Formulation Scientist Job at H.B. Fuller (St. Paul)

Food Scientist

The Food Scientist will provide technical expertise to new product development f...

Location

Canada , London

Salary:

Not provided

Cargill

Expiration Date

Until further notice

Requirements

Diploma/Certificate or bachelor’s degree in Food Science or equivalent experience
Experience working in a manufacturing environment
Two or more years of professional experience combined in the following areas: protein formulation development, ingredient functionality and product commercialization
Must be willing to participate in sensory evaluation of animal protein products
Minimum of two years of related work experience
Ability to travel up to 30% of the time, into US and Canada
Ability to support early or late hours or weekends as needed
Proficiency in Microsoft Office
Possess a valid, full Canadian Driver’s Licence in good standing, authorizing you to drive independently during the course of your employment
Must be legally entitled to work for Cargill in Canada

Job Responsibility

Identify product growth and new product opportunities
Participate in sensory evaluation of animal protein products with cross functional teams and with customers
Provide technical guidance and leadership on products, process development and improvement, and support for quality systems and regulatory oversight
Partner and stay connected with cross functional teams that include marketing, insights, sales, ops, food safety quality and regulatory
Provide findings and analysis with insights, research, and commercial brand to develop short- and long-term testing programs for experimental and commercial products and hybrids
Collaborate and build partnership with sales, business management and marketing partners to identify customer needs and translate these into new product development opportunities
Independently solve moderately complex issues with minimal supervision, while escalating more complex issues to appropriate staff
Other duties as assigned

What we offer

Relocation assistance and visa sponsorship will not be provided for this position

Fulltime

Data Scientist

We are seeking a data scientist to join our business intelligence team to help u...

Location

United States , Dallas

Salary:

Not provided

Select Minds

Expiration Date

Until further notice

Requirements

Bachelor’s degree in data science, data analytics, or related field
Master’s degree or Ph.D. in a quantitative field, such as statistics, computer science, mathematics, or engineering
Proficiency in Python, Java, or Kotlin
Knowledge of data science toolkits such as R, NumPy, and MatLab
Experience with big data analytics technologies such as Spark and Hadoop
Experience with data visualization tools such as D3.js and Tableau
Expertise in data mining and machine learning
Working knowledge of statistical models and business intelligence
Familiarity with cloud-based infrastructure
Ability to store and process unstructured data with NoSQL databases and machine learning models

Job Responsibility

Formulates and leads guided, multifaceted analytic studies against large volumes of data
Interprets and analyzes data using exploratory mathematic and statistical techniques based on the scientific method
Coordinates research and analytic activities utilizing various data points (unstructured and structured) and employ programming to clean, massage, and organize the data
Experiments against data points, provide information based on experiment results and provide previously undiscovered solutions to command data challenges
Leads all data experiments tasked by the Data Science Team
Coordinates with Data Engineers to build data environments providing data identified by Data Analysts, Data Integrators, Knowledge Managers, and Intel Analysts
Develops methodology and processes for prioritization and scheduling of projects
Analyzes problems and determines root causes
Defines company data assets (data models), spark, sparkSQL, and hiveSQL jobs to populate data models
Works closely with all business units and engineering teams to develop strategy for long term data platform architecture

Group Leader, Formulation Development & Manufacturing

This role is pivotal for delivering high-quality formulation and manufacturing s...

Location

Belgium

Salary:

Not provided

Mantell Associates

Expiration Date

Until further notice

Requirements

MSc or PhD in Pharmaceutical Sciences, Chemical Engineering, or a related discipline
significant hands-on experience in formulation development and GMP manufacturing
At least 8-10 years in the pharmaceutical industry, including experience working with oral and/or injectable dosage forms in GMP production settings
Proven leadership experience managing and mentoring scientific teams in both R&D and GMP production environments
In-depth knowledge of GMP regulations, drug product formulation, process optimization, tech transfer and regulatory documentation practices
Strong organizational, communication, and scientific reporting skills
capable of driving technical excellence in a growing team
Fluent in English

Job Responsibility

Lead, plan and oversee GMP production projects from formulation development through clinical batch manufacturing – ensuring deliverables are on time, within budget, and compliant with GMP standards
Translate project specs from Project Managers into actionable tasks for Development & GMP teams
supervise Associate Scientists in formulating and manufacturing oral and injectable dosage forms
Develop and refine formulation strategies, select excipients and delivery formats, and guide tech transfers from R&D to GMP production
Ensure documentation quality: master batch records, batch records, technical reports, GMP manufacturing reports
coach the team to maintain standards in non-conformance management and quality assurance alignment
Coordinate with QA / QP and supply chain to ensure availability of starting materials, manage deviations, and resolve GMP / compliance issues swiftly and effectively
Act as scientific & technical problem-solver: troubleshoot formulation, process, equipment, and compliance challenges when they arise
Represent the Formulation & GMP Manufacturing team in project core meetings
provide scientific input to clients and internal cross-functional teams

Fulltime

R&D Formulation Scientist

The Formulation Scientist under the direction of Process Development Director is...

Location

Spain , Leon

Salary:

Not provided

PCI Pharma Services

Expiration Date

Until further notice

Requirements

Master’s degree in pharmaceutics or a related scientific discipline
At least 5 years’ experience in formulation development of product formulations in solution, suspension, emulsion and lyophilized forms for small molecules and biological products, defining QTPPs and CQAs, selecting suitable form of API and designing characterization studies, compatibility, solubility, dissolution, physico-chemical stability, etc.
Good level of spoken English and Spanish
Very good written communication skills

Job Responsibility

Development of product formulations in solution, suspension, emulsion and lyophilized forms for small molecules and biological products (mAb: monoclonal antibodies
ADC: antibody drug conjugate
proteins, peptides, oligonucleotides and high potency products)
Define and update the QTPPs and CQAs of the formulation: efficacy, safety, stability, purity and potency, etc.
In partnership with the client aid in the selection of suitable form of API for final drug product through pre-formulation and formulation techniques e.g. polymorph, isomeric conformation, melting point, hygroscopicity, pH and logP, particle size
Evaluation and selection of excipients according to QTTP. Selection and concentration of the formulation excipients and definition of the CMA of the selected excipients
Design of tests to evaluate the behavior of excipients and APIs: characterization studies, compatibility, solubility, dissolution, physico-chemical stability, etc.
Application of DoE methodology to design, perform and analyze laboratory scale experiments for the optimization of formulations and their manufacturing processes
Selection, design and execution of supporting studies and documentation for the development of the project: general studies such as characterization, compatibility, robustness, stability, etc. and specific biological products studies such as freeze-thaw, shear stress, protein content, silicone compatibility, etc.
Selection of appropriate equipment, manufacturers and technologies for technical and manufacturing transfer. Perform tasks related to pre-clinical batches, including toxicological studies

What we offer

Competitive salary
Health insurance + reimbursement for medication
English classes
Discounts on various activities
Partnerships with gyms
Referral programme

Fulltime

R&D Student Worker/Internship- Light Duty

The Research and Development (R&D) Intern will help light duty engine oil group ...

Location

United States , Lexington

Salary:

Not provided

Valvoline Global

Expiration Date

Until further notice

Requirements

Currently enrolled in a Chemistry, Biology, or Engineering college program
Good team work mentality
Good communication skills
Good computer knowledge in Microsoft Office applications
The ability to occasionally lift and carry up to 40lbs

Job Responsibility

Following Valvoline RC 14001 rules to perform job safely
Getting familiar with our VLIMS system to collect and record data
Making formulation blending and collect viscosity metrics data
Performing bench top testing required for engine oils
Performing data analysis and communication with formulators and scientists
Other duties and responsibilities as determined by Valvoline from time to time in its sole discretion

Summer 2026 R&D Internship- Antifreeze

The Antifreeze Research and Development (R&D) Intern will compelete a 12 week in...

Location

United States , Lexington

Salary:

Not provided

Valvoline

Expiration Date

Until further notice

Requirements

Currently enrolled in a Chemistry, Biology, or Engineering college program
Good teamwork mentality
Good communication skills
Good computer knowledge in Microsoft Office applications
Ability to work independently with guidance and collaborate within a team setting
The ability to occasionally lift and carry up to 40lbs
Basic knowledge of PPE and lab safety protocols
Working in a laboratory environment with adherence to safety protocols, including use of required personal protective equipment (PPE)/ability to stand and walk for extended periods of time
Must be authorized to work in the U.S.

Job Responsibility

Following Valvoline RC 14001 rules to perform job safely
Demonstrate a strong commitment to laboratory safety, including proper use of PPE, safe chemical handling, and adherence to OSHA/EPA regulations
Getting familiar with our VLIMS system to collect and record data
Making formulation blends and collecting data on the blends and/or tests performed on the blends
Performing bench top testing as needed for antifreeze blends
Performing data analysis and communication with formulators and scientists
Familiarity with acid and bases and standard chemical reactions
Other duties and responsibilities as determined by Valvoline from time to time in its sole discretion.

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

Senior Scientist, Drug Formulation and Process Development

At Hemab you will join a clinical-stage biotech company on an exciting journey t...

Location

Denmark , København og omegn

Salary:

Not provided

Life Science Talent

Expiration Date

Until further notice

Requirements

Master’s degree or equivalent in e.g. pharmaceutical sciences, chemical engineering, biotechnology or biology
Minimum 5 years of industrial experience with complex subcutaneous therapeutics
Experience in early and late-stage development has been an integral part in developing and steering products through to market. Preferably with a demonstrated innovative approach
Possess expert knowledge in patient-centric liquid and lyophilized formulations, vial, syringe and combination product development, stability and in-use studies, specifications and justification of specification, process development, GMP fill and finish, technical transfer, and commercial stage manufacturing of complex products
Proven ability to work with outsourcing and managing of CMOs
Experience serving as CMC drug product responsible for multiple programs including drug delivery and combination products is a plus
Experience with regulatory and quality documentation according to cGMP practice
Negotiation, influence, and strong project management and interpersonal communication skills that facilitate collaboration across functions and with consultants and CMOs
A motivated self-starter who is resilient, capable of hitting the ground, running and excelling in a high-growth, entrepreneurial business environment. Proven ability to take initiative in a technical, multicultural global working environment, leading by example while having an inclusive, collaborative style
You work hard and are not afraid to have a little fun while you do so

Job Responsibility

Deliver subcutaneous formulations and drug and combination product manufacturing processes that meet the target product profile
Manage drug product cGMP clinical and commercial manufacturing for various modalities e.g peptides, siRNAs and biologics (antibodies notably), including formulation, process development, technology transfer, quality and life cycle management aspects
Contribute to the selection and management of CMOs for drug product formulation and process development, cGMP manufacture and supply of drug and drug-device combination products
Collaborate with cross-functional R&D partners to develop strategy and execute on activities
Lead, supervise and coordinate the work of CMOs, material suppliers, consultants and vendors as applicable to meet manufacturing development goals
Contribute to ensure that CMOs follow relevant regulatory standards
Support and write regulatory documentation and support interactions with Health Authorities
Other duties as assigned

Fulltime

Formulation Scientist

H.B. Fuller

Location:
United States , St. Paul

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
March 18, 2026

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Job Posted:March 18, 2026

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