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3 jobs found for warehouse work available call today start tomorrow in new jersey

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    • whippany, new jersey (remote)
    • contract
    • $42.85 - $50.41 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!   location: Whippany, New Jersey job type: Contract salary: $42.85 - 50.41 per hour work hours: 8 to 4 education: Bachelors   responsibilities: This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation. DEPARTMENT/TEAM DESCRIPTION Operational Excellence and Project Management in Global Medical Affairs (GMA), Oncology SBU is a global function which partners and collaborates with the MA Teams and Key Stakeholders (internal and external) to assist in achieving short and long term strategic goals while adhering to "LIFE" values (leadership, integrity, flexibility, efficiency). POSITION SUMMARY The Senior Contract Operations Excellence & PM Manager position is accountable for compliant and high quality management of GMA company-sponsored studies (both non and interventional), Investigator Initiated Research (IIR) and Investigator-Sponsored Collaborative Studies (ISCS) data acquisition projects, and Expanded Access Programs (EAPs) POSITION DUTIES & RESPONSIBILITIES Lead all aspects of clinical studies from planning to execution. Assigned studies include interventional, non-interventional and data acquisitions within Global Medical Affairs Oncology SBUOverall accountable for study management of assigned studies, serve as primary contact for CRO. Lead and manage multi-disciplinary cross functional team in all aspects of studies activities including but not limited to site start up, CRO/vendor selection and management, study-specific timelines and study executionCoordinate for fair market value assessment of study budgets; initiate and manage contracting process. Liaise with appropriate internal protocol review committees to ensure timely review, response and finalization of the protocol and protocol amendmentIIR and/or ISCS data acquisition projects. Responsibilities include chair conference calls, coordinate between team and IIR-sponsors on activities such as data review, query resolution and independent review of imaging scans, when applicable. Develop and manage overall project timelinesSupport GMA Medical Leads on overall delivery of the data generated from Oncology Non-Interventional Studies (NIS). Responsibilities include, but not limited to, monitor country/site selection and activation process, contribute in CRF design and review, study budget management, support Medical Leads on clinical data consistency review to ensure that data issues raised during medical and DM data review are adequately queried and resolvedManage study drug forecasting. Liaise with Clinical Supplies Management to ensure drug supply planning, labeling and distribution are executed timely and within applicable country and regional guidelinesAssist and/or lead in executing Expanded Access Programs within Oncology MA. Responsibilities include collaborate with country affiliates and Medical Experts as appropriate to ensure timely alignment and execution of country specific processes including permit license application, commercial product transition plan, and Real World Data (RWD) data generation when applicable  qualifications: SKILLS Extensive (7+ years) study management experience involving Phases 2 & 3 studies from planning through regulatory submission; regulatory submission experience a plusUnderstanding of the connection between protocol endpoints, study design, CRF design and data collection; clinical science backyard a plusAt least 5 years Oncology experience (can be outside of industry)Strong written, organizational, and computer (e.g. Excel, power point) skillsExcellent interpersonal and communication skills as candidate will interact with cross functional team members as well as liaise with external academic networks and cooperative groups from all over the global Preferences: Medical Affairs experience preferred REQUIREMENTS/PREFERENCES Education Requirement(s): Bachelor's degree required; life science preferredMasters in Science or Business Administration - preferred  skills: MS-EXCEL, Study Planning Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!   location: Whippany, New Jersey job type: Contract salary: $42.85 - 50.41 per hour work hours: 8 to 4 education: Bachelors   responsibilities: This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation. DEPARTMENT/TEAM DESCRIPTION Operational Excellence and Project Management in Global Medical Affairs (GMA), Oncology SBU is a global function which partners and collaborates with the MA Teams and Key Stakeholders (internal and external) to assist in achieving short and long term strategic goals while adhering to "LIFE" values (leadership, integrity, flexibility, efficiency). POSITION SUMMARY The Senior Contract Operations Excellence & PM Manager position is accountable for compliant and high quality management of GMA company-sponsored studies (both non and interventional), Investigator Initiated Research (IIR) and Investigator-Sponsored Collaborative Studies (ISCS) data acquisition projects, and Expanded Access Programs (EAPs) POSITION DUTIES & RESPONSIBILITIES Lead all aspects of clinical studies from planning to execution. Assigned studies include interventional, non-interventional and data acquisitions within Global Medical Affairs Oncology SBUOverall accountable for study management of assigned studies, serve as primary contact for CRO. Lead and manage multi-disciplinary cross functional team in all aspects of studies activities including but not limited to site start up, CRO/vendor selection and management, study-specific timelines and study executionCoordinate for fair market value assessment of study budgets; initiate and manage contracting process. Liaise with appropriate internal protocol review committees to ensure timely review, response and finalization of the protocol and protocol amendmentIIR and/or ISCS data acquisition projects. Responsibilities include chair conference calls, coordinate between team and IIR-sponsors on activities such as data review, query resolution and independent review of imaging scans, when applicable. Develop and manage overall project timelinesSupport GMA Medical Leads on overall delivery of the data generated from Oncology Non-Interventional Studies (NIS). Responsibilities include, but not limited to, monitor country/site selection and activation process, contribute in CRF design and review, study budget management, support Medical Leads on clinical data consistency review to ensure that data issues raised during medical and DM data review are adequately queried and resolvedManage study drug forecasting. Liaise with Clinical Supplies Management to ensure drug supply planning, labeling and distribution are executed timely and within applicable country and regional guidelinesAssist and/or lead in executing Expanded Access Programs within Oncology MA. Responsibilities include collaborate with country affiliates and Medical Experts as appropriate to ensure timely alignment and execution of country specific processes including permit license application, commercial product transition plan, and Real World Data (RWD) data generation when applicable  qualifications: SKILLS Extensive (7+ years) study management experience involving Phases 2 & 3 studies from planning through regulatory submission; regulatory submission experience a plusUnderstanding of the connection between protocol endpoints, study design, CRF design and data collection; clinical science backyard a plusAt least 5 years Oncology experience (can be outside of industry)Strong written, organizational, and computer (e.g. Excel, power point) skillsExcellent interpersonal and communication skills as candidate will interact with cross functional team members as well as liaise with external academic networks and cooperative groups from all over the global Preferences: Medical Affairs experience preferred REQUIREMENTS/PREFERENCES Education Requirement(s): Bachelor's degree required; life science preferredMasters in Science or Business Administration - preferred  skills: MS-EXCEL, Study Planning Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • ridgefield, new jersey
    • temp to perm
    • $22 - $23 per hour
    job summary: Compounding Associate - 4 OPENINGS Ridgefield, NJ 2 nd shift - 3:30pm - Midnight (M-F) Train on 1 st shift for 4 weeks. 7am - 3:30pm (M-F)   location: Ridgefield, New Jersey job type: Temporary salary: $22 - 23 per hour work hours: 3 to 11 education: High School   responsibilities: Compounding Associate will be responsible of the following: Verify all chemicals being added Closely follow compounding instructions Identify each chemical pre-weighed with information tag / initial Document all required information on batch card, verify and initial Follow all SOPs and WIs Keep compounding area clean and organized Follow all safety rules. Follow all GMP and company policies/procedures. Work on special projects as required   qualifications: Requirements High School Diploma or GED 2-5 years relevant blending or compounding experience, cosmetic or personal care setting preferred. Ability to read, understand, document and maintain records as required. Ability to handle multiple priorities in a fast-paced environment. Familiar with inventory control using RF scanning. Ability to lift up to 55 lbs. frequently   skills: GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: Compounding Associate - 4 OPENINGS Ridgefield, NJ 2 nd shift - 3:30pm - Midnight (M-F) Train on 1 st shift for 4 weeks. 7am - 3:30pm (M-F)   location: Ridgefield, New Jersey job type: Temporary salary: $22 - 23 per hour work hours: 3 to 11 education: High School   responsibilities: Compounding Associate will be responsible of the following: Verify all chemicals being added Closely follow compounding instructions Identify each chemical pre-weighed with information tag / initial Document all required information on batch card, verify and initial Follow all SOPs and WIs Keep compounding area clean and organized Follow all safety rules. Follow all GMP and company policies/procedures. Work on special projects as required   qualifications: Requirements High School Diploma or GED 2-5 years relevant blending or compounding experience, cosmetic or personal care setting preferred. Ability to read, understand, document and maintain records as required. Ability to handle multiple priorities in a fast-paced environment. Familiar with inventory control using RF scanning. Ability to lift up to 55 lbs. frequently   skills: GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • somerville, new jersey
    • contract
    • $20 - $25 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Somerville, New Jersey job type: Contract salary: $20 - 25 per hour work hours: 7 to 3 education: High School   responsibilities: Inspection of incoming components, materials, supplies, and outsourced finished goods utilized for the manufacture, shipment, and testing of products in accordance with component specifications and procedures.Utilizes component specifications to perform visual inspections, dimensional verifications, document reviews, and other standard quality control inspections to ensure items meet quality standards.Visual inspection of labeling, packaging, and inserts of final packaged product, in-house finished goods, to ensure conformance with product specification and proceduresDocuments results of inspection onto inspection record and in electronic system to determine acceptability of item for use, or transfer to QC Product Release.Ebeam inspectionDiscard activities as needed 80%  qualifications: Ability to work in a team environment2-4 years of experience working in quality required2-4 years of experience in a GMP environment performing related duties as listed in Principle Responsibilities and overall experience in regulated industry.Must be able to manually maneuver carts and material handling equipment weighing up to 50 lbs while wearing appropriate personal protective equipmentAbility to work varied schedule with some potential weekend, early morning or late evening hours, if needed.Excellent attention to detail and organizational skillsCustomer focusExperience with excel, word, etc.SAP ExperienceEducation and Experience High School/Secondary School/EquivalentAssociates or Bachelor's degree preferred   skills: Quality control, SOP, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Somerville, New Jersey job type: Contract salary: $20 - 25 per hour work hours: 7 to 3 education: High School   responsibilities: Inspection of incoming components, materials, supplies, and outsourced finished goods utilized for the manufacture, shipment, and testing of products in accordance with component specifications and procedures.Utilizes component specifications to perform visual inspections, dimensional verifications, document reviews, and other standard quality control inspections to ensure items meet quality standards.Visual inspection of labeling, packaging, and inserts of final packaged product, in-house finished goods, to ensure conformance with product specification and proceduresDocuments results of inspection onto inspection record and in electronic system to determine acceptability of item for use, or transfer to QC Product Release.Ebeam inspectionDiscard activities as needed 80%  qualifications: Ability to work in a team environment2-4 years of experience working in quality required2-4 years of experience in a GMP environment performing related duties as listed in Principle Responsibilities and overall experience in regulated industry.Must be able to manually maneuver carts and material handling equipment weighing up to 50 lbs while wearing appropriate personal protective equipmentAbility to work varied schedule with some potential weekend, early morning or late evening hours, if needed.Excellent attention to detail and organizational skillsCustomer focusExperience with excel, word, etc.SAP ExperienceEducation and Experience High School/Secondary School/EquivalentAssociates or Bachelor's degree preferred   skills: Quality control, SOP, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.

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