You are successfully logged out of your my randstad account

You have successfully deleted your account

Thank you for subscribing to your personalised job alerts.

8 jobs found in wisconsin

filter
    • verona, wisconsin
    • permanent
    • $42,000 - $52,000 per year
    job summary: Randstad is the #1 HR Services Company in the world and we are sourcing for a QC Chemist position in the Madison, WI area. The primary purpose of the QC Analytical Chemist is to provide support to the Production and Formulations Departments by analyzing pharmaceutical and/or cleaning samples. Support will be provided by analyzing samples using various procedures including, but not limited to, internal procedures, specifications, and analytical methods; compendial monographs, client procedures, and miscellaneous protocols. The QC Analytical Chemist is expected to understand basic internal procedures, and conduct analyses with some supervision after training is complete. This is a direct hire position and can start immediately.   location: Verona, Wisconsin job type: Permanent salary: $42,000 - 52,000 per year work hours: 8 to 4 education: Bachelors   responsibilities: Responsibilities: Ensures adherence to CPI Standard Operating Procedures, analytical methods, protocols, company standards, and applicable regulations.Analyzes pharmaceutical or cleaning samplesAbility to weigh samples, pipette, and prepare laboratory solutionsPerforms or assists with basic calibrationsMaintains a cGMP laboratory notebook, data, forms, and/or logbook.Assists in maintaining a clean, organized QC laboratory.Lifts/carries objects weighing up to 55 lbs.Follows all CPI cGMP practices, policies, and procedures.Follows all CPI safety practices, policies, and procedures.Other duties as assigned.  qualifications: Requirements: Bachelor's degree in Chemistry or related field.Experience with the use and troubleshooting of laboratory equipment desirable.Possesses good time management skills to complete assignments/projects in a timely manner with minimal supervision.Ability to establish and maintain effective working relationships with team members, co-workers, and/or clients. Working Conditions The QC Analytical Chemist works in a cGMP laboratory and production environment. Working in these environments will require working near skin irritants, electrical equipment, sharp instruments, toxic materials, and hazardous chemicals including controlled substances. Safety procedures must be followed to limit exposure.   skills: Quality control, SOP, Quality Assurance, Analytical Chemistry, Biology, Chemistry, GLP (Good Laboratory Practice), GMP (Good Manufacturing Practice), LIMS (Laboratory Information Management System 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: Randstad is the #1 HR Services Company in the world and we are sourcing for a QC Chemist position in the Madison, WI area. The primary purpose of the QC Analytical Chemist is to provide support to the Production and Formulations Departments by analyzing pharmaceutical and/or cleaning samples. Support will be provided by analyzing samples using various procedures including, but not limited to, internal procedures, specifications, and analytical methods; compendial monographs, client procedures, and miscellaneous protocols. The QC Analytical Chemist is expected to understand basic internal procedures, and conduct analyses with some supervision after training is complete. This is a direct hire position and can start immediately.   location: Verona, Wisconsin job type: Permanent salary: $42,000 - 52,000 per year work hours: 8 to 4 education: Bachelors   responsibilities: Responsibilities: Ensures adherence to CPI Standard Operating Procedures, analytical methods, protocols, company standards, and applicable regulations.Analyzes pharmaceutical or cleaning samplesAbility to weigh samples, pipette, and prepare laboratory solutionsPerforms or assists with basic calibrationsMaintains a cGMP laboratory notebook, data, forms, and/or logbook.Assists in maintaining a clean, organized QC laboratory.Lifts/carries objects weighing up to 55 lbs.Follows all CPI cGMP practices, policies, and procedures.Follows all CPI safety practices, policies, and procedures.Other duties as assigned.  qualifications: Requirements: Bachelor's degree in Chemistry or related field.Experience with the use and troubleshooting of laboratory equipment desirable.Possesses good time management skills to complete assignments/projects in a timely manner with minimal supervision.Ability to establish and maintain effective working relationships with team members, co-workers, and/or clients. Working Conditions The QC Analytical Chemist works in a cGMP laboratory and production environment. Working in these environments will require working near skin irritants, electrical equipment, sharp instruments, toxic materials, and hazardous chemicals including controlled substances. Safety procedures must be followed to limit exposure.   skills: Quality control, SOP, Quality Assurance, Analytical Chemistry, Biology, Chemistry, GLP (Good Laboratory Practice), GMP (Good Manufacturing Practice), LIMS (Laboratory Information Management System 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.
    • madison, wisconsin
    • permanent
    • $97,000 - $97,500 per year
    job summary: OUR TEAM: We are a motivated and caring team of individuals that support one another in providing quality assurance to existing products and new product development. We do this by partnering with our colleagues throughout the Promega organization, including Manufacturing, Quality Control, Research and Development, Marketing, Quality Systems, Technical Services, and others. JOB OBJECTIVE: Through their specified review, approval, and planning roles, QA Scientists apply their technical and quality system knowledge to assure internal and external customers that:   location: Madison, Wisconsin job type: Permanent salary: $97,000 - 97,500 per year work hours: 9 to 5 education: Bachelors   responsibilities: 1. Promega catalog and custom products meet their predetermined performance, process, and system requirements for quality. 2. Product and Process Changes and Quarantine disposition plans are implemented according to established procedures. 3. Technical literature (PPIs, labels, Technical Bulletins etc) are accurate and consistent. 4. Product performance claims and release criteria are based on objective data analysis. CORE DUTIES: Note that the emphasis placed on the essential duties listed here will vary by individual, depending on the focus and balance of that person's specific responsibilities. 1. Audit, data review, and approve product batch records for the next manufacturing step or availability in inventory. 2. Review and approve Manufacturing and Quality Control Protocols for catalog and custom products. 3. Review and approve product labels. 4. Establish and approve shelf-life assignments for catalog and custom products in cooperation with Manufacturing, Marketing, Regulatory Affairs and R&D staff. This includes approval of study design, data review, and change approval. 5. Review and approval of Technical Bulletins and Technical Manuals (performance and application claim accuracy and validity), including final release for publication. 6. Review and approve Promega Product Information (PPI) specification sheets and Certificates of Analysis; initiation, completion and issuance of these documents as required for custom products and some catalog products. 7. Assess the scope and inventory impact of nonconforming product situations; approving disposition plans of inventory product under quarantine; assisting in the disposition planning for nonconforming product in branch inventories. 8. Assist in the preparation, review and approval of design control documents. 9. Initiate, implement, review and/or approve Product and Process Change Plans. 10. Review, implement, and/or participate in Corrective and Preventive Action plans. 11. Review, implement, and participate in product and process validation planning. 12. Review, implement, and participate in complaint investigation planning. 13. Participate in process mapping and SOP development as directed. 14. Write SOPs as assigned. 15. Participate in team meetings to resolve planning and technical issues. Propose constructive solutions to existing problems. 16. Evaluate risks based on customer, technical, business and regulatory factors, provide options and recommendations to mitigate risk. 17. Consider basic regulatory requirements in product or process issues. 18. Demonstrates inclusion through their own words and actions and is accountable for a safe workspace. Acts with kindness, curiosity and respect for others. 19. Embracing and being open to incorporating Promega's 6 Emotional & Social Intelligence (ESI) core principles in daily work. 20. Understand and comply with ethical, legal and regulatory requirements applicable to our business. OCCASIONAL DUTIES: 1. Organize, facilitate, or lead meetings to discuss review findings and planning issues. 2. Represent Promega in support of technical sales at national and international trade shows and exhibitions, or attend relevant scientific meetings as requested. 3. Contact customers directly about quality issues or questions as directed. 4. Organize and implement training programs in areas of expertise and experience. 5. Participate in continuous improvement projects.   qualifications: KEY QUALIFICATIONS: 1. B.S. degree with a minimum of 7 years work experience in a relevant industry with quality control, quality assurance, or manufacturing responsibilities. 2. Working knowledge and direct application experience of the requirements of quality assurance systems in a manufacturing and/or product development or process development environment. 3. Proficiency with basic word processing and spreadsheet software programs. 4. Ability to apply basic statistical concepts to analytical data, process validation, and Quality Assurance activities. 5. A demonstrable track record of process improvement and effective procedure writing and revision. 6. Able to develop concise, clear and accurate written communication. 7. Proven ability to work constructively with a broad range of people. PREFERRED QUALIFICATIONS: 1. In-depth technical knowledge in genomics, protein analysis, or cellular analysis evidenced by peer-reviewed publications. 2. Work experience in Quality Assurance from a regulated industry. PHYSICAL DEMANDS: 1. Visual acuity required for physical inspection of finished product and raw materials and accompanying documentation. 2. Ability to wear basic safety apparel (safety glasses or goggles, lab coats, protective gloves). 3. Ability to use computers in an interactive manner for extended periods of time.   skills: Biology, Chemistry, 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.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: OUR TEAM: We are a motivated and caring team of individuals that support one another in providing quality assurance to existing products and new product development. We do this by partnering with our colleagues throughout the Promega organization, including Manufacturing, Quality Control, Research and Development, Marketing, Quality Systems, Technical Services, and others. JOB OBJECTIVE: Through their specified review, approval, and planning roles, QA Scientists apply their technical and quality system knowledge to assure internal and external customers that:   location: Madison, Wisconsin job type: Permanent salary: $97,000 - 97,500 per year work hours: 9 to 5 education: Bachelors   responsibilities: 1. Promega catalog and custom products meet their predetermined performance, process, and system requirements for quality. 2. Product and Process Changes and Quarantine disposition plans are implemented according to established procedures. 3. Technical literature (PPIs, labels, Technical Bulletins etc) are accurate and consistent. 4. Product performance claims and release criteria are based on objective data analysis. CORE DUTIES: Note that the emphasis placed on the essential duties listed here will vary by individual, depending on the focus and balance of that person's specific responsibilities. 1. Audit, data review, and approve product batch records for the next manufacturing step or availability in inventory. 2. Review and approve Manufacturing and Quality Control Protocols for catalog and custom products. 3. Review and approve product labels. 4. Establish and approve shelf-life assignments for catalog and custom products in cooperation with Manufacturing, Marketing, Regulatory Affairs and R&D staff. This includes approval of study design, data review, and change approval. 5. Review and approval of Technical Bulletins and Technical Manuals (performance and application claim accuracy and validity), including final release for publication. 6. Review and approve Promega Product Information (PPI) specification sheets and Certificates of Analysis; initiation, completion and issuance of these documents as required for custom products and some catalog products. 7. Assess the scope and inventory impact of nonconforming product situations; approving disposition plans of inventory product under quarantine; assisting in the disposition planning for nonconforming product in branch inventories. 8. Assist in the preparation, review and approval of design control documents. 9. Initiate, implement, review and/or approve Product and Process Change Plans. 10. Review, implement, and/or participate in Corrective and Preventive Action plans. 11. Review, implement, and participate in product and process validation planning. 12. Review, implement, and participate in complaint investigation planning. 13. Participate in process mapping and SOP development as directed. 14. Write SOPs as assigned. 15. Participate in team meetings to resolve planning and technical issues. Propose constructive solutions to existing problems. 16. Evaluate risks based on customer, technical, business and regulatory factors, provide options and recommendations to mitigate risk. 17. Consider basic regulatory requirements in product or process issues. 18. Demonstrates inclusion through their own words and actions and is accountable for a safe workspace. Acts with kindness, curiosity and respect for others. 19. Embracing and being open to incorporating Promega's 6 Emotional & Social Intelligence (ESI) core principles in daily work. 20. Understand and comply with ethical, legal and regulatory requirements applicable to our business. OCCASIONAL DUTIES: 1. Organize, facilitate, or lead meetings to discuss review findings and planning issues. 2. Represent Promega in support of technical sales at national and international trade shows and exhibitions, or attend relevant scientific meetings as requested. 3. Contact customers directly about quality issues or questions as directed. 4. Organize and implement training programs in areas of expertise and experience. 5. Participate in continuous improvement projects.   qualifications: KEY QUALIFICATIONS: 1. B.S. degree with a minimum of 7 years work experience in a relevant industry with quality control, quality assurance, or manufacturing responsibilities. 2. Working knowledge and direct application experience of the requirements of quality assurance systems in a manufacturing and/or product development or process development environment. 3. Proficiency with basic word processing and spreadsheet software programs. 4. Ability to apply basic statistical concepts to analytical data, process validation, and Quality Assurance activities. 5. A demonstrable track record of process improvement and effective procedure writing and revision. 6. Able to develop concise, clear and accurate written communication. 7. Proven ability to work constructively with a broad range of people. PREFERRED QUALIFICATIONS: 1. In-depth technical knowledge in genomics, protein analysis, or cellular analysis evidenced by peer-reviewed publications. 2. Work experience in Quality Assurance from a regulated industry. PHYSICAL DEMANDS: 1. Visual acuity required for physical inspection of finished product and raw materials and accompanying documentation. 2. Ability to wear basic safety apparel (safety glasses or goggles, lab coats, protective gloves). 3. Ability to use computers in an interactive manner for extended periods of time.   skills: Biology, Chemistry, 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.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.
    • green bay, wisconsin
    • permanent
    • $31,200 - $33,280 per year
    job summary: Summary/Objective Performs laboratory support responsibilities in a fast-paced production environment; preparation of microbiological samples & media, cleaning, waste disposal, and basic maintenance functions.   location: Green Bay, Wisconsin job type: Permanent salary: $31,200 - 33,280 per year work hours: 9 to 5 education: High School   responsibilities: Essential Functions Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. - Sterilize and dispose biohazardous waste according to established procedures. - Prepare media and reagents to support microbiology testing, ensuring products are documented, aliquoted, labelled and quality control specifications are met. - Perform and document routine laboratory maintenance tasks such as sample archiving, basic equipment monitoring, waste disposal and cleaning (laboratory and labware). - Assist Lab Techs in sample preparation and weighing of test items, as required. - Adhere to lab safety procedures and reporting standards. - Follow written Standard Operating Procedures and Work Instructions. - As needed, perform shipping/receiving duties and keep external/customer facing areas clear. - Other duties may be assigned to assist with the operations of the lab.   qualifications: Required Education and Experience - High School Diploma, or equivalent. - Demonstrates ability to work with a team. - Able to multitask. - Positive outlook with the ability to adapt to a changing environment.   skills: Sample Preparation 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: Summary/Objective Performs laboratory support responsibilities in a fast-paced production environment; preparation of microbiological samples & media, cleaning, waste disposal, and basic maintenance functions.   location: Green Bay, Wisconsin job type: Permanent salary: $31,200 - 33,280 per year work hours: 9 to 5 education: High School   responsibilities: Essential Functions Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. - Sterilize and dispose biohazardous waste according to established procedures. - Prepare media and reagents to support microbiology testing, ensuring products are documented, aliquoted, labelled and quality control specifications are met. - Perform and document routine laboratory maintenance tasks such as sample archiving, basic equipment monitoring, waste disposal and cleaning (laboratory and labware). - Assist Lab Techs in sample preparation and weighing of test items, as required. - Adhere to lab safety procedures and reporting standards. - Follow written Standard Operating Procedures and Work Instructions. - As needed, perform shipping/receiving duties and keep external/customer facing areas clear. - Other duties may be assigned to assist with the operations of the lab.   qualifications: Required Education and Experience - High School Diploma, or equivalent. - Demonstrates ability to work with a team. - Able to multitask. - Positive outlook with the ability to adapt to a changing environment.   skills: Sample Preparation 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.
    • green bay, wisconsin
    • permanent
    • $35,360 - $39,520 per year
    job summary: Summary/Objective Performs all aspects of routine and non-routine microbiological testing of food and environmental samples.   location: Green Bay, Wisconsin job type: Permanent salary: $35,360 - 39,520 per year work hours: 9 to 5 education: Bachelors   responsibilities: Essential Functions Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. - Perform microbiological analysis of food and environmental samples using conventional plating techniques as well as PCR and ELISA instrumentation. - Identify microorganisms by microscopic examination of physiological and cultural characteristics. - Perform cultural confirmations for pathogens. - Ensure accurate and complete traceability and documentation of testing activities performed, including LIMS result entry. - Review result for accuracy and suitability prior to approval, initiating additional testing per client requests if required. - Identify, communicate and document non-conformities with samples, instrumentation and methodologies, assisting with troubleshooting as assigned. - When required, assist with method verification activities as directed by assigned staff. - Perform routine and non-routine instrument maintenance and routine troubleshooting. - Referring to LIMS, ensure client expectations for turnaround time are met, communicating with Lead Microbiologists and Supervisor on status or potential delays. - Review of controlled documents and procedures - For methods within area of responsibility, provide training for other laboratory staff. - Participate in quality system activities, including maintenance of test and training records. - Identify and assist with implementation of process improvements - Adhere to lab safety procedures and reporting standards. - Follow written Standard Operating Procedures and Work Instructions. - Other duties may be assigned to assist with the operations of the lab.   qualifications: Required Education and Experience - Bachelor's Degree in Sciences, preferably Microbiology, plus 2 years in laboratory experience (or equivalent combination) - Ability to distinguish colors as required for Microbiological testing. - Demonstrated ability to work with a team. - Positive outlook with the ability to adapt to a changing environment   skills: Microbiology 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: Summary/Objective Performs all aspects of routine and non-routine microbiological testing of food and environmental samples.   location: Green Bay, Wisconsin job type: Permanent salary: $35,360 - 39,520 per year work hours: 9 to 5 education: Bachelors   responsibilities: Essential Functions Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. - Perform microbiological analysis of food and environmental samples using conventional plating techniques as well as PCR and ELISA instrumentation. - Identify microorganisms by microscopic examination of physiological and cultural characteristics. - Perform cultural confirmations for pathogens. - Ensure accurate and complete traceability and documentation of testing activities performed, including LIMS result entry. - Review result for accuracy and suitability prior to approval, initiating additional testing per client requests if required. - Identify, communicate and document non-conformities with samples, instrumentation and methodologies, assisting with troubleshooting as assigned. - When required, assist with method verification activities as directed by assigned staff. - Perform routine and non-routine instrument maintenance and routine troubleshooting. - Referring to LIMS, ensure client expectations for turnaround time are met, communicating with Lead Microbiologists and Supervisor on status or potential delays. - Review of controlled documents and procedures - For methods within area of responsibility, provide training for other laboratory staff. - Participate in quality system activities, including maintenance of test and training records. - Identify and assist with implementation of process improvements - Adhere to lab safety procedures and reporting standards. - Follow written Standard Operating Procedures and Work Instructions. - Other duties may be assigned to assist with the operations of the lab.   qualifications: Required Education and Experience - Bachelor's Degree in Sciences, preferably Microbiology, plus 2 years in laboratory experience (or equivalent combination) - Ability to distinguish colors as required for Microbiological testing. - Demonstrated ability to work with a team. - Positive outlook with the ability to adapt to a changing environment   skills: Microbiology 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.
    • verona, wisconsin
    • permanent
    • $40,000 - $50,000 per year
    job summary: Randstad is the #1 HR Services Company in the world and we are sourcing for a QC Analytical Chemist in the Madison, WI area. The ideal candidate will provide support to the Production and Formulations Departments by analyzing pharmaceutical and/or cleaning samples. Support will be provided by analyzing samples using various procedures including, but not limited to, internal procedures, specifications, and analytical methods; compendial monographs, client procedures, and miscellaneous protocols. The QC Analytical Chemist is expected to understand basic internal procedures, and conduct analyses with some supervision after training is complete. This is a direct hire position and can start immediately.   location: Verona, Wisconsin job type: Permanent salary: $40,000 - 50,000 per year work hours: 11 to 7 education: Bachelors   responsibilities: Responsibilities: Ensures adherence to CPI Standard Operating Procedures, analytical methods, protocols, company standards, and applicable regulations.Analyzes pharmaceutical or cleaning samplesAbility to weigh samples, pipette, and prepare laboratory solutionsPerforms or assists with basic calibrationsMaintains a cGMP laboratory notebook, data, forms, and/or logbook.Assists in maintaining a clean, organized QC laboratory.Lifts/carries objects weighing up to 55 lbs.Follows all CPI cGMP practices, policies, and procedures.Follows all CPI safety practices, policies, and procedures.Other duties as assigned.  qualifications: Requirements: Bachelor's degree in Chemistry or related field.Experience with the use and troubleshooting of laboratory equipment desirable.Possesses good time management skills to complete assignments/projects in a timely manner with minimal supervision.Ability to establish and maintain effective working relationships with team members, co-workers, and/or clients. Working Conditions The QC Analytical Chemist works in a cGMP laboratory and production environment. Working in these environments will require working near skin irritants, electrical equipment, sharp instruments, toxic materials, and hazardous chemicals including controlled substances. Safety procedures must be followed to limit exposure.   skills: Analytical Chemistry, Biology, Chemistry, GLP (Good Laboratory Practice), Laboratory Information Management Systems (LIMS), Sample Preparation, Sample Testing, Sanitation 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: Randstad is the #1 HR Services Company in the world and we are sourcing for a QC Analytical Chemist in the Madison, WI area. The ideal candidate will provide support to the Production and Formulations Departments by analyzing pharmaceutical and/or cleaning samples. Support will be provided by analyzing samples using various procedures including, but not limited to, internal procedures, specifications, and analytical methods; compendial monographs, client procedures, and miscellaneous protocols. The QC Analytical Chemist is expected to understand basic internal procedures, and conduct analyses with some supervision after training is complete. This is a direct hire position and can start immediately.   location: Verona, Wisconsin job type: Permanent salary: $40,000 - 50,000 per year work hours: 11 to 7 education: Bachelors   responsibilities: Responsibilities: Ensures adherence to CPI Standard Operating Procedures, analytical methods, protocols, company standards, and applicable regulations.Analyzes pharmaceutical or cleaning samplesAbility to weigh samples, pipette, and prepare laboratory solutionsPerforms or assists with basic calibrationsMaintains a cGMP laboratory notebook, data, forms, and/or logbook.Assists in maintaining a clean, organized QC laboratory.Lifts/carries objects weighing up to 55 lbs.Follows all CPI cGMP practices, policies, and procedures.Follows all CPI safety practices, policies, and procedures.Other duties as assigned.  qualifications: Requirements: Bachelor's degree in Chemistry or related field.Experience with the use and troubleshooting of laboratory equipment desirable.Possesses good time management skills to complete assignments/projects in a timely manner with minimal supervision.Ability to establish and maintain effective working relationships with team members, co-workers, and/or clients. Working Conditions The QC Analytical Chemist works in a cGMP laboratory and production environment. Working in these environments will require working near skin irritants, electrical equipment, sharp instruments, toxic materials, and hazardous chemicals including controlled substances. Safety procedures must be followed to limit exposure.   skills: Analytical Chemistry, Biology, Chemistry, GLP (Good Laboratory Practice), Laboratory Information Management Systems (LIMS), Sample Preparation, Sample Testing, Sanitation 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.
    • verona, wisconsin
    • permanent
    • $35,000 - $43,000 per year
    job summary: Randstad is the #1 HR Services Company in the world and we are sourcing for a QA Associate in the Madison, WI area. The ideal candidate will provide quality assurance support and leadership to the Production Department. The QA Associate I, Process Quality Inspector provides a strong floor presence and works directly with production supervision and operators to maintain quality of manufacturing operations. This is a direct hire position and can start immediately.   location: Verona, Wisconsin job type: Permanent salary: $35,000 - 43,000 per year work hours: 3 to 11 education: High School   responsibilities: Responsibilities: Works with Production personnel to ensure compliance of CPI practices, policies, and procedures. A significant focus on batch record and process compliance is expected. Performs routine review of in process production documents during processing to ensure accuracy and completeness.Performs routine inspections/audits on personnel, procedures, equipment, and products.Provides leadership to Production personnel on quality issues.Initiates deviations and documents initial investigations. May contribute to assessment of deviations under the direction of the supervisor.Contributes to quality investigations. Serves as lead investigator when assigned by the supervisor.Initiates, maintains, and dispositions non-conformances.Assists in training of Production personnel in company practices, policies, and procedures.Assists in the movement of controlled substances into/out of the controlled substance storage and processing areas.Performs sampling activities when assigned by the supervisor.Reviews unit logbooks and/or environmental monitoring data as assigned.Follows all CPI cGMP practices, policies, and procedures.Follows all CPI safety practices, policies, and procedures.Other duties as assigned.  qualifications: Requirements: High school diploma or equivalent required.2-3 years of industry quality or cGMP manufacturing experience required. Formal quality training may be substituted in place of experience.Knowledge of current Good Manufacturing Practices (cGMPs) preferred.Knowledge of a variety of cGMP manufacturing practices preferred (including fluid bed coating/granulation, capsule filling, milling, tableting)Strong attention to detail and problem solving skills required.Ability to read, write (legibly), and speak the English language at a level necessary for efficient job performance.Ability to establish and maintain effective working relationships with team members, co-workers, and/or clients.Ability to stand for extended periods of time and lift objects weighing up to 55 lbs.  skills: Quality control, SOP, Quality Assurance, 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.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: Randstad is the #1 HR Services Company in the world and we are sourcing for a QA Associate in the Madison, WI area. The ideal candidate will provide quality assurance support and leadership to the Production Department. The QA Associate I, Process Quality Inspector provides a strong floor presence and works directly with production supervision and operators to maintain quality of manufacturing operations. This is a direct hire position and can start immediately.   location: Verona, Wisconsin job type: Permanent salary: $35,000 - 43,000 per year work hours: 3 to 11 education: High School   responsibilities: Responsibilities: Works with Production personnel to ensure compliance of CPI practices, policies, and procedures. A significant focus on batch record and process compliance is expected. Performs routine review of in process production documents during processing to ensure accuracy and completeness.Performs routine inspections/audits on personnel, procedures, equipment, and products.Provides leadership to Production personnel on quality issues.Initiates deviations and documents initial investigations. May contribute to assessment of deviations under the direction of the supervisor.Contributes to quality investigations. Serves as lead investigator when assigned by the supervisor.Initiates, maintains, and dispositions non-conformances.Assists in training of Production personnel in company practices, policies, and procedures.Assists in the movement of controlled substances into/out of the controlled substance storage and processing areas.Performs sampling activities when assigned by the supervisor.Reviews unit logbooks and/or environmental monitoring data as assigned.Follows all CPI cGMP practices, policies, and procedures.Follows all CPI safety practices, policies, and procedures.Other duties as assigned.  qualifications: Requirements: High school diploma or equivalent required.2-3 years of industry quality or cGMP manufacturing experience required. Formal quality training may be substituted in place of experience.Knowledge of current Good Manufacturing Practices (cGMPs) preferred.Knowledge of a variety of cGMP manufacturing practices preferred (including fluid bed coating/granulation, capsule filling, milling, tableting)Strong attention to detail and problem solving skills required.Ability to read, write (legibly), and speak the English language at a level necessary for efficient job performance.Ability to establish and maintain effective working relationships with team members, co-workers, and/or clients.Ability to stand for extended periods of time and lift objects weighing up to 55 lbs.  skills: Quality control, SOP, Quality Assurance, 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.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.
    • green bay, wisconsin
    • permanent
    • $65,000 - $70,000 per year
    job summary: Summary/Objective Within the Microbiology department, this role is responsible for the coordination of lab staff in daily workflow organization and sample troubleshooting in addition to routine and non-routine sample analysis. Additionally, monitors lab operations such that quality and behavioral procedures are being followed, supporting management in general operational oversight.   location: Green Bay, Wisconsin job type: Permanent salary: $65,000 - 70,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: Essential Functions Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. - Plan and adjust daily laboratory workflow to meet the needs of sample volumes, client needs, and available staff. - Review and authorize test results, ensuring accuracy and traceability/documentation of activities performed. - Relay operational updates to management, communicating any customer impacts to Customer Service as appropriate. - Maintain technical proficiency and perform routine and non-routine microbiology analyses as required, including result interpretation. - Troubleshoot operation of equipment, assisting in maintenance as required. - Document and respond to QC failures, nonconformities & deviations and client out of specification results. - Participate in investigating non-conformances and development of corrective actions, working to implement required corrective actions at the bench level. - Perform and document training activities for department staff on all laboratory duties performed including safety procedures, general bench skills, method specific proficiencies and associated data system tasks. - Supports quality of lab operations by ensuring employees are following documented procedures and the team works to reduce non-conformances. - Participate in review and revision of applicable Standard Operating Procedures and Work Instructions. - Identify and assist with implementation of process improvements within the Microbiology Department. - Other duties may be assigned to assist with the operations of the lab.   qualifications: Required Education and Experience - Bachelor's degree, preferably in Microbiology, or Associates degree with equivalent work experience. - 2 years working in a commercial lab environment with various food samples and methodologies. - Ability to distinguish colors as required for Microbiology testing. - Demonstrated ability to work with a team. - Positive outlook with the ability to adapt to a changing environment.   skills: Microbiology 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: Summary/Objective Within the Microbiology department, this role is responsible for the coordination of lab staff in daily workflow organization and sample troubleshooting in addition to routine and non-routine sample analysis. Additionally, monitors lab operations such that quality and behavioral procedures are being followed, supporting management in general operational oversight.   location: Green Bay, Wisconsin job type: Permanent salary: $65,000 - 70,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: Essential Functions Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. - Plan and adjust daily laboratory workflow to meet the needs of sample volumes, client needs, and available staff. - Review and authorize test results, ensuring accuracy and traceability/documentation of activities performed. - Relay operational updates to management, communicating any customer impacts to Customer Service as appropriate. - Maintain technical proficiency and perform routine and non-routine microbiology analyses as required, including result interpretation. - Troubleshoot operation of equipment, assisting in maintenance as required. - Document and respond to QC failures, nonconformities & deviations and client out of specification results. - Participate in investigating non-conformances and development of corrective actions, working to implement required corrective actions at the bench level. - Perform and document training activities for department staff on all laboratory duties performed including safety procedures, general bench skills, method specific proficiencies and associated data system tasks. - Supports quality of lab operations by ensuring employees are following documented procedures and the team works to reduce non-conformances. - Participate in review and revision of applicable Standard Operating Procedures and Work Instructions. - Identify and assist with implementation of process improvements within the Microbiology Department. - Other duties may be assigned to assist with the operations of the lab.   qualifications: Required Education and Experience - Bachelor's degree, preferably in Microbiology, or Associates degree with equivalent work experience. - 2 years working in a commercial lab environment with various food samples and methodologies. - Ability to distinguish colors as required for Microbiology testing. - Demonstrated ability to work with a team. - Positive outlook with the ability to adapt to a changing environment.   skills: Microbiology 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.
    • green bay, wisconsin
    • permanent
    • $33,280 - $37,440 per year
    job summary: Summary/Objective Performs routine microbiological testing of food and environmental samples for under aseptic conditions for qualitative and quantitative parameters, focusing on sample preparation and plating responsibilities.   location: Green Bay, Wisconsin job type: Permanent salary: $33,280 - 37,440 per year work hours: 9 to 5 education: Associate   responsibilities: Essential Functions Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. - Perform sample set up, dilutions and plating activities on food and environmental samples following aseptic techniques and standard operating procedures. - Perform equipment monitoring and verification on basic laboratory items such as balances, fridges, incubators, pipettes, etc. - Identify, communicate and document non-conformities related to daily activities. - Support routine laboratory operations through tasks such as sample archiving, media preparation, cleaning and waste disposal. - Ensure accurate and complete traceability and documentation of testing activities performed. - Ensure samples are processed efficiently to meet client expectations for turnaround time. - Support assigned staff with investigations and implementation of corrective actions performing activities as directed. - Identify and assist with implementation of process improvements - For responsibilities within area of responsibility, provide training for other laboratory staff. - Adhere to lab safety procedures and reporting standards. - Follow written Standard Operating Procedures and Work Instructions. - Other duties may be assigned to assist with the operations of the lab   qualifications: Required Education and Experience - Minimum Associates Degree in Sciences or at least 2 years working in a commercial lab environment. - Demonstrated ability to work with a team. - Positive outlook with the ability to adapt to a changing environment   skills: Sample Preparation 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: Summary/Objective Performs routine microbiological testing of food and environmental samples for under aseptic conditions for qualitative and quantitative parameters, focusing on sample preparation and plating responsibilities.   location: Green Bay, Wisconsin job type: Permanent salary: $33,280 - 37,440 per year work hours: 9 to 5 education: Associate   responsibilities: Essential Functions Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. - Perform sample set up, dilutions and plating activities on food and environmental samples following aseptic techniques and standard operating procedures. - Perform equipment monitoring and verification on basic laboratory items such as balances, fridges, incubators, pipettes, etc. - Identify, communicate and document non-conformities related to daily activities. - Support routine laboratory operations through tasks such as sample archiving, media preparation, cleaning and waste disposal. - Ensure accurate and complete traceability and documentation of testing activities performed. - Ensure samples are processed efficiently to meet client expectations for turnaround time. - Support assigned staff with investigations and implementation of corrective actions performing activities as directed. - Identify and assist with implementation of process improvements - For responsibilities within area of responsibility, provide training for other laboratory staff. - Adhere to lab safety procedures and reporting standards. - Follow written Standard Operating Procedures and Work Instructions. - Other duties may be assigned to assist with the operations of the lab   qualifications: Required Education and Experience - Minimum Associates Degree in Sciences or at least 2 years working in a commercial lab environment. - Demonstrated ability to work with a team. - Positive outlook with the ability to adapt to a changing environment   skills: Sample Preparation 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.

Thank you for subscribing to your personalised job alerts.

explore over 8 jobs with randstad.

It looks like you want to switch your language. This will reset your filters on your current job search.