RD&A Process Scientist - Food Industry
Principal research scientist job in Clark, NJ
Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment.
About the role
The RDA Process Scientist performs research and development work with an operations focus which bridges the gap between RD&A Taste Innovation and KERRY's commercialization process. He/she will focus on process optimizations, scale-ups, solving regulatory and other hurdles to new products and technologies introductions. He/she will collaborate with other scientists (especially Taste Innovation team), engineers, maintenance, QC, sanitation, etc.
Key responsibilities
Work closely with Taste Innovation team to develop and scale up taste modulation products
Focus on solving the regulatory hurdles
Liaising with cross functional teams: engineering, research, technical, QC, sanitation, maintenance, and/or production staff, regulatory, procurement, etc.
Planning, organizing, and overseeing process or production trials
Suggests improvements or modifications to current processes
Generates ideas for new products and researches feasibility in terms of profitability, resource availability and compliance with regulations.
Adheres to Standard Operating Procedures (SOPs) and Cleaning In Place (CIP)
Keeps recording data log (flow rate, pressure, temperature, etc) and analyzing data
Writes and reads technical papers, reports, reviews, and specifications.
Qualifications and skills
Bachelor's or Master's in food process science, food engineering, agricultural science, engineering, material science or related science fields.
Experience in a food production environment or industrial laboratory Experience with upscaling of food manufacturing processes is a plus: moving from lab scale to industrial scale.
Knowledge of good manufacturing practice
Problem-solving skills, analytical skills, and attention to detail
Strong communication and interpersonal skills, able to work effectively as part of a team.
Excellent analytical, organizational, and multi-tasking skills.
The pay range for this position is $107,757 to $181,563 in Annual Salary. Kerry typically does not hire an individual at the top or near the top of the range, as we are a pay-for-performance company, and this range is set to continue to reward performance annually while in role. Compensation decisions are dependent on the facts and circumstances of each case. The specific compensation offered to a candidate within the above range may be influenced by a variety of factors including skills, qualifications, experience, and internal equity. Kerry offers a competitive benefits package, including medical, dental, vision, paid time off, a 401(k) plan with employee and company contribution opportunities, Employee Share Plan, Life, disability, and accident insurance, and tuition reimbursement. This job posting is anticipated to expire on Jan 30th, 2026.
Kerry is an equal opportunity employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age disability, protected veteran status or other characteristics protected by law. Kerry will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditional upon the successful completion of a background investigation and drug screen. Additional information can be found at: Know Your Rights: Workplace Discrimination is Illegal (dol.gov).
Beware of scams online or from individuals claiming to represent us. A Kerry employee will not solicit candidates through a non-Kerry email address or phone number. In addition, Kerry does not currently utilise video chat rooms (e.g., Google Hangouts) to conduct interviews. Refuse any request that asks you to provide payment to participate in the hiring process (e.g., purchasing a “starter kit,” investing in training, or something similar). Kerry will not ask you to pay any money at any point in the hiring process with the exception of reimbursable travel expenses. In addition, any payments made by Kerry will be from official firm accounts bearing the Kerry name.
Principal Scientist
Principal research scientist job in Elma, NY
The Principal Scientist will serve as a technical leader and subject matter expert, driving R&D strategy across alternative protein platforms-including plant-based proteins, precision fermentation, and emerging technologies. This role blends hands-on research with strategic leadership, ensuring our scientific platforms deliver transformative products that meet consumer needs and accelerate business growth. In this position, you will collaborate closely with the VP of Research to create novel ingredients, processes, and products with high potential for intellectual property (IP). Strong expertise in protein structure-function relationships, particularly in novel food systems, is essential.
Key Responsibilities
Lead the extraction, isolation, and characterization of new functional ingredients from plant raw materials using analytical techniques (HPLC-MS, SDS-PAGE, spectrophotometry, etc.).
Apply advanced soft matter science to develop differentiated structured foods through emulsification, gelation, foaming, crystallization, and related approaches.
Leverage AI and emerging technologies to design the next generation of healthy, functional foods with enhanced consumer experiences.
Develop and implement procedures to characterize proteins and biopolymers using materials science techniques (DSC, rheometry, laser diffraction).
Design and execute experiments, write SOPs and protocols for new procedures, analyze data, and prepare reports for review.
Continuously scout and evaluate advanced technologies aligned with strategic focus areas; generate insights on new ingredient platforms.
Lead high-impact research projects that result in patents and strengthen the company's innovation leadership.
Build and manage collaborations with academic researchers, analytical service providers, consultants, ingredient suppliers, equipment manufacturers, and IP partners.
Qualifications
Ph.D. in a scientific discipline (materials science, physics/biophysics, chemistry, physical chemistry, biological or chemical engineering, or related field) with 3-5 years of food industry research experience.
Hands-on expertise in characterizing and quantifying food ingredients (proteins, fats, carbohydrates, flavors, nutrients) using chemistry, rheology, texture analysis, and other advanced analytical methods.
Strong knowledge of industry-standard food processing techniques and ability to research, design, and implement disruptive technologies.
Demonstrated expertise in food texture development and emulsion formulation.
Proven ability to translate scientific insights into novel food processes and products.
Nice to Have (Not Required)
Experience with data analytics and machine learning.
Demonstrated track record of IP generation and patent development.
Salary Range: $120,000 - $150,000
Steuben Foods is committed to equal employment opportunity. We recruit, employ, train, compensate, and promote without regard to race, religion, color, national origin, age, sex, disability, protected veteran status, or any other basis protected by applicable federal, state, or local law.
Research Scientist
Principal research scientist job in Piscataway, NJ
Onsite in 909 River Road Piscataway, NJ 08854
Monday - Friday, 8am - 4pm (with some flexibility)
Reason for request: Lab development, stability, data integration/analysis work
JOB DESCRIPTION:
Perform appropriate Lab practices and procedures for making product formulation and testing of products. Follow product stability protocols. Maintain, monitor, validate and calibrate lab equipment, as necessary. Prepare reports, collect data analysis, and communicate progress and completion of tests to leadership. Maintain good record keeping habits.
Responsibilities include:
Lead the development and implementation of new toothpaste formulas for North America - under the hello and Tom's of Maine brands.
Be the R&D point of contact for commercial teams for hello and Tom's key innovation.
Lead experimental designs to help identity launch formulations and production processes.
Make lab and pilot batches of formulations for stability testing and customer sampling.
Support Pilot Plant batches by preparing batch sheets, requesting raw materials, pre-weighing materials and batch execution.
Support plant trial batches at various North America locations as needed.
Manage multiple stability studies at the lab, pilot and plant scale, working with support groups (analytical, flavor, micro, etc) to deliver samples and follow up on results.
Create/maintain all required R&D documentation to ensure flawless, high quality commercialization.
This may include R&D project timelines, formula databases, tech transfer checklists, proof of claims documents, registration documents, NODs, change control documents and technical justifications.
Manage independent projects and collaborate with cross-functional teams, leveraging diverse perspectives to achieve key project goals and influence beyond your network
Create and maintain all required documentation under GMP/GLP per FDA/ICH guidelines as required.
Validate new raw material suppliers and packaging as required.
Maintain a clean and organized working environment.
Work on multiple tasks with changing priorities.
Make day-to-day recommendations and escalate issues regarding formula development.
Stay abreast of supplier and competitor's new developments.
Abide by and follow all company standard operating procedures (SOPs) including those for product development, regulatory and safety.
Deliver effective presentations of technical data and project status.
Required Qualifications
Bachelor's or MS Degree in Chemistry, Chemical Engineering, Biochemistry, Food Science or related fields.
4+ years of experience developing and/or implementing consumer products.
Experience scaling up formulations from the lab through pilot or manufacturing scale.
Technical understanding of related chemistry and science (for example: active deliveries, emulsions, surfactants, rheology, liquid chemistry)
Strong knowledge of ingredient chemistry to be able to understand how the interdependencies and interactions of raw material components affect formulation and process performance
Able to multi-task and coordinate various simultaneous projects
Strong oral and written communication skills
Self-motivated but able to work well within a team environment
Knowledge of cGMP /GMP and GLP
Excellent computer skills (MS Office, Google suite, SAP, etc.)
Preferred Qualifications
Knowledge of equipment and procedures for making oral care formulations
Experience running stability studies for OTC/Drug products
Experience & understanding of producing formulations at the manufacturing scale.
Experience with claim substantiation.
Strong project planning and management experience
Knowledge of Regulatory environment in North America and across the globe
Knowledge of ICH/FDA guidelines for stability and testing of new drug products
Other Required Experience/Qualifications:
Previous laboratory experience preferred.
Must have hands-on experience with laboratory instruments.
Must be able to learn new procedures in a short period of time.
Must be able to follow SOPs and obtain reliable and accurate data.
Must be able to document data consistently and accurately.
Must be able to perform routine tasks daily
Principal Scientist, Complex Fluids & Surfaces
Principal research scientist job in Warren, NJ
Vantage Specialty Chemicals is seeking a highly skilled and results-driven Principal Scientist, Complex Fluids & Surfaces to lead a critical enabling platform that advances measurement science and mechanistic understanding across multiple business units. This high-impact senior role will apply fundamental colloid, interface, and surface science to drive technical excellence and deliver differentiated product solutions for consumer and industrial markets, including Personal Care, Food, and Surface Treatment. The Principal Scientist is a recognized technical authority responsible for independently leading, organizing, and executing complex research and development (R&D) projects with broad impact on organizational goals. Operating with substantial autonomy, this individual will develop novel methodologies, guide strategic scientific direction, and serve as the global subject matter expert in complex fluids and surfaces.
Key Responsibilities
Assume full technical responsibility for the design, execution, and coordination of major R&D projects and initiatives in colloid and surface science.
Plan and lead research addressing novel, complex, or controversial scientific problems with significant impact on product portfolios and long-term business strategies.
Act as global technical authority in measurement science, establishing worldwide liaison with internal and external experts to shape the company's strategic direction.
Develop and apply advanced methods in rheology, interfacial and surface analysis, and particle characterization to provide deep mechanistic understanding of complex fluids and formulated products.
Collaborate with R&D, process engineering, scale-up, and operations teams to apply measurement science to both product innovation and manufacturing process improvements.
Serve as:
Individual Contributor - Lead original, high-impact research, often resulting in new methodologies, inventions, or breakthrough innovations.
Staff Specialist - Act as the company-wide expert in applying advanced scientific principles to facilities, products, and technologies.
Translate measurement science into consumer-technical models linking physical properties of products with consumer experience and perception.
Guide the design, commissioning, and operation of laboratories for advanced instrumentation; ensure scientific instrumentation is maintained, calibrated, and continuously improved.
Train, mentor, and supervise junior scientists and technical staff in advanced methods and best practices.
Evaluate project outcomes, recommend shifts in strategy, and monitor emerging scientific fields to identify new opportunities.
Champion adherence to safety, compliance, and quality standards, while fostering an inclusive and collaborative culture of scientific excellence.
Qualifications
Ph.D. in Chemistry, Chemical Engineering, Polymer Science, or a related discipline; minimum 5-6 years of relevant industrial R&D experience.
Proven track record of technical leadership, innovation, and significant contributions to scientific advancement in complex fluids and surfaces.
Extensive hands-on experience with characterization of colloidal and multiphase systems, including viscoelastic surfactant solutions, polymer solutions, emulsions, microemulsions, dispersions, and lamellar liquid crystalline fluids.
Expertise in measurement science techniques, with emphasis on rheology for characterizing complex fluids and supporting structure-property and sensory modeling. Familiarity with oscillatory and steady shear methods, viscoelastic behavior, and flow analysis is desirable. Additional experience in tribology, viscometry, surface/interfacial tensiometry, contact angle analysis, foam stability, particle size characterization, and microscopy (PLM, fluorescence, SEM, TEM) is also valued.
Strong record of scientific impact through publications, patents, and professional engagement as a subject matter expert.
Experience in laboratory design, instrumentation operation, maintenance, and upgrades.
Demonstrated ability to mentor and develop junior technical talent.
Strong written and verbal communication skills, with experience presenting to technical and business audiences.
Authorized to work in the United States.
Applications and Product Development Senior Scientist
Principal research scientist job in Avenel, NJ
Applications & Product Development Senior Scientist:
Work directly for a Middlesex County, NJ area company that supplies high quality oils and specialty ingredients to the beverage industry.
Seeking a detail-oriented and motivated individual to join our team as an Application and Product Development Senior Scientist specializing in dairy and alternative dairy protein beverage development. As a Senior Scientist, you will play a crucial role developing and implementing innovative protein-based beverages with knowledge and understanding of dairy beverage production equipment and processes. This role requires excellent communication skills to successfully collaborate across multiple departments to deliver results in a team-oriented setting.
The Senior Scientist should be able to lead a team of Scientists and Technicians while meeting critical deadlines and delivering superior service to the clients.
Essential Duties and Responsibilities:
* Own and manage multiple projects developing stable cost-effective consumer products that meet customer expectations & project parameters including processing parameters, ingredient functionality, costs, regulatory constraints, and flavor tonality.
* Formulate new dairy beverage recipes, innovating with new flavors and ingredients, and developing process improvements.
* Develop protein beverage formulations from conceptualization to scale-up that meet taste, texture, stability, quality and process optimization.
* Be the subject matter expert in training more junior staff.
* Conduct routine laboratory tests to resolve technical challenges, ensure products meet performance, stability, quality and safety standards and communicate findings with R&D team and relevant stakeholders, including senior leadership.
* Conduct sensory evaluations and prototype evaluations with Applications and Flavor Team to ensure product consistency and quality.
* Accountable to monitor and maintain laboratory equipment and supplies, ensuring they are in proper working condition.
* Aid in vetting new and alternative ingredients in finished products.
* Leverage internal and external resources to bring insight, expertise, and efficiency into project executions and to improve team knowledge.
* Scale up lab-scale processes to pilot and production levels.
* Ability to travel both domestically and internationally to assist with scale up to support commercialization runs.
Education and/or Work Experience and Other Requirements:
* Bachelor's Degree in Food Science, Chemistry, or related field. Master's degree preferred.
* 8-12 years of experience working as a Scientist in the food and beverage industry.
* Strong knowledge of food science principles, regulations, and industry best practices.
* Flexibility to adapt to changing priorities and tight deadlines.
* Ability to work in a fast-paced and dynamic environment.
* Extensive knowledge of food and beverage testing techniques, equipment, and procedures.
* Knowledge of Good Manufacturing Practices (GMPs), food safety and quality control procedures.
* Excellent analytical, problem-solving, and critical-thinking skills, with keen attention to detail and accurate record keeping.
* Effective communication and interpersonal skills with the ability to effectively collaborate with team members and other departments, including outside clients and senior leadership.
* Ability to work independently and collaborate in a team environment.
Physical Requirements:
* Ability to lift and carry objects (up to 50 lbs.) and stand for extended periods of time.
Salary: $110-$120k plus benefits and bonus eligible
Apply Directly on LinkedIn or through our Website: https://search5.smartsearchonline.com/synerfac/jobs/jobdetails.asp?jo_num=116372&apply=yes&job Title=Applications%20&%20Product%20Development&city Zip=NJ&proximity=25&
Research Scientist IV
Principal research scientist job in Spring House, PA
Source One is a consulting services company and we're currently looking for the following individual to work as a consultant with our direct client, a global Pharmaceutical Manufacturing client in Spring House, PA.
No Third-Party, No Corp to Corp, No Sponsorship. Must be able to work in the US and must not require sponsorship for employment visa status now or in the future (e.g., FI, H1-B status)
Title: Research Scientist IV
Location: Spring House, PA
Onsite (Mon-Fri, 40 hours)
Contract Duration: 12 months, with likely extension
Pay Rate: $67.88 per hour (w2)
Key Responsibilities:
• Support membrane protein expression and purification.
• Conduct protein production, purification and characterization.
• Characterization and quality check of membrane proteins to support biotherapeutics development.
• Collaborate effectively in a multi-team environment.
• Contribute to both internal and external efforts in membrane protein production.
Education:
• Minimum of BS Degree with a minimum of 2-4 years of academic/industry experience or MS Degree with a minimum of 1-2 years is required.
Required Skills:
• Experience with membrane protein expression and optimization, purification, and characterization of proteins
• Well-versed with analytical characterization to determine quality, conformation, purity and stability
• Knowledge of protein expression construct design and optimization, and expression platforms
• Excellent communication skills to collaborate with internal and external partners
Preferred:
• Proficient in protein purification optimization, detergent screening, and reconstitutions into lipid nanodiscs
• Experience in independently operating AKTA FPLC and analytical HPLC instruments
• Experience in generating DNA/RNA constructs and or other tools as antigen for supporting antibody discovery
• Knowledge and experience with CROs for protein production
Principal Protein scientist
Principal research scientist job in Spring House, PA
Duration: 12Months
Required Skills
Role is 100% onsite in Spring House, PA
Bachelor's degree is required
#1 Required skill: Must have processing protein production, purification experience
#2 Required skill: Must have analytical characterization experience
Membrane protein experience, a huge plus
Must have 2-4 years of experience
Will attend group meetings
60%-70% of the role will be lab based work
Will do data capturing
Description:
Key Responsibilities:
Support membrane protein expression and purification.
Conduct protein production, purification and characterization.
Characterization and quality check of membrane proteins to support biotherapeutics development.
Collaborate effectively in a multi-team environment.
Contribute to both internal and external efforts in membrane protein production.
Qualifications
Minimum of BS Degree with a minimum of 2-4 years of academic/industry experience or MS Degree with a minimum of 1-2 years is required.
Experience and Skills:
Experience with membrane protein expression and optimization, purification, and characterization of proteins
Well-versed with analytical characterization to determine quality, conformation, purity and stability
Knowledge of protein expression construct design and optimization, and expression platforms
Excellent communication skills to collaborate with internal and external partners
Preferred:
Proficient in protein purification optimization, detergent screening, and reconstitutions into lipid nanodiscs
Experience in independently operating AKTA FPLC and analytical HPLC instruments
Experience in generating DNA/RNA constructs and or other tools as antigen for supporting antibody discovery
Knowledge and experience with CROs for protein production
About US Tech Solutions:
US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit ************************
US Tech Solutions is an Equal Opportunity Employer.All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Recruiter Details:
Name: I.Prudvi kumar
Email: *******************************
Internal Id: 25- 54564
Clinical Scientist
Principal research scientist job in Clark, NJ
Job Title: Scientist I - pharmacovigilance
Job Duration: 12 Months Contract - W2
Note:
Backfill
Onsite role
Job Description:
As a Scientist in our Post Market Safety & Cosmetovigilance team, your main responsibilities are:
• Prioritization of workload for US OTC/Medical Devices (MD) & Hospital visit cases, data entry, MedDRA coding and completion of case narratives of incoming potential Health Related Complaints (HRCs) into the Post-marketing Safety (PMS) database while ensuring completeness and legibility.
• Reconciliation of daily cases received from Consumer Care Center (CCC), identify missing cases, correct errors in the Salesforce database & notify CCC manager of discrepancies.
• Provide feedback using discretion regarding database issues or with case details that are documented by CCC and communicate database discrepancies.
• Support PMS team members with projects regarding completion of cases with missing data or formula numbers as needed and serve as a backup for preparing statistical reports.
• Perform data extractions for global PMS analyses and validate data.
• Provide ongoing training/feedback of operating tools coordinating with colleagues in France to ensure accuracy.
• Provide prompt queries of vendor's database to review all AEs received, notify appropriate partner contacts, review for potential quality-related complaints, notification of manufacturing sites, while maintaining appropriate recording and archiving of information.
• Conduct database and data entry training of PMS newcomers within the Americas zone.
• Ensure documentation management of departmental work files, including organization of department training documents, Quality Investigations, and maintenance of FDA correspondence.
• Review/update standard operating procedures (SOP) and work processes (WP) as needed.
• Participate in department presentations to CCC or other métiers.
• Ensures compliance with company policies, procedures, and standards.
• Ensuring prioritization of data entry workload (OTC/Hospital/MD cases), data exploitation/validation working with colleagues in Global Data Management, ensure department document retention, while working with other Sr. Scientists, Vigilance Coordinators & Head of Post-Marketing Safety.
To Succeed in this Position, You Have:
• A completed BS or MS in biology or a related field preferred with case processing experience & relevant data exploitation experience in pharmacovigilance.
• Minimum of 3-5 years of relevant experience.
• Experience in MedDRA coding preferred.
• Basic understanding of US Regulations pertaining to Post Marketing Safety preferred.
• Knowledge of medical terminology preferred.
• Excellent communication (verbal, written) and interpersonal skills required.
• Well organized while handling multiple projects simultaneously.
• Demonstrated skills in analyzing, reporting, and documenting information with strong attention to detail.
• Ability to work independently with minimum supervision in a matrix environment.
Clinical Scientist Data Reviewer
Principal research scientist job in Jersey City, NJ
6 month contract w/ renewal
3 days onsite in Jersey City, NJ
We are seeking a Clinical Scientist Data Reviewer that will support the scientific planning efforts and collaborate with Clinical Research, Pharmacovigilance and Clinical Operations in the execution of one or more clinical trials or significant aspects thereof. In this position, you will have the opportunity to demonstrate technical skills and scientific acumen as part of a cross-functional clinical development team. You will be a key contributor and supporter in the clinical science activities of evidence generation for regulatory approval and/or engagement with physicians, including protocol development, study implementation, data analysis and reporting of results. This role will be focused on the detailed and critical safety data review efforts from study start-up through final CSR. The Clinical Scientist Data Reviewer is a crucial role in analyzing and interpreting clinical trial data to ensure accuracy, integrity, and compliance with regulatory requirements. There is additional room for growth and leadership opportunities in this role.
Responsible for supporting specific aspects of clinical/scientific execution of clinical protocol(s). This may include:
Serving as a supportive clinical scientist data reviewer focused on safety, efficacy and critical data deliveries as part of the clinical trial team
Supporting the clinical study team as part of the clinical sciences functional line which is closely aligned with the medical monitoring team in review and interpretation of clinical data/medical protocol deviations in collaboration with Clinical Research and Pharmacovigilance (as well as other functional areas in this matrix environment)
Collaborating cross-functionally in the development of Protocol and related study materials (e.g., ICF documents / amendments); partnering with Clinical Operations on critical and key study deliverables
Ensure CRF design supports data collection in alignment with the Protocol in collaboration with Clinical Data Management/Programming
Collaborating cross-functionally to review clinical data to ensure quality, completeness, and integrity of trial conduct
Potential to provide tactical/scientific mentorship to other clinical scientists and move into Clinical Scientist lead role as well as focus on scientific growth and development
Responsible for assisting with the generation, analysis, and presentation of clinical data, including manuscripts, abstracts, and oral presentations (including authoring documents and slide preparation as appropriate)
Apply proficient analytical knowledge and skills to understand how program objectives and design impact data analysis; identifies risks and designs mitigation strategies
Promotes consistent first line medical/clinical data review techniques and conventions across studies/programs
Qualifications
6+ years of experience with a Post Graduate Degree or 8+ years of experience with a Bachelor's degree in a relevant scientific discipline.
Experience in clinical drug development experience, or a PhD, Pharm D, or RN degree is preferred.
Experience within oncology preferred
Solid knowledge of clinical research regulatory requirements (e.g., GCP and ICH)
Ability to manage multiple competing priorities with good planning, time management and prioritization skills
Strong analytical skills with the ability to interpret clinical trial data and synthesize conclusions
Proficient scientific expertise to propose, design, and execute clinical research and development studies, and authors documents related to clinical trials, such as medical monitoring plan, SAPs, informed consent and clinical components of the Clinical Study Reports
Interact with key stakeholders across Clinical Development functional areas
Role requires proactive approach, strategic thinking and leadership in driving toward clinical study goals
Influence opinions and decisions of internal and external customers / vendors, across functional areas
Problem solving, prioritization, conflict resolution and critical thinking skills
Strong communication, technical writing, and presentation skills experience
Analytical Scientist
Principal research scientist job in Somerset, NJ
Job Title: Analytical Scientist - Solid Oral Product Development
The Analytical Development Department is dedicated to the successful and timely development of new pharmaceutical solid oral products by providing essential analytical development services to clients. The Analytical Scientist will offer analytical support for the team, contributing to the evaluation, development, and validation of analytical methods with limited supervision. The role also involves conducting routine analyses of active pharmaceutical ingredients (APIs) and finished products using advanced laboratory techniques and instrumentation.
Specific Duties, Activities, and Responsibilities
Perform hands-on method development, improvement, and validation using techniques including, but not limited to: HPLC, GC, Dissolution, UV-Vis Spectroscopy, FTIR, Microscopy, and Particle Size Distribution (PSD).
Assist in complex analytical experiments such as unknown impurity identification and excipient compatibility studies.
Effectively prioritize activities to provide timely analytical support to product development initiatives.
Anticipate analytical challenges in the R&D development process and provide strategic long-term planning for method development and enhancement.
Support formulation development and technology transfer activities for assigned projects.
Investigate method performance and reliability, and conduct optimization studies as necessary.
Collaborate in the preparation of technical documents, including validation protocols and reports, stability protocols and reports, and analytical test procedures.
Education and Experience
Bachelor's degree (BS) in Chemistry, Biochemistry, or a related discipline with 6-8 years of pharmaceutical industry experience, or
Master's degree (MS) in Chemistry, Biochemistry, or a related discipline with 4+ years of pharmaceutical industry experience.
Knowledge/Skills
Solid working knowledge of GxP principles, regulatory (ICH) guidelines, and compendial (USP/EP/JP) requirements for generic product development.
Scientist 4 - Research and Development
Principal research scientist job in Spring House, PA
Immediate need for a talented Scientist 4 - Research and Development. This is a 12+ Months Contract opportunity with long-term potential and is located in Spring House, PA (Onsite). Please review the job description below and contact me ASAP if you are interested.
Job ID:25-94738
Pay Range: $57 - $67/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).
Key Responsibilities:
Support membrane protein expression and purification.
Conduct protein production, purification and characterization.
Characterization and quality check of membrane proteins to support biotherapeutics development.
Collaborate effectively in a multi-team environment.
Contribute to both internal and external efforts in membrane protein production.
Key Requirements and Technology Experience:
Skills-Experience in independently operating AKTA FPLC and analytical HPLC instruments.
Proficient in protein purification optimization, detergent screening, and reconstitutions into lipid nanodiscs.
Minimum of BS Degree with a minimum of 2-4 years of academic/industry experience or MS Degree with a minimum of 1-2 years is required.
Experience with membrane protein expression and optimization, purification, and characterization of proteins
Well-versed with analytical characterization to determine quality, conformation, purity and stability
Knowledge of protein expression construct design and optimization, and expression platforms
Excellent communication skills to collaborate with internal and external partners
Proficient in protein purification optimization, detergent screening, and reconstitutions into lipid nanodiscs
Experience in independently operating AKTA FPLC and analytical HPLC instruments
Experience in generating DNA/RNA constructs and or other tools as antigen for supporting antibody discovery
Knowledge and experience with CROs for protein production
Our client is a leading Pharmaceutical Industry and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration.
Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
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Analytical Scientist
Principal research scientist job in Middlesex, NJ
We are seeking an Analytical Scientist to join a reputable pharmaceutical manufacturing company to conduct routine and non-routine analyses of in-process materials, raw materials, environmental samples, finished goods, or stability samples.
** No Relocation, No C2C Candidates**
Pay: Up to $50/hour.
RESPONSIBILITIES:
Conduct and document chemical analyses for raw materials, in-process goods, and finished products.
Design, validate, and resolve issues with analytical methods, including HPLC for cleaning verification.
Collect and analyze equipment cleaning validation samples.
Prepare Certificates of Analysis, analytical reports, and maintain lab documentation.
Peer-review records and support OOS or OOT investigations as per SOPs.
Ensure compliance with SOPs, cGMPs, and regulatory requirements.
Assist with environmental monitoring and other tasks as assigned.
QUALIFICATIONS:
2 years hands-on method development experience (HPLC)
Knowledge of cGMPs, pharmacopeia (USP, EP), and regulatory standards (21 CFR Part 210/211/820, ISO).
Bachelor's in Chemistry-related discipline with 2+ years of analytical lab experience.
This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!
Associate Scientist
Principal research scientist job in Franklin, NJ
Develop, optimize, and qualify/validate molecular and cell-based assays, including multi-parameter flow cytometry, cell phenotyping, functional assays, cytokine assays (ELISA/MSD/Luminex), qPCR/dd PCR, VCN analysis, and related potency methods.
Culture and maintain primary human immune cells and engineered cell products; perform isolation, activation, expansion, and transduction/transfection workflows.
Independently design, execute, and analyze experiments; document results in ELNs; interpret data and present findings to cross-functional groups.
Support tech transfer of analytical methods into manufacturing/QC, including authoring SOPs, protocols, and technical reports.
Collaborate cross-functionally to support product characterization, comparability, process development, release testing, stability studies, and assay troubleshooting.
Dexian stands at the forefront of Talent + Technology solutions with a presence spanning more than 70 locations worldwide and a team exceeding 10,000 professionals. As one of the largest technology and professional staffing companies and one of the largest minority-owned staffing companies in the United States, Dexian combines over 30 years of industry expertise with cutting-edge technologies to deliver comprehensive global services and support.
Dexian connects the right talent and the right technology with the right organizations to deliver trajectory-changing results that help everyone achieve their ambitions and goals. To learn more, please visit ********************
Dexian is an Equal Opportunity Employer that recruits and hires qualified candidates without regard to race, religion, sex, sexual orientation, gender identity, age, national origin, ancestry, citizenship, disability, or veteran status.
Associate Scientist
Principal research scientist job in Lansdale, PA
Job Title: Scientist
Duration: 12 Months
Pay Rate: $32/hr on W2
Education:
• B.S. in Biology, Bio/chemistry, Bio/chemical Engineering, or related science or engineering field.
• At least 1yr of laboratory experience in Molecular Biology, Protein Biochemistry, and/or upstream process development.
The ideal candidate would possess:
• General laboratory skills, experience with aseptic manipulations, pipettes
• Experience in culturing microbial cells at different scales
• Experience in protein biochemistry and analytical methods (e.g. SDS-PAGE, Western Blot, ELISA)
• Basic knowledge of fermentation
• Experience using formulas and linking spreadsheets in Excel
• Highly computer literate. Capable of quickly learning and adapting to new computer programs. Strong computer, scientific, and organizational skills
• Excellent communication (oral and written) and attention to detail
• Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
• Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.
Additional Requirements:
• This position will require occasional off-hour and/or weekend work (10-20% of hours may be “off-shift”)
• This position will require work with Biosafety Level-1 organisms
Responsibilities:
Scientist responsibilities include, but are not limited to, the following:
• Prepare laboratory reagents, solutions, and culture media
• Perform lab-scale fermentation runs to meet different needs
• Set up process equipment for lab-scale experiments
• Perform analytical assays
• Analyze, collate, track, and report data back to client staff members
• Maintain records and test results following good laboratory practices (GLP) guidance
• Work independently and efficiently
• Document work clearly and perform tests accurately
• Communicate effectively with client staff members
Cell Therapy Process Development Scientist (Autologous)
Principal research scientist job in Spring House, PA
Our large pharmaceutical clients is seeking a Scientist to join their growing Process Development team within the Cell Therapy Development organization in Spring House, PA. This person will be focused on CAR-T cell manufacturing and will spend about 80% of their time in the lab setting up and running automation instruments for T cell manufacturing (primarily Prodigy), doing manipulation with cells, sampling, and making sure equipment is running properly. They will primarily be focused on process development in CAR-T and its transition to manufacturing. In this role, the successful candidate will be involved in process design, unit operation development, and parameter optimization studies resulting in the development of new production processes. Other responsibilities include:
Design and execute process development studies using sound scientific and engineering principles to develop and improve unit operations used for production of autologous T-cell therapies,
Identify, critically assess and evaluate opportunities to improve manufacturing outcomes such as improving success rate, throughput, reducing cost, process time and product quality of the final drug product.
Lead/contribute to the design and execution of phase-appropriate process development study plans, identifying process parameters and appropriate ranges to be assessed for optimal experimental design of the study.
Investigate improvements to current processes used for T-cell selection, activation, transduction and expansion together with their impact on critical quality attributes.
Author reports detailing experimental work and summarizing results, protocols, technical reports and SOPs.
Support technology transfer activities, writing protocols, reports, and performing and coordinating activities to support successful manufacturing
Qualifications:
Minimum of a Bachelor's Degree in a related field of study
Minimum of 2 years of process development for autologous cell therapy or CAR-T manufacturing
Prior experience working with bioreactors (preferably Xuri)
Salary: $80,000-$100,000 (flexible based on experience)
Hours: Monday-Friday, 8:00am-5:00pm
Hiring Method: Multiyear contract - After 1 year on contract, the individual will have the opportunity to apply for a permanent role or have their contract renewed for another year
PTO: 10 PTO days, 6 paid sick days annually & paid Holidays
Benefits: Medical, Dental, Vision and 401K plans available
Exact compensation may vary based on several factors, including skills, experience, and education.
Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.
Scientist I
Principal research scientist job in Point, PA
Johnson Service Group (JSG) is currently looking for a Scientist. This is a contract hire opportunity with one of the world's premier research-intensive biopharmaceutical company and is located in West Point PA. Pay: $32/hour What You'll Bring To The Table
A Bachelor's degree in Biology, Bio/chemistry, Bio/chemical Engineering, or a related science or engineering field
At least 1 year of laboratory experience in Molecular Biology, Protein Biochemistry, or upstream process development
Proficiency in aseptic techniques, pipetting, and microbial culturing at various scales
Hands-on experience with protein analytical methods such as SDS-PAGE, Western Blot, and ELISA
Basic understanding of fermentation processes
Strong computer skills, including Excel formulas and data management, with the ability to quickly learn new software
Excellent communication skills, both written and verbal, with keen attention to detail
Ability to work independently and collaboratively in a fast-paced, results-oriented environment
Self-motivated, adaptable, with a positive attitude and a commitment to quality
Additional Skills That Will Make You Stand Out:
Experience working with Biosafety Level-1 organisms
Familiarity with laboratory reagent preparation and process setup
Knowledge of Good Laboratory Practices (GLP)
Preferred Education and Experience:
Bachelor's degree in a scientific discipline
Minimum of one year laboratory experience in relevant scientific techniques and processes
Other Requirements:
Willingness to work occasionally outside regular hours, including some evenings and weekends (10-20%)
Ability to work safely with Biosafety Level-1 organisms
Strong organizational skills to maintain accurate records and documentation
Johnson Service Group, Inc. (JSG) is a North American leader in the staffing and consulting services industry, with over 35 years of experience investing in people and companies.
Johnson Service Group (JSG) is an Equal Opportunity Employer. JSG provides equal employment opportunities to all applicants and employees without regard to race, color, religion, sex, age, sexual orientation, gender identity, national origin, disability, marital status, protected veteran status, or any other characteristic protected by law.
#D400
Staff/Senior Staff Scientist
Principal research scientist job in Delaware, PA
Join our innovative preclinical research team and play a pivotal role in advancing Client therapies for inflammatory and dermatological diseases. As a Staff or Senior Staff Scientist, you will directly influence early-stage drug discovery programs, generating insights that shape treatments and improve patients lives. This position offers an exciting opportunity to combine scientific rigor with creativity in a collaborative, fast-paced environment.
Key Responsibilities
Design and execute biologically relevant assays to elucidate disease mechanisms and accelerate therapeutic discovery.
Analyze and interpret complex datasets to guide strategic decisions in discovery programs.
Perform advanced cellular and molecular biology assays using cutting-edge technologies.
Maintain accurate, detailed records of experimental procedures and results to ensure reproducibility and compliance.
Communicate findings effectively to cross-functional teams and leadership, influencing program direction.
Collaborate within a high-performing team while developing as an independent scientific contributor.
Qualifications
Education
Doctorate (Ph.D.) in Immunology, Biochemistry, Molecular Biology, Cell Biology, or related discipline.
Required Skills
Strong background in immunology or related biological sciences.
Proficiency in molecular and cellular techniques, including RT-PCR, Western blotting, ELISA, and sterile cell culture.
Proficiency in multi-color flow cytometry.
Excellent organizational skills with the ability to manage multiple priorities.
Outstanding written and verbal communication skills.
Demonstrated ability to work independently and collaboratively in a team environment.
Commitment to scientific rigor and delivering impactful research.
Preferred Qualifications
1-2 years experience in pharma industry or post-doctoral experience.
Experience with in-vivo disease models (rodents).
Familiarity with human immunology (innate and adaptive) and/or prior industry experience.
Hands-on experience with multiplex protein or RNA-based technologies.
Enthusiasm for fostering a culture of scientific curiosity and open collaboration.
Success Indicators
Delivery of high-quality, reproducible data within agreed timelines.
Effective contribution to in vivo studies and mechanistic research.
Clear, impactful communication of scientific findings to influence program milestones.
Kaztronix is an equal opportunity employer and does not discriminate on the basis of race, color, national origin, sex, age, religion, disability, veteran status or any other consideration made unlawful by federal, state or local laws. In addition, all human resource actions in such areas as compensation, employee benefits, transfers, layoffs, training and development are to be administered objectively, without regard to race, color, religion, age, sex, national origin, disability, veteran status or any other consideration made unlawful by federal, state or local laws.
By applying to the position, you acknowledge that your information will be used by Kaztronix in processing your application.
Senior Food Scientist
Principal research scientist job in Elma, NY
About the job
The position of Senior Food Scientist - Technical Solution is responsible for supporting technical aspects related to supporting customers in successful launch of their product through our facility. This includes, leading projects, creating new product formulas, managing pilot plant activities, working out technical challenges and providing formulation/technical support. The position requires a proactive, self-starter who is able to work independently with good decision-making skills while coordinating all information required to create and maintain the existing Steuben programs. This job also requires a team player with high standards of excellence and attention to detail.
Education/Prerequisites Requirements:
M.S. in Food Science or Food Related Discipline
Minimum 3-5 years of experience in ingredients research at a food or beverage company
Strong knowledge & experience with food chemistry, rheology and processing
Dairy formulation experience
Plant based product formulation experience
Knowledge of flavor and ingredient functionality and usage
Understanding of complex food matrices
Strong understanding of UHT processing
Excellent Planning & Organizing Skills
Ability to adapt to situations and responsibilities within an ever-growing business
Familiarity with Excel, Word, PowerPoint, Gantt Chart and PLM Stage Gate processes
Good Understanding of Food Safety
Analytical, detailed oriented individual
Ability to work with minimum supervision
Equipment/Training Knowledge:
Expertise in designing food/beverage formulations
Experience running Pilot Plant scale equipment
Member of the IFT
Any Industry certifications
Strong computer program(s) knowledge
Working knowledge for standard lab equipment
Experience working within Food Formulation & Labeling Software
Work Specifications - Responsibilities:
Primarily responsible for working with R&D and Quality in evaluating root cause for product stability in terms of product formulation and processing.
Responsible for technical support to Steuben Foods co-manufacturing partners
Key stake holder to successfully manage his/her projects to completion
Provide formulation support to 3rd party customers as needed
Attend plant trials as needed
Keep detailed accurate records
Operate pilot plant equipment if/when needed
Create reports for R&D/Ownership as needed
Attend R&D and other key meetings as a technical support role
Stay up to date on Regulatory Affairs and changes in the Food and Beverage labeling sectors
Work closely with Quality Compliance to help support SQF and FSMA initiatives
Work closely with Quality Control to help support internal Quality Programs and help create new Quality Programs
Work closely with Production to understand the equipment (processing, filling and blending) to help facilitate scale up of new and existing products
Help Facilitate improvements to resource infrastructure
Work in Excel, Word, PowerPoint and PLM Stage Gate programs
Work Closely with Purchasing/Procurement to ensure supply of new formulation ingredients
Schedule:
Monday - Friday
Extended schedule on major projects, as necessary
Availability by phone
Some travel required to attend trade shows and to support Business Development as needed
Salary Range: $120,000 - $150,000
Steuben Foods is committed to equal employment opportunity. We recruit, employ, train, compensate, and promote without regard to race, religion, color, national origin, age, sex, disability, protected veteran status, or any other basis protected by applicable federal, state, or local law.
Associate Scientist MSAT Advanced Therapies Validations
Principal research scientist job in Raritan, NJ
The Associate Scientist MSAT Advanced Therapies Validation is responsible for validating supporting processes, implementing improvements within commercial manufacturing, and managing the lifecycle of these processes. The Associate Scientist acts as a Subject Matter Expert for validation studies, particularly in optimizing commercial manufacturing of lentiviral vectors, and liaises with various stakeholder departments.
Responsibilities:
Contribute to Life Cycle Management (LCM) and New Technology Introduction for the site.
Execute validation of supporting processes (e.g.,mixing, sterilization, thermal processing, bio-decontamination).
Support the introduction of new technologies and digitalization projects through validation protocol execution.
Support the introduction of new materials via execution of validation protocols.
Validate process parameters (e.g., process hold times).
Contribute to Life Cycle Management projects.
Act as Subject Matter Expert for one or more validation categories. Leverage the global MSAT network to identify and implement best practices.
Author and review well-documented protocols and reports for all processes to be qualified/validated, in accordance with corporate/site guidelines, procedures, regulatory requirements, and industry best practices.
Coordinate and support the execution of validation studies that conform to site standards and client guidelines, while meeting quality requirements.
Support the site change control program by performing validation impact assessments and delivering the resulting implementation plan.
Investigate deviations associated with process validation activities and oversee pre-validation and validation activities resulting from technical changes.
Propose and formalize enhancements to qualification and validation processes and procedures to support process validation throughout the lifecycle and ensure program sustainability.
Assist with writing Quality Risk Assessments for existing and new or changed processes.
Ensure integration of global standards into local production processes.
Support complex investigations and risk assessments.
Act as SME during internal and external audits and inspections.
Experience:
Minimum of 2 years of relevant Manufacturing, Science, & Technology experience in the pharmaceutical industry.
Experience with cell therapy manufacturing or viral vector manufacturing.
GMP manufacturing and/or validation experience in pharmaceuticals.
Skills in communication, planning, documentation, risk management, root cause problem-solving, and knowledge management.
Understanding of regulatory requirements and industry guidelines for validation (e.g., FDA, EMA, ICH, ASTM, ISO, ISPE, PDA, etc.).
Affinity with process technology and digitalization in manufacturing.
Capable of successful delivery of local small projects, regional project work streams, or departmental programs under supervision. Selects applicable engineering/scientific tactics.
Works independently within scope, requiring general guidance.
Skills:
Stem Cell Therapy
Good Manufacturing Practices (GMP)
Drug Manufacturing
Education:
BSc in Biochemistry, Biotechnology, Chemical Engineering, or a related field.
Advanced degree (MSc/PhD) in Biochemistry, Biotechnology, Chemical Engineering.
About US Tech Solutions:
US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit ************************
US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Recruiter Details:
Name: Azhar
Email: ****************************
Internal Id: 25-53773
Associate Scientist - Biologics Discovery
Principal research scientist job in Spring House, PA
Our large pharmaceutical clients is seeking an Associate Scientist to join their growing Biophysics & Molecular Attributes Group in Spring House, PA. The Biophysics & Molecular Attributes Group within Biologics Discovery uses innovative biophysical, biochemical, and mass spectrometry based analytical tools to help select best therapeutic candidates for clinical development. You will be a critical member of the Higher Order Structure (HOS) team that characterizes developability attributes like thermal stability, chemical stability, solubility, and aggregation on a broad range of biologics platforms including monoclonal antibodies, multi-specific antibodies, antibody drug conjugates, antibody radio conjugates, and other therapeutic proteins. You will design and perform experiments using a variety of technologies like HPLC, DSF, DSC, cIEF, GXII, DLS, and more.
Key Responsibilities:
Execute automated methods for biophysical and structural characterization of antibody therapeutics. Integrate robotic liquid handling systems (e.g., Hamilton, Tecan) with analytical platforms to improve efficiency, consistency, and sample throughput.
Execute analytical analysis of biologics candidates using a wide variety of technologies such as size-exclusion HPLC, plate-based HIC/Heparin binding, DSF.
Evaluate results to deliver scientifically supported conclusions and recommendations that are documented in appropriate technical reports.
Maintain lab and equipment.
Collaborate with colleagues in the global organization to support discovery projects.
Assist in developing recommendations for improving standard procedures.
Qualifications:
Master's or Bachelor's Degree in a related field of study
Minimum of 1 year of protein/antibody analytical methods experience
Experience using HPLC, DSF or DLS
Salary: $70,000-$75,000 (flexible based on experience)
Hours: Monday-Friday, 8:00am-5:00pm
Hiring Method: Multiyear contract - After 1 year on contract, the individual will have the opportunity to apply for a permanent role or have their contract renewed for another year
PTO: 10 PTO days, 6 paid sick days annually & paid Holidays
Benefits: Medical, Dental, Vision and 401K plans available
Exact compensation may vary based on several factors, including skills, experience, and education.
Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.