3 jobs found in round lake, illinois

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    • round lake, illinois
    • contract
    • US$28.50 - US$33.53, per hour, $28.50 - 33.53 per hour
    • 8 to 4
    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. A longtime partner who prides itself on being a leader in many different practical manufacturing processes to better serve the entire population is renowned for pioneering new treatments for renal diseases, immune disorders, and more; the focus is on patient care. If you're looking to be a part of an impactful team, you won't be disappointed! location: Round Lake, Illinoisjob type: Contractsalary: $28.50 - 33.53 per hourwork hours: 8 to 4education: Bachelors responsibilities:This position is responsible for analytical testing, validation/verification, and/or transfer of test method supporting Pharmaceuticals parenteral products. Work will primarily support stability testing, but may also support new product development and/or sustaining product initiatives.Effectively contribute solid technical knowledge to a variety of projects within the relevant discipline with minimal assistance.Display basic technical understanding of related disciplines.Conduct routine/non-routine research and design experiments with minimal assistance.Conduct critical chemical, physical, and biological analyses on finished product stability samples. May also support testing of raw materials, initial, in-process, and final product samples from manufacturing facilities or department projects. Work under minimum supervision.Perform review of test data, which includes overall documentation practices. Perform review functions in LIMS or other computerized systems.Use sophisticated laboratory instrumentation and computer systems to collect and record data. May be required to be a system owner or conduct validations.Perform advanced biological and chemical assays requiring precise analytical skills and understanding of chemistry principles. Complete all testing, including special project / protocol testing in a timely and appropriate manner to meet project schedulesMaintain data integrity and ensure compliance with company SOPs and specifications, FDA, cGxP, and QSR regulations.Investigate deviations and write exception documents.Collaborate with other functions/departments to solve problems, increase efficiency, improve quality and provide product support.Maintain laboratory safety requirements, perform equipment maintenance/calibration, and troubleshoot basic instrument problems qualifications:Bachelors degree in relevant scientific discipline (e.g. chemistry, pharmaceutical sciences) with analytical chemistry laboratory coursework and at least 2-5 years of experience or advanced degree in Chemistry or Biological SciencesAnalytical chemistry instrumentation experience (e.g. HPLC, UPLC, UHPLC, GC, pH, KF, TOC, AA, GFAA, titration, etc.)Pharmaceutical GMP laboratory experience is desiredStability study execution and validation experience is desiredMust have good oral and written communication skills, strong analytical skills and be detail oriented.Proficient in advanced wet chemistry, volumetric preparation techniques and instrumental methods of analysisMust demonstrate effectiveness in ability to train others, leadership, organization, teamwork/interpersonal skills, results orientation, and task completionMust be able to handle multiple tasks concurrently and in a timely fashionPossess writing and computer skillsMust communicate effectively with managers, peers, and subordinatesInterpret available information and make recommendation to resolve technical challengesPhysical Activities and Requirements:Must be able to hand write and use computers for the majority of the work dayMust be able to transfer materials, mix solutions/product(s), open products, and perform laboratory testingMay require standing for extended periodsMust be able to lift up to 10 pounds routinelyThis work is subject to hazards including exposure to chemicals, drug products, and bacteria. This includes Penicillin, Cephalosporin, their related products and/or materialsMust not be allergic to Cephalosporin drugs skills: HPLC, Analytical Chemistry, 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.
    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. A longtime partner who prides itself on being a leader in many different practical manufacturing processes to better serve the entire population is renowned for pioneering new treatments for renal diseases, immune disorders, and more; the focus is on patient care. If you're looking to be a part of an impactful team, you won't be disappointed! location: Round Lake, Illinoisjob type: Contractsalary: $28.50 - 33.53 per hourwork hours: 8 to 4education: Bachelors responsibilities:This position is responsible for analytical testing, validation/verification, and/or transfer of test method supporting Pharmaceuticals parenteral products. Work will primarily support stability testing, but may also support new product development and/or sustaining product initiatives.Effectively contribute solid technical knowledge to a variety of projects within the relevant discipline with minimal assistance.Display basic technical understanding of related disciplines.Conduct routine/non-routine research and design experiments with minimal assistance.Conduct critical chemical, physical, and biological analyses on finished product stability samples. May also support testing of raw materials, initial, in-process, and final product samples from manufacturing facilities or department projects. Work under minimum supervision.Perform review of test data, which includes overall documentation practices. Perform review functions in LIMS or other computerized systems.Use sophisticated laboratory instrumentation and computer systems to collect and record data. May be required to be a system owner or conduct validations.Perform advanced biological and chemical assays requiring precise analytical skills and understanding of chemistry principles. Complete all testing, including special project / protocol testing in a timely and appropriate manner to meet project schedulesMaintain data integrity and ensure compliance with company SOPs and specifications, FDA, cGxP, and QSR regulations.Investigate deviations and write exception documents.Collaborate with other functions/departments to solve problems, increase efficiency, improve quality and provide product support.Maintain laboratory safety requirements, perform equipment maintenance/calibration, and troubleshoot basic instrument problems qualifications:Bachelors degree in relevant scientific discipline (e.g. chemistry, pharmaceutical sciences) with analytical chemistry laboratory coursework and at least 2-5 years of experience or advanced degree in Chemistry or Biological SciencesAnalytical chemistry instrumentation experience (e.g. HPLC, UPLC, UHPLC, GC, pH, KF, TOC, AA, GFAA, titration, etc.)Pharmaceutical GMP laboratory experience is desiredStability study execution and validation experience is desiredMust have good oral and written communication skills, strong analytical skills and be detail oriented.Proficient in advanced wet chemistry, volumetric preparation techniques and instrumental methods of analysisMust demonstrate effectiveness in ability to train others, leadership, organization, teamwork/interpersonal skills, results orientation, and task completionMust be able to handle multiple tasks concurrently and in a timely fashionPossess writing and computer skillsMust communicate effectively with managers, peers, and subordinatesInterpret available information and make recommendation to resolve technical challengesPhysical Activities and Requirements:Must be able to hand write and use computers for the majority of the work dayMust be able to transfer materials, mix solutions/product(s), open products, and perform laboratory testingMay require standing for extended periodsMust be able to lift up to 10 pounds routinelyThis work is subject to hazards including exposure to chemicals, drug products, and bacteria. This includes Penicillin, Cephalosporin, their related products and/or materialsMust not be allergic to Cephalosporin drugs skills: HPLC, Analytical Chemistry, 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.
    • round lake, illinois
    • contract
    • US$19.00 - US$21.06, per hour, $19.00 - 21.06 per hour
    • 7 to 3
    job summary:As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you! location: Round Lake, Illinoisjob type: Contractsalary: $19.00 - 21.06 per hourwork hours: 7 to 3education: High School responsibilities:The Supply Handler (SH) is responsible for executing all processes in production at while strictly adhering to cGMP, environmental health and safety guidelines, and any other related regulations which could apply; fully participates in both departmental projects and any quality working teams which may be applicable; under the general direction of the lead technician and the overall direction of the supervisor, is responsible for hands-on execution of all activities in the production area; initiates minor revisions to existing documents; troubleshoots simple existing procedures.Supports all local manufacturing operationsSupplies components, small parts, glassware, tubing, etc. to cell culture and purification areasOperates general production equipment (such as parts washers, autoclave, stir plates, etc.)Assures that Production Associates rotate to different stations every 30 minutesCoordinates break and lunch schedules for PAs in their inspection or packaging roomsCompletes relevant paperwork following GDP/GMP guidelinesManually cleans all portable equipment and small partsParticipates on Continuous Improvement TeamsReceives and distributes supplies into the production area as necessaryPerforms daily cleaning of the production area to maintain in GMP fashionPrepares media and buffer solutionsAssembles and operates filtration systemsReviews and revises pertinent documentation as appropriateTrains new and existing employees/contractors on procedures for which Supply Handler is qualified as trainerEmbodies thecompany's Leadership Behaviors: Be Positive. Be Accountable. Be Results-Driven. Be an Excellent Manager of Self and Others.May perform other duties as assigned qualifications:Requires AA degree with 0-2 years of production experience or high school diploma with 1-3 years of related manufacturing experienceMust be willing and able to work 12 hour shift in a 2-2-3 rotation. Shifts are 5am-5:30pm, 5:00pm - 5:30am.This position is a NIGHT Shift 12 hour.Must have good written and oral communication skills in the English languageStrong understanding of cGMP regulationsMust be able to speak, read, write, understand and follow detailed instructions (written and oral) in the English languageMust have 20/20 vision or better within arm's lengthMust NOT be colorblindMust be proficient in a variety of mathematical disciplines and be able to work with both the metric and USA standards of measurementFamiliarity with pharmaceutical production equipment including but not limited to autoclave, DP oven and CIP/SIPGood interpersonal skills and ability to work effectively and efficiently in a team environmentMust be willing and able to work overtime; position requires shift, weekend and holiday work; mandatory overtime will be required, typically 2 Saturdays per monthWill work in a clean room environment wearing special garments; personal protective equipment must be worn due to safety, cGMP and FDA requirementsKnowledge of basic chemical and biological safety proceduresMay require immunization before performing work within the manufacturing areaMust be able to lift, push, pull and/or carry up to 30 lbs.Repetitive motions with hands, wrists, turning head, bending at knees and waistWalking within and between production and packaging rooms, as well as throughout the entire plantMust be able to work in controlled environments requiring special gowning; will be required to follow gowning requirements and wear protective clothing over the head, face, hands, feet and bodyNo make-up, jewelry, contact lenses, nail polish or artificial fingernails may be worn in the manufacturing environmentMay work in a cold, wet environmentMust be able to work multiple shifts, including weekendsMust be able to work overtime as required, including SaturdaysMay be required to work in a confined areaWill be exposed to some Clean Room and cool/hot storage conditionsMay require immunization before performing work within the manufacturing area skills: GMP (Good Manufacturing Practice), Manufacturing OperationsEqual 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. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you! location: Round Lake, Illinoisjob type: Contractsalary: $19.00 - 21.06 per hourwork hours: 7 to 3education: High School responsibilities:The Supply Handler (SH) is responsible for executing all processes in production at while strictly adhering to cGMP, environmental health and safety guidelines, and any other related regulations which could apply; fully participates in both departmental projects and any quality working teams which may be applicable; under the general direction of the lead technician and the overall direction of the supervisor, is responsible for hands-on execution of all activities in the production area; initiates minor revisions to existing documents; troubleshoots simple existing procedures.Supports all local manufacturing operationsSupplies components, small parts, glassware, tubing, etc. to cell culture and purification areasOperates general production equipment (such as parts washers, autoclave, stir plates, etc.)Assures that Production Associates rotate to different stations every 30 minutesCoordinates break and lunch schedules for PAs in their inspection or packaging roomsCompletes relevant paperwork following GDP/GMP guidelinesManually cleans all portable equipment and small partsParticipates on Continuous Improvement TeamsReceives and distributes supplies into the production area as necessaryPerforms daily cleaning of the production area to maintain in GMP fashionPrepares media and buffer solutionsAssembles and operates filtration systemsReviews and revises pertinent documentation as appropriateTrains new and existing employees/contractors on procedures for which Supply Handler is qualified as trainerEmbodies thecompany's Leadership Behaviors: Be Positive. Be Accountable. Be Results-Driven. Be an Excellent Manager of Self and Others.May perform other duties as assigned qualifications:Requires AA degree with 0-2 years of production experience or high school diploma with 1-3 years of related manufacturing experienceMust be willing and able to work 12 hour shift in a 2-2-3 rotation. Shifts are 5am-5:30pm, 5:00pm - 5:30am.This position is a NIGHT Shift 12 hour.Must have good written and oral communication skills in the English languageStrong understanding of cGMP regulationsMust be able to speak, read, write, understand and follow detailed instructions (written and oral) in the English languageMust have 20/20 vision or better within arm's lengthMust NOT be colorblindMust be proficient in a variety of mathematical disciplines and be able to work with both the metric and USA standards of measurementFamiliarity with pharmaceutical production equipment including but not limited to autoclave, DP oven and CIP/SIPGood interpersonal skills and ability to work effectively and efficiently in a team environmentMust be willing and able to work overtime; position requires shift, weekend and holiday work; mandatory overtime will be required, typically 2 Saturdays per monthWill work in a clean room environment wearing special garments; personal protective equipment must be worn due to safety, cGMP and FDA requirementsKnowledge of basic chemical and biological safety proceduresMay require immunization before performing work within the manufacturing areaMust be able to lift, push, pull and/or carry up to 30 lbs.Repetitive motions with hands, wrists, turning head, bending at knees and waistWalking within and between production and packaging rooms, as well as throughout the entire plantMust be able to work in controlled environments requiring special gowning; will be required to follow gowning requirements and wear protective clothing over the head, face, hands, feet and bodyNo make-up, jewelry, contact lenses, nail polish or artificial fingernails may be worn in the manufacturing environmentMay work in a cold, wet environmentMust be able to work multiple shifts, including weekendsMust be able to work overtime as required, including SaturdaysMay be required to work in a confined areaWill be exposed to some Clean Room and cool/hot storage conditionsMay require immunization before performing work within the manufacturing area skills: GMP (Good Manufacturing Practice), Manufacturing OperationsEqual 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.
    • round lake, illinois
    • contract
    • US$19.00 - US$21.06, per hour, $19.00 - 21.06 per hour
    • 7 to 3
    job summary:As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you! location: Round Lake, Illinoisjob type: Contractsalary: $19.00 - 21.06 per hourwork hours: 7 to 3education: High School responsibilities:The Supply Handler (SH) is responsible for executing all processes in production at while strictly adhering to cGMP, environmental health and safety guidelines, and any other related regulations which could apply; fully participates in both departmental projects and any quality working teams which may be applicable; under the general direction of the lead technician and the overall direction of the supervisor, is responsible for hands-on execution of all activities in the production area; initiates minor revisions to existing documents; troubleshoots simple existing procedures.Supports all local manufacturing operationsSupplies components, small parts, glassware, tubing, etc. to cell culture and purification areasOperates general production equipment (such as parts washers, autoclave, stir plates, etc.)Assures that Production Associates rotate to different stations every 30 minutesCoordinates break and lunch schedules for PAs in their inspection or packaging roomsCompletes relevant paperwork following GDP/GMP guidelinesManually cleans all portable equipment and small partsParticipates on Continuous Improvement TeamsReceives and distributes supplies into the production area as necessaryPerforms daily cleaning of the production area to maintain in GMP fashionPrepares media and buffer solutionsAssembles and operates filtration systemsReviews and revises pertinent documentation as appropriateTrains new and existing employees/contractors on procedures for which Supply Handler is qualified as trainerEmbodies thecompany's Leadership Behaviors: Be Positive. Be Accountable. Be Results-Driven. Be an Excellent Manager of Self and Others.May perform other duties as assigned qualifications:Requires AA degree with 0-2 years of production experience or high school diploma with 1-3 years of related manufacturing experienceMust be willing and able to work 12 hour shift in a 2-2-3 rotation. Shifts are 5am-5:30pm, 5:00pm - 5:30am.This position is a NIGHT Shift 12 hour.Must have good written and oral communication skills in the English languageStrong understanding of cGMP regulationsMust be able to speak, read, write, understand and follow detailed instructions (written and oral) in the English languageMust have 20/20 vision or better within arm's lengthMust NOT be colorblindMust be proficient in a variety of mathematical disciplines and be able to work with both the metric and USA standards of measurementFamiliarity with pharmaceutical production equipment including but not limited to autoclave, DP oven and CIP/SIPGood interpersonal skills and ability to work effectively and efficiently in a team environmentMust be willing and able to work overtime; position requires shift, weekend and holiday work; mandatory overtime will be required, typically 2 Saturdays per monthWill work in a clean room environment wearing special garments; personal protective equipment must be worn due to safety, cGMP and FDA requirementsKnowledge of basic chemical and biological safety proceduresMay require immunization before performing work within the manufacturing areaMust be able to lift, push, pull and/or carry up to 30 lbs.Repetitive motions with hands, wrists, turning head, bending at knees and waistWalking within and between production and packaging rooms, as well as throughout the entire plantMust be able to work in controlled environments requiring special gowning; will be required to follow gowning requirements and wear protective clothing over the head, face, hands, feet and bodyNo make-up, jewelry, contact lenses, nail polish or artificial fingernails may be worn in the manufacturing environmentMay work in a cold, wet environmentMust be able to work multiple shifts, including weekendsMust be able to work overtime as required, including SaturdaysMay be required to work in a confined areaWill be exposed to some Clean Room and cool/hot storage conditionsMay require immunization before performing work within the manufacturing area skills: GMP (Good Manufacturing Practice), Manufacturing OperationsEqual 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. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you! location: Round Lake, Illinoisjob type: Contractsalary: $19.00 - 21.06 per hourwork hours: 7 to 3education: High School responsibilities:The Supply Handler (SH) is responsible for executing all processes in production at while strictly adhering to cGMP, environmental health and safety guidelines, and any other related regulations which could apply; fully participates in both departmental projects and any quality working teams which may be applicable; under the general direction of the lead technician and the overall direction of the supervisor, is responsible for hands-on execution of all activities in the production area; initiates minor revisions to existing documents; troubleshoots simple existing procedures.Supports all local manufacturing operationsSupplies components, small parts, glassware, tubing, etc. to cell culture and purification areasOperates general production equipment (such as parts washers, autoclave, stir plates, etc.)Assures that Production Associates rotate to different stations every 30 minutesCoordinates break and lunch schedules for PAs in their inspection or packaging roomsCompletes relevant paperwork following GDP/GMP guidelinesManually cleans all portable equipment and small partsParticipates on Continuous Improvement TeamsReceives and distributes supplies into the production area as necessaryPerforms daily cleaning of the production area to maintain in GMP fashionPrepares media and buffer solutionsAssembles and operates filtration systemsReviews and revises pertinent documentation as appropriateTrains new and existing employees/contractors on procedures for which Supply Handler is qualified as trainerEmbodies thecompany's Leadership Behaviors: Be Positive. Be Accountable. Be Results-Driven. Be an Excellent Manager of Self and Others.May perform other duties as assigned qualifications:Requires AA degree with 0-2 years of production experience or high school diploma with 1-3 years of related manufacturing experienceMust be willing and able to work 12 hour shift in a 2-2-3 rotation. Shifts are 5am-5:30pm, 5:00pm - 5:30am.This position is a NIGHT Shift 12 hour.Must have good written and oral communication skills in the English languageStrong understanding of cGMP regulationsMust be able to speak, read, write, understand and follow detailed instructions (written and oral) in the English languageMust have 20/20 vision or better within arm's lengthMust NOT be colorblindMust be proficient in a variety of mathematical disciplines and be able to work with both the metric and USA standards of measurementFamiliarity with pharmaceutical production equipment including but not limited to autoclave, DP oven and CIP/SIPGood interpersonal skills and ability to work effectively and efficiently in a team environmentMust be willing and able to work overtime; position requires shift, weekend and holiday work; mandatory overtime will be required, typically 2 Saturdays per monthWill work in a clean room environment wearing special garments; personal protective equipment must be worn due to safety, cGMP and FDA requirementsKnowledge of basic chemical and biological safety proceduresMay require immunization before performing work within the manufacturing areaMust be able to lift, push, pull and/or carry up to 30 lbs.Repetitive motions with hands, wrists, turning head, bending at knees and waistWalking within and between production and packaging rooms, as well as throughout the entire plantMust be able to work in controlled environments requiring special gowning; will be required to follow gowning requirements and wear protective clothing over the head, face, hands, feet and bodyNo make-up, jewelry, contact lenses, nail polish or artificial fingernails may be worn in the manufacturing environmentMay work in a cold, wet environmentMust be able to work multiple shifts, including weekendsMust be able to work overtime as required, including SaturdaysMay be required to work in a confined areaWill be exposed to some Clean Room and cool/hot storage conditionsMay require immunization before performing work within the manufacturing area skills: GMP (Good Manufacturing Practice), Manufacturing OperationsEqual 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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