Scientist Jobs in West Deptford, NJ

Franklin Biolabs emerges from the esteemed legacy of Dr. Jim Wilson's laboratory, a beacon of innovation in vector technology for over three decades. Building on this rich heritage, Franklin Biolabs is poised to redefine the landscape of the global genetic medicines industry. As a Contract Research Organization (CRO), Franklin Biolabs offers a comprehensive suite of services spanning from discovery through clinical manufacturing. Our goal is to empower our partners by providing unparalleled solutions that drive the advancement of genetic medicines. Leveraging decades of expertise and a commitment to excellence, we bridge the gap between groundbreaking research and ensuring that transformative therapies reach those who need them most. Job Summary As an Upstream GMP Scientist I you will have a strong background in cell culture and bioreactor operations at pilot and GMP scale, preferably in rAAV production. You will receive processes transferred into GMP, and author batch records, SOPs as well as deviation investigations. You will execute GMP processes in appropriate grade clean rooms trained in gowning and all relevant GMP processes and procedures. Personnel in this position will mentor and train associates as well. Unlike traditional manufacturing personnel, our model aims to train GMP personnel to be process science experts as well and there will be times when they will work closely with PD/MS&T to perform development work as well. The Upstream GMP Scientist I will have mastered the skills and responsibilities of a GMP Associate Scientist and will be mastering the skills and responsibilities of a GMP Scientist. Qualifications B.S. in Biology, Biochemistry, Engineering or related field preferred but not required with 3-5 years' experience. Understanding of relevant science and proficiency in laboratory/GMP space techniques. Strong attention to detail and ability to document activities and follow protocols. Preparation of buffers and solutions. Comfort with routine calculations, tracking and interpreting data. Proficient with Microsoft Office, lab and equipment software. Familiarity with statistical analysis software preferred. Ability to follow GMP and execute in GMP environment when needed. Mastered GMP execution of all relevant areas. Understands regulations applicable to area and how to conduct deviation investigations. Understanding of GMP materials controls, facilities, and equipment. Strong problem-solving skills, planning and mitigation of risks. Strong understanding of data measurements and variability. Ability to troubleshoot and involve/communicate with management and QA as required. Involved in technology transfer. Strong communication, ability to present and write technical instructions and deviation reports. Ability to train and assist Associate level scientists. Analyze data and interpret results to identify trends and work with development scientists to make improvements. Assist in preparing documents for regulatory submissions. Strong understanding of cell culture and bioreactor operations. Strong understanding of in-process monitoring equipment, probes and assays. Understanding of analytics testing results, including AAV quality and purity. Proficiency in AAV production, and an understanding of stability and impact of process variable on AAV yield and quality. Application note Franklin Biolabs is not accepting unsolicited resumes from search or staffing firms. All resumes submitted by search or staffing firms to any employee at Franklin Biolabs via email, the Internet, or directly without a valid written search agreement for this role will be deemed the sole property of Franklin Biolabs and no fee will be paid in the event the candidate is hired

Our large pharmaceutical client is seeking a Scientist to join the Immunomics team within the R&D Immunology Translational Science organization in Spring House, PA. The Immunology Therapeutic Area is focused on developing new cutting-edge therapies to treat dermatology, GI, and rheumatic diseases. This team is responsible for generating Next Generation Sequencing (NGS) data and passing it to the computational group for analysis. The role of this lab-based Scientist will primarily be focused on Next Generation Sequencing (NGS) including QC of RNA. Main responsibilities include: * Extracting RNA from tissue, cells, blood * RNAseq library preparation using Roche Kapa kits and sc RNAseq library preparation using 10X Genomics kits * QC of RNA/DNA samples using qPCR, Agilent TS and updating team with progress of library generation/QC * Lab sample/freezer management The ideal candidate will have strong molecular biology skills and hands-on experience in the lab doing RNA QC work. They will also need to demonstrate strong attention to detail and organization as they will be responsible for hundreds of samples at any given time. REQUIRED SKILLS AND EXPERIENCE -Bachelor's or Master's Degree in Biology or related field -3+ years of experience in the lab with Next Generation Sequencing (NGS) -RNA sequencing experience -Pipetting skills NICE TO HAVE SKILLS AND EXPERIENCE -Single cell experience -Tecan automation experience -Experience working with tissues -Olink experience -Immunology experience -Experience working with frozen PPMC -Flow cytometry Compensation: $40-48/hr 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.

Bioanalytical Associate- Wilmington, Delaware This role will focus on supporting in-vitro ADME (Absorption, Distribution, Metabolism, and Excretion) studies and plasma sample analysis in preclinical drug development. The successful candidate will play a pivotal role in the analysis and interpretation of bioanalytical data to support early-stage drug discovery. Key Responsibilities: Support ADME Studies: Conduct routine ADME assays, such as protein binding and metabolic stability, to generate key data supporting drug development decisions. Plasma Sample Analysis: Prepare and analyze plasma samples for pharmacokinetic studies, including the measurement of drug concentration, metabolite profiling, and related biomarkers. Data Interpretation & Reporting: Analyze data sets, provide scientific interpretation, and communicate results to cross-functional teams in a clear and concise manner. Record-Keeping: Maintain concise and accurate records of all study activities in accordance with industry guidelines and company policies. Troubleshooting and Continuous Improvement: Troubleshoot assay issues, propose corrective actions, and implement process improvements to enhance the efficiency and reliability of bioanalytical data. Qualifications: Bachelor's degree in Analytical Chemistry, Biochemistry, or a related field. 1+ years of hands-on lab experience in bioanalysis, with a focus on ADME/PK studies and plasma sample analysis. Technical Expertise: Hands-on lab experience with ADME screening assays, such as protein binding and microsomal stability. Experience with plasma sample bioanalysis in support of non-clinical pharmacokinetic studies. Experience with LC-MS/MS, HPLC, UPLC, and related analytical techniques for the quantification and characterization of drug candidates in biological samples is a plus. Strong analytical and troubleshooting skills with the ability to interpret complex datasets. Preferred Qualifications: Familiarity with drug discovery and development, especially within preclinical research. Experience with quantitative LC-MS/MS bioanalytical techniques and ABSciex mass spectrometers. Knowledge of relevant bioanalytical software (e.g., Analyst, Prism) is a plus.

Key responsibilities: Employee will be expected to participate in all aspects of department visual inspection program, including preparation of the inspection suite, stocking of related supplies, performance of inspection of injectable products, completion of associated logbooks and batch documentation, and storage of finished product. Individual can pass color-blindness and vision testing (must achieve 20/20 with or without vision correction such as glasses or contact lenses). Must be able to pass visual appearance testing method competencies within 90 days of hire. When not inspecting, employee will be asked to complete training in and perform functions in manufacturing operations, which may include vial washing, component rinsing and preparation, Container Closure Integrity testing, and other manufacturing tasks as requested. Employee will also assist with department consumables storage and stocking programs. Employee may be asked to perform administrative tasks such as procedure revision, template revision, records filing, records archiving, and other tasks as needed. All job functions will be performed according to procedure and in accordance with cGMP, Standard Operating Procedures, and safety codes and regulations. Identifies risks to business for consideration by management. Assist and contribute to GMP and safety self-inspection activities. Accountable for delivering innovation in the Clinical Supply Chain to deliver cost savings, reduce risk and improve service. Accountable for reporting and maintaining metrics as appropriate. Zero instances of data falsification or data integrity issues by staff. Employee has basic computer skills including Word, Outlook, and ability to navigate simple website interfaces. Education and Experience: Bachelor's degree in lab sciences such as Chemistry, Biochemistry, Material Science, Immunology, Biology, Molecular Biology or similar Knowledge, Skills and Abilities: Application of knowledge and leveraging of continuous improvement activities utilizing available tools where applicable that support continued adherence with industry regulations,

Hi, My name is Gaurav and I am a recruiter with Net2Source Inc. Our direct client is looking to hire a Scientist - II (Associate) - PA/NJ Only Only in their growing team. Please find below the job description. Title : Scientist - II (Associate) Location : Lower Gwynedd, PA 19002 or Rahway NJ 07065 Duration : 12 months Rate : $35/hr on W2 without any benefits Key skills: • HPLC and dissolution experience is required. • Analytical chemistry background is required. • Empower expertise is preferred • Pharma industry is preferred Description • We are currently seeking a temporary scientist for an immediate onsite position within the Analytical Sciences (AS) laboratory within Science and Technology at Organon. • The successful candidate will be expected to perform analytical testing of drug products and APIs under the supervision of a senior scientist. • The candidate will have a good understanding of the technical, regulatory, and GMP needs related to drug product development. • The position will report to the Senior Leadership of the Analytical Sciences laboratory. • Strong technical background with a problem-solving skill set as well as the ability to work in teams are considered essential. Position Responsibilities: • Perform analytical testing (e.g., HPLC/UPLC and dissolution) of drug products • Perform data analysis (chromatography/spectroscopy) and present them to the team in a timely manner Qualifications Education and experience: BS with 4-6 years or MS with 1-3 years or Ph.D with 0-2 years of relevant experience in Analytical Chemistry. Required Experience and Skills • Hands-on analytical laboratory experience-e.g., wet chemistry, chromatography. • Expertise in Liquid Chromatography (HPLC/UPLC) and dissolution • Hands-on experience with chromatographic integration and with Empower software (or other chromatographic data acquisition systems) and Electronic Laboratory Notebook (ELN) • Experience collecting and analyzing raw data, preparing graphs and other visualization tools to help interpret results • Demonstrated strong verbal as well as written communication skills and ability to work in an interdisciplinary team environment. Preferred Experience and Skills: • Expertise in UV. • Working knowledge of laboratory GMP, quality, compliance and data integrity requirements and related recent industry trends • Working knowledge of troubleshooting analytical techniques (e.g., chromatography, dissolution, spectroscopy, etc). • Demonstrated ability to work independently in the laboratory • Working knowledge of statistics and tools, e.g., statistical data treatment and/or Excel or Minitab. • Experienced in conducting comparative and or multi-media dissolution studies. Thanks Gaurav Gupta Sr. Pharma Recruiter *************************** **************

Upstream Associate Scientist - Contract - King of Prussia, PA Proclinical is working alongside a global pharmaceutical who are seeking an Upstream Associate Scientist to join our team in King of Prussia, PA. Primary Responsibilities: In this role, you will focus on completing daily manufacturing tasks, documenting activities, and ensuring all production activities are safe and compliant. This position requires a strong ability to work within a highly matrixed organization and multi-functional team environment. Skills & Requirements: Ability to work in a highly matrixed organization. Ability to multi-task within a multi-functional team environment. Troubleshooting skills. Capable of following written instructions and clear written communication skills. Computer literacy. Familiarity with basic scientific principles and experience in routine bench work and/or instrumental analysis. Ability to author, revise, and/or support SOPs, change controls, and deviations. Bachelor of Science degree in Chemical Engineering, Biology, Chemistry, or other engineering or scientific field. The Upstream Associate Scientist's responsibilities will be: Complete daily manufacturing tasks per standard operating procedures and batch document instructions. Document all manufacturing activities clearly and accurately. Ensure all production activities are completed in a safe and compliant manner. Maintain and prepare high-quality documentation. Dispense large and small amounts of raw materials. Perform CIP (Clean-in-Place) and SIP (Sterilize-in-Place) of product tanks. Work with hazardous materials under appropriate safety procedures. Perform other functions as necessary or as assigned. If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at j.cerchio@proclinical.com Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer. INDSCIC

Responsibilities: Should be able to work flexible hours; Setup process equipment for lab-scale experiments. Prepare laboratory reagents, solutions and culture media. Perform lab-scale downstream processing of vaccine process intermediates. Perform process monitoring assays. Analyze, collate, track, and report data back to client staff members. Maintain records and test results following good laboratory practices (GLP). Work independently and efficiently. Document work clearly and perform tests accurately. Communicate effectively with client staff members. Qualifications: Education: B.S. in Bio/ Chemical Engineering, Biochemistry, or related science. 0-5 years work experience with at least six months related laboratory experience preferably performing biologics purification steps. General laboratory skills, experience with pipettes. Operation of tangential flow filtration experience is preferred. Experience using formulas and linking spreadsheets in Excel. 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.

Job Title: Senior Scientist, Formulation - Biologics We are seeking a highly skilled and motivated Senior Scientist to join our Formulation Development team, focused on the development of Biologics including mAbs, ADCs, and fusion proteins. The ideal candidate will hold a PhD in a relevant scientific discipline, with a minimum of 2 years of industry experience in Biologics formulation. In this role, the Senior Scientist will be responsible for the design, optimization, and scale-up of protein formulations, stability studies, and drug product development for Biologic therapeutics. Key Responsibilities: Lead formulation development efforts for biologics, including monoclonal antibodies (mAbs), ADCs, and fusion proteins, focusing on stability, solubility, and compatibility with various delivery systems. Design, execute, and analyze experiments to optimize protein formulations, including buffer selection, excipient compatibility, and process conditions. Conduct stability testing under accelerated, real-time, and stress conditions to assess formulation integrity, stability, and compatibility. Work closely with cross-functional teams, including Analytical Development, Process Development, and Quality Control, to ensure alignment and consistency of formulations through the product development lifecycle. Drive the development of scalable and robust formulations for clinical and commercial manufacturing, ensuring compatibility with large-scale production methods. Provide scientific leadership in the resolution of complex formulation challenges during early and late-stage development. Author technical documentation, including formulation protocols, study reports, and data analysis for internal and regulatory submissions. Stay current with scientific trends and industry developments related to biologics formulation, particularly in the areas of mAbs, ADCs, and fusion proteins. Mentor and guide junior scientists and associates in formulation development best practices. Qualifications: PhD in Biochemistry, Molecular Biology, Chemical Engineering, Pharmaceutical Sciences, or a related field. Minimum of 2 years of industry experience in biologics formulation, with expertise in monoclonal antibodies (mAbs), ADCs, fusion proteins, or other protein-based therapeutics. Strong understanding of protein chemistry, stability, and formulation strategies. Proficiency in analytical techniques used for protein characterization and stability assessment (e.g., HPLC, SEC, DSC, DLS, FTIR, UV-Vis, etc.). Experience in conducting stability studies and interpreting data to assess shelf life, degradation pathways, and formulation performance. Familiarity with biopharmaceutical manufacturing processes, scale-up, and cGMP requirements. Ability to troubleshoot complex formulation issues and collaborate with cross-functional teams. Excellent written and verbal communication skills, with the ability to present complex data to internal and external stakeholders. .

Job Title: Biophysics Research Associate Hours: 40 hours/week, Monday to Friday, 8:00 AM - 5:00 PM (flexible schedule) We are seeking a motivated Scientific Service Specialist 1 to join the Biophysics group within our R&D team in Upper Providence, PA. This role involves generating and analyzing biophysical assay data to support drug discovery efforts, specifically focusing on protein characterization and protein-ligand binding analysis. The ideal candidate will work closely with protein biochemists and structural biologists, contributing to high-quality data generation and supporting the transformation of data acquisition and integration within the team. Daily Responsibilities: Conduct biophysical assays and data analysis to support the drug discovery pipeline, including protein characterization and protein-ligand binding assays. Work in a matrix team environment, collaborating with cross-functional business partners to achieve project objectives. Organize, interpret, and present experimental results at group meetings. Perform routine laboratory maintenance and ensure compliance with safety protocols and ethical standards. Maintain an electronic laboratory notebook to document experiments and results. Ensure proper inventory management by routinely checking and maintaining laboratory supplies. Follow detailed protocols and maintain high standards of notetaking and data documentation. Ensure compliance with all R&D data integrity practices, safety codes, and environmental regulations. Working Environment: Work will be primarily in a laboratory setting, with potential exposure to hazardous materials, requiring the use of personal protective equipment (PPE). The job pace may be fast, with high demands for job completion. Employee may be required to manage hazardous waste in compliance with company and regulatory standards. Skills and Qualifications: Education: BS in a life sciences discipline (e.g., biophysics, analytical chemistry, biochemistry). Experience: Laboratory research experience, preferably in quantitative or analytical sciences. Technical Skills: Strong practical knowledge of protein biochemistry and biophysics. Experience with biophysical analysis techniques such as thermal stability analysis, microscale thermophoresis, surface plasmon resonance, and hydrogen deuterium exchange mass spectrometry is highly desirable. Proficiency in curve fitting, regression analysis, mathematical modeling, or other quantitative data analysis techniques. Familiarity with working with purified proteins for biophysical analysis, enzymology, or structural biology. Additional Skills: Ability to handle, store, label, and ensure the safety of scientific materials and data. Strong communication skills with the ability to summarize and present findings to a varied audience. Strong data handling skills, including acquisition, manipulation, and documentation of experimental data. Physical Demands: Ability to remain stationary for more than 25% of the time. Regular movement within the lab, including bending, squatting, and reaching for instruments or materials. Must be able to lift and move up to 25 pounds regularly, and occasionally up to 100 pounds. Specific vision abilities required include close-range observation, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus for detailed work with instruments. Success/Performance Metrics: Successful completion of assigned biophysical assays with high accuracy and timely delivery of data. Effective collaboration with cross-functional teams to achieve project objectives. Clear, concise communication of experimental results and findings to both technical and non-technical audiences. Soft Skills: Strong communication skills, both written and verbal. Proficient in scientific data handling, including acquisition, manipulation, and visualization of experimental data. Ability to work independently and as part of a collaborative team.

The Scientific Team at Russell Tobin & Associates is hiring a Biophysics Scientist for a world-class client in Collegeville, PA 19426 Required top skills: -Biophysical Assays & Data Analysis -Bachelor's degree (BS) in a life sciences discipline, such as biophysics, analytical chemistry, or biochemistry. -Experience in laboratory research, especially in quantitative or analytical science fields, is preferred. (Not Mandatory) -knowledge of protein biochemistry and biophysics Additional Details: -3+ months contract with Possibility for extension or conversion to FTE Based on business need -Pay: $30 to $34/ hr

· Lab Operations responsibilities include but are not limited to: · Coordination and management of instrument onboarding and validation · GMP record keeping · Chamber management · Lab safety and housekeeping · Software validation · Be able to coordinate activities with internal and external operations and service teams, service providers, IT, site quality, and analysts to ensure lab operation activities are completed and compliant. Responsibilities: · Strong verbal communication skills are required. Demonstrates excellent interpersonal skills (written and oral) and the ability to work in a cross-functional customer-focused environment is required. Must have demonstrated ability to drive completion of activities in a timely manner. Experience: · Experience with lab operation activities in a GMP environment is required. · Ability to work with limited guidance to plan, execute, and follow through with work assignments is expected. · Experience with electronic laboratory notebook is preferred. · Minimum of 1 or more years related industry experience managing laboratory equipment. Skills: · Facilitating instrument preventive maintenance, calibration, and repairs; may include some hands-on maintenance and calibration duties Education: · Bachelor's degree or equivalent, in Chemistry, Biochemistry or related subject area 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: 24- 26358

The Upstream Process Development Associate is involved in the execution of recombinant adeno-associated viral vector (rAAV) production processes. The Associate will executes experiments, aggregates and reviews experimental data, verifies data in technical reports and works under supervision of senior technical leads. He/she will be responsible for: Culturing mammalian cells in shake flask and benchtop bioreactors. Support lab operational activities for rAAV cell culture studies in stirred tank bioreactors including AMBR15 and/or AMBR250 bioreactors. Execute experimental designs; collect and format data for analyses in support of technical platform development objectives. Compile data analysis summaries and present to appropriate project teams Contribute to the authoring of lab procedures, data analysis summaries, and support data verification and other relevant process documentation. Maintaining an accurate laboratory notebook following ALCOA+ principles. Ensuring work conforms to applicable quality and safety standards. Support maintenance and troubleshooting of laboratory equipment. Other duties as assigned including but not limited to contributing to lab organization and cleanliness, consumables stocking, and routine equipment maintenance.

LHH Recruitment Solutions has a Development Chemist opening for our client in the Burlington, NJ area. This direct hire role allows you to collaborate with numerous departments to facilitate new formulations for new compounds through customer specifications in accordance with regulations. This direct hire role allows you to collaborate closely with the research and development team to facilitate quality control, trials, and issuance of new formulations. Candidates MUST have a minimum of 3 years' professional experience in rigid formulation with polyvinyl chloride and familiar with extrusion and/or injection molding. This fully on-site position requires a bachelor's degree preferably in a chemistry or related field and a minimum 3-year development experience. Ideal candidates will have extensive experience in PVC material application as well as a proven track record of understanding and utilization of surface to interface properties a s well as surface characterization. You will be responsible for customer interfacing as well. Salary range: $75,000 to $80,000 DOE. Job Summary: Conduct development work for new compounds in new product developments, and improves current compounds in performance, efficiency, and price competitiveness in accordance with all regulatory requirements. Responsibilities: Analyze compounds and manage corresponding data tracking. Define and determine physical and chemical properties for compounds. Oversee development and issuance of new formulations for new compounds based on requirements and specifications from clientele. Conduct investigation of new and old formulations in replacement of raw materials to enhance performance and minimize cost. Maintain quality standards. Responsible overseeing raw material substitutions as required. Collaborate with HSE in updating and maintaining SDS. Prepare technical data information for customers. Generate ideas for new product development. Manage tests performed with accuracy, completeness and in regulatory compliance. Make recommendations regarding for production line or production lines and trial formulations. Attend and oversee production trials to ensure formulations are being utilized as intended. Attends monthly QA/QC meetings as scheduled. Attend customer trial(s) per request from R&D Manager to validate the performance of the new compound and make necessary adjustments per customer trial(s) feedback. Collaborate internally with various departments for R&D related issues. Provides technical support internally/externally to Production, QC/QA, Sales and customers as needed. Responsible for managing regulatory files including, but not limited to, NSF and UL qualifications and certifications. Annual audit participation. Oversee monitoring of equipment to ensure safety precautions are being followed. Assist in ISO Audits. Assist in creating, maintaining, and updating of R&D ISO documents. Required Qualifications: Bachelor's degree (B.S.) in chemistry - NOT BIOLOGY. Minimum of three years of relevant experience in a manufacturing environment of PVC Material. Highly preferred - experience in a PVC (Polyvinyl Chloride) compounding setting. ASQ Certified Quality Engineer, with a desired ASQ Six Sigma Green Belt highly preferred. Possesses in-depth knowledge of quality control/quality assurance procedures and legal standards. Proven expertise in chemistry relating to surface-interface properties as well as surface characterization. Proficiency in Microsoft Excel and competence in other Microsoft Office 365 applications or related programs. Effective promoter of positive culture and relationships utilizing clear and positive communication across the board. Highly detail oriented. Expert in time management, capable of working under pressure as well as meeting deadlines. Excellent verbal and written communication skills. Oversee task prioritization and delegation when necessary. This posting is a representative sample of the types of roles we typically place with our clients. Depending on the specific client, location, and role, the salary range is estimated to be $75,000 to $80,000 DOE and benefits may include medical, dental, vision, 401k+match and PTO.

Innovative company is seeking an innovative and team-oriented surfactant and water treatment chemist in their facility located in the Philadelphia area. Chemist will be responsible for R&D projects covering a variety of formulation development and modification as well as leachate, condensate treatability study. The position will work closely with other R&D and QC Chemists as well as manufacturing technicians. This position will be located in West Chester, PA and report to the VP of Technology. Essential Functions & Responsibilities: Set-up internal standard test procedures New product development Leachate, condensate treatability study using various physical/chemical as well as biological processes. Scope, design and execute product performance improvement projects Formulation tailoring for unique customer specifications Operating bench scale or pilot scale leachate, condensate treatment systems Conduct water quality analysis. Support Manufacturing, Quality, Sales and Product Management functions Operation of analytical and application equipment Developing and implementation of quality control specifications and standards Project management and documentation including laboratory notebook documentation and project report writing Strong laboratory skills required including both scientific practices and housekeeping Job Specifications: Bachelors of Science in Chemistry, Chemical Engineering (or related technical discipline) is preferred. Candidates with other relevant industry experience may be considered 5 or more years lab experience in product development/application is desirable Experience in operating bench scale or pilot scale water treatment system is desirable. Foam formulation experience is required Understanding of polymer chemistry and structure property relationships Strong mechanical aptitude Experience in data collection, manipulation and analysis (Microsoft Suite, etc.) Company offers a salary of 90-115K, bonus opportunities, extensive benefits package.

High Complexity Blood Bank Hiring CLS Evenings or Baylor Shift Nights (Fri-Sun) Performs blood bank testing and stat lab testing Must have high volume blood bank experience Full benefits and competitive compensation Permanent position with job security MUST have ASCP certification For more information please send your resume directly to or call/text me at

A well-established company with offices in Moorestown, NJ is currently looking for qualified environmental engineers, scientists, and geologists to work with our existing team of Environmental Consulting professionals on diverse and interesting projects throughout the United States. Extensive Knowledge of Phase I Environmental Site Assessments, and soil and groundwater investigations. Requirements Our ideal candidate will possess the following skills and attributes: Bachelor's degree in geology, environmental science, engineering, or related field required. 1-3 years' experience working on Phase I Environmental Site Assessments, and soil and groundwater investigations. 40-hour OSHA HAZWOPER and current 8-hour refresher. Excellent verbal and written communication skills. Strong computer skills, including Microsoft Office. Attention to detail. Resourcefulness and initiative. Strong work ethic. Ability to work independently and contribute to a team. Willingness to travel to jobsites across New Jersey, New York, and Pennsylvania, and sometimes nationally; and Willingness to perform a variety of assignments on short notice and on weekends (occasionally) if needed. This position will be based in our Moorestown, NJ offices Property Solutions offers competitive salary and excellent benefits package (medical, dental, and vision, coverage, 401K). We also offer the opportunity to work on a variety of projects. We offer the opportunity for advancement based on performance.

Our large pharmaceutical client is seeking an Associate Scientist to join their growing team within the R&D Immunology Translational Science organization in Spring House, PA. The Immunology Therapeutic Area is focused on developing new cutting-edge therapies to treat dermatology, GI, and rheumatic diseases. This team is responsible for generating Next Generation Sequencing (NGS) data and passing it to the computational group for analysis. The role of this lab-based Scientist will primarily be focused on Next Generation Sequencing (NGS) including QC of RNA, normalizing the RNA, bringing it down to specific concentration, then moving into library prep. The ideal candidate will have strong molecular biology skills and hands-on experience in the lab doing RNA QC work. They will also need to demonstrate strong attention to detail and organization as they will be responsible for hundreds of samples at any given time. Qualifications: Bachelor's or Master's Degree in Biology or related field 3+ years of experience in the lab with Next Generation Sequencing (NGS) RNA sequencing experience Salary: $75,000-$100,000 (flexible based on experience) Hours: Monday-Friday, 8:00am-4:30pm 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 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.

Employee will be expected to participate in all aspects of department visual inspection program, including preparation of the inspection suite, stocking of related supplies, performance of inspection of injectable products, completion of associated logbooks and batch documentation, and storage of finished product. Individual can pass color-blindness and vision testing (must achieve 20/20 with or without vision correction such as glasses or contact lenses). Must be able to pass visual appearance testing method competencies within 90 days of hire. When not inspecting, employee will be asked to complete training in and perform functions in manufacturing operations, which may include vial washing, component rinsing and preparation, Container Closure Integrity testing, and other manufacturing tasks as requested. Employee will also assist with department consumables storage and stocking programs. Employee may be asked to perform administrative tasks such as procedure revision, template revision, records filing, records archiving, and other tasks as needed. Assist and contribute to GMP and safety self-inspection activities.

Director of Clinical Research Scientist - Contract - Wilmington, DE Proclinical is recruiting for an experienced and dedicated Director to head up the Clinical Research team. Primary Responsibilities: This role will work closely with physicians within Clinical Development to support clinical research programs. The successful candidate will be required to focus on developing protocols, contributing to program strategies, and drafting clinical scientific documents. This position requires a proactive approach to data review and collaboration with various stakeholders. Skills & Requirements: Degree in a scientific or life-sciences field; Pharm.D. or Ph.D. preferred. Minimum of 8 years of experience in research with at least 5 years of drug development experience are required. Alternative drug development experience will be considered. Ability to work independently and manage multiple tasks in a fast-paced environment. Excellent written and oral communication skills. Strong analytical abilities. Willingness to travel up to 20% as needed. The Director of Clinical Research Scientist's responsibilities will be: Develop protocols for clinical studies. Contribute to program strategy development for assigned compounds/programs. Draft and review clinical scientific documents such as INDs, Investigator Brochures, and Health Authority submissions. Provide clinical input into eCRF design, SAP, and TLFs. Collaborate with study team members to review study data and identify trends. Represent clinical development on project teams. Develop relationships with consultants and external experts for protocol feedback. Lead the creation of study abstracts, posters, presentations, and manuscripts. Serve as a liaison to project teams, CROs, and clinical sub-teams. Maintain updated knowledge of the competitive landscape and evolving standards of care. If you are having difficulty in applying or if you have any questions, please contact Mike Raletz at m.raletz@proclinical.com Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer. INDCR