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7 jobs found in lake forest, california

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    • buena park, california
    • permanent
    • $115,000 - $130,000 per year
    job summary: We are the #1 HR Services Company in the world and we are sourcing for a Sr. Research Scientist in the greater Los Angeles, CA area. The ideal candidate will be passionate about ensuring the sound science of our nutrition products, along with developing relevant and meaningful product and program solutions that address key customer needs in the health and wellness space. This is a direct hire position and can start immediately.   location: Buena Park, California job type: Permanent salary: $115,000 - 130,000 per year work hours: 8 to 4 education: Masters   responsibilities: What's special about this team: The Health Seekers Platform is a cross-functional product development team comprised of formulation, process engineering, package engineering, and nutrition investigations. The team's work focuses on innovation and delivery of new products for our targeted product platform and the 40+ age segment -vision health, bone health, immunity, etc. Working with this technical team, you will develop with an open innovation mindset, working both internally and through external partnerships to offer creative & engaging product offerings. Your teamwork will continue to position the team as the leading direct selling company in the world by offering innovative product solutions for our targeted nutrition category. You will add energy and inspiration to a strong technical team! What's special about this role: As a Senior Nutrition Research & Clinical Investigator on this team, you will evaluate scientific research to support the Nutrilite global product portfolio and provide scientific credibility to differentiate Nutrilite products from competitors. Your role will require you to work on front end research, helping to identify relevant mechanisms of action and outcomes, and to partner with internal teams and/or external partners to advance ingredient and product technologies. If clinical studies are warranted, you will develop protocols, identify the appropriate CRO or academic partner, oversee study execution and results analysis, and then translate the results into consumer-friendly and regulatory acceptable claims and stories which support the efficacy of our products. Your background in both nutrition science and clinical research will be showcased in the role. Your work will maintain the high credibility of the Nutrilite brand and will offer a highly visible role, providing patent and publication opportunities, in addition to the ability to travel globally, meeting and sharing expert insights about Nutrilite products, nutrition, and health. If you have a passion for health and wellness, enjoy translating complex nutrition science into efficacious, experiential products, and the ability to share your expertise with clients and customers around the world, this role can offer a strong platform to spotlight your talent!   qualifications: Required qualifications: Minimum 3 - 6 years of experience in nutrition research and product claim substantiationAdvanced degree (MS or PhD) in Bioscience, Nutrition Science, or related scientific disciplineProven exposures incorporating functional botanicals and botanically derived bioactives into product profile designAbility to translate complex scientific and technical concepts into consumer appropriate language, ideally with compelling visuals, to enable communication and understanding of the science underlying the productInterpersonal skills to influence and inspire both internal and external audiencesExperience leading clinical studies in an industry setting is helpfulBasic understanding of global regulations in the nutraceutical industry is preferredIndustry awareness with knowledge of trends and innovation desiredRD (Registered Dietician) Certification, ACRP (Association of Clinical Research Professionals) Certification, or naturopathic background helpful  skills: Biology, Food Product Development 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.EOEDisclaime 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: We are the #1 HR Services Company in the world and we are sourcing for a Sr. Research Scientist in the greater Los Angeles, CA area. The ideal candidate will be passionate about ensuring the sound science of our nutrition products, along with developing relevant and meaningful product and program solutions that address key customer needs in the health and wellness space. This is a direct hire position and can start immediately.   location: Buena Park, California job type: Permanent salary: $115,000 - 130,000 per year work hours: 8 to 4 education: Masters   responsibilities: What's special about this team: The Health Seekers Platform is a cross-functional product development team comprised of formulation, process engineering, package engineering, and nutrition investigations. The team's work focuses on innovation and delivery of new products for our targeted product platform and the 40+ age segment -vision health, bone health, immunity, etc. Working with this technical team, you will develop with an open innovation mindset, working both internally and through external partnerships to offer creative & engaging product offerings. Your teamwork will continue to position the team as the leading direct selling company in the world by offering innovative product solutions for our targeted nutrition category. You will add energy and inspiration to a strong technical team! What's special about this role: As a Senior Nutrition Research & Clinical Investigator on this team, you will evaluate scientific research to support the Nutrilite global product portfolio and provide scientific credibility to differentiate Nutrilite products from competitors. Your role will require you to work on front end research, helping to identify relevant mechanisms of action and outcomes, and to partner with internal teams and/or external partners to advance ingredient and product technologies. If clinical studies are warranted, you will develop protocols, identify the appropriate CRO or academic partner, oversee study execution and results analysis, and then translate the results into consumer-friendly and regulatory acceptable claims and stories which support the efficacy of our products. Your background in both nutrition science and clinical research will be showcased in the role. Your work will maintain the high credibility of the Nutrilite brand and will offer a highly visible role, providing patent and publication opportunities, in addition to the ability to travel globally, meeting and sharing expert insights about Nutrilite products, nutrition, and health. If you have a passion for health and wellness, enjoy translating complex nutrition science into efficacious, experiential products, and the ability to share your expertise with clients and customers around the world, this role can offer a strong platform to spotlight your talent!   qualifications: Required qualifications: Minimum 3 - 6 years of experience in nutrition research and product claim substantiationAdvanced degree (MS or PhD) in Bioscience, Nutrition Science, or related scientific disciplineProven exposures incorporating functional botanicals and botanically derived bioactives into product profile designAbility to translate complex scientific and technical concepts into consumer appropriate language, ideally with compelling visuals, to enable communication and understanding of the science underlying the productInterpersonal skills to influence and inspire both internal and external audiencesExperience leading clinical studies in an industry setting is helpfulBasic understanding of global regulations in the nutraceutical industry is preferredIndustry awareness with knowledge of trends and innovation desiredRD (Registered Dietician) Certification, ACRP (Association of Clinical Research Professionals) Certification, or naturopathic background helpful  skills: Biology, Food Product Development 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.EOEDisclaime 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.
    • lake forest, california
    • contract
    • $80 - $85.71 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. 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: Lake Forest, California job type: Contract salary: $80.00 - 85.71 per hour work hours: 9 to 5 education: Associate   responsibilities: Review of documents to support continued market access of Company medical device products Assist colleagues in preparation of clinical focused regulatory documents and agreements Participation in Cross Functional team meetings on product development and regulatory documents Review literature and assist in creation of abstracts, presentations and publications of Company internal studies/Company sponsored studies Creation of documents as references for summary of Company internal studies  qualifications: Bachelor's Degree or equivalent years of directly related experience; (Assoc.+9 yrs; M.S.+2 yrs; PhD+0 yrs)MEDICAL DEVICEREGULATORY DOCUMENTSMEDICAL WRITINGCDMAThe ability to fluently read, write, understand and communicate in English5 Years of Relevant ExperienceLifecycle Management experience, understanding of documents required for CE Marking Ophthalmic experience strongly desired, especially in posterior segment Medical writing a plus  skills: GCP (Good Clinical Practice), Regulatory Briefing Documents, Submissions 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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. 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: Lake Forest, California job type: Contract salary: $80.00 - 85.71 per hour work hours: 9 to 5 education: Associate   responsibilities: Review of documents to support continued market access of Company medical device products Assist colleagues in preparation of clinical focused regulatory documents and agreements Participation in Cross Functional team meetings on product development and regulatory documents Review literature and assist in creation of abstracts, presentations and publications of Company internal studies/Company sponsored studies Creation of documents as references for summary of Company internal studies  qualifications: Bachelor's Degree or equivalent years of directly related experience; (Assoc.+9 yrs; M.S.+2 yrs; PhD+0 yrs)MEDICAL DEVICEREGULATORY DOCUMENTSMEDICAL WRITINGCDMAThe ability to fluently read, write, understand and communicate in English5 Years of Relevant ExperienceLifecycle Management experience, understanding of documents required for CE Marking Ophthalmic experience strongly desired, especially in posterior segment Medical writing a plus  skills: GCP (Good Clinical Practice), Regulatory Briefing Documents, Submissions 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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.
    • lake forest, california
    • contract
    • $38 - $43.48 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. 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: Lake Forest, California job type: Contract salary: $38.00 - 43.48 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Assist with preparing technical documents, legalized documents and letters in support of international regulatory submissions.Assist with set-up and preparation of EU Technical Files.Organize and support renewals of international licenses.Support various activities associated with implementation of the EU Medical Device Regulation.  qualifications: Bachelor's degree or 5 years equivalent experience in medical devices. Excellent writing skills.Regulatory affairs knowledge and experience in medical devices.Self-starter with ability to work independently on basic tasks and under direction by more experienced staff on more complex assignments/tasks.Proficient in MS Office applications.Ability to work hours outside 8am-5pm Pacific time in order to support international colleagues is preferred. Proficiency in Veeva application desired.  skills: MS-WORD, MS-EXCEL, MS-Powerpoint, Submissions 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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. 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: Lake Forest, California job type: Contract salary: $38.00 - 43.48 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Assist with preparing technical documents, legalized documents and letters in support of international regulatory submissions.Assist with set-up and preparation of EU Technical Files.Organize and support renewals of international licenses.Support various activities associated with implementation of the EU Medical Device Regulation.  qualifications: Bachelor's degree or 5 years equivalent experience in medical devices. Excellent writing skills.Regulatory affairs knowledge and experience in medical devices.Self-starter with ability to work independently on basic tasks and under direction by more experienced staff on more complex assignments/tasks.Proficient in MS Office applications.Ability to work hours outside 8am-5pm Pacific time in order to support international colleagues is preferred. Proficiency in Veeva application desired.  skills: MS-WORD, MS-EXCEL, MS-Powerpoint, Submissions 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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.
    • lake forest, california
    • contract
    • $25 - $30 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. 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: Lake Forest, California job type: Contract salary: $25 - 30 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Assist with preparing and coordinating documents to be legalized in support of international regulatory submissions.Support and prepare technical documents for international registrations.Support Regulatory Affairs organization by processing invoices, processing legal documents, ordering supplies, and performing other administrative activities as needed.  qualifications: Bachelor's degree or equivalent experience is preferred.Self-starter with ability to work independently under pressure and react quickly to changing priorities.Proficient in MS Office applications.Ability to work hours outside 8am-5pm Pacific Time in order to support international colleagues is preferred.Licensed notary by the State of California is preferred.Knowledge/experience of medical devices is preferred.   skills: MS-WORD, MS-EXCEL, MS-Powerpoint 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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. 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: Lake Forest, California job type: Contract salary: $25 - 30 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Assist with preparing and coordinating documents to be legalized in support of international regulatory submissions.Support and prepare technical documents for international registrations.Support Regulatory Affairs organization by processing invoices, processing legal documents, ordering supplies, and performing other administrative activities as needed.  qualifications: Bachelor's degree or equivalent experience is preferred.Self-starter with ability to work independently under pressure and react quickly to changing priorities.Proficient in MS Office applications.Ability to work hours outside 8am-5pm Pacific Time in order to support international colleagues is preferred.Licensed notary by the State of California is preferred.Knowledge/experience of medical devices is preferred.   skills: MS-WORD, MS-EXCEL, MS-Powerpoint 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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.
    • irvine, california
    • contract
    • $35 - $40.52 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: Irvine, California job type: Contract salary: $35.00 - 40.52 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Looking for a team player with strong QC lab experience in a cGMP environment.   qualifications: Bachelor's degree (or above) in biology or chemistry strongly preferred, with 6-10 years industry experience;Six to ten years' experience in the lab in chemistry in a GMP pharmaceutical manufacturing and/or development environment.Industry experience in chromatography data collection/processing software. Empower preferred.Industry experience in GMP documentation and working in a GMP environment.Experience with release and stability analytical data reviewFamiliarity with TrackWise preferredExperience with investigations and non-conformance writing and reviewAbility to work closely with QC analysts to generate Standard Operating Procedures, protocols and reports, including validation protocols and reportsAbility execute laboratory testing, if needed, to support the QC lab activities  skills: Quality control, 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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: Irvine, California job type: Contract salary: $35.00 - 40.52 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Looking for a team player with strong QC lab experience in a cGMP environment.   qualifications: Bachelor's degree (or above) in biology or chemistry strongly preferred, with 6-10 years industry experience;Six to ten years' experience in the lab in chemistry in a GMP pharmaceutical manufacturing and/or development environment.Industry experience in chromatography data collection/processing software. Empower preferred.Industry experience in GMP documentation and working in a GMP environment.Experience with release and stability analytical data reviewFamiliarity with TrackWise preferredExperience with investigations and non-conformance writing and reviewAbility to work closely with QC analysts to generate Standard Operating Procedures, protocols and reports, including validation protocols and reportsAbility execute laboratory testing, if needed, to support the QC lab activities  skills: Quality control, 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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.
    • buena park, california
    • permanent
    • $100,000 per year
    job summary: In partnership with Amway, we are conducting a direct hire search for a Sensory and Consumer Research Scientist! Amway is a $9B Global Leader in Nutrition and Wellness. This role is part of the team at their Nutrilite Center of Excellence in Buena Park, CA. Enjoy a hybrid schedule and 3-day weekends! This team works four 10-hour days M-Th.   location: Buena Park, California job type: Permanent work hours: 8 to 4 education: Bachelors   responsibilities: In this role, you will design and execute sensory and consumer research for nutrition products (including supplements, food and beverage) to serve both adult and child consumers. You will identify and interpret customer needs and insights to enable the team to make consumer-focused decisions.   qualifications: BS Degree in Food Science, Nutrition, or a related discipline with sensory science focus3 years' experience in nutrition or food sensory research and consumer product researchDemonstrated experience leading sensory and consumer research (experience working with children preferred) including designing experiments, gathering, analyzing, and translating data into meaningful recommendationsExperience overseeing the design and execution of various consumer product tests (ie. central location tests, descriptive analysis, discrimination testing, and qualitative/observational methodologies, etc)Statistical experimental design and analysis skills for interpreting complex data and translating into business support materialsExperience as active contributor on food/nutrition product development teamsExperience in Human Centered Design preferred  skills: Sensory Analysis 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.EOEDisclaime 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: In partnership with Amway, we are conducting a direct hire search for a Sensory and Consumer Research Scientist! Amway is a $9B Global Leader in Nutrition and Wellness. This role is part of the team at their Nutrilite Center of Excellence in Buena Park, CA. Enjoy a hybrid schedule and 3-day weekends! This team works four 10-hour days M-Th.   location: Buena Park, California job type: Permanent work hours: 8 to 4 education: Bachelors   responsibilities: In this role, you will design and execute sensory and consumer research for nutrition products (including supplements, food and beverage) to serve both adult and child consumers. You will identify and interpret customer needs and insights to enable the team to make consumer-focused decisions.   qualifications: BS Degree in Food Science, Nutrition, or a related discipline with sensory science focus3 years' experience in nutrition or food sensory research and consumer product researchDemonstrated experience leading sensory and consumer research (experience working with children preferred) including designing experiments, gathering, analyzing, and translating data into meaningful recommendationsExperience overseeing the design and execution of various consumer product tests (ie. central location tests, descriptive analysis, discrimination testing, and qualitative/observational methodologies, etc)Statistical experimental design and analysis skills for interpreting complex data and translating into business support materialsExperience as active contributor on food/nutrition product development teamsExperience in Human Centered Design preferred  skills: Sensory Analysis 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.EOEDisclaime 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.
    • irvine, california
    • permanent
    • $80,000 - $90,000 per year
    job summary: Exciting opportunity to join a growing pharmaceutical company as a Regulatory Affairs Specialist with lots of room to grow you career!   location: Irvine, California job type: Permanent salary: $80,000 - 90,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: Provides regulatory assistance during the ANDA / NDA submission and approval process.Assists in company Standard Operating Procedures (SOP's) development and review.Develop and assess strategies for regulatory approvals for NDAs and ANDAs by providing input for product development through commercialization.Assists in reviewing documents for regulatory compliance necessary for the acceptability of quality documentation for submission filing.Assists in developing pre-approval compliance activities during manufacturing of submission batches.Performs label development and reviews for compliance.Monitors impact of changing regulations on submissions.Monitors and submits applicable reports to regulatory authorities as required.Maintains annual licenses, registrations, listings and patent information as required.Prepare annual reports for NDA / ANDAs by scheduling and coordinating receipt of documentation/information, preparing cover pages describing changes made to an application and tracking progress of their preparation.Review of documents and interacting with multiple departments (QA, Manufacturing, Project Management, Engineering, PD, etc.) which provide information and documentation utilizing the change control database to ensure accurate reporting to FDA.Assist in maintaining approved NDA / ANDAs current by requesting revisions to technical documentation as part of the annual report preparation process.Provide a critical detailed review of technical documentation including labeling, distribution reports, analytical procedures, product specifications, manufacturing and packaging batch records, in-process specifications, etc. prior to FDA submission.Assist in the preparation, revision and approval of labeling.Assist in the preparation and submission of required post approval reports such as field alert reports, periodic adverse drug experience reports etc. Ensures product safety issues and product-associated events are reported to regulatory agencies.Ensures compliance with product post-marketing approval requirements, annual reports, drug listings, labeling, pharmacopeia changes (pre and post approval), etc.Reviews regulatory aspects of contracts with customers.Provides regulatory support for product recalls and recalls communications.  qualifications: Bachelor's degree in science field (Biology, Chemistry, Microbiology, and Pharmacy).10+ years' of experience in a regulatory function within pharmaceuticals (preferred) or medical products; experience in quality assurance and/or compliance may be considered.Certification such as RAC from the Regulatory Affairs Professionals Society preferred.Experience with electronic regulatory submissions.Knowledge of USP, and Code of Federal Regulations 21 CFR 111, 11, 210, and 211. FDA/ICH guidance and the regulatory process pertaining to drug development and approval.Able to handle multiple high priority assignments.Advanced technical writing skills and acute attention to detail.Ability to read and interpret complex technical documents. Ability to write comprehensive reports.Strong communication skills, both written and verbal.Able to build rapport at all levels of the organization as well as with external contacts.  skills: NDA, Regulatory Affairs Strategy, Submissions 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.EOEDisclaime 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: Exciting opportunity to join a growing pharmaceutical company as a Regulatory Affairs Specialist with lots of room to grow you career!   location: Irvine, California job type: Permanent salary: $80,000 - 90,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: Provides regulatory assistance during the ANDA / NDA submission and approval process.Assists in company Standard Operating Procedures (SOP's) development and review.Develop and assess strategies for regulatory approvals for NDAs and ANDAs by providing input for product development through commercialization.Assists in reviewing documents for regulatory compliance necessary for the acceptability of quality documentation for submission filing.Assists in developing pre-approval compliance activities during manufacturing of submission batches.Performs label development and reviews for compliance.Monitors impact of changing regulations on submissions.Monitors and submits applicable reports to regulatory authorities as required.Maintains annual licenses, registrations, listings and patent information as required.Prepare annual reports for NDA / ANDAs by scheduling and coordinating receipt of documentation/information, preparing cover pages describing changes made to an application and tracking progress of their preparation.Review of documents and interacting with multiple departments (QA, Manufacturing, Project Management, Engineering, PD, etc.) which provide information and documentation utilizing the change control database to ensure accurate reporting to FDA.Assist in maintaining approved NDA / ANDAs current by requesting revisions to technical documentation as part of the annual report preparation process.Provide a critical detailed review of technical documentation including labeling, distribution reports, analytical procedures, product specifications, manufacturing and packaging batch records, in-process specifications, etc. prior to FDA submission.Assist in the preparation, revision and approval of labeling.Assist in the preparation and submission of required post approval reports such as field alert reports, periodic adverse drug experience reports etc. Ensures product safety issues and product-associated events are reported to regulatory agencies.Ensures compliance with product post-marketing approval requirements, annual reports, drug listings, labeling, pharmacopeia changes (pre and post approval), etc.Reviews regulatory aspects of contracts with customers.Provides regulatory support for product recalls and recalls communications.  qualifications: Bachelor's degree in science field (Biology, Chemistry, Microbiology, and Pharmacy).10+ years' of experience in a regulatory function within pharmaceuticals (preferred) or medical products; experience in quality assurance and/or compliance may be considered.Certification such as RAC from the Regulatory Affairs Professionals Society preferred.Experience with electronic regulatory submissions.Knowledge of USP, and Code of Federal Regulations 21 CFR 111, 11, 210, and 211. FDA/ICH guidance and the regulatory process pertaining to drug development and approval.Able to handle multiple high priority assignments.Advanced technical writing skills and acute attention to detail.Ability to read and interpret complex technical documents. Ability to write comprehensive reports.Strong communication skills, both written and verbal.Able to build rapport at all levels of the organization as well as with external contacts.  skills: NDA, Regulatory Affairs Strategy, Submissions 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.EOEDisclaime 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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