 years of experience in the job offered or in a process development-related occupation. Position requires 3 years of experience in the following: 1. Mass spectrometry knowledge in mechanism of different ionization techniques, configuration of mass spectrometry platforms by different vendors including Waters, Thermo Fisher, or Agilent, and gas-phase ion chemistry for structural elucidation
2. Sample preparation including liquid-liquid extraction and solid phase microextraction for qualitative and quantitative analysis of both small molecules and large molecules
3. Analytical techniques including FT-IR (Fourier-transform infrared spectroscopy), NMR (nuclear magnetic resonance), and UV (ultraviolet–visible spectroscopy)
4. Chromatography and related separation techniques including RP-HPLC (reversed phase high-performance liquid chromatography) and GC (gas chromatography)
5. High-throughput analysis in processing multidimensional mass spectrometry-based data and implementing statistical analysis and interpreting statistical results
and 6. Software applications including ChemDraw, Xcalibur, or ChemStation and programming language for data processing including Python or Matlab.

Job Responsibility

Lead analytical method development, validation and trouble-shooting for drug substances and drug products and in-process testing for synthetic small molecules and/or synthetic peptide testing and characterization
Define analytical control strategies and implement methodologies for development of late phase clinical programs
Collaborate closely with drug substance and drug product process development colleagues to achieve project objectives
Lead and mentor a group of analysts in supporting process development
Provide career development guidance to the team members
Provide concise summary to cross-functional leadership for endorsement of key decisions
Oversee activities at contract manufacturing and testing sites
Author technical reports and analytical Chemistry, Manufacturing and Controls (CMC) sections in regulatory documents
Address analytical and product quality inquiries from health authorities
Supervises direct reports

What we offer

stock
retirement
medical
life and disability insurance
eligibility for an annual bonus
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

Fulltime

Associate Scientist Foods Product Development

As a member of the Condiments R&D team, you will support the R&D activities requ...

Location

United States , Englewood Cliffs

Salary:

59300.00 - 88900.00 USD / Year

Unilever

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Food Science, Food Engineering, Chemistry, Chemical Engineering, or a related field
1+ years of experience in food product development, R&D, or a similar technical role (internships or traineeships are highly valued)
Basic knowledge of food formulation, ingredients functionality, and processing techniques
Hands-on experience with laboratory testing, prototype development, or pilot plant work
Familiarity with food safety, quality standards, and regulatory requirements (labeling knowledge is a plus)
Exposure to cross-functional teamwork and ability to manage multiple priorities in a fast-paced environment
Strong analytical and problem-solving skills, with a structured approach to experimentation and data interpretation

Job Responsibility

Execute agreed R&D activities to deliver the brand’s program, ranging from innovation, product superiority and margin enhancement
Works as a member of a cross-functional project team to deliver projects on time in full
Independently design products against simple product briefs, design/execute test protocols for the various technical aspects of projects as required (e.g., prototype development and scale-up, shelf-life testing, analytical testing, etc.)
Lead the process of specification/label creation in SAP PLM from the request to the approved status
Actively participate and/or represent R&D in cross functional meetings
Assess feasibility of new ideas and troubleshoot activities where formulation knowledge is essential
Support technical investigations using root-cause analysis and problem-solving techniques as required for existing and new products
Develop and maintain effective working relationships with R&D, Supply Chain and Marketing teams, customers, suppliers, and key stakeholders

What we offer

Health insurance (including prescription drug, dental, and vision coverage)
Retirement savings benefits
Life insurance and disability benefits
Parental leave
Sick leave
Paid vacation and holidays
Access to numerous voluntary benefits
Bonus eligible
Long-Term Incentive (LTI) eligible

Fulltime

Analytical and Materials Scientist

Viatris is seeking an Analytical & Materials Scientist to join our Analytical Co...

Location

United Kingdom , Sandwich

Salary:

33000.00 - 37000.00 GBP / Year

SRG

Expiration Date

Until further notice

Requirements

Relevant scientific A Levels, BTEC Level 3, equivalent qualifications, or substantial practical experience
Ability to organise tasks, follow analytical methods, and deliver high‑quality results on time
Strong teamwork skills and the ability to collaborate effectively within a laboratory environment
Understanding of basic chemistry principles
Good IT skills, including Microsoft Excel, Word, and PowerPoint
Strong written and verbal communication skills
Genuine enthusiasm for working in a lab-based role
1 year of experience in industry (placement or work experience)

Job Responsibility

Conduct analytical testing to support product development, clinical trials, and regulatory submissions
Execute experiments that deepen scientific understanding in analytical and materials science, contributing to method development and formulation activities
Perform analysis related to product stability, development, and scale‑up processes
Process and interpret data, highlighting any anomalies and working with supervisors to investigate where needed
Maintain clear and accurate laboratory documentation in line with data integrity and good documentation practices
Support project delivery through additional tasks such as laboratory housekeeping, ordering, and shipment of samples
Comply with all relevant policies and procedures, including those relating to EHS, GMP, GCP, Quality, and Compliance
Undertake other duties assigned in line with the level and scope of the role

Fulltime

Research Scientist

Form part of a group of technical experts (SMEs) responsible for the continuity,...

Location

Malta , Marsa

Salary:

36800.00 EUR / Year

Baxter

Expiration Date

Until further notice

Requirements

Strong knowledge of product lifecycle management, including development, stability, clinical, registration, process transfer, manufacturing, and supply
Strong leadership and team management skills, with the ability to guide, delegate, and develop team members
Proven ability to lead cross-functional and cross-regional teams
Excellent interpersonal and communication skills, with the ability to present within technical and leadership forums
Strong technical writing capability for reports and scientific documentation
Advanced problem-solving, critical thinking, and analytical skills to address complex technical challenges
Demonstrated ability to lead projects to successful outcomes and work across disciplines
Self-motivated, resourceful, flexible, and able to manage multiple priorities
Fluent in English
Bachelor’s degree (EQF Level 6) in a scientific discipline (Chemistry, Biology, Pharmaceutics, Chemical Engineering, or related) with 8+ year experience, or Master’s degree (EQF Level 7) with 4+ year experience, or PhD (EQF Level 8) with 1+ year experience

Job Responsibility

Manage routine and complex changes for the on-market Clinical Nutrition (pharmaceutical) portfolio
Mentor/lead a team of scientists responsible for lifecycle design and change execution activities for on-market products
Provide direction on prioritization, technical problem solving, and process clarification, ensuring alignment with organizational objectives
Plan, organize and execute product changes in compliance with global regulatory and quality requirements
Lead cross-functional teams and facilitate decision-making to ensure timely project delivery
Apply advanced scientific and cross-functional knowledge to drive outcomes
Utilize project management tools to manage timelines, risks, and budgets, while identifying and resolving issues impacting delivery
Establish and maintain metrics to track operational performance and KPIs
Communicate progress and results to management and Senior Leadership Team (SLT) as required
Drive market enhancements and operational improvements

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
competitive benefits
discretionary bonuses
and/or long-term incentive

Fulltime

Research Scientist

This is where new knowledge is discovered. Baxter’s Research and Development tea...

Location

Malta , Marsa

Salary:

36800.00 EUR / Year

Baxter

Expiration Date

Until further notice

Requirements

Bachelor’s degree (EQF Level 6) in a scientific discipline (Chemistry, Biology, Pharmaceutics, Chemical Engineering, or related) with 8+ year experience, or Master’s degree (EQF Level 7) with 4+ year experience, or PhD (EQF Level 8) with 1+ year experience
Relevant experience in the pharmaceutical or other regulated industry, with a broad background in product development and lifecycle management
Strong knowledge of product lifecycle management, including development, stability, clinical, registration, process transfer, manufacturing, and supply
Strong leadership and team management skills, with the ability to guide, delegate, and develop team members
Proven ability to lead cross-functional and cross-regional teams
Excellent interpersonal and communication skills, with the ability to present within technical and leadership forums
Strong technical writing capability for reports and scientific documentation
Advanced problem-solving, critical thinking, and analytical skills to address complex technical challenges
Demonstrated ability to lead projects to successful outcomes and work across disciplines
Self-motivated, resourceful, flexible, and able to manage multiple priorities

Job Responsibility

Manage routine and complex changes for the on-market Clinical Nutrition (pharmaceutical) portfolio
Mentor/lead a team of scientists responsible for lifecycle design and change execution activities for on-market products
Provide direction on prioritization, technical problem solving, and process clarification, ensuring alignment with organizational objectives
Plan, organize and execute product changes in compliance with global regulatory and quality requirements
Lead cross-functional teams and facilitate decision-making to ensure timely project delivery
Apply advanced scientific and cross-functional knowledge to drive outcomes
Utilize project management tools to manage timelines, risks, and budgets, while identifying and resolving issues impacting delivery
Establish and maintain metrics to track operational performance and KPIs
Communicate progress and results to management and Senior Leadership Team (SLT) as required
Drive market enhancements and operational improvements

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
Competitive benefits
Discretionary bonuses
Long-term incentive

Fulltime

Research Scientist

Form part of a group of technical experts (SMEs) responsible for the continuity,...

Location

Malta , Marsa

Salary:

36800.00 EUR / Year

Baxter

Expiration Date

Until further notice

Requirements

Bachelor’s degree (EQF Level 6) in a scientific discipline (Chemistry, Biology, Pharmaceutics, Chemical Engineering, or related) with 8+ year experience, or Master’s degree (EQF Level 7) with 4+ year experience, or PhD (EQF Level 8) with 1+ year experience
Relevant experience in the pharmaceutical or other regulated industry, with a broad background in product development and lifecycle management
Familiarity with analytical techniques and/or process engineering is advantageous
Strong knowledge of product lifecycle management, including development, stability, clinical, registration, process transfer, manufacturing, and supply
Strong leadership and team management skills, with the ability to guide, delegate, and develop team members
Proven ability to lead cross-functional and cross-regional teams
Excellent interpersonal and communication skills, with the ability to present within technical and leadership forums
Strong technical writing capability for reports and scientific documentation
Advanced problem-solving, critical thinking, and analytical skills to address complex technical challenges
Demonstrated ability to lead projects to successful outcomes and work across disciplines

Job Responsibility

Manage routine and complex changes for the on-market Clinical Nutrition (pharmaceutical) portfolio
Mentor/lead a team of scientists responsible for lifecycle design and change execution activities for on-market products
Provide direction on prioritization, technical problem solving, and process clarification, ensuring alignment with organizational objectives
Plan, organize and execute product changes in compliance with global regulatory and quality requirements
Lead cross-functional teams and facilitate decision-making to ensure timely project delivery
Apply advanced scientific and cross-functional knowledge to drive outcomes
Utilize project management tools to manage timelines, risks, and budgets, while identifying and resolving issues impacting delivery
Establish and maintain metrics to track operational performance and KPIs
Communicate progress and results to management and Senior Leadership Team (SLT) as required
Drive market enhancements and operational improvements

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Process Development Senior Associate

At Amgen, if you feel like you’re part of something bigger, it’s because you are...

Location

United States , Cambridge

Salary:

85306.00 - 103484.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Master’s degree or (foreign equivalent) in Chemical Engineering, Bioengineering, Analytical Chemistry, Biochemistry or a related field & completion of a university-level course, research project, internship, thesis, or one year of experience in the following: 1. Analytical chemistry experience for small molecules, and completion of project deliverables including: designing and conducting targeted metabolomics experiments, extracting and analyzing results via dedicated software: ChemStation, MassHunter, or MassAnalyzer
2. Analytical method development (chromatography and mass spectrometry), related technologies and instrumentation including: U/HPLC, GC, or LC-MS
3. Method qualification and transfer for analytical instruments, along with data analysis and statistical evaluation of experimental results
4. Application analytical instrument troubleshooting across different platforms: Waters, Agilent, or Sciex, and problem solving of such technologies
5. Implementing Standard Operating Procedures in a laboratory environment in accordance with GLP standards
and 6. Maintaining a laboratory notebook.

Job Responsibility

Conduct experiments, analyze results, and implement process improvements to enhance efficiency and product quality
Design, develop, and optimize manufacturing processes
Collaborate closely with a team of analysts and scientists
Responsible for the technical aspects of developing analytical tools to gain understanding of quality attributes in product and process for late phase synthetic small molecule, synthetic peptide, and siRNA programs
Utilize platform and in-depth product attribute knowledge to advance Amgen products and ensure success through pivotal clinical phases to marketing authorization application
Develop, optimize, and execute analytical methods for synthetic small molecules, synthetic peptide, and SiRNA release testing and process characterization
Collaborate closely with drug substance process development team to achieve project objectives and provide analytical data to support drug substance product development.

What we offer

stock
retirement
medical
life and disability insurance
eligibility for an annual bonus
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

Fulltime

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Analytical Chemistry Development Scientist 1

Job Description

Job Responsibility

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