Scientist - I (Assistant)
Talent Software Services, Inc.
**
Rahway, New Jersey
Basic
Posted about 10 hours ago
Qualifications
Minimum Education Requirements
B.S. or M.S. degree, or equivalent, in Pharmaceutical Sciences, Chemical Engineering, Biochemistry, Chemistry, or a related field is required.
Experience:
Bachelor s with 2 3 years or master s with 1 2 years of experience.
Required Skills and Experience
Excellent hands-on laboratory skills in pharmaceutical formulation, sterile product development, process development, or a related field.
Strong written and verbal communication skills.
Self-driven, independent, meticulous in execution, organized, attentive to timelines, and motivated to learn.
Ability to work effectively as part of a team and interface with cross-functional scientific professionals.
Desired Skills and Experience
Experience with biologics and sterile formulation.
Pharmaceutical industry experience in formulation and/or process development.
Understanding of formulation and aseptic processes in a non-GMP/GLP environment.
Experience with process development and benchtop unit operations, including mixing, pumping, filtration, and lyophilization.
Familiarity with additional biophysical or biochemical analytical methods such as DLS, DSC, DSF, SDS-PAGE, or UV/Vis.
Ability to manage multiple priorities in a fast-paced environment and adapt to changing project needs.
Statistical software such as JMP
Previous pharmaceutical, biologics, or *** experience
Position Details: This is a one-year, on-site role in Rahway, New Jersey.
Responsibilities
The Formulation Scientist will provide hands-on support to the *** Sterile Formulation Sciences team at the Rahway site. The primary focus of the position will be project work supporting sterile pharmaceutical product development, with emphasis on formulation composition, process development, and laboratory execution. The selected candidate will contribute to the design, preparation, testing, analysis, and documentation of formulation compositions and process definitions while collaborating with cross-functional scientific and operational partners.
Primary Responsibilities
Design and execute hypothesis-driven formulation and process-development experiments for sterile pharmaceutical products.
Prepare common formulation buffers, reagents, and execute development batches/fill finish in appropriate containers using appropriate aseptic techniques and Good Laboratory Practices, as applicable.
Support processing activities for solution or lyophilized formulations, or other dosage-form preparation techniques as required.
Conduct formulation characterization and selected analytical studies, including pH, osmolality, viscosity, particle-size measurements, dynamic light scattering, and HPLC.
Support stability and stress studies; analyze data, summarize findings, and document conclusions in laboratory notebooks, protocols, and technical reports.
Draft, review, and execute protocols supporting laboratory batches and process-development activities.
Maintain clear, accurate, and contemporaneous laboratory records.
Support laboratory readiness through equipment care, material preparation, and maintenance of a clean and organized working environment.
Collaborate with cross-functional partners, including analytical operations, manufacturing, and other scientific teams, to meet project timelines and deliverables.
Continuously learn and apply relevant literature, methods, and technologies to improve formulation compositions and processes.
Perform all work safely and in compliance with applicable site procedures and safety policies.
Minimum Education Requirements
B.S. or M.S. degree, or equivalent, in Pharmaceutical Sciences, Chemical Engineering, Biochemistry, Chemistry, or a related field is required.
Experience:
Bachelor s with 2 3 years or master s with 1 2 years of experience.
Required Skills and Experience
Excellent hands-on laboratory skills in pharmaceutical formulation, sterile product development, process development, or a related field.
Strong written and verbal communication skills.
Self-driven, independent, meticulous in execution, organized, attentive to timelines, and motivated to learn.
Ability to work effectively as part of a team and interface with cross-functional scientific professionals.
Desired Skills and Experience
Experience with biologics and sterile formulation.
Pharmaceutical industry experience in formulation and/or process development.
Understanding of formulation and aseptic processes in a non-GMP/GLP environment.
Experience with process development and benchtop unit operations, including mixing, pumping, filtration, and lyophilization.
Familiarity with additional biophysical or biochemical analytical methods such as DLS, DSC, DSF, SDS-PAGE, or UV/Vis.
Ability to manage multiple priorities in a fast-paced environment and adapt to changing project needs.
Statistical software such as JMP
Previous pharmaceutical, biologics, or *** experience
Position Details: This is a one-year, on-site role in Rahway, New Jersey.
Responsibilities
The Formulation Scientist will provide hands-on support to the *** Sterile Formulation Sciences team at the Rahway site. The primary focus of the position will be project work supporting sterile pharmaceutical product development, with emphasis on formulation composition, process development, and laboratory execution. The selected candidate will contribute to the design, preparation, testing, analysis, and documentation of formulation compositions and process definitions while collaborating with cross-functional scientific and operational partners.
Primary Responsibilities
Design and execute hypothesis-driven formulation and process-development experiments for sterile pharmaceutical products.
Prepare common formulation buffers, reagents, and execute development batches/fill finish in appropriate containers using appropriate aseptic techniques and Good Laboratory Practices, as applicable.
Support processing activities for solution or lyophilized formulations, or other dosage-form preparation techniques as required.
Conduct formulation characterization and selected analytical studies, including pH, osmolality, viscosity, particle-size measurements, dynamic light scattering, and HPLC.
Support stability and stress studies; analyze data, summarize findings, and document conclusions in laboratory notebooks, protocols, and technical reports.
Draft, review, and execute protocols supporting laboratory batches and process-development activities.
Maintain clear, accurate, and contemporaneous laboratory records.
Support laboratory readiness through equipment care, material preparation, and maintenance of a clean and organized working environment.
Collaborate with cross-functional partners, including analytical operations, manufacturing, and other scientific teams, to meet project timelines and deliverables.
Continuously learn and apply relevant literature, methods, and technologies to improve formulation compositions and processes.
Perform all work safely and in compliance with applicable site procedures and safety policies.
Scientist - II (Associate)
Talent Software Services, Inc.
**
Rahway, New Jersey
Basic
Posted about 10 hours ago
Qualifications
Minimum Education Requirements
B.S. or M.S. degree, or PHD in Pharmaceutical Sciences, Chemical Engineering, Biochemistry, Chemistry, or a related field is required.
Experience:
Bachelor s with 5+ years, Master s with 3+ years, or PhD with 0 1 year of exeprience.
Required Skills and Experience
Excellent hands-on laboratory skills in pharmaceutical formulation, sterile product development, process development, or a related field.
Strong written and verbal communication skills.
Self-driven, independent, meticulous in execution, organized, attentive to timelines, and motivated to learn.
Ability to work effectively as part of a team and interface with cross-functional scientific professionals.
Desired Skills and Experience
Experience with biologics and sterile formulation.
Pharmaceutical industry experience in formulation and/or process development.
Understanding of formulation and aseptic processes in a non-GMP/GLP environment.
Experience with process development and benchtop unit operations, including mixing, pumping, filtration, and lyophilization.
Familiarity with additional biophysical or biochemical analytical methods such as DLS, DSC, DSF, SDS-PAGE, or UV/Vis.
Ability to manage multiple priorities in a fast-paced environment and adapt to changing project needs.
Statistical software such as JMP
Previous pharmaceutical, biologics, or *** experience
Position Details: This is a one-year, on-site role in Rahway, New Jersey.
Responsibilities
The Formulation Scientist will provide hands-on support to the *** Sterile Formulation Sciences team at the Rahway site. The primary focus of the position will be project work supporting sterile pharmaceutical product development, with emphasis on formulation composition, process development, and laboratory execution. The selected candidate will contribute to the design, preparation, testing, analysis, and documentation of formulation compositions and process definitions while collaborating with cross-functional scientific and operational partners.
Primary Responsibilities
Design and execute hypothesis-driven formulation and process-development experiments for sterile pharmaceutical products.
Prepare common formulation buffers, reagents, and execute development batches/fill finish in appropriate containers using appropriate aseptic techniques and Good Laboratory Practices, as applicable.
Support processing activities for solution or lyophilized formulations, or other dosage-form preparation techniques as required.
Conduct formulation characterization and selected analytical studies, including pH, osmolality, viscosity, particle-size measurements, dynamic light scattering, and HPLC.
Support stability and stress studies; analyze data, summarize findings, and document conclusions in laboratory notebooks, protocols, and technical reports.
Draft, review, and execute protocols supporting laboratory batches and process-development activities.
Maintain clear, accurate, and contemporaneous laboratory records.
Support laboratory readiness through equipment care, material preparation, and maintenance of a clean and organized working environment.
Collaborate with cross-functional partners, including analytical operations, manufacturing, and other scientific teams, to meet project timelines and deliverables.
Continuously learn and apply relevant literature, methods, and technologies to improve formulation compositions and processes.
Perform all work safely and in compliance with applicable site procedures and safety policies.
Minimum Education Requirements
B.S. or M.S. degree, or PHD in Pharmaceutical Sciences, Chemical Engineering, Biochemistry, Chemistry, or a related field is required.
Experience:
Bachelor s with 5+ years, Master s with 3+ years, or PhD with 0 1 year of exeprience.
Required Skills and Experience
Excellent hands-on laboratory skills in pharmaceutical formulation, sterile product development, process development, or a related field.
Strong written and verbal communication skills.
Self-driven, independent, meticulous in execution, organized, attentive to timelines, and motivated to learn.
Ability to work effectively as part of a team and interface with cross-functional scientific professionals.
Desired Skills and Experience
Experience with biologics and sterile formulation.
Pharmaceutical industry experience in formulation and/or process development.
Understanding of formulation and aseptic processes in a non-GMP/GLP environment.
Experience with process development and benchtop unit operations, including mixing, pumping, filtration, and lyophilization.
Familiarity with additional biophysical or biochemical analytical methods such as DLS, DSC, DSF, SDS-PAGE, or UV/Vis.
Ability to manage multiple priorities in a fast-paced environment and adapt to changing project needs.
Statistical software such as JMP
Previous pharmaceutical, biologics, or *** experience
Position Details: This is a one-year, on-site role in Rahway, New Jersey.
Responsibilities
The Formulation Scientist will provide hands-on support to the *** Sterile Formulation Sciences team at the Rahway site. The primary focus of the position will be project work supporting sterile pharmaceutical product development, with emphasis on formulation composition, process development, and laboratory execution. The selected candidate will contribute to the design, preparation, testing, analysis, and documentation of formulation compositions and process definitions while collaborating with cross-functional scientific and operational partners.
Primary Responsibilities
Design and execute hypothesis-driven formulation and process-development experiments for sterile pharmaceutical products.
Prepare common formulation buffers, reagents, and execute development batches/fill finish in appropriate containers using appropriate aseptic techniques and Good Laboratory Practices, as applicable.
Support processing activities for solution or lyophilized formulations, or other dosage-form preparation techniques as required.
Conduct formulation characterization and selected analytical studies, including pH, osmolality, viscosity, particle-size measurements, dynamic light scattering, and HPLC.
Support stability and stress studies; analyze data, summarize findings, and document conclusions in laboratory notebooks, protocols, and technical reports.
Draft, review, and execute protocols supporting laboratory batches and process-development activities.
Maintain clear, accurate, and contemporaneous laboratory records.
Support laboratory readiness through equipment care, material preparation, and maintenance of a clean and organized working environment.
Collaborate with cross-functional partners, including analytical operations, manufacturing, and other scientific teams, to meet project timelines and deliverables.
Continuously learn and apply relevant literature, methods, and technologies to improve formulation compositions and processes.
Perform all work safely and in compliance with applicable site procedures and safety policies.
Formulation Scientist
Genesis10
**
Rahway, New Jersey
Basic
Posted about 10 hours ago
Aptask Global Workforce (AGW) is seeking a Formulation Scientist for an Onsite position with a Pharmaceutical Company located in Rahway, NJ. This is a 12+ month contract opportunity.
This position will provide hands-on support to our client's Sterile Formulation Sciences team. The primary focus will be project work supporting sterile pharmaceutical product development, with an emphasis on formulation composition, process development, and laboratory execution. The selected candidate will contribute to the design, preparation, testing, analysis, and documentation of formulation compositions while collaborating with cross-functional partners.
Responsibilities:
- Design and execute hypothesis-driven formulation and process-development experiments for sterile pharmaceutical products
- Prepare common formulation buffers, reagents, and execute development batches/fill finish in appropriate containers using appropriate aseptic techniques and Good Laboratory Practices, as applicable
- Support processing activities for solution or lyophilized formulations, or other dosage-form preparation techniques as required
- Conduct formulation characterization and selected analytical studies, including pH, osmolality, viscosity, particle-size measurements, dynamic light scattering, and HPLC
- Support stability and stress studies; analyze data, summarize findings, and document conclusions in laboratory notebooks, protocols, and technical reports
- Draft, review, and execute protocols supporting laboratory batches and process-development activities
- Maintain clear, accurate, and contemporaneous laboratory records
- Support laboratory readiness through equipment care, material preparation, and maintenance of a clean and organized working environment
- Collaborate with cross-functional partners, including analytical operations, manufacturing, and other scientific teams, to meet project timelines and deliverables
- Continuously learn and apply relevant literature, methods, and technologies to improve formulation compositions and processes
- Perform all work safely and in compliance with applicable site procedures and safety policies
Requirements:
- B.S. or M.S. degree, or equivalent, in Pharmaceutical Sciences, Chemical Engineering, Biochemistry, Chemistry, or a related field
- Bachelor's with 2–3 years or Master's with 1–2 years of experience
- Excellent hands-on laboratory skills in pharmaceutical formulation, sterile product development, process development, or a related field
- Strong written and verbal communication skills
- Self-driven, independent, meticulous in execution, organized, attentive to timelines, and motivated to learn
- Ability to work effectively as part of a team and interface with cross-functional scientific professionals
Desired skills:
- Experience with biologics and sterile formulation
- Pharmaceutical industry experience in formulation and/or process development
- Understanding of formulation and aseptic processes in a non-GMP/GLP environment
- Experience with process development and benchtop unit operations, including mixing, pumping, filtration, and lyophilization
- Familiarity with additional biophysical or biochemical analytical methods such as DLS, DSC, DSF, SDS-PAGE, or UV/Vis
- Ability to manage multiple priorities in a fast-paced environment and adapt to changing project needs
- Statistical software such as JMP
Pay range: up to $32.14 per hour
Only candidates available and ready to work directly as Aptask Global Workforce (AGW) employees will be considered for this position.
If you have the described qualifications and are interested in this exciting opportunity, apply today!
Aptask Global Workforce (AGW)
ApTask Global Workforce (AGW) is a certified Minority and Veteran workforce solutions company. AGW delivers operational, clinical, lab and professional talent with a strong focus on healthcare and life sciences. The company supports clients with reliable staffing, program expertise and a commitment to quality, speed and consistent delivery.
Benefits of working with ApTask Global Workforce include:
- Medical
- Dental
- Vision
- Sick Pay (for applicable states/municipalities)
Our team stays close to the process and is here to guide you every step of the way. To learn more, please visit our website (url removed).
ApTask Global Workforce is an Equal Opportunity Employer. Candidates will receive consideration without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability or status as a protected veteran.
Formulation Scientist
Genesis10
**
Rahway, New Jersey
Basic
Posted about 10 hours ago
Aptask Global Workforce (AGW) is seeking a Formulation Scientist for an Onsite position with a Pharmaceutical Company located in Rahway, NJ. This is a 12+ month contract opportunity.
This position provides hands-on support to the Sterile Formulation Sciences team. The primary focus of the role is project work supporting sterile pharmaceutical product development, with an emphasis on formulation composition, process development, and laboratory execution. The selected candidate will contribute to the design, preparation, testing, analysis, and documentation of formulation compositions while collaborating with cross-functional scientific and operational partners.
Responsibilities:
- Design and execute hypothesis-driven formulation and process-development experiments for sterile pharmaceutical products
- Prepare common formulation buffers, reagents, and execute development batches/fill finish in appropriate containers using appropriate aseptic techniques and Good Laboratory Practices
- Support processing activities for solution or lyophilized formulations, or other dosage-form preparation techniques as required
- Conduct formulation characterization and selected analytical studies, including pH, osmolality, viscosity, particle-size measurements, dynamic light scattering, and HPLC
- Support stability and stress studies; analyze data, summarize findings, and document conclusions in laboratory notebooks, protocols, and technical reports
- Draft, review, and execute protocols supporting laboratory batches and process-development activities
- Maintain clear, accurate, and contemporaneous laboratory records
- Support laboratory readiness through equipment care, material preparation, and maintenance of a clean and organized working environment
- Collaborate with cross-functional partners, including analytical operations, manufacturing, and other scientific teams, to meet project timelines and deliverables
- Continuously learn and apply relevant literature, methods, and technologies to improve formulation compositions and processes
- Perform all work safely and in compliance with applicable site procedures and safety policies
Requirements:
- B.S. or M.S. degree, or PhD in Pharmaceutical Sciences, Chemical Engineering, Biochemistry, Chemistry, or a related field
- Bachelor's with 5+ years, Master's with 3+ years, or PhD with 0–1 year of experience
- Excellent hands-on laboratory skills in pharmaceutical formulation, sterile product development, process development, or a related field
- Strong written and verbal communication skills
- Self-driven, independent, meticulous in execution, organized, attentive to timelines, and motivated to learn
- Ability to work effectively as part of a team and interface with cross-functional scientific professionals
Desired skills:
- Experience with biologics and sterile formulation
- Pharmaceutical industry experience in formulation and/or process development
- Understanding of formulation and aseptic processes in a non-GMP/GLP environment
- Experience with process development and benchtop unit operations, including mixing, pumping, filtration, and lyophilization
- Familiarity with additional biophysical or biochemical analytical methods such as DLS, DSC, DSF, SDS-PAGE, or UV/Vis
- Ability to manage multiple priorities in a fast-paced environment and adapt to changing project needs
- Statistical software such as JMP
- Previous experience in the pharmaceutical or biologics industry
Pay range: up to $53.45 per hour
Only candidates available and ready to work directly as Aptask Global Workforce (AGW) employees will be considered for this position.
If you have the described qualifications and are interested in this exciting opportunity, apply today!
Aptask Global Workforce (AGW)
ApTask Global Workforce (AGW) is a certified Minority and Veteran workforce solutions company. AGW delivers operational, clinical, lab and professional talent with a strong focus on healthcare and life sciences. The company supports clients with reliable staffing, program expertise and a commitment to quality, speed and consistent delivery.
Benefits of working with ApTask Global Workforce include:
- Medical
- Dental
- Vision
- Sick Pay (for applicable states/municipalities)
Our team stays close to the process and is here to guide you every step of the way. To learn more, please visit our website (url removed).
ApTask Global Workforce is an Equal Opportunity Employer. Candidates will receive consideration without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability or status as a protected veteran.
Process Development Scientist
Nesco Resource, LLC
**
Mapleton, Illinois
Basic
Posted about 10 hours ago
Will consider interns
Addtional medical screenings needed - must be able to lift 50 lbs
Must have hands on lab experience
RESPONSIBILITIES
Hands-On Synthesis / Product & Process Development
Oleochemical synthesis
100 mL to 4L reaction scale, working with pressurized equipment
Interpretation of analytical results (provided by QC laboratory)
Raw Material receiving to shipping Final Product
Process development and Plant support for the Care Solutions product lines at the Mapleton Plant
New Product Introduction (NPI) Work
Investigating and developing corrective actions for chemistry-based production problems
Qualification of new raw materials
Administrative Activities (project management, safety, training, meetings, etc.)
Bi-monthly reports and ongoing project summaries
Regular (monthly) company required training
Regular group meetings that require written updates and presentations
Leadership based Collaboration (Data interpretation, coaching, education)
Working with other team members to help interpret reaction/ analytical results
be a role model in safe working behavious
REQUIREMENTS -
Ph.D. (preferred) in chemistry or related field with at least two years of experience or MS/BS with at least five years of experience
Attention to safety and safe work practices in an industrial chemical laboratory including work with hazardous substances
Industrial synthesis and/or process optimization experience, especially related to fatty acid, hydrogenation and/or amine chemistry
Experience with high pressure equipment is preferred
Experience with wet chemistry analytics, IR and NMR is preferred
Good communication and presentation skills; ability to work within cross-regional and cross-cultural teams
Comprehensive technical and chemical knowledge, ability to analyze R&D and production data and trends to identify problems and provide technical guidance
Utilize Microsoft 365 for data analysis, documentation, reporting and presentation
Strong and proactive verbal communication skills
Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.
Nesco Resource 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.
Addtional medical screenings needed - must be able to lift 50 lbs
Must have hands on lab experience
RESPONSIBILITIES
Hands-On Synthesis / Product & Process Development
Oleochemical synthesis
100 mL to 4L reaction scale, working with pressurized equipment
Interpretation of analytical results (provided by QC laboratory)
Raw Material receiving to shipping Final Product
Process development and Plant support for the Care Solutions product lines at the Mapleton Plant
New Product Introduction (NPI) Work
Investigating and developing corrective actions for chemistry-based production problems
Qualification of new raw materials
Administrative Activities (project management, safety, training, meetings, etc.)
Bi-monthly reports and ongoing project summaries
Regular (monthly) company required training
Regular group meetings that require written updates and presentations
Leadership based Collaboration (Data interpretation, coaching, education)
Working with other team members to help interpret reaction/ analytical results
be a role model in safe working behavious
REQUIREMENTS -
Ph.D. (preferred) in chemistry or related field with at least two years of experience or MS/BS with at least five years of experience
Attention to safety and safe work practices in an industrial chemical laboratory including work with hazardous substances
Industrial synthesis and/or process optimization experience, especially related to fatty acid, hydrogenation and/or amine chemistry
Experience with high pressure equipment is preferred
Experience with wet chemistry analytics, IR and NMR is preferred
Good communication and presentation skills; ability to work within cross-regional and cross-cultural teams
Comprehensive technical and chemical knowledge, ability to analyze R&D and production data and trends to identify problems and provide technical guidance
Utilize Microsoft 365 for data analysis, documentation, reporting and presentation
Strong and proactive verbal communication skills
Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.
Nesco Resource 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.
Oral Formulation Scientist- # 26-23653
US Tech Solutions, Inc.
**
New Brunswick, New Jersey
Basic
Posted about 10 hours ago
Duration: 12 months ( contract extension possibility )
Description:
Work Schedule: Mon-Fri(normal business hours)
- The Scientist is responsible for supporting studies to establish oral solid formulations. This includes execution of laboratory and pilot plant work, design experimental formulation studies, and conduct material characterization and formulation testing.
Required Competencies :
Knowledge, Skills, and Abilities:
- Knowledge of formulation development.
- Knowledge of oral product processing - blending, tableting, encapsulation etc.
- Knowledge of data trending and tracking, including use of statistical analysis software a plus.
- Demonstrate advanced problem-solving ability / mentality, technical adeptness and logical thinking.
- Ability to communicate honestly, transparently, and effectively with peers, department management and cross functional peers.
- Requires a bachelor’s degree in science or engineering or related engineering discipline (advanced degree preferred).
- Minimum 1 year of relevant work experience
- An equivalent combination of education and experience may substitute.
- Previous experience working in oral formulation development and processing required.
- Experience in oral formulation preparation and testing techniques preferred.
- Conduct development activities related to developing oral formulations
- Conduct oral product batch processing, material characterization and formulation testing.
- Design and optimize formulation using design of experience approach.
- The incumbent will be working 10% to 20% of the time in an office environment.
- The incumbent will be working 80% to 90% of the time in a manufacturing and/or laboratory setting.
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 (url removed) .
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.
AI Statement: By applying, you acknowledge that AI-assisted tools may be used during hiring.
IND01
#LI-AS140
Scientist III # 26-23800
US Tech Solutions, Inc.
**
Rockford, Illinois
Basic
Posted about 10 hours ago
Duration: 18 Months
Job description:
Summary:
The Organic Chemist / Scientist will play a critical role in the Fatty Acid project by developing, optimizing, scaling, and documenting synthetic and purification processes for priority lipid and fatty-acid-related raw materials used to support cell-culture media production. The role will focus initially on fatty acids and lipids and fatty acids and lipids, with potential expansion to other priority materials. The scientist will apply strong multi-step organic synthesis, lipid chemistry, purification, and analytical characterization skills to establish robust processes that meet internal raw-material specifications and are suitable for scale-up and transfer to manufacturing.
Key Responsibilities:
Minimum Requirements / Qualifications:
Preferred Qualifications:
Success Measures:
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 (url removed) .
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.
AI Statement: By applying, you acknowledge that AI-assisted tools may be used during hiring.
IND01
#LI-AS140
Job description:
Summary:
The Organic Chemist / Scientist will play a critical role in the Fatty Acid project by developing, optimizing, scaling, and documenting synthetic and purification processes for priority lipid and fatty-acid-related raw materials used to support cell-culture media production. The role will focus initially on fatty acids and lipids and fatty acids and lipids, with potential expansion to other priority materials. The scientist will apply strong multi-step organic synthesis, lipid chemistry, purification, and analytical characterization skills to establish robust processes that meet internal raw-material specifications and are suitable for scale-up and transfer to manufacturing.
Key Responsibilities:
- Design, plan, and independently execute laboratory experiments for synthesis and process development of fatty acids, glycerides, phospholipids, and related lipid molecules.
- Develop and optimize synthetic routes for priority materials, including fatty acids and lipids, with emphasis on yield, purity, reproducibility, scalability, and raw-material availability.
- Develop and optimize purification strategies for intermediates and final products using normal-phase and reverse-phase chromatography, preparative HPLC/flash chromatography, crystallization, extraction, precipitation, and other appropriate techniques.
- Characterize starting materials, intermediates, impurities, and final products using HPLC, LC-MS/MS or MS, NMR, FT-IR, UV/VIS, ELSD/CAD, and other applicable analytical techniques.
- Investigate impurity profiles and troubleshoot synthesis, purification, stability, and recovery issues that could prevent materials from meeting internal specifications.
- Perform feasibility studies using lower-purity or alternate-source starting materials and define process conditions required to achieve target product quality.
- Support scale-up from laboratory development to gram/hundreds-of-gram scale and develop processes suitable for transfer to Rockford manufacturing operations.
- Partner with Analytical Development to establish or refine purity and identity methods and ensure analytical methods are fit for process-development decisions.
- Support preparation of material for internal evaluation, packaging/formulation activities, process validation, and manufacturing transfer as required by the project.
- Write experimental protocols, development reports, batch/process instructions, technical summaries, and documentation supporting testing, validation, and production.
- Maintain complete and accurate laboratory records and ensure traceability of experimental conditions, calculations, raw data, observations, deviations, and conclusions.
- Work cross-functionally with R&D, Analytical, Operations, Quality, Procurement/Sourcing, and project-management teams; communicate technical results, risks, recommendations, and project status to stakeholders.
- Adhere to departmental quality systems, chemical hygiene, EHS requirements, and safe laboratory practices.
Minimum Requirements / Qualifications:
- M.S. or Ph.D. in Organic Chemistry, Medicinal Chemistry, Chemical Sciences, or a closely related scientific discipline; Bachelor's degree with substantial directly relevant industrial synthetic chemistry experience may also be considered.
- Strong hands-on experience in organic synthesis, reaction optimization, and multi-step synthesis.
- Demonstrated experience with purification of complex organic molecules using chromatography and other preparative purification techniques.
- Hands-on experience interpreting HPLC, LC-MS/MS or MS, NMR, and FT-IR data for reaction monitoring, identity confirmation, purity assessment, and impurity troubleshooting.
- Ability to independently troubleshoot reactions and purification processes and design efficient experiments to resolve technical problems.
- Experience documenting experimental work in a manner suitable for process development, technology transfer, and regulated or quality-controlled environments.
- Ability to work independently while contributing effectively in a cross-functional project team.
- Excellent written, verbal, data-presentation, and technical communication skills.
Preferred Qualifications:
- Industrial experience with lipid chemistry, fatty-acid chemistry, glycerides, phospholipids, surfactants, or detergent-like molecules.
- Experience with synthesis or purification of phosphatidylcholines, diacylglycerols, or structurally related lipid molecules.
- Hands-on experience with Biotage Isolera/Selekt or comparable flash/preparative chromatography systems.
- Experience with CAD or ELSD detection for lipid/non-chromophoric compound analysis.
- Experience scaling synthetic chemistry processes from small-scale feasibility experiments to gram or hundreds-of-gram quantities.
- Experience in reagent/raw-material product development, process validation, change control, or transfer of R&D processes to manufacturing.
- Working knowledge of raw-material specifications, supplier qualification, and technical evaluation of alternate-source materials.
Success Measures:
- Development milestones completed according to the project plan.
- Target materials consistently meet required identity and purity specifications.
- Processes demonstrate acceptable yield, reproducibility, scalability, and operational practicality.
- Technical risks and deviations are identified early, investigated scientifically, and communicated with clear mitigation plans.
- Complete development documentation supports successful transfer to Operations and subsequent qualification/validation activities.
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 (url removed) .
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.
AI Statement: By applying, you acknowledge that AI-assisted tools may be used during hiring.
IND01
#LI-AS140
In Vivo Scientist
Eurofins USA PSS Insourcing Solutions
**
West Point, Pennsylvania
Basic
Posted 1 day ago
Job Description
Role Overview
We are seeking a highly motivated In Vivo Scientist to contribute to discovery research. This position will focus on HIV research, including virus production, characterization, and support of HIV discovery efforts.
Key Responsibilities
- Lead the design, execution, optimization, and characterization of HIV production workflows. As well as inventory management.
- Conduct HIV discovery research using primary human cells (PBMCs, CD4+ T cells) and immortalized cell lines (THP-1, Jurkat, MT-4).
- Perform and analyze experiments utilizing multi-parameter flow cytometry (2 colors or more), RT-qPCR, PCR, ELISA, and MSD multiplex assays.
- Generate and characterize stable cell lines expressing proteins of interest.
- Support in vivo studies, including tissue collection and processing, and perform ex vivo viral RNA isolation from tissues and/or blood samples.
- Analyze and interpret experimental data, communicate findings, and contribute to project strategy and execution.
Scientist II
The Fountain Group LLC
**
North Chicago, Illinois
Basic
Posted 1 day ago
Bill: $78.27
Pay: $55-52
Spread:(phone number removed)
Duration:6 months
Length of Assignment – 6 months
On-Site Position
First Shift, Mon-Fri, 8am – 5pm (possibility of earlier than 8am depending on job tasks)
What are the top 3-5 skills, experience or education required for this position:
1. Quantitative mass spectrometry experience
2. Attention to detail
3. Demonstrated proficiency using different extraction conditions
4. Team oriented
5. Experience with automated liquid handlers is a plus
Purpose:
Investigate, identify, develop, and optimize new methods and techniques to generate reliable and reproducible data in a timely manner. Read and adapt scientific literature to accomplish assignments and demonstrate broad and versatile technical expertise within discipline.
Responsibilities:
• Independently design and conduct critical experiments that further project goals.
• Implement and may innovate new experimental protocols/techniques.
• Understand the goal and maintain a high proficiency in his/her projects as well as the overall program.
• Interpret results and draw conclusions from own multistage experiments, note significant deviations, then suggest, design, and pursue relevant experiments.
• Understand relevant scientific literature and apply theoretical framework to solving problems within scientific discipline in a timely manner.
• Perform routine and complex tasks competently and independently and generate reliable and consistent results.
• Impact projects mostly through lab and/or pilot plant-based activities.
• Responsible for compliance with all applicable Corporate and Divisional policies and procedures.
• Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable.
Qualifications:
• Bachelor's Degree or equivalent education, or Master's Degree or equivalent education with years of experience.
• Theoretical and practical knowledge to carry out the job functions.
Experience Level:
3-5 Years.
Bussiness Unit:
R&D-Development Science (RDDS)
Cost Allocation:
6003|CC|RDI QTAS LC ((phone number removed))
Pay: $55-52
Spread:(phone number removed)
Duration:6 months
Length of Assignment – 6 months
On-Site Position
First Shift, Mon-Fri, 8am – 5pm (possibility of earlier than 8am depending on job tasks)
What are the top 3-5 skills, experience or education required for this position:
1. Quantitative mass spectrometry experience
2. Attention to detail
3. Demonstrated proficiency using different extraction conditions
4. Team oriented
5. Experience with automated liquid handlers is a plus
Purpose:
Investigate, identify, develop, and optimize new methods and techniques to generate reliable and reproducible data in a timely manner. Read and adapt scientific literature to accomplish assignments and demonstrate broad and versatile technical expertise within discipline.
Responsibilities:
• Independently design and conduct critical experiments that further project goals.
• Implement and may innovate new experimental protocols/techniques.
• Understand the goal and maintain a high proficiency in his/her projects as well as the overall program.
• Interpret results and draw conclusions from own multistage experiments, note significant deviations, then suggest, design, and pursue relevant experiments.
• Understand relevant scientific literature and apply theoretical framework to solving problems within scientific discipline in a timely manner.
• Perform routine and complex tasks competently and independently and generate reliable and consistent results.
• Impact projects mostly through lab and/or pilot plant-based activities.
• Responsible for compliance with all applicable Corporate and Divisional policies and procedures.
• Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable.
Qualifications:
• Bachelor's Degree or equivalent education, or Master's Degree or equivalent education with years of experience.
• Theoretical and practical knowledge to carry out the job functions.
Experience Level:
3-5 Years.
Bussiness Unit:
R&D-Development Science (RDDS)
Cost Allocation:
6003|CC|RDI QTAS LC ((phone number removed))
Analytical Research and Development Scientist
On-Board Companies
**
Somerset, New Jersey
Basic
Posted 3 days ago
On-Board Services is hiring an Analytical Research and Development Scientist in Somerset, NJ
For immediate consideration please send your resume to (url removed)Subject Line: Position Title and State you are located
About Us:
On-Board Services, Incorporated is an on-site contract service provider for a local manufacturing entity providing full time positions to our employees. We offer benefits as well as 401k.
Position Details:
Title: Analytical Research and Development Scientist
Position Type: contract with additional opportunity contingent upon performance and continued business need
Job Location: Somerset, NJ
Shift: 1st
Benefits: 401K, Dental insurance, Life Insurance, Medical Insurance, Vision Insurance, PTO
Compensation: $35-$40/HR Role Summary The Analytical Research and Development Chemist will work with an assigned project team in the laboratory to analyze and develop HPLC and GC methods for assay, impurity, dissolution, residual solvents testing, and particle size distribution of active pharmaceutical ingredients, excipients, and finished dosage forms. Essential Duties and Responsibilities
- Perform method development, method validation, and stability testing, including report writing, for various dosage forms including tablets, hard gelatin capsules, oral/topical liquids, oral suspensions, powder for oral suspensions, and nasal products with minimal supervision
- Support the Product Development team in developing new products
- Identify and characterize unknown impurities in drug products and drug substances
- Independently perform analytical testing and troubleshooting to achieve desired results
- Conduct elemental impurity testing using ICP-MS and ICP-OES
- Troubleshoot analytical issues and recommend solutions
- Maintain accurate laboratory documentation and reports
- Perform additional duties as assigned
- Bachelor’s degree in Chemistry, Biology, or a related scientific field required; Master’s degree preferred
- 3–10 years of experience working as an R&D Chemist within the pharmaceutical industry
- Hands-on experience with HPLC, GC, dissolution testing, particle size distribution, and related analytical techniques
- Experience with pharmaceutical method development, method validation, and stability testing
- Ability to write technical reports suitable for regulatory submissions with minimal supervision
- Strong organizational skills and attention to detail
- Ability to work independently and collaboratively in a fast-paced laboratory environment
- Ability to occasionally lift up to 20 pounds
- Work is primarily performed in a laboratory environment involving chemicals, reagents, and solvents
Apply Today!
On-Board was founded in 1976 by Robert L. Wilson to provide Engineering and Design services to the chemical manufacturing industry. Today, On-Board is a thriving privately held family of companies with services including: Consulting, Professional Engineering, Industrial Maintenance and Facility Management, Contracted Manufacturing and Production Services, as well as Temporary Staffing and Recruiting throughout North America.
The On-Board Family of Companies conducts operations through its Corporate Headquarters located in East Windsor, NJ along with Regional Offices in New Castle, DE and Wake Forest, NC. On-Board’s Mission is to provide “Flexible Service by applying the talents of our people, work processes and technology to meet our clients’ expectations in a Safe, Responsible and Dependable manner.”
On-Board Companies provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, religion, sex, national origin, age, disability or genetics.
JD# (phone number removed)
INDOJ