Astrix jobs in Lakewood, NJ - 29 jobs

Repair/Maintenance & Installation Piscataway, New Jersey, US + Added - 02/12/2025 Apply for Job Pay Rate Low: 35 | Pay Rate High: 40 **High Pressure Boiler Operator** **2nd shift: M-F, 3pm-11pm** **Pay: $35-40/hour** We're seeking a skilled Boiler Operator to manage and maintain high-pressure boilers and related equipment in compliance with safety standards. You'll play a critical role in ensuring consistent steam generation, troubleshooting issues, and supporting operational efficiency. **Key Responsibilities** + **Monitor and Operate** : Oversee high-pressure boilers, adjusting controls to maintain optimal steam and pressure levels. + **Inspect and Maintain** : Conduct routine inspections and preventive maintenance on boiler systems, pumps, compressors, and controls. + **Troubleshoot** : Diagnose and resolve equipment issues promptly to minimize downtime. + **Record Keeping** : Maintain accurate logs of operations, maintenance, and safety checks. + **Collaborate** : Work with engineering and maintenance teams on process improvements. + **Safety Compliance** : Follow all safety, health, and environmental regulations. + **Emergency Support** : Assist with emergency response efforts related to boiler systems as needed. **Qualifications** + High school diploma or equivalent; technical training in boiler operation preferred. + Valid High-Pressure Boiler Operator's License or equivalent certification. + 2+ years of experience in high-pressure boiler operation, preferably in an industrial or biotech setting. + Familiarity with boiler control systems, steam distribution, and safety protocols. + Strong problem-solving skills and attention to detail. + Ability to read technical documents and work independently or with a team. **Working Conditions** + Active, on-your-feet role in an industrial environment. + May involve shift work, including nights and weekends. + Exposure to high temperatures, noise, and hazardous conditions (safety gear provided). Ready to take on a vital role in maintaining our facility's operations? Apply today! This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you! INDBH We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Manufacturing Red Bank, New Jersey, US + Added - 05/02/2025 Apply for Job Our client is an innovative biotechnology company dedicated to unlocking new possibilities in viral gene therapy through genomics-driven discovery. Focused on delivering transformative solutions for individuals with genetic disorders, they are seeking a highly motivated **Sr. Process Development Associate** to join their team. This is an exciting opportunity to contribute to groundbreaking advancements in gene therapy and make a meaningful impact on patients' lives. **Pay Rate:** $45 - $55/hr **Key Responsibilities:** + Design and implement bench-scale operations for downstream purification processes. + Analyze experimental data to generate clear, detailed technical reports that outline process performance and validation results. + Work closely with multidisciplinary teams, including formulation development, manufacturing, and quality assurance, to scale up and ensure compliance with processes. + Assess and interpret process data, presenting key findings on product quality and performance to various teams. + Maintain accurate and thorough records of all activities in an Electronic Laboratory Notebook (ELN). + Assist in drafting and reviewing technical reports, Standard Operating Procedures (SOPs), and other process documentation. + Engage in process transfer activities, ensuring smooth scale-up and process transitions. **Qualifications:** + B.S. or M.S. in Chemical Engineering, Biochemical Engineering, Biochemistry, or related discipline. + 2-6 years of relevant experience in purification process development or a comparable role. + Strong expertise in chromatography systems and control software, particularly Akta and UNICORN. + Experience in performing analytical and characterization assays, along with proficiency in Microsoft Office Suite (Excel, PowerPoint, Word). _This role offers the chance to be at the cutting edge of gene therapy and contribute to life-changing innovations. Apply today to join a passionate team dedicated to making a difference!_ We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Clinical Red Bank, New Jersey, US + Added - 30/01/2025 Apply for Job We are seeking a highly motivated and detail-oriented **Specimen Processor** to join our client's dynamic team in Kennewick, WA! In this role, you will play a key part in specimen collection, processing, and data entry, all while adhering to strict protocols and regulations. If you're passionate about working in a fast-paced laboratory environment and contributing to meaningful work, we want to hear from you! **Pay Rate:** $17-$19/hr **Responsibilities:** + Handle and process specimens for toxicology and medical laboratory testing. + Follow procedures to identify every patient specimen with a two-step ID process. + Troubleshoot and resolve sample or order errors according to established guidelines. + Communicate with other departments to resolve specimen issues. + Operate computer systems to enter patient data, track specimens, and retrieve test results. + Maintain documentation, including patient medical records and quality records, ensuring accuracy. + Assist in ordering laboratory supplies and maintaining appropriate inventory levels. **Requirements:** + High School Diploma or GED. + Must meet CLIA regulations to perform waived testing. + Laboratory experience. We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Science & Research Red Bank, New Jersey, US + Added - 05/02/2025 Apply for Job We are looking for a highly motivated, independent, and creative **Bioinformatics Analyst** to join a dynamic and collaborative team in the field of computational research. An individual in this position will support the analysis of sequencing data from pre-clinical studies with a focus on identifying mechanisms of action and potential biomarkers. **Pay Rate:** $50-$65/hr **Responsibilities:** + Conduct comprehensive analysis of Next-Generation Sequencing (NGS) data, including bulk RNA-seq and single-cell genomic studies. + Serve as an analyst on NGS projects, progressing from data exploration and normalization to differential gene expression and pathway analysis. + Produce insightful data visualizations and present findings to team members in an accessible, compelling format. + Enhance existing code to generate targeted plots and analyses from project data or perform individual study analyses as needed. **Required Skills and Qualifications:** + PhD in bioinformatics, genomics, computational biology, or a closely related field. + Strong computational and statistical analysis skills, with proficiency in Linux-based servers. + Advanced expertise in with high level scripting language like Python or R + Experience handling large datasets, including performing batch effect detection, normalization, and adjusting for confounders and covariates. + Experience with analysis of genomic and/or epigenomic NGS data _If you are passionate about applying computational methods to solve real-world problems in immunology and drug discovery, we encourage you to apply for this exciting opportunity!_ We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Clinical Red Bank, New Jersey, US + Added - 02/06/2025 Apply for Job At Astrix, we're expanding our team to support a diverse range of clients across various industries. We're seeking talented Medical Writers with experience in pharmacovigilance to join us! Our partners range from emerging biotech firms to established pharmaceutical companies. Opportunities are available both remotely and on-site throughout the country! **Responsibilities:** + Prepare and review pharmacovigilance documents including: + Periodic Safety Update Reports (PSURs/PBRERs) + Risk Management Plans (RMPs) + Development Safety Update Reports (DSURs) + Clinical safety narratives + Signal evaluation and benefit-risk assessment reports + Ensure all documents are compliant with regulatory guidelines (ICH, EMA, FDA, etc.), internal SOPs, and quality standards. + Collaborate with cross-functional teams including drug safety, regulatory affairs, clinical development, and biostatistics. + Interpret and synthesize complex clinical and safety data into accurate, concise, and scientifically sound documentation. + Contribute to the development and maintenance of standard operating procedures (SOPs) and templates for pharmacovigilance documents. + Monitor regulatory updates and industry trends to ensure documents remain compliant with changing guidelines. **Qualifications:** + Bachelor's degree in Life Sciences, Pharmacy, Medicine, or a related field; advanced degree (MS, PhD, PharmD, MD) preferred. + Minimum of 3 years of experience in medical writing with a focus on pharmacovigilance or regulatory affairs. + Strong knowledge of drug safety regulations and pharmacovigilance systems. + Proficiency with safety databases, literature databases (e.g., PubMed, Embase), and standard writing tools (e.g., Microsoft Word, Excel). + Excellent written and verbal communication skills with attention to detail. + Ability to manage multiple projects and work independently under tight deadlines.This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!\#INDBH We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Manufacturing Red Bank, New Jersey, US + Added - 20/03/2025 Apply for Job We are looking for an enthusiastic and driven **Manufacturing Associate I** to join our client's innovative team in the biotechnology industry. In this key role, you will be responsible for the formulation of biochemical solutions and play an integral part in the production process. _This is a fantastic opportunity to contribute to cutting-edge work in a fast-paced, dynamic environment, ensuring the creation of high-quality products that make a real impact. If you're passionate about biotechnology and eager to be part of a growing team, we'd love for you to apply and help us drive success!_ **Location:** South San Francisco, CA **Pay Rate:** $25-$35/hr **Key Responsibilities:** + Formulate biochemical solutions at both liter and mL scale + Operate and troubleshoot automation equipment to support manufacturing processes + Adhere to Good Manufacturing Practices (GMP) to maintain product quality and safety + Follow Standard Operating Procedures (SOPs) to ensure consistent and accurate production + Accurately complete manufacturing batch records to document the production process + Utilize ERP systems to track inventory, production schedules, and materials + Perform pipetting tasks with precision and accuracy + Use Microsoft Excel, Word, and Google Sheets for data entry, documentation, and analysis + Conduct PCR (Polymerase Chain Reaction) processes as part of quality control **Qualifications:** + Experience in manufacturing, preferably in a biochemistry or biotechnology setting + Strong understanding of GMP and SOPs + Proficiency with ERP systems and data management tools + Experience with pipetting and biochemical solution formulation + Familiarity with PCR techniques is preferred + Proficient in Microsoft Excel, Word, and Google Sheets **Additional Skills & Attributes:** + Strong attention to detail and organizational skills + Ability to work effectively in a team-oriented environment + Good communication skills and a proactive attitude + Willingness to learn and adapt to new processes and technologies We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Smithers PDS LLC (Pharmaceutical Development Services) brings new drugs to market by providing pre-clinical and clinical services for all phases of drug development. PDS works with customers to develop new methods, validate existing methods, as well as performing the assays necessary to analyze samples from patients on more than 100 clinical trials. PDS is seeking a Lab Support Technician to work in our Ewing, NJ site. This role will perform routine instrument maintenance according to established SOPs, ensure stock for general lab consumables, create and submit orders for projects, and review data. Must be able to work independently as well as in a team setting. Must be able to communicate and coordinate efficiently to meet deadlines. Salary for range for this position is $19.39 - 24.23 per hour. Salary and job title will be commensurate with experience and qualifications. Position is hourly and non-exempt. Smithers PDS offers a comprehensive health insurance package including a choice of 3 medical plans, dental insurance, vision insurance, 401K retirement plan and PTO. Qualifications: High School diploma, 2 plus years' prior relevant experience and at least 12 months laboratory experience preferred. Strong attention to detail. Proficient with basic computer applications such as email, MS Word and Excel. Primary Responsibilities: Reviews laboratory workload and prepares schedules in conjunction with laboratory manager. Independently performs equipment maintenance (daily - annual) as per SOPs. Schedule and coordinate equipment calibration/preventative maintenance to be performed in-house or by vendor technician. Receives and logs in daily shipments and stores appropriately. Obtain quotes, submit requisitions for lab and project supplies. Notifies Project Managers and/or Laboratory Supervisor of quality issues and documents appropriately. Ensures adequate inventory/supplies are stocked for lab use. Prepare wash buffers for equipment maintenance. Maintain glassware. Assign and track storage for critical reagents in refrigerators and freezers according to established system. Ability to function effectively in a team-oriented atmosphere. Works independently when necessary. Documents activities and records observations regarding sample preparation in accordance with GLPs, SOPs, and protocol. Ability to produce high quality data while working under the pressure of strict deadlines. Independently reviews data, performs laboratory QC of equipment logs and identifies potential problems. Recognizes deviations from normal situations and results, resolves problems within area of expertise, and informs supervisor when the problem is outside of their scope, experience, or authority. Responsible for recommending process improvements and/or revising SOPs/Forms. Responsible for training lab personnel. Independently responds to client/QA audits and documents deviations. Additional Position Responsibilities Performs technical procedures such as pipetting as required. Additional Requirements Practices universal safety precautions and wear appropriate personal protective equipment. Ability to produce high quality data while working under the pressure of strict deadlines. Excellent written and oral communication skills. Ability to multi-task and participate in multiple studies concurrently. Overtime, weekend, and holiday work as required. #PharmaJobs #LI - MV1

Science & Research Red Bank, New Jersey, US + Added - 20/03/2025 Apply for Job We are seeking a highly skilled **Organic Chemist** with expertise in **surfactant synthesis** and **molecular biology** to join our team. This position offers a unique opportunity to work on cutting-edge projects within the biotechnology and chemical industries, focusing on the synthesis of surfactants and contributing to various molecular biology applications. If you are passionate about organic chemistry and have a strong background in both synthesis and molecular biology, we would love to hear from you! **Location:** South San Francisco, CA **Pay Rate:** $35-50/hr **Key Responsibilities:** + Synthesize surfactants using organic chemistry techniques, ensuring high purity and yield + Conduct research and development to optimize surfactant synthesis processes + Apply molecular biology techniques to support projects in protein expression, gene cloning, and DNA/RNA manipulation + Collaborate with cross-functional teams to design experiments, analyze data, and solve technical challenges + Maintain accurate and detailed records of all experimental procedures, results, and observations + Stay up-to-date with the latest advancements in organic chemistry, surfactant synthesis, and molecular biology + Assist in troubleshooting and improving lab processes and protocols **Qualifications:** + Bachelor's or Master's degree in Organic Chemistry, Biochemistry, or related field + Proven experience in surfactant synthesis and organic synthesis techniques + Strong background in molecular biology, including PCR, cloning, protein expression, and genetic manipulation + Excellent laboratory skills and the ability to work independently and collaboratively + Ability to design and execute experiments, analyze results, and communicate findings effectively + Strong problem-solving and critical-thinking abilities + Proficiency in using laboratory equipment, software tools, and data analysis **Preferred Skills:** + Experience with bioconjugation techniques and surfactant-based formulations + Familiarity with advanced molecular biology techniques (e.g., CRISPR, RNAi, etc.) + Strong communication skills and a proactive, team-oriented attitude We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Repair/Maintenance & Installation Middlesex County, New Jersey, US + Added - 22/01/2026 Apply for Job Pay Rate Low: 30.00 | Pay Rate High: 38.00 The Industrial Maintenance Mechanic is responsible for maintaining and repairing facility equipment, handling both electrical and mechanical projects, and ensuring regular preventive maintenance is completed. **Type:** Direct Hire **Location:** Middlesex County, NJ **Pay:** $30 - $38/HR DOE **Shift Information:** + 3rd Shift: Monday - Friday, 11:00 PM - 7:30 AM with required training on 1 st (7:00 AM - 3:30 PM) **Key Responsibilities** + Diagnose, repair, and maintain manufacturing and production equipment. + Perform preventive maintenance on motors, conveyors, pneumatic and hydraulic systems, and other machinery. + Install and calibrate new injection molding or similar plastic molding equipment. + Use hand and power tools to complete repairs and ensure equipment reliability. + Identify and correct safety hazards to maintain a safe work environment. + Manage maintenance resources efficiently and complete additional tasks as needed. **Qualifications** + High School Diploma/GED + 2+ years of experience as an industrial mechanic (preferred). + Working knowledge of pneumatics, hydraulics, and mechanical schematics. + Strong troubleshooting, communication, and teamwork skills. + Able to lift up to 50 lbs and work overtime or weekends as required. _This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!_ _INDBH_ We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Clinical Red Bank, New Jersey, US + Added - 06/02/2025 Apply for Job Astrix has been partnered with the Life Sciences industries for over 28 years and we deliver top talent to companies focused in: Pharmaceutical, Biotechnology, Diagnostics, Medical Devices, Food & Beverage, Nutraceutical, and more. If you're a top tier candidate seeking new opportunities, we highly encourage you to apply to this job posting. Types of positions that our team is regularly supporting: + Clinical Research Associates/Clinical Research Coordinators + Clinical Trial Managers + Clinical Project Manager + Site Start Up Specialists + Clinical Data Manager + Clinical Development Associates + SAS Programmer + and more! We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Laboratory Middlesex County, New Jersey, US + Added - 22/01/2026 Apply for Job Pay Rate Low: 22.00 | Pay Rate High: 22.00 Our Client, a global leader in personal care and household products, is seeking a Lab Technician to join their growing team. This is a great opportunity to work with one of the world's fastest growing consumer packaged goods companies. **Type:** Contract **Pay:** $22/hr **Responsibilities:** + Prepare consumer product formulations, measure pH, specific gravity and viscosity, perform stability tests, product performance evaluation, fragrance evaluation by test panels, record keeping and housekeeping. + Conduct all applicable testing relating to product care in the product group. **Requirements:** + BS in Chemistry or Biochemistry + Hands on laboratory experience preferred (can be from school) + Preference is for experience with wet chemistry (pH, viscosity, titrations, etc.) + Must be comfortable lifting up to 40 lbs + Must be able to work in a fast paced, high priority environment + Must have strong work ethic and attention to detail _This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!_ INDBH We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Supply Chain & Logistics Rahway, , NONE + Added - 23/01/2026 Apply for Job A great medical equipment manufacturing company in Union County, NJ, is looking for an Account Manager, who plays a key role in delivering exceptional service to clients, optimizing workflows, and managing top accounts. **Location:** Union County, NJ **Type:** Direct Hire **Pay:** $25-$30/hr (Direct Hire) **Hours:** Monday - Friday, 8:00 AM - 5:00 PM **Summary:** The Account Representative is responsible for providing high-quality service to internal and external customers, leveraging deep product knowledge and effective communication with team members across the organization. This role is highly transactional and includes quoting, order processing, and responding to inbound customer inquiries. **Key Responsibilities:** + Produce and deliver accurate customer quotations and proposals. + Process customer orders, ensuring pricing, drawings, shipping, and order details are correct. + Communicate with customers regarding discrepancies or questions. + Collaborate with Master Scheduling and other departments to ensure orders move efficiently. + Attend daily production meetings and follow up on order status. + Solve problems independently using company resources, documentation, and prior knowledge. + Perform other duties as assigned, including temporary receptionist support when needed. **Qualifications:** + High school diploma required; BA preferred. + Minimum 3 years customer service experience in a manufacturing or B2B environment. + Strong organizational, verbal, and written communication skills. + Proficiency in Microsoft Excel, Word, and Outlook. + Ability to work independently and collaboratively across teams. + Professional appearance and demeanor; attention to detail. + Bilingual Spanish skills are a plus but not required.INDBH\#LI-CS1 We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Engineering Red Bank, New Jersey, US + Added - 06/02/2025 Apply for Job Astrix has been partnered with the Life Sciences industries for over 28 years and we deliver top talent to companies focused in: Pharmaceutical, Biotechnology, Diagnostics, Medical Devices, Food & Beverage, Nutraceutical, and more. If you're a top tier candidate seeking new opportunities, we highly encourage you to apply to this job posting. Types of positions that our team is regularly supporting: + Process Engineer + Chemical Engineer + Manufacturing Engineer + MS&T Engineer + Electrical Engineer + Mechanical Engineer + Field Service Engineer + Environmental Engineer + R&D Engineer + Quality Engineer + and more! We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Repair/Maintenance & Installation Piscataway, New Jersey, US + Added - 22/01/2026 Apply for Job Pay Rate Low: 70000 | Pay Rate High: 83000 Join our client's team as a Senior HVAC Operator supporting critical facility systems in a GMP-regulated biotech environment. In this role, you will operate, monitor, and maintain HVAC and BMS systems to ensure precise climate control and building performance. You'll troubleshoot and repair chillers, air handlers, ventilation systems, and other HVAC components while also performing routine inspections and preventive maintenance on process equipment such as bioreactors and fermenters. **Type:** Direct Hire **Location:** Middlesex County, NJ **Pay:** $70,000 - $83,000 **Key Responsibilities:** + Operate, monitor, and maintain HVAC and BMS systems to ensure optimal climate control and building performance. + Troubleshoot, diagnose, and repair HVAC components, including chillers, air handling units, and ventilation systems. + Perform routine inspections and preventive maintenance on process equipment such as bioreactors, fermenters, and support systems. + Maintain and update records of maintenance activities, system performance logs, and operational procedures. + Collaborate with the facilities and engineering teams to implement upgrades and improvements to HVAC, BMS, and process equipment. + Support validation and qualification efforts of new and existing equipment in compliance with GMP and regulatory requirements. + Respond to equipment alarms and emergencies, providing timely and effective solutions to maintain uninterrupted operations. + Ensure compliance with safety standards and participate in safety training and protocols. + Provide technical guidance and training to junior technicians and operators as needed. **Qualifications:** + High school diploma or equivalent; technical degree or certification in HVAC, mechanical systems, or a related field preferred. + Minimum 5 years of experience working with HVAC, BMS, and process equipment in a biotech or pharmaceutical environment. + Proficiency in operating and troubleshooting Building Management Systems + Strong understanding of HVAC principles, process equipment operations, and related mechanical systems. + Knowledge of GMP, FDA, and other regulatory standards relevant to biotech facilities. + Strong analytical and problem-solving skills. + Excellent communication and teamwork abilities. + Ability to work flexible hours, including nights and weekends, as needed. _This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!_ INDBH We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Manufacturing & Utilities Middlesex County, New Jersey, US + Added - 27/01/2026 Apply for Job Pay Rate Low: 33.00 | Pay Rate High: 40.00 Opportunity for an experienced Water System Operator to continue their career with our client who has a global footprint in both R&D and manufacturing within the biopharma industry. The Water Systems Operator will be responsible for the operation, monitoring, and maintenance of purified water (PW) and Water for Injection (WFI) systems within a GMP-regulated biotechnology or biopharmaceutical manufacturing facility. This role ensures all water and clean steam systems operate reliably, efficiently, and in full regulatory compliance to support continuous manufacturing operations. The ideal candidate will have strong technical skills, mechanical aptitude, and attention to detail in maintaining high-purity utility systems. **Location:** Middlesex County, NJ **Shifts:** 1st, 2nd, & 3rd shift options available - must have flexibility to rotate weekends Key Responsibilities + Operate, monitor, and maintain WFI, purified water, and clean steam systems, ensuring consistent quality and availability for manufacturing operations. + Perform routine sampling, testing, and data logging of water systems in compliance with GMP and USP requirements. + Conduct preventive and corrective maintenance on water system components, including RO units, EDI systems, heat exchangers, pumps, valves, filters, and distribution loops. + Monitor system performance trends, respond to alarms or deviations, and take corrective actions to prevent downtime. + Support validation, calibration, and change control activities related to water and utility systems. + Maintain accurate, compliant documentation in accordance with SOPs, GMP, and FDA regulations. + Collaborate cross-functionally with Facilities, Engineering, and Quality teams to investigate issues and implement improvements. + Participate in on-call rotations and weekend coverage to support 24/7 facility operations. Qualifications + Minimum Education: High School Diploma or equivalent required. + Experience: Minimum 2 years operating or maintaining WFI, purified water, or clean utility systems in a GMP-regulated biotech, biopharma, or pharmaceutical environment. + Strong understanding of water generation and distribution principles, including reverse osmosis (RO), electrodeionization (EDI), and distillation. + Working knowledge of GMP, USP, and FDA requirements governing clean utilities. + Ability to read and interpret P&IDs, system schematics, and technical manuals. + Strong mechanical aptitude, attention to detail, and proactive problem-solving skills. + Excellent communication and teamwork abilities. + Shift flexibility required - ability to work rotating weekends and participate in after-hours support as needed. This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you! \#LI-KR1 INDBH We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Science & Research Monroe Township, New Jersey, US + Added - 21/01/2026 Apply for Job Pay Rate Low: 38 | Pay Rate High: 45 We are seeking an Analytical Scientist to join a reputable pharmaceutical manufacturing company to conduct routine and non-routine analyses of in-process materials, raw materials, environmental samples, finished goods, or stability samples. _** No Relocation, No C2C Candidates**_ **Pay:** Up to $45/hour. **RESPONSIBILITIES:** + Conduct and document chemical analyses for raw materials, in-process goods, and finished products. + Design, validate, and resolve issues with analytical methods, including HPLC for cleaning verification. + Collect and analyze equipment cleaning validation samples. + Prepare Certificates of Analysis, analytical reports, and maintain lab documentation. + Peer-review records and support OOS or OOT investigations as per SOPs. + Ensure compliance with SOPs, cGMPs, and regulatory requirements. + Assist with environmental monitoring and other tasks as assigned. **QUALIFICATIONS:** + 2 years hands-on method development experience (HPLC) + Knowledge of cGMPs, pharmacopeia (USP, EP), and regulatory standards (21 CFR Part 210/211/820, ISO). + Bachelor's in Chemistry-related discipline with 2+ years of analytical lab experience. This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you! INDBH We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Engineering Princeton, New Jersey, US + Added - 26/02/2025 Apply for Job Our Client, a global leader in personal care and household products, is seeking a Process Engineer to join their growing team. This is a great opportunity to work with one of the world's fastest growing consumer packaged goods companies. **Key Responsibilities** + Lead process development, including pilot plant design, operation, and data analysis. + Support projects by writing process trial documentation and reports. + Work cross functionally with R&D to develop and improve products + Conduct feasibility studies of product/process + Participate in process validation and cGMP implementation. + Test process changes, troubleshoot issues, and offer plant support. **Education & Experience** + B.S. or M.S. in Chemical, Materials, or similar + 2+ years of relevant experience. Pay: $38-42/hr This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you! We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Manufacturing & Utilities Middlesex County, New Jersey, US + Added - 13/01/2026 Apply for Job Pay Rate Low: 33.00 | Pay Rate High: 40.00 Our client is a cutting-edge biopharmaceutical organization advancing the boundaries of complex drug development, this firm specializes in creating high-quality, affordable therapeutic solutions is seeking a Facilities Technician to join their growing team! The Facilities Technician will be responsible for maintaining and supporting facility and equipment operations within a GMP biotechnology manufacturing environment. Located in Middlesex County, NJ All shifts are available **Contract to hire** **Pay:** $33-40/hour **Key Responsibilities** + Perform routine and emergency maintenance on facility systems, including **HVAC, boilers, chillers, air compressors, and cold storage units** (freezers, refrigerators, incubators). + Monitor and maintain **building utilities** and **environmental control systems** to support GMP production areas. + Conduct **preventive maintenance** and calibration checks on **bioreactors, shakers, centrifuges, pumps, and supporting lab or process equipment** . + Troubleshoot equipment and system issues to minimize downtime and ensure uninterrupted operations. + Support installation, qualification, and commissioning of new or upgraded equipment and utilities. + Maintain accurate and timely documentation in accordance with **GMP, SOPs, and company policies** . + Collaborate with Manufacturing, Quality, and Engineering to ensure compliance and equipment readiness. + Participate in after-hours or weekend on-call rotations as needed to support 24/7 facility operations. **Qualifications** + **Minimum High School Diploma required.** + **Minimum 2+ years of relevant experience** in facilities or equipment maintenance within a **GMP-regulated biotech, biopharma, or pharmaceutical** environment. + Hands-on experience with **HVAC systems, chillers, boilers, and cold storage** equipment. + Strong working knowledge of **bioreactors, shakers, and related laboratory/process systems** . + Familiarity with **GMP documentation, calibration, and validation principles** . + Ability to read and interpret technical drawings, P&IDs, and equipment manuals. + Excellent troubleshooting, communication, and teamwork skills. **"This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!"** **\#INDBH** \#LI-DNP We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Manufacturing Rahway, New Jersey, NONE + Added - 25/01/2026 Apply for Job Pay Rate Low: 30 | Pay Rate High: 37 **A precision manufacturer with 50 years of expertise in life-changing medical components is seeking skilled Precision CNC Machinists to join their growing team. All shifts available!** **Schedule/Pay/Experience:** + 1 st shift : 7a-3p, 30-34 + 2 nd shift: 3p-11p, 30-34 + 3 rd shift: 11p-7a, 34-37 **Location** : Rahway, New Jersey **Why join our team?** + Competitive pay! + Extensive benefits package (Health, Dental, Vision, Life, Short-Term Disability, Accident & Critical Care) + PTO, paid holidays, and 401(k) with match **Responsibilities:** + Programming, setup, and operation of machines + Read and interpret complex part drawings. Turn drawings into functional parts. **Requirements:** + High school diploma or equivalent + 4+ years of experience operating CNC machines specifically with centerless grinding OR tight tolerances + Must have experience setting up, operating, and adjusting machines + Desire to learn and grow + Great attention to detail **_We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!_** INDBH \#LI-DNP We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.