Referso Jobs

Scientist

Axelon Services Corporation · Posted Nov 9, 2026

Open

Charles City, Iowa, United States
On-site
Contract
$35–$52 per hour
5+ years

Scientist

Axelon Services Corporation · Posted Nov 9, 2026

Open

Charles City, Iowa, United States
On-site
Contract
$35–$52 per hour
5+ years

Superviseur, Purification IGIV Supervisor

Grifols · Posted Nov 9, 2026

Open

Montreal, Quebec, Canada
1–3 years

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Supervisor overseeing daily manufacturing shift activities in the IGIV Purification area of Grifols Canada Therapeutics (GCT) facility, ensuring quality, safety, delivery, and productivity objectives are met.

Responsibilities

Lead and direct daily manufacturing shift activities ensuring all tasks are assigned and followed up
Ensure quality or preventative maintenance notifications are issued and investigated in a timely manner
Ensure manufacturing schedules, products and materials are delivered
Train IGIV Purification personnel on process activities, safety requirements and cGMP requirements
Identify technical and non-technical development gaps and implement plans and targets

Requirements

Diplôme collégial ou technique
Baccalauréat en sciences
Baccalauréat en génie

Skills

cGMP Good Documentation Practices automated control systems OSHA EPA FDA regulations

Process Engineer

Catalent · Posted Nov 9, 2026

Open

Swindon, Wiltshire, United Kingdom
On-site
Full-time · Senior

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Lead product transfers, process development, and validation activities to ensure successful product introduction.

Compensation

Competitive Salary – Reflecting your experience and skills.

Responsibilities

Lead product transfers, process development, and validation activities
Develop process specifications, optimize manufacturing processes, and drive continuous improvement
Provide technical expertise to resolve process issues and improve operational performance
Ensure equipment, processes, and documentation meet GMP, regulatory, and quality standards
Manage project priorities and resources to achieve business objectives and timelines

Requirements

Degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering, Engineering, or a related discipline
Nice to have: Design of Experiments (DoE)
Nice to have: Statistical analysis
Nice to have: Leading projects

Skills

Pharmaceutical manufacturing Product development Life sciences Oral solid dosage (OSD) formulation

Senior Scientist – Product Development

DuPont · Posted Sep 2, 2026

Open

Richmond, Virginia, United States
Senior

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Lead and execute product innovation programs for Tyvek® portfolio, translating breakthrough science into differentiated products and driving commercialization.

Responsibilities

Lead and execute product innovation programs that strengthen the technical value proposition and market position of Tyvek® products.
Serve as a product technology leader, partnering with Marketing, Product Management, Application Development, Manufacturing, and Engineering teams to identify growth opportunities and develop market participation strategies.
Translate manufacturing process capabilities into differentiated product features and customer value propositions.
Develop deep mechanistic understanding of the relationship between material structure, processing conditions, and product performance.
Design and drive experimental programs involving flash-spinning technology, polymers, additives, and advanced material systems to support new product development.

Requirements

PhD or Master's degree in Chemistry, Polymer Science, Materials Science, Chemical Engineering, Mechanical Engineering, or a related technical discipline.
Nice to have: 3+ years of experience spanning product development, manufacturing, process scale-up, technical service, regulatory, quality, or commercial-facing technical roles.
Nice to have: German language capabilities

Skills

Manager, Contract Manufacturing

Insmed Incorporated · Posted Sep 11, 2026

Open

Remote, United States
Remote
Full-time · Manager
$124K–$161K per year
5+ years

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Responsible for the development, optimization, scale-up, and routine execution of manufacturing operations for pharmaceutical products, with a focus on on-site supervision at CMOs.

Compensation

$124,000.00-161,000.00 Annual

Responsibilities

CMO Oversight: Real-time and on-site supervision of CMO execution of routine manufacturing as well as technology transfer, optimization, new equipment install, and process validation activities
Design, develop, and optimize manufacturing processes for pharmaceutical APIs and formulations; with an emphasis on particle engineering via spray drying and low fill weight powder encapsulation
Contribute to the transition of spray drying and other drug product processes from pilot and commercial scale at primary and secondary CMOs
Troubleshoot spray drying and other drug product process equipment, ensuring efficiency and compliance with GMP regulations
Develop and execute validation protocols (IQ, OQ, PQ) for spray drying and other drug product processes

Requirements

Bachelor’s degree
Nice to have: capsule filling
Nice to have: blister primary packaging

Skills

pharmaceutical process engineering manufacturing

Senior Process Engineer

FMC Corporation · Posted Nov 9, 2026

Open

Schaffhausen, Schaffhausen, Switzerland
Senior
10+ years

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Senior Process Engineer

Responsibilities

Provide senior chemical engineering expertise and technical leadership across process development, scale-up and commercial manufacturing.
Partner with chemistry teams to develop safe, scalable and cost-effective processes, leading scale-up from laboratory to commercial production.
Lead process engineering and design activities, including process modelling, mass and energy balances, equipment requirements and capital project support.
Drive technology innovation and step-change improvements to enhance manufacturing efficiency, capacity and competitiveness.
Lead engineering activities for technology transfer, site adaptation, commissioning and start-up at internal and external manufacturing sites.

Requirements

Master’s degree in chemical engineering
PhD

Skills

process scale-up process design technology transfer commercial manufacturing mass and energy balances

Associate Scientist - Downstream Process Development

Lilly · Posted Nov 6, 2026

Open

Boston, Massachusetts, United States
Full-time · Associate
$72K–$189K per year
5+ years

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Lead development and optimization of downstream purification processes supporting viral vector programs from research through preclinical development.

Compensation

$72,000 - $189,200

Responsibilities

Lead development, optimization, and scale-up of downstream purification workflows for viral vectors.
Design and implement purification strategies using Iodixanol and CsCl density gradient ultracentrifugation, affinity chromatography, ion-exchange chromatography (AEX/CEX), membrane chromatography, and polishing operations.
Lead AKTA-based chromatography workflow development and process intensification initiatives.
Develop scalable downstream platform approaches to support rapid material generation and process consistency across programs.
Independently design experiments, analyze data, interpret results, and present technical conclusions to multi-functional teams and leadership.

Requirements

Bachelor’s degree in biology, biochemistry, chemical engineering, biotechnology, or related scientific field
Master’s/PhD
Nice to have: CsCl and iodixanol ultracentrifugation
Nice to have: Affinity chromatography
Nice to have: Ion-exchange chromatography

Skills

ultracentrifugation

Senior Scientist - Industrial Biotechnology & Fermentation Innovation

IFF · Posted Nov 6, 2026

Open

Grasse, Provence-Alpes-Côte d'Azur, France
Senior

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Lead scientific innovation in industrial biotechnology and fermentation for natural ingredients in flavor and fragrance.

Responsibilities

Develop innovative microbial and fermentation-based approaches to create natural ingredients for flavor and fragrance applications.
Translate sensory and product development objectives into biotransformation and microbial production strategies.
Identify, evaluate, and optimize microorganisms capable of producing high-value compounds from plant-based raw materials and agricultural by-products.
Explore emerging technologies in industrial biotechnology, fermentation science, biocatalysis, and biomass valorization.
Support analytical, biochemical, and sensory evaluation of fermentation-derived ingredients.

Requirements

PhD in Industrial Biotechnology, Microbiology, Fermentation Sciences, Food Biotechnology, Bioprocess Engineering, or a related scientific discipline.
Nice to have: French language skills
Nice to have: experience in flavor & fragrance
Nice to have: botanical ingredients
Nice to have: natural extracts

Skills

microbial cultivation fermentation processes

Associate Director, Strategic Manufacturing Solutions (DSP)

Celonic AG · Posted Nov 5, 2026

Open

Basel
Manager
5–7 years

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Lead technical and operational aspects of downstream biologics manufacturing, ensuring GMP compliance and process robustness.

Responsibilities

Review and assess current processes
Document new processes
Lead technology transfer to GMP sites
Support production planning and troubleshooting
Identify regulatory gaps and recommend solutions

Requirements

PhD or Master’s degree in biochemistry, biology, pharmaceutical sciences, engineering or related field

Skills

Downstream Processing Chromatography TFF/UFDF Viral clearance Filtration Process scale-up Process characterization Validation Troubleshooting

Scientist II

RepliGen Corporation · Posted Nov 3, 2026

Open

Marlborough, Massachusetts, United States
$113K–$163K per year
2+ years

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Support the development and commercialization of next-generation ultrafiltration and microfiltration membrane technologies for bioprocessing applications.

Compensation

The estimated base salary range for this role, based in the United States of America is $113,000-$163,000. Compensation decisions are dependent on several factors including, but not limited to an individual's ,qualifications, location, internal equity, and alignment with market data. Additionally, employees are eligible to participate in one of our variable cash programs (bonus or commission) and eligible roles may receive equity as part of the compensation package.

Responsibilities

Develop ultrafiltration and microfiltration membranes and membrane manufacturing processes from concept through commercialization, with a focus on product performance, manufacturability, and customer needs.
Execute new product development activities including process development, design verification, validation, scale-up, and technology transfer, taking ownership of deliverables and project outcomes.
Evaluate membrane formulations, process improvements, and emerging technologies to enhance product performance and manufacturability, bringing forward new ideas and approaches to technical challenges.
Design, execute, and analyze laboratory and pilot-scale experiments to address technical challenges, make informed decisions, and support project objectives.
Support validation activities using quality and manufacturing tools including DFMEA, PFMEA, IQ/OQ/PQ, control plans, and process verification methodologies, maintaining a strong commitment to quality, integrity, and compliance.

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