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Floater Phlebotomist - East NJ. We are seeking a skilled and experienced Floater Phlebotomist to join our team in East New Jersey.

Job Title: Oncology Registered Nurse. We are seeking a dedicated Oncology Registered Nurse to administer a range of treatments including chemotherapy, biotherapy, antibiotics, and injections, while managing symptoms and educating patients. Proficiency in oncology nursing and infusion therapies.

Proficiency in x-ray technology. Licensed by the State of New Jersey Department of Environmental Protection Bureau of X-ray Compliance. Registered by the American Registry of Radiologic Technologists (ARRT).

Job Description Job Title: Entry Level Cell & Gene Therapy Associate Book a time to connect here: The Cell & Gene Therapy Associate will assist in clean room qualifications, manage supplies and materials for clean room operations, and perform aseptic gowning to enter and work in clean room environments. The role involves processing cells and samples, including cultures, cryopreservation, and manipulation of cell products using aseptic techniques. Previous experience in GMP practices and adherence to SOPs is essential. This position will be based in clinical manufacturing labs. Responsibilities • Assist in clean room qualification by helping to burden clean rooms for testing., • Run supplies and materials as needed for clean room operation and processing., • Aseptically gown to enter clean room and assist with qualifications., • Work within manufacturing to process cells and samples., • Process cultures, cryopreserve, and manipulate cell products using aseptic techniques., • Perform any processing and testing required to produce and assess safe and efficacious products., • Experience in a biology lab, either academic or industry., • Proficiency in aseptic techniques., • Familiarity with GMP practices., • Ability to work in a fast-paced environment., • Associates or Bachelor's degree in biology or related scientific field is a plus., • Experience in cell-based biology lab environments., • Ability to work flexibly on shifts, including weekends. The role is based in a clinical manufacturing lab, reporting to Operations Managers and part of a large team of operators. Training will be provided extensively in aseptic gowning for clean room work. Initial training occurs Monday to Friday from 8am to 4pm for the first 2-3 months. Flexibility is required for shifts, which may include working Saturdays and Sundays, with potential shift times extending as late as 2:30am. The work schedule includes four ten-hour shifts once permanent, specifically Thursday-Friday and Sunday-Monday. Job Type & Location This is a Permanent position based out of Allendale, NJ. Pay and Benefits The pay range for this position is $29.78 - $29.78/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job DescriptionJob Title: Quality Control Technician – Color Evaluation Lab Job Description The Quality Control Technician works in a textile color evaluation laboratory, assessing production samples to ensure they meet pre-approved color standards. This role focuses on visually evaluating color, establishing and applying color tolerances, and making clear pass/fail decisions that directly impact production quality. The technician collaborates closely with other lab staff and quality control teams to maintain consistent, high-quality color standards across all production lots. Responsibilities • Receive and gather production samples for color evaluation in the lab., • Conduct visual assessments of textile colors to determine whether products meet pre-approved color standards., • Establish and apply appropriate color tolerances when evaluating production lots., • Make clear pass/fail decisions on production lots based on color quality and adherence to standards., • Articulate and communicate color decisions, including the reasons for pass or fail outcomes, to relevant stakeholders., • Maintain accurate records of evaluations and decisions, ensuring thorough documentation of color assessments., • Input comments, evaluation data, and decisions into Microsoft Excel spreadsheets with attention to detail., • Work alongside the quality control laboratory team using a benchtop spectrophotometer to ensure QC requirements are achieved., • Collaborate and communicate effectively with other lab technicians and quality control inspectors to support consistent quality standards., • Perform inspection and quality control activities related to color, samples, and laboratory procedures as needed.Essential Skills, • Strong color acuity and the ability to accurately distinguish subtle color differences., • Ability to pass the Farnsworth-Munsell 100 Hue Test with a Superior rating (score less than 16)., • Comfort working in a laboratory environment, including handling samples and lab equipment., • Basic proficiency in Microsoft Excel for data entry and recordkeeping., • Superior written and verbal communication skills for explaining color decisions and documenting results., • Experience or familiarity with quality control and inspection processes., • Ability to work collaboratively with lab technicians and quality control inspectors.Additional Skills & Qualifications, • Experience with laboratory work in textiles, color, chemistry, or a related field., • Familiarity with benchtop spectrophotometers and color measurement equipment., • Background in quality control, inspections, or laboratory sample evaluation., • Experience entering and managing data in Excel and maintaining organized records., • Strong interpersonal and people skills to support a collaborative, community-focused environment.Work Environment This role is based in a textile color evaluation laboratory that focuses on color quality for production lots. The work is performed on a first-shift schedule, typically from 7:00 a.m. to 3:30 p.m. The environment is lab-based, requiring comfort around laboratory equipment, samples, and quality control instruments such as a benchtop spectrophotometer. The workplace culture is described as very friendly and kind, promoting a strong sense of community and collaboration. The organization operates in a highly specialized niche within the color and textiles industry and offers opportunities to grow into other roles over time. Dress is appropriate for a professional lab setting, with an emphasis on safety and practicality. Job Type & Location This is a Contract to Hire position based out of Carlstadt, NJ. Pay and Benefits The pay range for this position is $20.00 - $23.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Description Job Title: R&D Formulation Scientist – Capsules, Tablets, and Powders Job Description The R&D Formulation Scientist – Capsules develops and optimizes formulations for nutraceutical products across multiple dosage forms, including capsules, oils, waters, soft gels, powders, and granulations. This role partners closely with Sales, Customers, Sourcing, and Purchasing to translate product requirements into robust, scalable formulations while ensuring material availability and cost efficiency. The scientist performs hands-on work in the product development laboratory, utilizes advanced analytical instrumentation, and troubleshoots technical issues to support high-quality, sustainable products that promote health and wellness. This position offers significant growth potential as the R&D function expands and provides opportunities to move into leadership and people management over time. Responsibilities • Partner closely with Sales and Customers to understand product requirements and technical needs and translate them into effective formulation strategies., • Develop and optimize formulations for oils, waters, soft gels, two-piece capsules, powders, and granulations within the nutraceutical and dietary supplement space., • Apply expertise in powder, liquid, and capsule formulations to create stable, manufacturable, and high-quality products., • Collaborate with Sourcing and Purchasing teams to ensure timely material availability, cost efficiency, and appropriate raw material selection., • Troubleshoot technical formulation issues, identify root causes, and implement effective, data-driven solutions., • Assist with analytical testing and quality assessments to ensure products meet specifications and regulatory and internal quality standards., • Perform hands-on experimental work in the Product Development laboratory, including batching, blending, encapsulation, and related lab-scale processes., • Utilize analytical instrumentation such as gas chromatography (GC), high-performance liquid chromatography (HPLC), and inductively coupled plasma mass spectrometry (ICP-MS) to support formulation development and analytical chemistry needs., • Support quality control activities by evaluating raw materials, intermediates, and finished products, including those involving fish oils and other nutraceutical ingredients., • Evaluate laboratory capabilities, identify opportunities for future R&D expansion, and recommend new technologies, methods, or equipment to enhance innovation., • Contribute to new product development projects from concept through commercialization, including experimental design, data analysis, and documentation., • Collaborate effectively with a predominantly Spanish-speaking laboratory team, using translation tools as needed to maintain clear communication and teamwork., • Maintain accurate records of experiments, methods, and results in accordance with internal procedures and good laboratory practices., • Work cross-functionally with Quality, Manufacturing, and other internal stakeholders to ensure formulations are scalable and suitable for production., • Bachelor’s degree in Food Science, Chemistry, or a related field., • 3+ years of R&D formulation experience, preferably in nutraceuticals or dietary supplements., • Proven expertise in formulation of powders, liquids, and capsules., • Bilingual skills, particularly Spanish, are a plus but not required., • Interest in purpose-driven work focused on high-quality, ethically sourced, and sustainable products. 401K, holiday, vacation and sick time offered to internal employees. Will have potential to grow into a leadership role - the R&D department is new and there will be room to expand to R&D formulators that report to them. Workplace Type This is a fully onsite position in Clifton,NJ. Application Deadline This position is anticipated to close on Apr 24, 2026. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through: • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Description Job Title: Civil Engineer Job Description This Civil Engineer role focuses on managing and delivering a wide range of land development and infrastructure projects, from small-scale to large-scale, in a safe, timely, and sustainable manner. You will work on predominantly mixed-use residential and urban projects, using modern design tools and collaborating closely with internal teams and external stakeholders. The position offers strong professional growth, a supportive team environment, and a stable organization with excellent benefits and work-life balance. Responsibilities • Manage, design, develop, and maintain construction and land development projects from concept through completion, ensuring safe, timely, and sustainable delivery., • Conduct on-site investigations and gather field data, including reviewing maps, reports, tests, drawings, and other technical documentation., • Perform technical and feasibility studies and prepare design plans and blueprints that meet all relevant technical specifications and regulatory requirements., • Assess potential project risks, materials, and costs, and incorporate these considerations into design and planning decisions., • Provide engineering advice and creatively resolve emerging problems or deficiencies during design and construction., • Oversee and mentor junior staff, supporting their professional development and ensuring high-quality work output., • Liaise with a variety of stakeholders, including clients, consultants, and regulatory agencies, to coordinate approvals and project progress., • Prepare and hand over completed structures, systems, and services for operational use, ensuring all requirements are met., • Monitor project progress, track milestones, and compile clear and timely project status reports., • Manage project budgets, including estimating costs and overseeing the purchase of equipment and materials., • Ensure full compliance with applicable guidelines, permits, safety regulations, and industry standards., • 1–4 years of proven working experience in civil engineering., • Bachelor’s or Master’s degree in Civil Engineering., • Civil Engineering background with a strong foundation in land development and infrastructure design., • Excellent knowledge of design and visualization software such as AutoCAD and Civil 3D or similar tools., • Hands-on experience with AutoCAD for revising, updating, and refining engineering designs., • Experience with stormwater design, including tools such as Civil 3D and HydroCAD, or similar stormwater modeling software., • Proficiency in site layout and site design, including grading, drainage, and utility design., • Experience with erosion control design and preparation of related plans and details., • Familiarity with obtaining and coordinating regulatory approvals for civil engineering projects., • Project management skills, including planning, organizing, and tracking project tasks and deliverables., • Supervision skills to guide and mentor junior team members effectively., • Strong communication and interpersonal skills to collaborate with team members and external stakeholders., • Professional Engineer (PE) license is a plus., • Experience with Revit and AutoCAD Civil 3D for multidisciplinary coordination and advanced civil design., • Experience specifically in stormwater design and modeling using tools such as HydroCAD or equivalent., • background in mixed-use residential projects, particularly in urban environments., • Familiarity with project work in dense urban areas similar to Newark, Jersey City, and Paterson., • Strong problem-solving abilities with a creative approach to design challenges and field issues. You will work in a newly built office space located in a remodeled former bank building with abundant natural light and a modern layout. The team is composed of a energetic staff with an average age of around 26, fostering a collaborative and dynamic culture. The project portfolio consists primarily of mixed-use residential developments, with a significant portion of work focused on urban projects in cities such as Newark, Jersey City, and Paterson. After the first month, you may work from home two days per week and will receive your own computer and VPN access to support remote work. The organization emphasizes stability and employee retention, with a long history of no layoffs and strong benefits, including substantial insurance coverage, a 4% 401(k) match, paid time off, and paid major holidays, as well as regular social events that support team cohesion and a positive work atmosphere. Job Type & Location This is a Permanent position based out of Montclair, NJ. Pay and Benefits The pay range for this position is $60000.00 - $80000.00/yr. 401k, hybrid, medical, dental, and vision covered Workplace Type This is a hybrid position in Montclair,NJ. Application Deadline This position is anticipated to close on Apr 23, 2026. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through: • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Description Job Title: QC Microbiology Analyst Job Description As a QC Microbiology Analyst, you will be responsible for environmental monitoring in a clean room or GMP environment. This role involves micro sampling, personnel sampling, surface plating, and equipment monitoring. You will work extensively with the MODA database and receive comprehensive EM training. Additionally, you will analyze and read plates after incubation and conduct testing for active air viables, passive air viables, and surface viables. Responsibilities • Perform environmental monitoring within clean room or GMP environment., • Conduct micro sampling, personnel sampling, and surface plating., • Work with the MODA database for data management and reporting., • Receive and apply extensive EM training., • Monitor and maintain equipment., • Analyze and interpret microbiological plates after incubation., • 1+ year of environmental monitoring experience., • Experience working in an aseptic or GMP environment., • 1-3 years of experience with sampling, personnel monitoring, and surface plating., • Proficiency in aseptic techniques and basic microbiology knowledge., • Bachelor's degree in a related scientific field., • Knowledge of microbiology techniques., • Gowning certification., • Experience with cleaning, incubation, and sub-culturing., • This role requires working in a clean room aseptic environment., • The position is available on the 2nd shift with the following schedules: Sunday to Wednesday from 3:30am to 2:00pm, and Wednesday to Saturday from 3:30pm to 2:00am., • Initial training will be conducted on the first shift from Monday to Friday, 8:00am to 4:30pm, for 4-6 weeks. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Description Description Summary of Position: The Senior Manager in Statistics responsible for perform statistical activities in clinical trials from protocol development to final study report and statistical activities in drug in-licensing, regulatory filings and marketing. Duties and Responsibilities: • Review protocol, understand study requirements, prepare statistical sections, design study elements including sample size calculation, analysis methods, study duration, etc., • Review CRF, database design, and edit check specs, • Review study quality surveillance plan and monitor study conduct, • Prepare and/or review SAP, TFL shells and specifications for variable derivation, • Work closely with Statistical Programmers and Clinical Data Manager in identify data quality issues for key efficacy and safety variables, • Provide statistical and validation support for statistical analysis, analysis datasets and TFL, • Review study report, manuscripts and other documents related to statistics, • Work on responses to health authorities and execute new analysis required for responses, review statistical inputs for regulatory documents, • Perform other ad-hoc statistical activities as needed, • Works effectively with cross functional groups, study team, and vendors. Proactively control and monitor timelines related to statistics and statistical programming, • Participates in monitoring CRO activities and reviewing CRO deliverables, • Other duties as assigned Supervision Exercised: N/A Qualifications: Education Preferred: • Ph.D or MS in Statistics or Biostatistics Work Experience: • Minimum of 4 years (Ph. D) or 6 years (MS) Pharmaceutical/CRO industry experience, • Excellent knowledge of SAS computer package, • Excellent knowledge of industry standards, such as the ICH guidelines, CDISC data structures and FDA guidelines, • Excellent organizational skills, time management, and ability to meet established deadlines., • Excellent communication and interpersonal skills to effectively interface with others, • Exceptional interpersonal skills and problem-solving capabilities, • Ability to work independently and collaboratively, • Ability to provide leadership for the CRO statisticians and statistical programmers Physical and Mental Requirements: • Ability to multitask, • Adapts to change, • Maintain composure under pressure, • Ability to follow verbal or written instructions and use of effective verbal communications, • Adapts change, adjust change and grasps information quickly, • Examine and observe details Skills Audit, Gcp, cro audit, tmf, edc Top Skills Details Audit,Gcp,cro audit,tmf,edc Additional Skills & Qualifications Please ensure that candidates meet all requirement below prior to submitting them! • Ph.D or MS in Statistics or Biostatistics, • Minimum of 4 years (Ph. D) or 6 years (MS) Pharmaceutical/CRO industry experience, • Excellent knowledge of SAS computer package, • Excellent knowledge of industry standards, such as the ICH guidelines, CDISC data structures and FDA guidelines, • Excellent organizational skills, time management, and ability to meet established deadlines, • Excellent communication and interpersonal skills to effectively interface with others, • Ability to work independently and problem-solve, • Ability to provide leadership for the CRO statisticians and statistical programmers Experience Level Intermediate Level Job Type & Location This is a Contract position based out of Paramus, NJ. Pay and Benefits The pay range for this position is $87.00 - $93.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Description Description Summary of Position: The Senior Manager in Statistics responsible for perform statistical activities in clinical trials from protocol development to final study report and statistical activities in drug in-licensing, regulatory filings and marketing. Duties and Responsibilities: • Review protocol, understand study requirements, prepare statistical sections, design study elements including sample size calculation, analysis methods, study duration, etc., • Review CRF, database design, and edit check specs, • Review study quality surveillance plan and monitor study conduct, • Prepare and/or review SAP, TFL shells and specifications for variable derivation, • Work closely with Statistical Programmers and Clinical Data Manager in identify data quality issues for key efficacy and safety variables, • Provide statistical and validation support for statistical analysis, analysis datasets and TFL, • Review study report, manuscripts and other documents related to statistics, • Work on responses to health authorities and execute new analysis required for responses, review statistical inputs for regulatory documents, • Perform other ad-hoc statistical activities as needed, • Works effectively with cross functional groups, study team, and vendors. Proactively control and monitor timelines related to statistics and statistical programming, • Participates in monitoring CRO activities and reviewing CRO deliverables, • Other duties as assigned Work Experience: • Minimum of 4 years (Ph. D) or 6 years (MS) Pharmaceutical/CRO industry experience, • Excellent knowledge of SAS computer package, • Excellent knowledge of industry standards, such as the ICH guidelines, CDISC data structures and FDA guidelines, • Excellent organizational skills, time management, and ability to meet established deadlines., • Excellent communication and interpersonal skills to effectively interface with others, • Exceptional interpersonal skills and problem-solving capabilities, • Ability to work independently and collaboratively, • Ability to provide leadership for the CRO statisticians and statistical programmers Physical and Mental Requirements: • Ability to multitask, • Adapts to change, • Maintain composure under pressure, • Ability to follow verbal or written instructions and use of effective verbal communications, • Adapts change, adjust change and grasps information quickly, • Examine and observe details Additional Skills & Qualifications • Ph.D or MS in Statistics or Biostatistics, • Minimum of 4 years (Ph. D) or 6 years (MS) Pharmaceutical/CRO industry experience, • Excellent knowledge of SAS computer package, • Excellent knowledge of industry standards, such as the ICH guidelines, CDISC data structures and FDA guidelines, • Excellent organizational skills, time management, and ability to meet established deadlines, • Excellent communication and interpersonal skills to effectively interface with others, • Ability to work independently and problem-solve Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Description Job Title: Aseptic Technician - 3rd Shift Job Description We are seeking an attentive and dedicated Aseptic Technician to join our team. The role involves washing glassware and medical components, performing aseptic cleaning and packaging of products, and maintaining aseptic samples in an ISO-6 & 7 cleanroom environment. You will be responsible for ensuring adherence to GMP standards while executing tasks with precision and accuracy. Responsibilities • Wash glassware and medical components using designated equipment., • Work in an ISO-6 & 7 cleanroom environment while wearing required PPE., • Perform aseptic cleaning and packaging of products., • Maintain aseptic samples and ensure GMP compliance., • Monitor process systems and equipment for proper operation., • Perform daily and weekly preventative maintenance tasks; assist maintenance team as needed., • Participate in safety committees and adhere to all safety rules and regulations., • Accurately complete required documentation for all tasks., • Clean, sanitize, and disinfect workstations before and after use., • Perform additional tasks as assigned by supervisor., • Aseptic technique and sterilization expertise., • Experience in laboratory and cleanroom environments., • Industry experience of 1-2 years in pharmaceutical, CGMP, and sterile processing., • Good documentation practices and understanding of GMP., • Punctuality, flexibility, and a strong work ethic. The role requires working in ISO level 6 & 7 cleanrooms, with gowning for 6-10 hours at a time, including breaks. The position is scheduled for the 2nd shift, Monday through Friday, from 2 PM to 10:30 PM. Our team is growing with new expansions, offering potential for career growth and a dynamic work environment. Job Type & Location This is a Contract to Hire position based out of Fairfield, NJ. Pay and Benefits The pay range for this position is $23.00 - $24.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Description Job Title: R&D Formulation Scientist – Tablets, and Powders (Nutraceutical) Top Must Have: Need to come from the Nutraceutical industry, working with vitamins and dietary supplements! Job Description The R&D Formulation Scientist – develops and optimizes formulations for nutraceutical products across multiple dosage forms, including, oils, waters, soft gels, powders, and granulations. This role partners closely with Sales, Customers, Sourcing, and Purchasing to translate product requirements into robust, scalable formulations while ensuring material availability and cost efficiency. The scientist performs hands-on work in the product development laboratory, utilizes advanced analytical instrumentation, and troubleshoots technical issues to support high-quality, sustainable products that promote health and wellness. This position offers significant growth potential as the R&D function expands and provides opportunities to move into leadership and people management over time. Responsibilities • Partner closely with Sales and Customers to understand product requirements and technical needs and translate them into effective formulation strategies., • Develop and optimize formulations for oils, waters, soft gels, two-piece capsules, tablets, powders, and granulations within the nutraceutical and dietary supplement space., • Apply expertise in powder, liquid, and tablet formulations to create stable, manufacturable, and high-quality products., • Collaborate with Sourcing and Purchasing teams to ensure timely material availability, cost efficiency, and appropriate raw material selection., • Troubleshoot technical formulation issues, identify root causes, and implement effective, data-driven solutions., • Assist with analytical testing and quality assessments to ensure products meet specifications and regulatory and internal quality standards., • Perform hands-on experimental work in the Product Development laboratory, including batching, blending, encapsulation, and related lab-scale processes., • Utilize analytical instrumentation such as gas chromatography (GC), high-performance liquid chromatography (HPLC), and inductively coupled plasma mass spectrometry (ICP-MS) to support formulation development and analytical chemistry needs., • Support quality control activities by evaluating raw materials, intermediates, and finished products, including those involving fish oils and other nutraceutical ingredients., • Evaluate laboratory capabilities, identify opportunities for future R&D expansion, and recommend new technologies, methods, or equipment to enhance innovation., • Contribute to new product development projects from concept through commercialization, including experimental design, data analysis, and documentation., • Collaborate effectively with a predominantly Spanish-speaking laboratory team, using translation tools as needed to maintain clear communication and teamwork., • Maintain accurate records of experiments, methods, and results in accordance with internal procedures and good laboratory practices., • Work cross-functionally with Quality, Manufacturing, and other internal stakeholders to ensure formulations are scalable and suitable for production., • Bachelor’s degree in Food Science, Chemistry, or a related field., • 3+ years of R&D formulation experience, preferably in nutraceuticals or dietary supplements., • Proven expertise in formulation of powders, liquids, and tablets., • Bilingual skills, particularly Spanish, are a plus but not required., • Interest in purpose-driven work focused on high-quality, ethically sourced, and sustainable products. 401K, holiday, vacation and sick time offered to internal employees. Will have potential to grow into a leadership role - the R&D department is new and there will be room to expand to R&D formulators that report to them. Workplace Type This is a fully onsite position in Clifton,NJ. Application Deadline This position is anticipated to close on Apr 28, 2026. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through: • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job Description Description Support lab operations, data integrity, and compliance responsible for scientific accuracy, regulatory adherence, and lab workflow Support and maintain LIMS integrations and instrument interfaces Enhance, develop, and maintain SQL Server database systems Create management and data reports using Crystal Reports and/or Microsoft Access Develop customized electronic data deliverables (EDD) in CSV, tab‑delimited, and Excel formats Troubleshoot and maintain Access VBA programs Provision, install, configure, and maintain computer systems and infrastructure Develop and maintain regulatory reporting formats Skills Chemistry, Laboratory, Lims, Quality control, Qc analysis, R&d lab, Labware, rcra Top Skills Details Chemistry,Laboratory,Lims Additional Skills & Qualifications 2+ years of experience with Clinisys Element LIMS (v6 or v7) strong technical expertise in databases, reporting tools, and system configuration Experience Level Intermediate Level Job Type & Location This is a Contract to Hire position based out of Wayne, NJ. Pay and Benefits The pay range for this position is $43.00 - $58.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job DescriptionJob Title: Quality Control Associate I - 1st Shift (Tues-Sat) Job Description Join a dynamic team where you will perform essential testing and analysis to support the development of methods for flow cytometry and cell analysis. You will engage in cell culture, cell counting, and quality control analysis, providing valuable input to improve workflow and laboratory activities. As a key member of our team, you will also help train and oversee new employees, ensuring the accurate execution of company and client test methods to guarantee the safety and efficacy of cellular products. Responsibilities • Execute test methods and procedures for cellular products according to company and client guidelines., • Perform maintenance, monitoring, and troubleshooting of laboratory equipment, ensuring routine start-ups and shutdowns are completed., • Document and report test results for products or materials following CGMP and GTP guidelines., • Organize laboratory supplies and maintain a clean and orderly lab environment., • Assist in equipment and method qualification and validation activities., • Cross-train in methods for multiple clients to enhance lab efficiency., • Upload data in real-time to shared drives or client SharePoint sites., • Prepare reagents and media, and respond to equipment alarms., • Investigate and report on out-of-specification, out-of-trend, and non-conforming test results., • Initiate, investigate, and prepare deviation reports with supervisor input., • Document training and manage the shipping of test samples to contract laboratories., • Communicate effectively with coworkers, departments, management, and clients., • Assist in training other Quality Control technicians.Essential Skills, • 2 years of experience performing flow cytometry assays and endotoxin testing., • 1-2 years of experience with cell culture., • Experience in a quality control setting with test methodologies., • Proficiency in microbiology test methods and equipment use., • Bachelor's or Master's degree in a related scientific field.Additional Skills & Qualifications, • Experience in CGMP/GTP environments is preferred., • Prior laboratory experience in cell counting methodologies is advantageous., • Experience in clinical laboratory, microbiology, hematology, blood banking, or immunology., • Proficiency with Microsoft Office and Visio software., • Experience with paper-based testing and documentation.Work Environment The role operates on a 1st shift schedule from Tuesday to Saturday, 6 AM to 2:30 PM. Training occurs Monday to Friday, 8 AM to 4:30 PM. You will work in an aseptic quality environment as part of the Analytical Team, reporting to a quality control manager. Flexibility is required, as cell and gene therapy processes may experience delays. The position involves a collaborative setting with opportunities for growth and development within the company. Job Type & Location This is a Contract to Hire position based out of Allendale, NJ. Pay and Benefits The pay range for this position is $30.00 - $31.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

Job DescriptionJob Title: Quality Control Associate I Job Description As a Quality Control Associate I, you will perform testing to develop methods for flow cytometry and analysis. You will engage in cell culture and cell counting to ensure quality control and help analyze flow methods and complexity testing. Your role will involve providing input to improve workflow and laboratory activity and offering training and oversight to new team members. Responsibilities • Execute company and client test methods and procedures of cellular products to ensure safety and efficacy., • Perform maintenance, monitoring, and troubleshooting of laboratory equipment., • Test, document, and report results for products or materials following CGMP and GTP guidelines., • Organize the lab and manage supplies efficiently., • Perform cleanings of laboratory equipment as per SOP., • Assist in equipment and method qualification/validation activities., • Cross-train in methods for multiple clients to enhance lab efficiency., • Upload data in real-time to shared drives or client SharePoint sites., • Prepare reagents and media., • Respond to equipment alarms using the Linc Alarm Report system., • Troubleshoot malfunctioning equipment and provide insights based on experience., • Investigate out-of-specification, out-of-trend, aberrant, and non-conforming test results., • Initiate, investigate, and prepare deviation reports with supervisor input., • Brainstorm and implement corrective and preventive actions., • Document training and execute shipping test samples to contract laboratories., • Complete all documentation according to SOPs in line with CGMP and GDP., • Communicate effectively with coworkers, departments, management, and clients., • Assist in training other Quality Control technicians.Essential Skills, • Flow cytometry and cell culture expertise., • 1-2 years of experience in performing flow cytometry assays and endotoxin testing., • 1-2 years of cell culture experience., • Experience in quality control settings., • Proficiency in clinical and commercial production support., • Familiarity with process checkpoint, stability, and release analytical testing.Additional Skills & Qualifications, • Bachelor's or Master's degree in a related scientific field., • Experience with microbiology test methods., • Experience in training and leading others in the lab., • Experience in a CGMP/GTP environment is preferred., • Prior industrial experience in cell count methodologies is preferred., • 2-4 years of experience in a Quality Control laboratory setting or the biopharmaceutical industry., • Proficiency with Microsoft Office and Visio.Work Environment This position operates on a Sun-Thurs second shift schedule from 2:30 PM to 11:00 PM. Initial training occurs Monday through Friday from 8:00 AM to 4:30 PM. Flexibility is required as work hours may vary. You will work within an aseptic quality environment, alongside scientists and other associates. The role involves electronic-based SOPs and paper-based testing and documentation. The company fosters a collaborative environment with opportunities for growth, project management, and leadership roles. Job Type & Location This is a Contract to Hire position based out of Allendale, NJ. Pay and Benefits The pay range for this position is $30.00 - $31.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

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Delivering with Uber is an alternative to a part-time or full-time job and can get you earning cash quickly.Delivering with Uber allows you to earn quick cash while maintaining the flexibility your schedule requires (gig, part-time, full-time, seasonal, hourly, or temporary).With Uber, you can cash

Delivering with Uber is an alternative to a part-time or full-time job and can get you earning cash quickly.Delivering with Uber allows you to earn quick cash while maintaining the flexibility your schedule requires (gig, part-time, full-time, seasonal, hourly, or temporary).With Uber, you can cash

About Actalent Actalent is a global leader in engineering and sciences services. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through: * Hiring diverse talent * Maintaining an inclus

Delivering with Uber is an alternative to a part-time or full-time job and can get you earning cash quickly.Delivering with Uber allows you to earn quick cash while maintaining the flexibility your schedule requires (gig, part-time, full-time, seasonal, hourly, or temporary).With Uber, you can cash

Actalent is a global leader in engineering and sciences services and talent solutions. Canada, Asia and Europe, Actalent serves many of the Fortune 500.

Delivering with Uber is an alternative to a part-time or full-time job and can get you earning cash quickly.Delivering with Uber allows you to earn quick cash while maintaining the flexibility your schedule requires (gig, part-time, full-time, seasonal, hourly, or temporary).With Uber, you can cash

Delivering with Uber is an alternative to a part-time or full-time job and can get you earning cash quickly.Delivering with Uber allows you to earn quick cash while maintaining the flexibility your schedule requires (gig, part-time, full-time, seasonal, hourly, or temporary).With Uber, you can cash

Delivering with Uber is an alternative to a part-time or full-time job and can get you earning cash quickly.Delivering with Uber allows you to earn quick cash while maintaining the flexibility your schedule requires (gig, part-time, full-time, seasonal, hourly, or temporary).With Uber, you can cash

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. Actalent is an equal opportunity employer. Actalent is a global leader in engineering and sciences services.

Delivering with Uber is an alternative to a part-time or full-time job and can get you earning cash quickly.Delivering with Uber allows you to earn quick cash while maintaining the flexibility your schedule requires (gig, part-time, full-time, seasonal, hourly, or temporary).With Uber, you can cash

Delivering with Uber is an alternative to a part-time or full-time job and can get you earning cash quickly.Delivering with Uber allows you to earn quick cash while maintaining the flexibility your schedule requires (gig, part-time, full-time, seasonal, hourly, or temporary).With Uber, you can cash

Delivering with Uber is an alternative to a part-time or full-time job and can get you earning cash quickly.Delivering with Uber allows you to earn quick cash while maintaining the flexibility your schedule requires (gig, part-time, full-time, seasonal, hourly, or temporary).With Uber, you can cash

Delivering with Uber is an alternative to a part-time or full-time job and can get you earning cash quickly.Delivering with Uber allows you to earn quick cash while maintaining the flexibility your schedule requires (gig, part-time, full-time, seasonal, hourly, or temporary).With Uber, you can cash

Delivering with Uber is an alternative to a part-time or full-time job and can get you earning cash quickly.Delivering with Uber allows you to earn quick cash while maintaining the flexibility your schedule requires (gig, part-time, full-time, seasonal, hourly, or temporary).With Uber, you can cash

Delivering with Uber is an alternative to a part-time or full-time job and can get you earning cash quickly.Delivering with Uber allows you to earn quick cash while maintaining the flexibility your schedule requires (gig, part-time, full-time, seasonal, hourly, or temporary).With Uber, you can cash

Delivering with Uber is an alternative to a part-time or full-time job and can get you earning cash quickly.Delivering with Uber allows you to earn quick cash while maintaining the flexibility your schedule requires (gig, part-time, full-time, seasonal, hourly, or temporary).With Uber, you can cash

Delivering with Uber is an alternative to a part-time or full-time job and can get you earning cash quickly.Delivering with Uber allows you to earn quick cash while maintaining the flexibility your schedule requires (gig, part-time, full-time, seasonal, hourly, or temporary).With Uber, you can cash