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Our client, a leading healthcare organization, is seeking a talented Certified Medical Assistant to join their team across Westchester!.Monitor patient arrival and assist with patient flow, ensuring that patients and visitors are greeted promptly and courteously.Escort patients to exam rooms, monito

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).

Hiring a Bilingual Phlebotomist!. The Bilingual Phlebotomist provides expert support in blood collection and specimen preparation while ensuring patients feel comfortable and informed throughout the process.

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

Job Description Description Work location: Leonia NJ Work Schedule: M-F 8am -4:30pm POSITION SUMMARY Under the direction of the Supervisor Quality Lab Services the Technician Quality is responsible for performing routine laboratory support functions cleaning of glassware and general housekeeping. Non-routine duties are performed in a learning capacity under direct supervision. Responsibilities are focused on less complex testing and support functions. KEY RESPONSIBILITIES: - Perform qualitative analysis of samples. - Conduct routine and laboratory support functions such as preparation of media reagents and standard solutions stocking and distributing supplies and equipment and collecting washing and storing glassware. As required maintains related notes and records. - Makes and records observations performs calculations collects and may assist in preparing data for evaluation. Keeps Supervisor informed of work status. - Prioritizes workload and meets scheduled timelines. - Informs Supervisor of equipment and supply needs required to avoid delays in testing. - Reports results of assignments and maintains and performs related record keeping in compliance with approved regulatory policies and standards to meet quality and accuracy requirements. Follows and complies with all appropriate SOPs QPs GMPs and safety and health requirements as applicable. - Demonstrate good housekeeping practices to minimize analytical mix-ups potential laboratory contamination and safety hazards. Understanding and handling of hazardous materials and waste using proper and safe techniques. Selected qualified associates at the discretion of the Quality Control Management will be responsible for handling hazardous waste management. - Assists higher level technical and scientific personnel as needed to learn more advanced techniques equipment instrumentation and procedures specific to the Quality Control Department. - Display ability in interpreting and evaluating atypical/OOS results and immediately report them to Supervisor. - Show versatility and be able to work as a part of a team when required. - Other duties as assigned. EXPERIENCE AND EDUCATION REQUIREMENTS - High School diploma or general education degree GED required. - Bachelors degree in chemistry or other closely related discipline preferred. - 0 to 1 years of laboratory experience. PREFERRED SKILLS - Ability to learn analytical skills. - Good time management skills and have the ability to meet deadlines. - Must be willing to work under extreme pressures and work Overtime if required. - Ability to write simple correspondence and have good verbal communication skills. - Basic mathematical skills. - Good computer skills i.e. Word Excel. - Exhibit positive attitude towards work and responsibilities. - Must be able to organize generated data evaluate and interpret the results when compared to specifications ADDITIONAL NOTES PHYSICAL DEMANDS: Work environment may be exposed to powders chemicals and allergens peanuts tree nuts milk dairy eggs wheat gluten soy fish and shellfish - Standing - Lifting Job Type & Location This is a Contract position based out of Leonia, NJ. Pay and Benefits The pay range for this position is $18.00 - $20.00/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: Phlebotomist Job Description The Phlebotomist provides expertise in blood draws and specimen preparation, ensuring minimal discomfort to patients across a wide demographic. This role is crucial to our commitment to delivering high-quality care for our patients and those of our partners. Responsibilities • Perform blood draws, label specimens, and centrifuge them., • Record maintenance data and perform decontamination., • Update patient information accurately., • Collect and store specimens according to established procedures., • Explain venipuncture and other specimen collection processes clearly and courteously., • Demonstrate techniques using straight needles and/or butterfly needles., • Understand and execute physicians' orders., • Match laboratory requisition forms to specimen tubes and handle specimens as required by test orders., • Check all test requisitions or computer labels against scripts to ensure accuracy., • Package specimens for transport., • Store specimens according to required temperatures and procedures to maintain specimen integrity., • Comply with OSHA and DEP regulations., • Wear appropriate attire and attend annual department trainings., • Answer telephone inquiries and read laboratory results.Essential Skills, • Phlebotomy expertise, including blood draw and specimen processing., • Experience with straight needle techniques., • 2-3 years of experience with drawing blood., • Strong administrative skills and attention to detail.Additional Skills & Qualifications, • Experience with infant draws is a plus., • Pediatric experience is beneficial.Work Environment The role offers a dynamic work environment, ideal for candidates who enjoy a change of scenery and in-state travel. The work schedule is Monday to Friday, 8am-5pm, with every other Saturday required. The position does not include holidays or vacation time. Job Type & Location This is a Contract to Hire position based out of Mount Vernon, NY. Pay and Benefits The pay range for this position is $20.00 - $22.00/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 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 Job Title: Microbiologist Book for immediate consideration: More than one year is overqualified * Job Description The Microbiologist will conduct routine microbiological testing and analysis for water, bulk pharmaceutical chemicals, and drug products. Responsibilities include collecting samples, preparing standards/controls, media, and sample solutions, and maintaining appropriate records. Responsibilities • Collect purified water samples from various USP Purified Water Loops used to manufacture or test drug products., • Perform microbiological testing on water, bulk pharmaceutical chemicals, drug products, and components, as well as finished products., • Conduct method suitability testing on finished products using traditional methods according to procedures, document results, and report appropriately., • Prepare media used in the microbiological testing of bulk pharmaceutical chemicals, drug products, and components., • Analyze and read microbiological test results while ensuring proper data integrity and adherence to GLP/GMP principles., • Perform growth promotion testing for purchased and prepared media., • Sample raw materials and/or finished products for microbial testing., • Prepare laboratory investigation reports, excursions, and/or non-conformance evaluations., • Collect environmental samples for microbiological analysis., • Conduct aseptic samplings for evaluation of compressed air and cleaning/sanitization processes., • Perform basic identification of microorganisms (Gram stain)., • Maintain the cleanliness and organization of the laboratory., • Prepare samples for shipment to an outside contract laboratory for microbiological testing., • Perform related support activities and duties as assigned., • Follow all Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements., • Perform laboratory tasks using general microbiological laboratory techniques and procedures., • Follow internal sampling methods and quality control systems., • Perform general mathematics (addition/subtraction/multiplication/division, dilutions, proportions, percentages)., • Proficiency in microbiological testing, aseptic techniques, and gram staining., • Bachelor’s degree in Biology, Microbiology, or a related science field from an accredited college or university., • 6 months to 1 year of related laboratory work experience in a regulated environment., • Ability to multi-task and manage time effectively., • Strong communication and customer service skills. 5% Target Bonus annually Medical, Dental, Vision, 401k match, etc. Workplace Type This is a fully onsite position in Orangeburg,NY. Application Deadline This position is anticipated to close on Apr 16, 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: Quality Assurance Technician Book for immediate interests: *Must have QA experience within GMP environment Job Description: As a Quality Assurance Technician, you will perform daily inspections of all production lines to ensure compliance with Good Manufacturing Practices (GMPs) and company standards. You will document inspection information accurately on the Daily Inspection Report (DIR) and ensure all manufacturing specifications are correct and complete. Your role will involve inspecting work areas, monitoring in-process finished products, collecting data and samples, and determining final product disposition. Responsibilities • Perform daily inspections of production lines to ensure GMP compliance., • Document all inspection details including lot numbers, fill weights, and defects., • Ensure manufacturing specifications for components, labeling, and products are correct., • Inspect work areas for removal of previous products and verify readiness., • Monitor, sample, and inspect finished products for quality through appropriate tests., • Collect data and samples to support product disposition decisions., • Determine and verify final product disposition and apply disposition labels., • Identify and report discrepancies to Production and Quality teams., • Perform AQL inspections and execute Rework protocols as needed., • Initiate and log LIMS and Retain Samples, and print specifications from ERP systems., • Collect and ship samples as required by customers or Manufacturing Instructions., • Collect stability samples and execute Trials and Validations., • Review documentation for accuracy prior to submission to QA Release team., • Act as Lead QA Inspector in absence, ensuring proper production floor coverage., • Identify continuous improvement opportunities and promote a culture of quality., • 3+ years of quality experience in a regulated environment., • Strong understanding of GMPs, quality systems, and regulated manufacturing environments., • Working knowledge of AQL inspection standards and in-process quality control methods., • Familiarity with batch documentation and manufacturing specifications., • Proficiency in Microsoft Office Suite and ability to learn quality-related systems., • Experience with in-process quality inspections, line clearances, and documentation review., • Experience supporting trials, validations, rework activities, and sample collection., • Ability to interpret and follow SOPs, Work Instructions, and product specifications., • Excellent documentation accuracy and attention to detail., • Associate’s Degree in a scientific, technical, or related field, or equivalent experience., • Experience in a regulated industry (e.g., FDA, EPA), preferably in manufacturing or QA roles., • Prior exposure to continuous improvement and deviation identification., • Solid organizational, multitasking, and time-management skills. Medical Dental Vision Accidental/Life 401k + match Holidays, Vacation & Sick Time Workplace Type This is a fully onsite position in Orangeburg,NY. Application Deadline This position is anticipated to close on Apr 16, 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 QC Lab Technician Candidates must be local to NY and readily available to start - 1+ year of experience is overqualified Job Description: Perform analyses of Clinical Chemistry, Critical Care, Coagulation, and Microbiology controls and reagents using automated and manual techniques per SOPs, QC Monographs, and GMP standards. Conduct raw material, in-process, and finished product testing; interpret results and determine pass/fail. Maintain GMP compliant documentation and perform product stability, proficiency, environmental, and water system testing. Perform routine preventive maintenance, troubleshooting, cleaning, and equipment calibration. Execute microbial testing per SOPs and QC Monographs. Manage lab supplies, monitor storage conditions and expiration dates, and properly dispose of hazardous/biohazardous materials. Keep saved product samples organized and update charts and logs that track testing trends and routine lab records. Responsibilities • Perform analyses of Clinical Chemistry, Critical Care, Coagulation, and Microbiology controls and reagents., • Conduct raw material, in-process, and finished product testing., • Interpret test results and determine pass/fail status., • Maintain GMP compliant documentation., • Perform product stability, proficiency, environmental, and water system testing., • Conduct routine preventive maintenance, troubleshooting, cleaning, and equipment calibration., • Execute microbial testing as per SOPs and QC Monographs., • Manage laboratory supplies, monitor storage conditions, and expiration dates., • Dispose of hazardous/biohazardous materials properly., • Proficiency in laboratory techniques and biochemistry., • Experience in quality control., • BS/BA in Biology, Biochemistry, Chemistry, or Medical Technology., • 3 to 6 months of research experience (academic, internship, co-op, or industry)., • Knowledge of Chemistry and Microbiology., • BS/BA in Biology, Biochemistry, Chemistry, or Medical Technology. If you are interested please book a virtual meeting here: Job Type & Location This is a Contract position based out of Orangeburg, NY. Pay and Benefits The pay range for this position is $22.00 - $22.00/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 QC Lab Technician Candidates must be local to NY and readily available to start - 1+ year of experience is overqualified PLease use this link to book a meeting to learn more: Work Environment: The role operates on a 2nd shift schedule, from Monday to Friday, 2:00 PM to 10:30 PM. Job Description: Perform analyses of Clinical Chemistry, Critical Care, Coagulation, and Microbiology controls and reagents using automated and manual techniques per SOPs, QC Monographs, and GMP standards. Conduct raw material, in-process, and finished product testing; interpret results and determine pass/fail. Maintain GMP compliant documentation and perform product stability, proficiency, environmental, and water system testing. Perform routine preventive maintenance, troubleshooting, cleaning, and equipment calibration. Execute microbial testing per SOPs and QC Monographs. Manage lab supplies, monitor storage conditions and expiration dates, and properly dispose of hazardous/biohazardous materials. Keep saved product samples organized and update charts and logs that track testing trends and routine lab records. Responsibilities • Perform analyses of Clinical Chemistry, Critical Care, Coagulation, and Microbiology controls and reagents., • Conduct raw material, in-process, and finished product testing., • Interpret test results and determine pass/fail status., • Maintain GMP compliant documentation., • Perform product stability, proficiency, environmental, and water system testing., • Conduct routine preventive maintenance, troubleshooting, cleaning, and equipment calibration., • Execute microbial testing as per SOPs and QC Monographs., • Manage laboratory supplies, monitor storage conditions, and expiration dates., • Dispose of hazardous/biohazardous materials properly., • Proficiency in laboratory techniques and biochemistry., • Experience in quality control., • BS/BA in Biology, Biochemistry, Chemistry, or Medical Technology., • 3 to 6 months of research experience (academic, internship, co-op, or industry)., • Knowledge of Chemistry and Microbiology., • BS/BA in Biology, Biochemistry, Chemistry, or Medical Technology. Job Type & Location This is a Contract position based out of Orangeburg, NY. Pay and Benefits The pay range for this position is $22.00 - $22.00/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

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

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