9 jobs found in missouri

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    • kansas city, missouri
    • permanent
    • US$40,000 - US$45,000, per year, $40k - 45k per year + none
    • 8 am - 5 pm
    Are you detail-oriented and good at coordinating a number of moving parts at once? Our client in the Southeast Kansas City area is looking to hire an administrative assistant to support multiple departments within the organization. Candidates who are a fit for this role will have experience providing administrative support and be comfortable working in MS Excel and Powerpoint. Responsibilitiesprovide administrative support to the VP of Sales and Marketing, as well as the Plant Manager maintain calendars and schedules answer the phones and cover for the receptionist when she is gone run reports for inventory assist with managing the maintenance of fleet cars assist with creating power point presentations pull an maintain sales reports SkillsClerical WorkSwitchboard OperationGreeting CustomersAdministrative Duties (2 years of experience is required)Multi-taskingAnswering PhonesMicrosoft OfficeMaintaining CalendarsScheduling AppointmentsCreating PresentationsEducationBachelorsQualificationsYears of experience: 2 yearsExperience level:ExperiencedShift: FirstWorking hours: 8 AM - 5 PMRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
    Are you detail-oriented and good at coordinating a number of moving parts at once? Our client in the Southeast Kansas City area is looking to hire an administrative assistant to support multiple departments within the organization. Candidates who are a fit for this role will have experience providing administrative support and be comfortable working in MS Excel and Powerpoint. Responsibilitiesprovide administrative support to the VP of Sales and Marketing, as well as the Plant Manager maintain calendars and schedules answer the phones and cover for the receptionist when she is gone run reports for inventory assist with managing the maintenance of fleet cars assist with creating power point presentations pull an maintain sales reports SkillsClerical WorkSwitchboard OperationGreeting CustomersAdministrative Duties (2 years of experience is required)Multi-taskingAnswering PhonesMicrosoft OfficeMaintaining CalendarsScheduling AppointmentsCreating PresentationsEducationBachelorsQualificationsYears of experience: 2 yearsExperience level:ExperiencedShift: FirstWorking hours: 8 AM - 5 PMRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
    • kansas city, missouri
    • temp to perm
    • US$16.00 - US$16.00, per hour, $16 per hour + none
    • 8 am - 5 pm
    A valued client of Randstad's is actively seeking customer service representatives.****This is a work-from-home opportunity if you reside in the following states: AZ, MD, SC, NV, TX and FL. ****Position entails receiving inbound calls to sell insurance plans and place outbound calls for member outreach or to welcome new members.If you are qualified and interested, please apply to this job posting and email your resume to megan.perri@randstadusa.comResponsibilitiesMust meet all requirements to obtain and maintain a state licensed advisor status. Client provides all necessary training and pays for all training classes to obtain health insurance licensing as well as license renewal fees while you are employed.Absorb, retain and explain a working knowledge of product plans and general Medicare informationAssist callers quickly and professionally by fielding inbound calls to sell health insurance plans with set sales techniquesPlace outbound calls for member outreach and welcome calls to new membersProvide accurate information to prospects using quality and compliance standardsCommunicate effectively with prospects and plan members over the phone and with co-workers and management personnel.Proficiently work with Windows and comfortably navigating between websites to assist callers requesting informationWork on a computer 8 or more hours per daySkillsHealth Insurance PoliciesCUSTOMER ORDERS/SALESInsuranceEnrolled AgentSalesEducationHigh School (required)QualificationsYears of experience: 0 yearsExperience level:Entry LevelShift: FirstWorking hours: 8 AM - 5 PMRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
    A valued client of Randstad's is actively seeking customer service representatives.****This is a work-from-home opportunity if you reside in the following states: AZ, MD, SC, NV, TX and FL. ****Position entails receiving inbound calls to sell insurance plans and place outbound calls for member outreach or to welcome new members.If you are qualified and interested, please apply to this job posting and email your resume to megan.perri@randstadusa.comResponsibilitiesMust meet all requirements to obtain and maintain a state licensed advisor status. Client provides all necessary training and pays for all training classes to obtain health insurance licensing as well as license renewal fees while you are employed.Absorb, retain and explain a working knowledge of product plans and general Medicare informationAssist callers quickly and professionally by fielding inbound calls to sell health insurance plans with set sales techniquesPlace outbound calls for member outreach and welcome calls to new membersProvide accurate information to prospects using quality and compliance standardsCommunicate effectively with prospects and plan members over the phone and with co-workers and management personnel.Proficiently work with Windows and comfortably navigating between websites to assist callers requesting informationWork on a computer 8 or more hours per daySkillsHealth Insurance PoliciesCUSTOMER ORDERS/SALESInsuranceEnrolled AgentSalesEducationHigh School (required)QualificationsYears of experience: 0 yearsExperience level:Entry LevelShift: FirstWorking hours: 8 AM - 5 PMRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
    • jefferson city, missouri
    • temp to perm
    • US$34.00 - US$36.50, per hour, $34.00 - 36.50 per hour
    • 9 to 5
    job summary:Perform a variety of clinical procedures to collect, record, report and interpret data on patients enrolled and/or seeking enrollment in clinical studies according to the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP). Assist with daily workload planning. location: Jefferson City, Missourijob type: Temporarysalary: $34.00 - 36.50 per hourwork hours: 9 to 5education: High School responsibilities:Provide clinical research support to investigators to prepare for and execute assigned research studies, including: Review study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research dataAttend all relevant study meetings; Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical researchRecruit and screen patients for clinical trials and maintain subject screening logsOrient research subjects to the study, including the purpose of the study, procedures, and protocol issues such as timelines for visitsDesign and maintain source documentation based on protocol requirements; Schedule and execute study visits and perform study proceduresCollect, record and maintain research subject study data according to study protocol and SOPs, preserving quality control for content, accuracy and completenessHandle lab testing and analysis, including preparation of specimen collection tubes and lab logisticsMonitor subject safety and report adverse reactions to appropriate medical personnelCorrespond with research subjects and troubleshoot study-related questions or issuesParticipate in huddles to confirm daily study tasks are assigned to team members and are executed to the expected standardsAssist with study data quality checking and query resolution.Perform a variety of complex clinical research procedures including but not limited to ECG, sample collection, spirometry, vital signs, dose verification, cannulation and cardiac telemetry monitoring.Record, report and interpret study findings appropriately to develop a study-specific database.Assist investigator in verifying that research study objectives are met on time, within budget and according to applicable protocol requirements, clinical research regulations and quality standards.Provide training to new investigator site staff members on study-specific topics and requirements.Assist in maintaining adherence to investigator site staff training requirements by auditing and maintaining training records.Prepare for and attend study monitoring visits, study audits, and regulatory inspections with clinical research regulatory agencies.Assist research site with coverage planning related to staffing and scheduling for research projects. qualifications:High school diploma (A BS would be a plus) or educational equivalent and relevant work experience in a clinical environment or medical setting; or equivalent combination of education, training and experience Applicable certifications and licenses as required by the company, country, state, and/or other regulatory bodies.Must have experience working as a research coordinator at a clinical research site with hands on patient facing contactKnowledge of clinical trials; 3-5 years experience in patient facing clinical research experience.In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules Knowledge of medical terminologySkilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word Excellent interpersonal skillsAbility to pay close attention to detailAbility to establish and maintain effective working relationships with coworkers, managers and clients skills: CSREqual 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.
    job summary:Perform a variety of clinical procedures to collect, record, report and interpret data on patients enrolled and/or seeking enrollment in clinical studies according to the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP). Assist with daily workload planning. location: Jefferson City, Missourijob type: Temporarysalary: $34.00 - 36.50 per hourwork hours: 9 to 5education: High School responsibilities:Provide clinical research support to investigators to prepare for and execute assigned research studies, including: Review study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research dataAttend all relevant study meetings; Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical researchRecruit and screen patients for clinical trials and maintain subject screening logsOrient research subjects to the study, including the purpose of the study, procedures, and protocol issues such as timelines for visitsDesign and maintain source documentation based on protocol requirements; Schedule and execute study visits and perform study proceduresCollect, record and maintain research subject study data according to study protocol and SOPs, preserving quality control for content, accuracy and completenessHandle lab testing and analysis, including preparation of specimen collection tubes and lab logisticsMonitor subject safety and report adverse reactions to appropriate medical personnelCorrespond with research subjects and troubleshoot study-related questions or issuesParticipate in huddles to confirm daily study tasks are assigned to team members and are executed to the expected standardsAssist with study data quality checking and query resolution.Perform a variety of complex clinical research procedures including but not limited to ECG, sample collection, spirometry, vital signs, dose verification, cannulation and cardiac telemetry monitoring.Record, report and interpret study findings appropriately to develop a study-specific database.Assist investigator in verifying that research study objectives are met on time, within budget and according to applicable protocol requirements, clinical research regulations and quality standards.Provide training to new investigator site staff members on study-specific topics and requirements.Assist in maintaining adherence to investigator site staff training requirements by auditing and maintaining training records.Prepare for and attend study monitoring visits, study audits, and regulatory inspections with clinical research regulatory agencies.Assist research site with coverage planning related to staffing and scheduling for research projects. qualifications:High school diploma (A BS would be a plus) or educational equivalent and relevant work experience in a clinical environment or medical setting; or equivalent combination of education, training and experience Applicable certifications and licenses as required by the company, country, state, and/or other regulatory bodies.Must have experience working as a research coordinator at a clinical research site with hands on patient facing contactKnowledge of clinical trials; 3-5 years experience in patient facing clinical research experience.In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules Knowledge of medical terminologySkilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word Excellent interpersonal skillsAbility to pay close attention to detailAbility to establish and maintain effective working relationships with coworkers, managers and clients skills: CSREqual 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.
    • chesterfield, missouri
    • contract
    • US$22.14 - US$26.05, per hour, $22.14 - 26.05 per hour
    • 9 to 5
    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. With therapeutic areas that include Oncology, Vaccines, and Rare Diseases, our partner aims to make treatments streamlined, easily accessible, and globally produced. If you share their goal of approaching healthcare in a novel way, look no further - apply for your dream job now! location: Chesterfield, Missourijob type: Contractsalary: $22.14 - 26.05 per hourwork hours: 9 to 5education: Bachelors responsibilities:The scientist filling this position will work within a highly-matrixed team setting on a variety of modalities including vaccines, viral constructs, therapeutic proteins, and monoclonal antibodies. The contractor will work in a cGMP testing environment performing sample testing and method qualification. Work skills required: Experience with DNA techniques (qPCR) and/or ELISA is required. Intermediate proficiency in Microsoft Office (Excel, Word, and Outlook) is required. Must be able to understand and follow standard operating procedures.POSITION RESPONSIBILITIES:- Analytical testing by qPCR and/or ELISA in a cGMP environment**- Analysis and documentation of results- Routine lab duties (ex. reagent preparation, consumable stocking) qualifications:EDUCATION AND EXPERIENCE:Preferred education is a bachelor's degree with 1-3 years of experience in DNA techniques (qPCR) and/or ELISA.TECHNICAL SKILLS REQUIREMENTS:- qPCR and/or ELISA (required)**- Proficiency in Microsoft Office (Excel and Word) Required- cGMP experience (preferred)- LIMS experience (preferred skills: PCR, 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.
    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. With therapeutic areas that include Oncology, Vaccines, and Rare Diseases, our partner aims to make treatments streamlined, easily accessible, and globally produced. If you share their goal of approaching healthcare in a novel way, look no further - apply for your dream job now! location: Chesterfield, Missourijob type: Contractsalary: $22.14 - 26.05 per hourwork hours: 9 to 5education: Bachelors responsibilities:The scientist filling this position will work within a highly-matrixed team setting on a variety of modalities including vaccines, viral constructs, therapeutic proteins, and monoclonal antibodies. The contractor will work in a cGMP testing environment performing sample testing and method qualification. Work skills required: Experience with DNA techniques (qPCR) and/or ELISA is required. Intermediate proficiency in Microsoft Office (Excel, Word, and Outlook) is required. Must be able to understand and follow standard operating procedures.POSITION RESPONSIBILITIES:- Analytical testing by qPCR and/or ELISA in a cGMP environment**- Analysis and documentation of results- Routine lab duties (ex. reagent preparation, consumable stocking) qualifications:EDUCATION AND EXPERIENCE:Preferred education is a bachelor's degree with 1-3 years of experience in DNA techniques (qPCR) and/or ELISA.TECHNICAL SKILLS REQUIREMENTS:- qPCR and/or ELISA (required)**- Proficiency in Microsoft Office (Excel and Word) Required- cGMP experience (preferred)- LIMS experience (preferred skills: PCR, 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.
    • st louis, missouri
    • contract
    • US$19.00 - US$21.00, per hour, $19 - 21 per hour
    • 7 to 3
    job summary:Technician of Quality$19-$21 (no flex)Shift is Monday thru Friday 7am-3:30pm. Weekend work may be required to meet business needs or schedules. location: Saint Louis, Missourijob type: Contractsalary: $19 - 21 per hourwork hours: 7 to 3education: Bachelors responsibilities:Job Summary:This role is responsible for carrying out approved microbiological techniques and methodologies, preparing samples, and performing analytical and microbial testing of food products, ingredients, environmental samples, and other sample matrices.Responsibilities:- Apply aseptic technique in all work conducted- Documentation of sample preparation, quality control and analytical activities- Prepare and analyze samples for pathogens, indicator organisms, probiotics, and other microbes- Accurately perform testing methods and read testing results- Responsible for the completion of required training to progress to more complex tasks qualifications:Minimum Qualifications:- BS in Microbiology or a Life Science.- Knowledge of aseptic technique- 2+ years of laboratory experience in a commercial food testing analytical laboratory preferred- Must possess Knowledge of ISO 17025 or GLPs preferred- General knowledge and experience in microbiological testingPhysical Demands:- Must have full dexterity of hands and fingers to operate a computer and carry out required testing and tasks- Capable of keeping up with a fast-paced, goal-oriented team- Color vision and depth perception necessary- Occasional lifting of up to 50lbs skills: GLP (Good Laboratory 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.
    job summary:Technician of Quality$19-$21 (no flex)Shift is Monday thru Friday 7am-3:30pm. Weekend work may be required to meet business needs or schedules. location: Saint Louis, Missourijob type: Contractsalary: $19 - 21 per hourwork hours: 7 to 3education: Bachelors responsibilities:Job Summary:This role is responsible for carrying out approved microbiological techniques and methodologies, preparing samples, and performing analytical and microbial testing of food products, ingredients, environmental samples, and other sample matrices.Responsibilities:- Apply aseptic technique in all work conducted- Documentation of sample preparation, quality control and analytical activities- Prepare and analyze samples for pathogens, indicator organisms, probiotics, and other microbes- Accurately perform testing methods and read testing results- Responsible for the completion of required training to progress to more complex tasks qualifications:Minimum Qualifications:- BS in Microbiology or a Life Science.- Knowledge of aseptic technique- 2+ years of laboratory experience in a commercial food testing analytical laboratory preferred- Must possess Knowledge of ISO 17025 or GLPs preferred- General knowledge and experience in microbiological testingPhysical Demands:- Must have full dexterity of hands and fingers to operate a computer and carry out required testing and tasks- Capable of keeping up with a fast-paced, goal-oriented team- Color vision and depth perception necessary- Occasional lifting of up to 50lbs skills: GLP (Good Laboratory 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.
    • bridgeton, missouri
    • temp to perm
    • US$16.72 - US$16.72, per hour, $16.72 - 16.72 per hour + none
    • 10 pm - 6 am
    Performs set-up and operation of the machine to support production.  Maintains the work area and equiptment in a clean and orderly manorMeet and follow prescribed safety regulationsClosley supervised involving routine, repetative tasksStay current on safety rules, and adhere to established specifications when performing production operationsMeet and exceed output and quality goals as defined by managerRequires high school diploma or GED, and minimal experience of 3 yearsWillingness to complete a drug test and background checkUnderstand basic mathAbility to work effectively on a teamAbility to communicate effectively with peers and managementAbility to work wiht basic computer programsPhysical requirements required for production environmentResponsibilitiesReceive and count stock items, and record data manually or using computer. Pack and unpack items to be stocked on shelves in stockrooms, warehouses, or storage yards. Verify inventory computations by comparing them to physical counts of stock, and investigate discrepancies or adjust errors. Store items in an orderly and accessible manner in warehouses, tool rooms, supply rooms, or other areas. Mark stock items using identification tags, stamps, electric marking tools, or other labeling equipment. Clean and maintain supplies, tools, equipment, and storage areas in order to ensure compliance with safety regulations. Keep records on the use and/or damage of stock or stock handling equipment. Examine and inspect stock items for wear or defects, reporting any damage to supervisors. Determine proper storage methods, identification, and stock location based on turnover, environmental factors, and physical capabilities of facilities. The essential functions of this role include:working in a smoke free environmentworking in a non-temperature controlled environmentstanding for 8 hours at one timeSkillsInventory AuditingProblem SolvingPackingpickingVerbal CommunicationWritten Communicationteam playerAccount Reconciliationdetail orientedMonth-End CloseEducationHigh School (required)QualificationsYears of experience: 5 yearsExperience level:Entry LevelShift: ThirdWorking hours: 10 PM - 6 AMRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
    Performs set-up and operation of the machine to support production.  Maintains the work area and equiptment in a clean and orderly manorMeet and follow prescribed safety regulationsClosley supervised involving routine, repetative tasksStay current on safety rules, and adhere to established specifications when performing production operationsMeet and exceed output and quality goals as defined by managerRequires high school diploma or GED, and minimal experience of 3 yearsWillingness to complete a drug test and background checkUnderstand basic mathAbility to work effectively on a teamAbility to communicate effectively with peers and managementAbility to work wiht basic computer programsPhysical requirements required for production environmentResponsibilitiesReceive and count stock items, and record data manually or using computer. Pack and unpack items to be stocked on shelves in stockrooms, warehouses, or storage yards. Verify inventory computations by comparing them to physical counts of stock, and investigate discrepancies or adjust errors. Store items in an orderly and accessible manner in warehouses, tool rooms, supply rooms, or other areas. Mark stock items using identification tags, stamps, electric marking tools, or other labeling equipment. Clean and maintain supplies, tools, equipment, and storage areas in order to ensure compliance with safety regulations. Keep records on the use and/or damage of stock or stock handling equipment. Examine and inspect stock items for wear or defects, reporting any damage to supervisors. Determine proper storage methods, identification, and stock location based on turnover, environmental factors, and physical capabilities of facilities. The essential functions of this role include:working in a smoke free environmentworking in a non-temperature controlled environmentstanding for 8 hours at one timeSkillsInventory AuditingProblem SolvingPackingpickingVerbal CommunicationWritten Communicationteam playerAccount Reconciliationdetail orientedMonth-End CloseEducationHigh School (required)QualificationsYears of experience: 5 yearsExperience level:Entry LevelShift: ThirdWorking hours: 10 PM - 6 AMRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
    • bridgeton, missouri
    • temp to perm
    • US$16.72 - US$16.72, per hour, $16.72 - 16.72 per hour + none
    • 2 pm - 10 pm
     Performs set-up and operation of the machine to support production.  Maintains the work area and equiptment in a clean and orderly manorMeet and follow prescribed safety regulationsClosley supervised involving routine, repetative tasksStay current on safety rules, and adhere to established specifications when performing production operationsMeet and exceed output and quality goals as defined by managerRequires high school diploma or GED, and minimal experience of 3 yearsWillingness to complete a drug test and background checkUnderstand basic mathAbility to work effectively on a teamAbility to communicate effectively with peers and managementAbility to work wiht basic computer programsPhysical requirements required for production environmentResponsibilitiesReceive and count stock items, and record data manually or using computer. Pack and unpack items to be stocked on shelves in stockrooms, warehouses, or storage yards. Verify inventory computations by comparing them to physical counts of stock, and investigate discrepancies or adjust errors. Store items in an orderly and accessible manner in warehouses, tool rooms, supply rooms, or other areas. Mark stock items using identification tags, stamps, electric marking tools, or other labeling equipment. Clean and maintain supplies, tools, equipment, and storage areas in order to ensure compliance with safety regulations. Keep records on the use and/or damage of stock or stock handling equipment. Examine and inspect stock items for wear or defects, reporting any damage to supervisors. Determine proper storage methods, identification, and stock location based on turnover, environmental factors, and physical capabilities of facilities. The essential functions of this role include:working in a smoke free environmentworking in a non-temperature controlled environmentstanding for 8 hours at one timeSkillsInventory AuditingProblem SolvingPackingpickingVerbal CommunicationWritten Communicationteam playerAccount Reconciliationdetail orientedMonth-End CloseEducationHigh School (required)QualificationsYears of experience: 5 yearsExperience level:Entry LevelShift: SecondWorking hours: 2 PM - 10 PMRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
     Performs set-up and operation of the machine to support production.  Maintains the work area and equiptment in a clean and orderly manorMeet and follow prescribed safety regulationsClosley supervised involving routine, repetative tasksStay current on safety rules, and adhere to established specifications when performing production operationsMeet and exceed output and quality goals as defined by managerRequires high school diploma or GED, and minimal experience of 3 yearsWillingness to complete a drug test and background checkUnderstand basic mathAbility to work effectively on a teamAbility to communicate effectively with peers and managementAbility to work wiht basic computer programsPhysical requirements required for production environmentResponsibilitiesReceive and count stock items, and record data manually or using computer. Pack and unpack items to be stocked on shelves in stockrooms, warehouses, or storage yards. Verify inventory computations by comparing them to physical counts of stock, and investigate discrepancies or adjust errors. Store items in an orderly and accessible manner in warehouses, tool rooms, supply rooms, or other areas. Mark stock items using identification tags, stamps, electric marking tools, or other labeling equipment. Clean and maintain supplies, tools, equipment, and storage areas in order to ensure compliance with safety regulations. Keep records on the use and/or damage of stock or stock handling equipment. Examine and inspect stock items for wear or defects, reporting any damage to supervisors. Determine proper storage methods, identification, and stock location based on turnover, environmental factors, and physical capabilities of facilities. The essential functions of this role include:working in a smoke free environmentworking in a non-temperature controlled environmentstanding for 8 hours at one timeSkillsInventory AuditingProblem SolvingPackingpickingVerbal CommunicationWritten Communicationteam playerAccount Reconciliationdetail orientedMonth-End CloseEducationHigh School (required)QualificationsYears of experience: 5 yearsExperience level:Entry LevelShift: SecondWorking hours: 2 PM - 10 PMRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
    • saint louis, missouri
    • contract
    • US$39.38 - US$46.33, per hour, $39.38 - 46.33 per hour
    • 9 to 5
    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. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now! location: Saint Louis, Missourijob type: Contractsalary: $39.38 - 46.33 per hourwork hours: 9 to 5education: Bachelors responsibilities:The SCES Q manager Person in Plant acts as the day-to-day liaison with internal and external customers for quality related activities.- Ensure GMP compliance of products manufactured and/or tested at a contract facility.- Ensure all aspects of product manufacturing and/or testing are reviewed versus establishedquality standards and the applicable marketing authorizations.- Manage Quality Systems, e.g. change control, deviations, complaints, and product investigations.- Modify, review, and ensure contractor quality standards and protocols for processing materials into partially finished or finished product meet Sanofi and GMP requirements.- Contribute to the completion of milestones associated with specific projects.- Release product in accordance with approved specifications and procedures.- Monitor contractor compliance via GxP documentation review and on-site visits/audits.- Implement methods and procedures for inspecting, testing, and evaluating the precision and accuracy of products and production equipment.- Compile data and write summaries for periodic product reviews, investigations, complaints, and deviations.- Distribute applicable contractor documentation for Regulatory, Validation, and Subject Matter Expert review.- Interact with multi-functional internal and external project teams to ensure compliance.- Respond to technical and quality issues and handle schedule and/or process-related conflicts.- Demonstrate understanding of applicable US and global regulations related to manufacture of medicinal products (small molecules and biologics).- Monitor contractor performance to established Key Performance Indicators (KPI) and report adverse trends.Additional Responsibilities- May assist in vendor selection and evaluation.- Provide QA project manager support for change controls and other projects.- Develop and manage Quality Technical Agreements between Sanofi and the contractor- Participate in contractor quality audits and verify any actions taken by the contractor in response to audit observations are completed satisfactorily.- Support program for maintaining performance metrics. qualifications:Bachelor's degree and 10+ years of experience working in a cGxP or other regulated environment, with 3+ years of experience in a Quality role. skills: Project Management, MS-WORD, MS-EXCEL, MS-Powerpoint, MS-ProjectEqual 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.
    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. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now! location: Saint Louis, Missourijob type: Contractsalary: $39.38 - 46.33 per hourwork hours: 9 to 5education: Bachelors responsibilities:The SCES Q manager Person in Plant acts as the day-to-day liaison with internal and external customers for quality related activities.- Ensure GMP compliance of products manufactured and/or tested at a contract facility.- Ensure all aspects of product manufacturing and/or testing are reviewed versus establishedquality standards and the applicable marketing authorizations.- Manage Quality Systems, e.g. change control, deviations, complaints, and product investigations.- Modify, review, and ensure contractor quality standards and protocols for processing materials into partially finished or finished product meet Sanofi and GMP requirements.- Contribute to the completion of milestones associated with specific projects.- Release product in accordance with approved specifications and procedures.- Monitor contractor compliance via GxP documentation review and on-site visits/audits.- Implement methods and procedures for inspecting, testing, and evaluating the precision and accuracy of products and production equipment.- Compile data and write summaries for periodic product reviews, investigations, complaints, and deviations.- Distribute applicable contractor documentation for Regulatory, Validation, and Subject Matter Expert review.- Interact with multi-functional internal and external project teams to ensure compliance.- Respond to technical and quality issues and handle schedule and/or process-related conflicts.- Demonstrate understanding of applicable US and global regulations related to manufacture of medicinal products (small molecules and biologics).- Monitor contractor performance to established Key Performance Indicators (KPI) and report adverse trends.Additional Responsibilities- May assist in vendor selection and evaluation.- Provide QA project manager support for change controls and other projects.- Develop and manage Quality Technical Agreements between Sanofi and the contractor- Participate in contractor quality audits and verify any actions taken by the contractor in response to audit observations are completed satisfactorily.- Support program for maintaining performance metrics. qualifications:Bachelor's degree and 10+ years of experience working in a cGxP or other regulated environment, with 3+ years of experience in a Quality role. skills: Project Management, MS-WORD, MS-EXCEL, MS-Powerpoint, MS-ProjectEqual 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.
    • st louis, missouri
    • contract
    • US$18.00 - US$19.00, per hour, $18 - 19 per hour
    • 9 to 5
    job summary:Behavior Data Acquisition Technician - Entry level - COLLEGE GRADS 5 Openings (3 Remote roles and 2 roles must be local and work onsite) 18 month contract. location: Saint Louis, Missourijob type: Contractsalary: $18 - 19 per hourwork hours: 9 to 5education: Bachelors responsibilities:POSITION DESCRIPTIONActively seeking five skilled and dynamic technicians excited about the opportunity to improve the health and wellness of pets by acquiring pet data through use of pet IoT products in-homes and in our world-leading research centers. This person will be a member on an agile team with a global responsibility and will have the opportunity to play a central role and wear many hats.The Global Digital Solutions Group is responsible to develop the algorithms and AI that deliver personalized behavior, health, wellness and nutrition insights from a pet's acquired data. These positions are part of the team responsible for the collection of the high quality pet-training data (sensor data, labelled video and other data in time-series) used as the primary input supporting data scientist development of the insight-generating AI within commercial IoT, diagnostic and other digital products. qualifications:QUALIFICATIONS:- Bachelor's degree from an accredited college/university in Biology, Zoology, Psychology, Animal Science or related discipline, with an emphasis in Animal Behavior, or experience in collection/labeling of behavioral data from video/sensors- Experience using behavior coding software (e.g., Noldus, Mangold) or processes (e.g., direct labeling in Excel or custom software) to label behavior from video footage- Ability to work with internal/external customers to assess needs, aid, and resolve problems, using excellent problem-solving skills and verbal/written communication to non-technical audiences skills: Biology, 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.
    job summary:Behavior Data Acquisition Technician - Entry level - COLLEGE GRADS 5 Openings (3 Remote roles and 2 roles must be local and work onsite) 18 month contract. location: Saint Louis, Missourijob type: Contractsalary: $18 - 19 per hourwork hours: 9 to 5education: Bachelors responsibilities:POSITION DESCRIPTIONActively seeking five skilled and dynamic technicians excited about the opportunity to improve the health and wellness of pets by acquiring pet data through use of pet IoT products in-homes and in our world-leading research centers. This person will be a member on an agile team with a global responsibility and will have the opportunity to play a central role and wear many hats.The Global Digital Solutions Group is responsible to develop the algorithms and AI that deliver personalized behavior, health, wellness and nutrition insights from a pet's acquired data. These positions are part of the team responsible for the collection of the high quality pet-training data (sensor data, labelled video and other data in time-series) used as the primary input supporting data scientist development of the insight-generating AI within commercial IoT, diagnostic and other digital products. qualifications:QUALIFICATIONS:- Bachelor's degree from an accredited college/university in Biology, Zoology, Psychology, Animal Science or related discipline, with an emphasis in Animal Behavior, or experience in collection/labeling of behavioral data from video/sensors- Experience using behavior coding software (e.g., Noldus, Mangold) or processes (e.g., direct labeling in Excel or custom software) to label behavior from video footage- Ability to work with internal/external customers to assess needs, aid, and resolve problems, using excellent problem-solving skills and verbal/written communication to non-technical audiences skills: Biology, 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.

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