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Job Description QC Analyst I–III Relocation Package Available (U.S. Citizens Only) Global Life Science Hub is recruiting on behalf of a rapidly growing biopharmaceutical company in New Jersey seeking QC Analysts (Levels I–III) to join their expanding Quality Control team. This is an exciting opportunity to contribute to the development and manufacturing of biologics in a state-of-the-art GMP facility, with a full relocation package offered for qualified U.S. citizens willing to move to New Jersey. Role Overview: As a QC Analyst, you will play a key role in performing analytical and microbiological testing to ensure product quality and compliance with regulatory standards. The role requires a minimum of 1 year of hands-on QC or GMP laboratory experience in the pharmaceutical/biotechnology industry. Key Responsibilities: • Perform analytical and/or microbiological testing of raw materials, in-process samples, and finished products under GMP., • Execute assays such as PCR, ELISA, HPLC, flow cytometry, and cell-based assays (depending on level and background)., • Support method qualification, validation, and transfer activities., • Document and review laboratory results in accordance with ALCOA+ and data integrity standards., • Contribute to deviation investigations, CAPAs, and change controls., • Maintain, calibrate, and operate laboratory instruments to ensure readiness for use., • Participate in audits, inspections, and continuous improvement initiatives. Requirements: • Bachelor’s or Master’s degree in Biology, Biotechnology, Chemistry, or related field., • Minimum of 1 year QC or GMP laboratory experience is required., • Analyst I: 1–2 years QC experience., • Analyst II: 2–4 years QC experience in GMP biopharma., • Analyst III: 4–6+ years QC experience with expertise in analytical/cell-based methods and mentoring., • Strong knowledge of GMP, FDA, and ICH guidelines., • Detail-oriented with strong documentation and organizational skills. Why Apply? • Competitive compensation and benefits package., • Relocation package offered exclusively to U.S. citizens willing to relocate to New Jersey., • Career development opportunities across QC levels with exposure to biologics and cell/gene therapy., • Join a collaborative and growing biopharma company shaping the future of medicine.

Overview Join our team as a day shift, full-time, Pathology Unit Histotechnologist in Montclair, NJ. You may be eligible for a sign on bonus of $5,000. Why Join Us? Thrive in a People-First Environment and Make Healthcare Better • Thrive: We empower our team with career growth opportunities, tuition assistance, and resources that support your wellness, education, and financial well-being., • People-First: We prioritize your well-being with paid time off, comprehensive health benefits, and a supportive, inclusive culture where you are valued and cared for., • Make Healthcare Better: We use advanced technology to support our team and enhance patient care., • The Histotechnologist functions as a professional who assumes responsibility and accountability for pre-analytical specimen preparation and processing, embedding, microtomy, and maintaining the equipment under the direction of the Histology/Pathology department leadership, Pathologist, or designee. The position may also perform specimen grossing of surgically removed tissue under the supervision of the Pathologist., • This job description reflects the essential function of the position, and it is not to be assumed that the principal functions are the only duties to be performed., • Other duties may arise and be carried out as assigned to meet quality standards expected for patient care. Job Requirements: Experience within a clinical or anatomic pathology department. * 6 months’ experience as a Histotechnician. Pay Range Minimum: $29.48/Hr. Rate of pay is determined based on experience and education, and may include other pay components such as differentials and call pay based on role.

Job Description LABORATORY MANAGER 1.0 Corporate Job Title Laboratory Manager 2.0 Reporting Relationships Branch Manager for day-to-day laboratory responsibilities and Laboratory Director for quality systems responsibilities. 3.0 Position Summary Manages and coordinates laboratory functions for the branch. Provides guidance, leadership and training to laboratory staff on routine matters. Responsible for taking the necessary steps to ensure that all laboratory functions and resources are run safely, accurately and efficiently. 4.0 Minimum Requirements • Requires a B.S. (preferable Chemistry degree) with a minimum of five years general laboratory experience or three years experience in a petroleum laboratory., • Must possess managerial and inter-personal skills., • Must be able to distinguish color., • Must pass pulmonary test for respirator use. 5.0 Responsibilities • Acts as the liaison between Laboratory Coordinator and general laboratory staff with respective Branch Manager, Operations Department and Laboratory Director., • Works closely with Operations Department to obtain day-to-day analytical testing requirements based upon nominations received from clients in order to provide accurate, reliable results on a timely basis. Works directly with customers for laboratory submitted samples if required., • Ensures that laboratory staff and visitors follow all documented safety requirements as defined by the company safety program., • Uses judgment and discretion in directing, coordinating and scheduling the work activities of laboratory staff consistent with accepted operating practices and procedures, including periods during non-working hours, weekends and holidays., • Receives, compiles, and verifies the data resulting from laboratory analyses and ensures accurate and complete preparation of applicable reports as per standard procedures., • Works in conjunction with the Laboratory Director to maintain internal quality control / quality assurance program to ensure the use of standard laboratory practices., • Works with laboratory staff to analyze and compile round robin and quality control sample results to ensure operating efficiency of process and/or testing equipment., • Ensures the laboratory has the equipment and supplies necessary to meet customer demands and established quality program. Manages equipment and supply inventory, including scheduled preventive maintenance requirements of the equipment. Coordinates the replacement or repair of faulty equipment or supplies as needed., • Responsible for the maintenance and control of the sample retain area, including standard cradle-to-grave sample requirements and waste disposal., • Ensures that laboratory staff is qualified to perform necessary testing and meets the training / refresher training requirements of the quality system. Ensures Test Method Assessments, • (TMA’s) are conducted as per the required procedure and schedule., • Using advanced knowledge gained in the laboratory, identifies the root causes of quality system problems (customer, specifications or Camin Cargo system) in respective areas of responsibility and uses good judgment to independently troubleshoot, initiate, recommend, and/or implement timely solutions to the problems. 6.0 Fitness for Duty – Physical Demands Workday may consist of 8-12 hours however this can vary day to day and shift to shift. Some of the retain work is performed outdoors, wearing full Personal Protective Equipment (PPE), and could include possible exposure to high and low temperatures for a prolonged duration of time. Laboratory work is normally performed indoors under climate-controlled conditions. All times listed in the table below are approximate. • Maximum Lift-Floor to knee; Knuckle to waist; Waist to shoulder Weight Up to 45 lbs.- Duration/Day Up to 1 hours. • Walking Weight Up to 45 lbs. -Duration/Day Up to 10 hours • Pushing-Pulling Weight Variable-Duration/Day Up to 1 hour • Carrying Weight Up to 45 lbs.- Duration/Day Up to 2 hours • Ascend/Descend Ladder/Stair Weight Up to 45 lbs.- Duration/Day Up to 1 hour • Extended Reach Weight Up to 45 lbs.- Duration/Day Up to 1 hour • Standing Weight Up to 45 lbs.- Duration/Day Up to 12 hours • Crouch/Squat/Knee Weight Up to 45 lbs.- Duration/Day Up to 1 hour • Tool use Weight 5-8 lbs.- Duration/Day Up to 1 hour • Sitting Weight 5-8 lbs. -Duration/Day Up to 6 hours • Driving Weight N/A- Duration/Day Up to 6 hours All are required to perform this position This document contains Confidential and Proprietary information which is the property of Camin Cargo Control. None of the information contained herein may be disclosed, reproduced, distributed or used without prior written consent from Camin. All rights reserved.

Job Description Key Responsibilities: 1. Formulation Development: o Develop and optimize pest control formulations, including insecticides, rodenticides, repellents, and larvicides. o Tailor formulations to meet efficacy, safety, environmental, and regulatory requirements. 2. Product Testing and Evaluation: o Conduct laboratory and field tests to evaluate product effectiveness against target pests. o Assess physical and chemical stability, efficacy, and environmental impact under various conditions. 3. Regulatory Compliance: o Ensure formulations comply with local, national, and international regulatory standards (e.g., EPA, EU regulations). o Prepare and submit technical documentation for regulatory approval. 4. Research and Innovation: o Explore and integrate emerging active ingredients, delivery systems, and sustainable practices into product development. o Stay informed about new technologies and advancements in pest control chemistry. 5. Process Improvement: o Collaborate with manufacturing teams to scale up formulations and optimize production processes. o Troubleshoot issues during scale-up and recommend improvements for quality control. 6. Documentation and Reporting: o Maintain accurate lab records, including experimental design, data analysis, and findings. o Prepare detailed technical reports and present research results to internal and external stakeholders. 7. Collaboration and Teamwork: o Work with cross-functional teams, including biology, regulatory, and marketing teams, to ensure product success. o Liaise with suppliers and external research organizations as needed. Qualifications: Education and Experience: • Bachelor's, Master's, or PhD in Chemistry, Biochemistry, Agricultural Science, or a related field., • 2+ years of experience in pesticide formulation, pest control product development, or related fields preferred. Technical Skills: • Strong knowledge of pesticide chemistry, toxicology, and modes of action., • Experience with analytical techniques such as HPLC, GC-MS, or FTIR for active ingredient analysis. • Familiarity with encapsulation, emulsification, and other delivery technologies. Soft Skills: • Excellent problem-solving and analytical thinking abilities., • Strong written and verbal communication skills., • Ability to work effectively in a team-oriented and fast-paced environment. Preferred Qualifications: • Experience with biodegradable and environmentally friendly pest control solutions., • Knowledge of integrated pest management (IPM) practices and their implementation. We’re proud of the investments we’ve made in our team, having grown from four to 1000 employees and evolving into one of the leading recruitment and staffing solution providers in the industry. Our recruiters and account managers are passionate about connecting qualified professionals with the right positions in small, medium, and large companies. Our Services W3Global understands the natural ups and downs of an organization’s staffing needs. We are continuously adapting to industry and economic changes to find the right candidates. We specialize in placing permanent, direct, contract, and temporary positions for companies of any size. Our recruiting services include sourcing, recruiting, screening, interview management, salary negotiations, training, and onboarding. We are committed to helping organizations redefine their recruitment process by delivering our SaaS-based proprietary application tracking system software. Our Expertise W3Global has been delivering staffing solutions for nearly two decades; we know which recruiting strategies work best. Our expert team is committed to developing a customized solution to fit your company’s unique needs. As a W3Global client, you’ll also receive personalized assistance from a seasoned team of staffing specialists. We are committed to providing both technical support and industry expertise to simplify the hiring process. We know that your time matters. W3Global will help you streamline the hiring process, getting it done and getting it right.W3Global was established in 2006 in Fremont, CA with a vision: simplify the recruiting process and develop an industry-disrupting platform to connect candidates with clients. Our cutting-edge Applicant Tracking System enables us to find the right person for the right job, creating value for job seekers and employers. While W3Global initially focused on IT staffing, we have expanded the business to serve many other industries, including accounting and finance, legal, engineering, human resources, government and more.\r\n\r\nWe’re proud of the investments we’ve made in our team, having grown from four to 1000 employees and evolving into one of the leading recruitment and staffing solution providers in the industry. Our recruiters and account managers are passionate about connecting qualified professionals with the right positions in small, medium, and large companies.\r\n\r\nOur Services\r\nW3Global understands the natural ups and downs of an organization’s staffing needs. We are continuously adapting to industry and economic changes to find the right candidates.\r\n\r\nWe specialize in placing permanent, direct, contract, and temporary positions for companies of any size. Our recruiting services include sourcing, recruiting, screening, interview management, salary negotiations, training, and onboarding.\r\n\r\nWe are committed to helping organizations redefine their recruitment process by delivering our SaaS-based proprietary application tracking system software.\r\n\r\nOur Expertise\r\nW3Global has been delivering staffing solutions for nearly two decades; we know which recruiting strategies work best. Our expert team is committed to developing a customized solution to fit your company’s unique needs.\r\n\r\nAs a W3Global client, you’ll also receive personalized assistance from a seasoned team of staffing specialists. We are committed to providing both technical support and industry expertise to simplify the hiring process. We know that your time matters. W3Global will help you streamline the hiring process, getting it done and getting it right.

Job DescriptionDescription: length of assignment: 6 months Work hours per day: 8 hours (Monday through Friday; 40 hours/week) Interview Process: Teams (other arrangements possible as needed) Job Responsibilities: • Perform analysis of samples and raw materials using chromatographic, spectroscopic, wet chemistry, physical testing and other analytical techniques. Techniques utilized include specific gravity, viscosity, potentiometric titrations, Karl Fisher, TLC, pH, liquid chromatography, gas chromatography, FTIR, others., • Apply existing test methods and procedures to complete the required analytical testing., • Collects, process and interpret accurately results, derive conclusions based on sound science, and prepare reports to effectively communicate results and findings to key stakeholders (audience with and without scientific backgrounds)., • Perform root cause analyses for non-conformance events related to laboratory testing., • Communicate effectively with management regarding testing statuses of projects., • Adhere to written procedures and practices to ensure good quality, compliance, and safety., • Ability to quickly adapt to changes, delays, or other unexpected events, and prioritize the work to ensure on time delivery of results and critical project milestones., • Communicate effectively with management regarding testing statuses of projects., • Adhere to written procedures and laboratory practices to ensure good quality and compliance., • Adhere to site and department’s health and safety guidelines and maintain personal and shared workspace., • Adapt to changes, delays, or other unexpected events, and prioritize the work to ensure on time delivery of results and critical project milestones. Qualifications: • Bachelor’s degree in Chemistry, or related field, with 1-3 years of professional experience, • Working knowledge of pH, TLC, Auto-titrators, FT-IR, Karl Fisher, Viscosity, and along with other wet chemistry analysis., • HPLC experience (preferred) and GC experience, • Strong written and verbal communication skills required., • Demonstrate ability to work in a diverse environment to manage multiple projects simultaneously and meet timelines., • Capability of working independently as well as working in a fast paced team driven environment, • Excellent bench skills and organization while maintaining a safe work environment., • Experience with Empower, ELN and LIMS software preferred Interview Process: Teams (other arrangements possible as needed) Job Responsibilities: • Perform analysis of samples and raw materials using chromatographic, spectroscopic, wet chemistry, physical testing and other analytical techniques. Techniques utilized include specific gravity, viscosity, potentiometric titrations, Karl Fisher, TLC, pH, liquid chromatography, gas chromatography, FTIR, others., • Apply existing test methods and procedures to complete the required analytical testing., • Collects, process and interpret accurately results, derive conclusions based on sound science, and prepare reports to effectively communicate results and findings to key stakeholders (audience with and without scientific backgrounds)., • Perform root cause analyses for non-conformance events related to laboratory testing., • Communicate effectively with management regarding testing statuses of projects., • Adhere to written procedures and practices to ensure good quality, compliance, and safety., • Ability to quickly adapt to changes, delays, or other unexpected events, and prioritize the work to ensure on time delivery of results and critical project milestones., • Communicate effectively with management regarding testing statuses of projects., • Adhere to written procedures and laboratory practices to ensure good quality and compliance., • Adhere to site and department’s health and safety guidelines and maintain personal and shared workspace., • Adapt to changes, delays, or other unexpected events, and prioritize the work to ensure on time delivery of results and critical project milestones. Qualifications: • Bachelor’s degree in Chemistry, or related field, with 1-3 years of professional experience, • Working knowledge of pH, TLC, Auto-titrators, FT-IR, Karl Fisher, Viscosity, and along with other wet chemistry analysis., • HPLC experience (preferred) and GC experience, • Strong written and verbal communication skills required., • Demonstrate ability to work in a diverse environment to manage multiple projects simultaneously and meet timelines., • Capability of working independently as well as working in a fast paced team driven environment, • Excellent bench skills and organization while maintaining a safe work environment., • Experience with Empower, ELN and LIMS software preferred, • Basic knowledge of the Microsoft Office Suite

Job Description POSITION SUMMARY Clinical laboratory technologist means a clinical laboratory practitioner who, pursuant to established and approved protocols of the department of health, performs clinical laboratory procedures and examinations and any other tests or procedures conducted by a clinical laboratory, including maintaining equipment and records, and performing quality assurance activities related to examination performance, and which require the exercise of independent judgment and responsibility, as determined by the department. Perform and report results on a variety of analytical tests and procedures of patient specimen samples according to established laboratory policies and procedures PRINCIPAL DUTIES AND RESPONSIBILITES Demonstrates knowledge and perform tests in one or more of the laboratory subspecialties, e.g. chemistry, immunology, microbiology, or hematology Demonstrates ability to coordinate multiple tasks with precision and flexibility to provide accurate and precise test results within the minimum turnaround time established for the laboratoryOperates various laboratory instruments involved in specimen testing and result reporting including performing all required quality control tests per shift or as necessary Follows the laboratory procedures for specimen handling and processing, test analysis, reporting and maintaining records for patient test results Performs qualitative and quantitative tests and examinations using various analyzers and/or manual methods on specimen sources such as blood, urine, and other body fluids using established procedures Identifies problems that may adversely affect test performance or reporting of test results and either corrects the problem or immediately notifies the lead laboratory technologist Follow the laboratory established corrective action policy and procedure, whenever test system is not within the laboratory’s established acceptable levels of performance Performs established quality assurance procedures (quality control testing, instrument function checks and calibrations), maintains appropriate documentation and reports irregularities Documents all quality control activities, instrument procedural calibrations, and maintenance performed Adheres and complies with laboratory infection control policies and procedures Actively participates in ongoing testing with the standards of accrediting agencies. Maintains records that demonstrate proficiency testing samples were tested in the same manner as a patient specimen sample Participate in the laboratory’s quality assurance and improvement program Assesses the accuracy and validity of obtained test results by applying knowledge of relevant scientific principles, recognizes changes that are critical to patient care, and identifies probable cause for irregular and atypical findings Performs required maintenance of equipment and performs troubleshooting procedures necessary to correct situations Maintains records of tests and examinations and final results for all record functions and inquiries related to patient care Prepare reports assigned by the supervisor or manager Troubleshoots instruments and resolves technical problems whenever possible, documents corrective action, and reports problems to the supervisor Train newly hired personnel when necessary Check inventory levels to maintain stock when needed Equipment knowledge: Beckman DXI 800, DXI 9000 Abbott Alinity CI DXH 900 with slide maker/ slide stainer DXC AU 700 Diasorin XL Phadia 250, 1000 DXU840M, AX 4030 IQ 200 AX 4030 Sebia Capi 3 Tera/Octa ACL Top 350\ Alcor iSed Cellavision POSITION REQUIREMENTS New York State licensure ( preferred) ASCP Certification highly recommended Basic computer skills PHYSICAL DEMANDS Involves standing, walking, sitting and bending May include lifting, carrying, pushing and pulling objects Company DescriptionLincoln Reference Laboratory is one of the largest independent, general diagnostic laboratories, located in Linden NJ. We take pride in delivering quality service since 2004 for a broad range of medical diagnostic testing in our new and advanced facility. We cover industry leading medical testing in Molecular Oncology, Hematology, Histopathology, and Chemistry. Excellence and specificity of patient testing is our highest priority! Our facility in New Jersey provides an array of services in molecular oncology, diagnostic blood testing, toxicology, GI testing, RPP, Urovysion Fish, H.Pylori breath test, BRCA 1/2 and so much more. All testing is done in-house, which increases turnaround time. Looking at the patient’s susceptibility to illness on a genetic level provides physicians with greater insight into improving patient care. Our state-of-the-art instrumentation and highly skilled and licensed technologists provide quality results and consultation. For many years our experienced pathologists offer their expertise in the oversight of diagnostic cases from all tissue specimens. We provide a full range of histology services, including grossing, processing, embedding, microtome, routine, and special staining. We ensure properly prepared tissues and slides to provide accurate diagnoses. We are highly experienced technologists, who are registered and licensed by NY and other states in US. We use latest, state-of-the-art, medical equipment and instrumentation in the preparation of specimens, and we guarantee strictest quality assurance mechanisms are implemented to maintain consistency and precision. For all our client’s convenience, we offer a web-based reporting tool to get testing results. You can now securely access results virtually anywhere and at any time. At Lincoln Diagnostics LLC, we can guarantee fast responses to your concerns and immediate action should you wish to receive them. Certifications National Women Business Owners Corporation (NWBOC)Lincoln Reference Laboratory is one of the largest independent, general diagnostic laboratories, located in Linden NJ. We take pride in delivering quality service since 2004 for a broad range of medical diagnostic testing in our new and advanced facility. We cover industry leading medical testing in Molecular Oncology, Hematology, Histopathology, and Chemistry. Excellence and specificity of patient testing is our highest priority!\r\n\r\nOur facility in New Jersey provides an array of services in molecular oncology, diagnostic blood testing, toxicology, GI testing, RPP, Urovysion Fish, H.Pylori breath test, BRCA 1/2 and so much more. All testing is done in-house, which increases turnaround time. Looking at the patient’s susceptibility to illness on a genetic level provides physicians with greater insight into improving patient care.\r\n\r\nOur state-of-the-art instrumentation and highly skilled and licensed technologists provide quality results and consultation. For many years our experienced pathologists offer their expertise in the oversight of diagnostic cases from all tissue specimens. We provide a full range of histology services, including grossing, processing, embedding, microtome, routine, and special staining. We ensure properly prepared tissues and slides to provide accurate diagnoses.\r\n\r\nWe are highly experienced technologists, who are registered and licensed by NY and other states in US. We use latest, state-of-the-art, medical equipment and instrumentation in the preparation of specimens, and we guarantee strictest quality assurance mechanisms are implemented to maintain consistency and precision.\r\n\r\nFor all our client’s convenience, we offer a web-based reporting tool to get testing results. You can now securely access results virtually anywhere and at any time. At Lincoln Diagnostics LLC, we can guarantee fast responses to your concerns and immediate action should you wish to receive them.\r\n\r\nCertifications\r\nNational Women Business Owners Corporation (NWBOC)

**This is a first shift opportunity, Monday-Friday. JOB DESCRIPTION • A client of ours is looking for an analytical stability chemist to join their team in Florham Park, NJ. This person will be supporting the analytical department through method development, validation/transfer, while managing stability studies for all the brands/products within this company's umbrella. They will be responsible for routine analytical work (HPLC, GC instrumentation), protocol and report writing, and adapting methods for formulation or packaging changes. They will ensure stability compliance for both new and existing product/formulas. REQUIRED SKILLS AND EXPERIENCE -1-2 years of experience in a lab -BS degree in Chemistry, biochemistry, chemistry related -Experience working in a regulated lab; pharma or CPG -HPLC and/or GC experience -Wet chemistry experience NICE TO HAVE SKILLS AND EXPERIENCE -Experience in CPG (lotions, skincare) -Experience troubleshoot -Experience preparing technical documents -Experience in GMP environment

POSITION SUMMARY: Looking for candidates at Chemist I, II and III levels responsible for carrying out analytical method validation/verification activities and testing for Oral Solids, Oral Liquids, Topicals and Powders. MAJOR DUTIES/RESPONSIBILITIES: • Develop/Validate/Verify analytical (HPLC, GC, ICP-MS/OES, other) methods for assay and impurities determination in drug substances and drug products., • Perform wet chemistry and chromatographic testing for raw materials and products under development phase, • Perform stability studies for drug products in development phase and generate reports, • Develop and validate cleaning methods and generated study protocols and reports, • Prepare relevant protocols, reports, and final methods, • Maintain proper instrument calibration status, • Ensure that work is carried out safely and in compliance with the organization’s quality system, • Ensure that quality documentation is generated and updated to reflect current best practice in a timely manner., • Perform peer review at Chemist III level, not required if you’re applying for Chemist I/II levels., • Perform other duties as assigned. MINIMUM/PREFERRED REQUIREMENTS: Education: Bachelor or Master’s degree in science or Pharmaceutics. Experience: Bachelor’s with 2-7 years of experience in a generic pharmaceutical analytical lab. Master’s is preferred. Candidates shall be considered for different positions based on educational qualification and experience. Good understanding of cGMPs is a must for experienced candidates. PHYSICAL DEMANDS/ENVIRONMENTAL CONDITIONS: • Laboratory and office environment, • Able to lift about 25 pounds., • Able to stand and or sit for longer period of time. On-site, Full-time, Day Shift

POSITION SUMMARY: Analytical Chemist will be engaged in the different laboratory testing using a range of analytical equipment and techniques within GMP laboratory. MAJOR DUTIES/RESPONSIBILITIES: • Perform assigned testing including but not limited to the physical, chemical tests per in-house written procedures and compendial monograph for the raw materials, active pharmaceutical ingredients, in-process, finished and stability products, using various wet chemistry, physical and instrumental techniques such as LC, GC, UV-Vis Spectrophotometer, dissolution, IR, Particle Size Analyzer, KF Auto titrator, Bulk Density, and other routine QC instruments., • Document work clearly and perform tests accurately. Record data and results as specified in documentation procedures., • Maintain proper laboratory logbooks, notebooks and other records all the time. Report and participate in the deviations and investigations. · Perform laboratory related other duties as assigned. MINIMUM/PREFERRED REQUIREMENTS: Education: Bachelor’s Degree in Science/Chemistry Experience: Based on the position level, must require minimum 2-10 years prior experience working in the Quality Control Laboratory in a cGMP environment, preferably in pharmaceutical industry. Hands on Empower-3 experience is plus. QC experience in Generic Pharmaceutical industries would be preferable Knowledge in Good Documentation practices. Knowledge in USP/ FDA BENEFITS: Offers a comprehensive benefits package to employees

BS degree in Chemistry, biochemistry, chemistry related. A client of ours is looking for an analytical stability chemist to join their team in Florham Park, NJ.

BS degree in Chemistry, biochemistry, chemistry related. A client of ours is looking for an analytical stability chemist to join their team in Florham Park, NJ.

EDUCATION AND QUALIFICATIONS: * Bachelor's degree in a life science discipline; Chemistry strongly preferred * Minimum of 3 years of successful sales experience with relevant analytical instruments, including: * Chromatography (GC and HPLC) * Mass Spectrometry (GCMS and LCMS Single Quadrupoles) *

The Principal Scientist is a senior scientific role tasked with working closely with the group Director to define group strategy and to lead a team of scientists in solving complex analytical problems at the interface of biology, chemistry, and lab informatics disciplines to enable development of bi

Title: Expert Science & Technology - Analytical Development. Minimum: BA/BS or MS in biology, chemistry, biochemistry, microbiology or other related science. Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation,

Expert Science & Technology Analytical Development. Minimum: BA/BS or MS in biology, chemistry, biochemistry, microbiology or other related science. Skills Desired Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simul

Our company is seeking an exceptional individual for a technical leadership position within the Supply Analytical Sciences (SAS) - Analytical Chemistry in Development and Supply (ACDS) organization located in the US. Technical Leadership Position In Supply Analytical Sciences. The individual will al

Perform basic chemistry tasks such as pipetting, volumetric measurements, and the utilization of analytical balances. To find out more about EMSL Analytical, Inc. Laboratory Technician II (Chemistry).

Analytical Chemist will be engaged in the different laboratory testing using a range of analytical equipment and techniques within GMP laboratory. Perform assigned testing including but not limited to the physical, chemical tests per in-house written procedures and compendial monograph for the raw m

Other related fields include, but are not limited to: Microbiology, Cell Biology, Genetics, Physiology, Biochemistry, Molecular Biology, Biotechnology, Environmental Science. Chemistry Expert - AI Trainer (Ph.

Application of a wide variety of analytical testing techniques such as, microscopy and spectroscopy techniques including, UV/Vis, FT-IR, Raman, NIR, SEM/EDX, particle sizing and counting, and wet chemistry. Bench" experience in forensics investigational work or analytical chemistry preferred. Microa

Complete analytical testing on in-process and finished product samples.

Is an oncology technology and insights business dedicated to transforming the fight against cancer.Part of, Ontada was founded on the core belief that precise insights - delivered exactly at the point of need - can save more patients' lives.We conn Research Scientist, Oncology, Research, Scientist,

Responsible for specimen accessioning, specimen preparation, computer data entry and reporting, quality assurance surveys, routine laboratory assignments, and any other tasks assigned by the Director.Provides training to staff on accessioning policies/procedures and assists in developing related pol

Postdoctoral Research Associate.Distinguished Professor, Civil & Environmental Engineering.The Center for Natural Resources (CNR) at the New Jersey Institute of Technology (NJIT) position is offered on the Main Campus of NJIT in Newark, 20 minutes from downtown New York City.The s

Complete analytical testing on in-process and finished product samples.

Other related fields include, but are not limited to: Microbiology, Cell Biology, Genetics, Physiology, Biochemistry, Molecular Biology, Biotechnology, Environmental Science.

Aya Healthcare has an immediate opening for the following position: Medical Lab Technician in Newark, NJ.We’ll work with you to build the healthcare career of your dreams.Whether you want a job close to home or across the country, we’ve got you.Requirements: Required Skills: ABO/Rh/Antibody Scre

A client of ours in Florham Park, NJ is looking for a clinical research scientist to join their team.This individual will be responsible for managing clinical and non-clinical studies and assist with inventory management, labeling, returns and tracking shipping of clinical test materials.They will b

Job Title: Laboratory Technician.Location: East Hanover NJ 07936.Work Hours 20-25 hours per week.Seeking a Part-Time Lab Contractor.Research & Development (R&D) team.This role will focus on assisting with various lab tasks, including sample management, shipping, safety compliance, and general lab up

Department: Reporting To: Program Manager.About Cogent Infotech At Cogent Infotech, we believe in creating opportunities that empower individuals and transform organizations.With over 21 years of excellence in consulting and talent solutions, we pride ourselves on building inclusive workplaces and d

Work Schedule: M-F(Normal business hours).Responsible for handling of test samples throughout the sample lifecycle from receipt to disposal.Maintains inventory and support distribution of QC sample and materials to appropriate functional groups as scheduled or requested.Handle test samples and retai

Schedule: 3x8-Hour 23:00 - 07:30.Skills: ABO/Rh/Antibody Screen & ID, AHG Crossmatch, Antibody Typing: Tube Method, Antigen Typing, Blood Banking Procedures, Blood Irradiation, Cold Agglutinins, Cord Blood Evaluation, Crossmatch-Immediate Spin/IgG, Direct Coombs (DAT), Electronic Crossmatch, Indirec

A leading R&D team is seeking a part-time Laboratory Technician to assist with lab operations, shipping coordination, and sample management.This role is essential for maintaining lab efficiency and supporting cross-functional departments including R&D, Marketing, and Sales.Support routine R&D, Marke

Laboratory Technician - Engineering.Faculty is eligible for Tenure Track?.Functions and Responsibilities.Under the supervision of the Chairperson of Mathematics, Engineering Technologies and Computer Sciences Division or designee, the Laboratory Technician is responsible for the maintenance, prepara

Master's degree Polymer Chemistry, Materials Science, Chemistry, or other relevant science discipline with 5 years of experience Required OR. Polymer Chemistry, Materials Science, Chemistry, or other relevant science discipline with 3 years experience Preferred.

To find out more about EMSL Analytical, Inc.

Postdoctoral Fellow - Natural Language Processing (NLP) And Artificial Intelligence (AI).Postdoctoral Fellow - Natural Language Processing (NLP) And Artificial Intelligence (AI) 50% Onsite 50% Remote Responsibilities: Utilizes supervised or unsupervised methods, learning from vast amounts of unlabel

Osmo is a digital olfaction company, on a mission to give computers a sense of smell to improve the health and wellbeing of human life.Why? Our sense of smell both enriches and saves lives, and has a deep and direct connection to our emotions and memory.This foundational understanding of smell's imp

Analytical Chemist will be engaged in the different laboratory testing using a range of analytical equipment and techniques within GMP laboratory. Perform assigned testing including but not limited to the physical, chemical tests per in-house written procedures and compendial monograph for the raw m

I am interested in laboratory operations and analytical methods.

BS degree in Chemistry, biochemistry, chemistry related. A client of ours is looking for an analytical stability chemist to join their team in Florham Park, NJ. This person will be supporting the analytical department through method development, validation/transfer, while managing stability studies

Complete analytical testing on in-process and finished product samples.

Strong analytical background, strategic thinking and problem-solving skills, with the ability to translate complex data into actionable insights and aligning them with business priorities for therapeutic areas to drive impactful results.

Founded in 1998 and headquartered in Farmington Hills, MI, Kyyba has a global presence delivering high-quality resources and top-notch recruiting services, enabling businesses to effectively respond to organizational changes and technological advances.At Kyyba, the overall well-being of our employee

Engineering Lab Technician AO7157972.Top skills: Exposure to measuring instruments and data acquisition tools, general mechanical and electrical knowledge, ability to assemble/craft prototypes using general workshop tools, attention to detail, observation skills Schedule: Fully onsite.Key Responsibi

Post Doctoral Research Associate.Chair, Biological Sciences Biological Sciences.The Fluid Locomotion Laboratory at the New Jersey Institute of Technology, led by Prof.Brooke Flammang, invites applications for a postdoctoral research associate position in the field of underwater attachment mechanics

Seeking a part-time lab contractor to provide essential support to our research & development (R&D) team.This role will focus on assisting with various lab tasks, including sample management, shipping, safety compliance, and general lab upkeep.The ideal candidate will be detail-oriented, possess exc

Postdoctoral Research Associate.Distinguished Professor, Civil & Environmental Engineering.The Center for Natural Resources (CNR) at the New Jersey Institute of Technology (NJIT) has an immediate opening for multiple postdoc positions in the area of modeling water flow in rivers and estuaries as sub

Job Description: 100% Onsite Work Schedule: M-F (Normal Business Hours) Position Summary: Responsible for handling of test samples throughout the sample lifecycle from receipt to disposal.Maintains inventory and support distribution of QC sample and materials to appropriate functional groups as sche

Seeking a Part-Time Lab Contractor to provide essential support to our Research & Development (R&D) team.This role will focus on assisting with various lab tasks, including sample management, shipping, safety compliance, and general lab upkeep.The ideal candidate will be detail-oriented, possess str

Position Summary: Responsible for handling of test samples throughout the sample lifecycle from receipt to disposal.Maintains inventory and supports distribution of QC sample and materials to appropriate functional groups as scheduled or requested.Handle test samples and retains throughout the sampl

High school diploma or equivalent required.Experience in a lab environment.Seeking a Part-Time Lab Contractor to provide essential support to our Research & Development (R&D) team.This role will focus on assisting with various lab tasks and contributing to the success of our projects.

Job Description: This is where the detailed job description goes.It provides an overview of the role and responsibilities expected.Focus on the key tasks and what the company is looking for in a candidate.Remove any redundant headers or mentions of "job details" or "job post".Requirements: List the

Experience with broad range of analytical toolkits, such as SQL, Spark, Scikit-Learn, and XGBoost.

At Real we're always looking for new and ambitious people to help deliver exceptional service levels, change the lives of the candidates we represent and partner with some of the world's best pharmaceutical, biotechnology and medical companies.As specialists in recognising talent we pride ourselves

Our Authentication Centers (warehouses) are where the magic happens! The Art & Science of Real comes to life within our facilities located in New Jersey and Arizona combining the knowledge of hundreds of luxury experts with cutting-edge, proprietary technology.As consigned goods travel into our fac

Purpose And Scope Of Position: The Associate Scientist/Engineer is responsible for leading investigation reports in support of S12 CAR T operations.This includes execution of thorough root cause investigations, interviewing personnel, hypothesis testing and interpretation of results, authoring inves

Onsite Position Summary The Assistant Scientist position will be part of the Biologics Downstream Development department in Summit, NJ that is responsible for early and late stage process development of client's growing biologics pipeline.The candidate will be responsible for developing efficient, r