3 jobs found in melrose park, illinois

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    • melrose park, illinois
    • contract
    • US$15.00 - US$17.00, per hour, $15 - 17 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. 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: Melrose Park, Illinoisjob type: Contractsalary: $15 - 17 per hourwork hours: 8 to 4education: High School responsibilities:Be able to articulate work related issues clearly and effectively to management and peers.Maintains the glassware (washing, drying, and organizing).Receives and delivers laboratory samples for In-Process and Finished Product from the Production Department.Verifies Semi-Finished Product sample counts and receipts in QC Chemistry prior to use.Receives and verifies QA issued documentation for QC Chemistry prior to use.Performs monthly water collection from Deionized Water Ports for delivery to Microbiology Department.Performs monthly Medical Air testing.Reviews Weekly Environmental Monitoring System (EMS) Reports.Maintains accurate records of all work performed with respect to a given project. Ensures documentation meets facility audit as well as cGMP or GLP requirements.Manages work and time based on departmental priorities using own judgement and objective reasoning.Performs good housekeeping practices and follows safety related policies. Makes recommendations.Assures all training on SOPs, Policies and other items as required, are completed on time per policy.Performs additional duties and responsibilities as assigned. qualifications:High school diploma/GED.Basic verbal and written communication (in English) skills are necessary.Working knowledge of cGMP's preferred.Must be able to support Production requirements (i.e. work weekends or holidays if necessary).Must be able to work with Antineoplastic Materials. skills: GLP (Good Laboratory Practice), 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. 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: Melrose Park, Illinoisjob type: Contractsalary: $15 - 17 per hourwork hours: 8 to 4education: High School responsibilities:Be able to articulate work related issues clearly and effectively to management and peers.Maintains the glassware (washing, drying, and organizing).Receives and delivers laboratory samples for In-Process and Finished Product from the Production Department.Verifies Semi-Finished Product sample counts and receipts in QC Chemistry prior to use.Receives and verifies QA issued documentation for QC Chemistry prior to use.Performs monthly water collection from Deionized Water Ports for delivery to Microbiology Department.Performs monthly Medical Air testing.Reviews Weekly Environmental Monitoring System (EMS) Reports.Maintains accurate records of all work performed with respect to a given project. Ensures documentation meets facility audit as well as cGMP or GLP requirements.Manages work and time based on departmental priorities using own judgement and objective reasoning.Performs good housekeeping practices and follows safety related policies. Makes recommendations.Assures all training on SOPs, Policies and other items as required, are completed on time per policy.Performs additional duties and responsibilities as assigned. qualifications:High school diploma/GED.Basic verbal and written communication (in English) skills are necessary.Working knowledge of cGMP's preferred.Must be able to support Production requirements (i.e. work weekends or holidays if necessary).Must be able to work with Antineoplastic Materials. skills: GLP (Good Laboratory Practice), 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.
    • melrose park, illinois
    • contract
    • US$15.00 - US$19.00, per hour, $15 - 19 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. 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: Melrose Park, Illinoisjob type: Contractsalary: $15 - 19 per hourwork hours: 9 to 5education: Bachelors responsibilities:The Q.A. Record Specialist is responsible for management and maintenance of master documents for manufacturing, packaging and testing. The QA Record Specialist assists management with respect to accomplishing projects, meeting commitments, developing departmental systems and overall assurance of accurate and appropriate processing of Master Batch Record documentation, issuance of batch records, testing specifications and laboratory records.Analyzes and coordinates scheduled production batches to assure availability of complete and accurate manufacturing documents.Prioritizes the issuance of all necessary and appropriate documents for each scheduled product, calculates and assigns product expiration date, assures critical information such as product I.D., strength.Implements revisions to master batch records by accurately incorporating changes as specified by the approved document change request (DCR).Recognizes and resolves documentation discrepancies. Communicates any such occurrence and corrective action to Manager and other QA Record Specialist.Assists management in the orientation of and provides training for newly-hired QA Record Specialists.Manages documentation-related projects to support the needs of management.Manages a central file of Master Records that provides the facility with comprehensive historical records of all master formula documents and corresponding change control records.Develops appropriate batch records to meet the documentation requirements of validation protocols, special studies, component qualification.May attend weekly production scheduling meeting and assures timely completion and issuance of all documents required for scheduled production. Monitors the approved Production Schedule on a continuous basis to assure timely response to changing requirements.Performs other duties and responsibilities as delegated by QA Documentation/MQA Disposition Management. qualifications:Undergraduate degree (preferably Chemistry or Biology) or appropriate combination of education, training and experience.3-5 years experience in the pharmaceutical industry.Excellent communication, writing and proofreading skills.Computer skills required.Excellent verbal and written communication skills required. skills: MS-WORD, MS-EXCEL, Biology, Chemistry, QC ReviewEqual 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: Melrose Park, Illinoisjob type: Contractsalary: $15 - 19 per hourwork hours: 9 to 5education: Bachelors responsibilities:The Q.A. Record Specialist is responsible for management and maintenance of master documents for manufacturing, packaging and testing. The QA Record Specialist assists management with respect to accomplishing projects, meeting commitments, developing departmental systems and overall assurance of accurate and appropriate processing of Master Batch Record documentation, issuance of batch records, testing specifications and laboratory records.Analyzes and coordinates scheduled production batches to assure availability of complete and accurate manufacturing documents.Prioritizes the issuance of all necessary and appropriate documents for each scheduled product, calculates and assigns product expiration date, assures critical information such as product I.D., strength.Implements revisions to master batch records by accurately incorporating changes as specified by the approved document change request (DCR).Recognizes and resolves documentation discrepancies. Communicates any such occurrence and corrective action to Manager and other QA Record Specialist.Assists management in the orientation of and provides training for newly-hired QA Record Specialists.Manages documentation-related projects to support the needs of management.Manages a central file of Master Records that provides the facility with comprehensive historical records of all master formula documents and corresponding change control records.Develops appropriate batch records to meet the documentation requirements of validation protocols, special studies, component qualification.May attend weekly production scheduling meeting and assures timely completion and issuance of all documents required for scheduled production. Monitors the approved Production Schedule on a continuous basis to assure timely response to changing requirements.Performs other duties and responsibilities as delegated by QA Documentation/MQA Disposition Management. qualifications:Undergraduate degree (preferably Chemistry or Biology) or appropriate combination of education, training and experience.3-5 years experience in the pharmaceutical industry.Excellent communication, writing and proofreading skills.Computer skills required.Excellent verbal and written communication skills required. skills: MS-WORD, MS-EXCEL, Biology, Chemistry, QC ReviewEqual 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.
    • melrose park, illinois
    • contract
    • US$25.00 - US$27.50, per hour, $25.00 - 27.50 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. 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: Melrose Park, Illinoisjob type: Contractsalary: $25.00 - 27.50 per hourwork hours: 9 to 5education: Bachelors responsibilities:Performs accurate routine chemical testing as well as chromatographic methods of analysis (HPLC, GC, TLC, AA) to meet departmental objectives.Audits chemistry SOP's and updates and writes new procedures to ensure compliance and accuracy.Assists in the formal training of lab personnel on topics such as GMP, safety, antineoplastic and new employee training.Provides technical support for methods validations.Applies computer experience to perform data collection and analysis of testing data to meet objectives of department.Performs troubleshooting of instrumentation by applying problem solving skills and sourcing out literature or vendors if necessary. Assist Associate Chemist personnel troubleshooting difficulties.Maintains accurate records of all work performed with respect to a given project. Ensure documentation meets facility audit as well as cGMP or GLP requirements.Establishes work priorities based on schedule needs using own judgment and objective reasoning. qualifications:Possess a B.S. in Chemistry. Typically requires 3-6 years of related experience in pharmaceutical industry. Must have hands-on experience and knowledge of chromatographic methods of analysis (HPLC, GC, TLC, AA). Familiarity with cGMP and Federal regulations.HPLC experience is a must, GMP experience is a bonus skills: HPLC, 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. 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: Melrose Park, Illinoisjob type: Contractsalary: $25.00 - 27.50 per hourwork hours: 9 to 5education: Bachelors responsibilities:Performs accurate routine chemical testing as well as chromatographic methods of analysis (HPLC, GC, TLC, AA) to meet departmental objectives.Audits chemistry SOP's and updates and writes new procedures to ensure compliance and accuracy.Assists in the formal training of lab personnel on topics such as GMP, safety, antineoplastic and new employee training.Provides technical support for methods validations.Applies computer experience to perform data collection and analysis of testing data to meet objectives of department.Performs troubleshooting of instrumentation by applying problem solving skills and sourcing out literature or vendors if necessary. Assist Associate Chemist personnel troubleshooting difficulties.Maintains accurate records of all work performed with respect to a given project. Ensure documentation meets facility audit as well as cGMP or GLP requirements.Establishes work priorities based on schedule needs using own judgment and objective reasoning. qualifications:Possess a B.S. in Chemistry. Typically requires 3-6 years of related experience in pharmaceutical industry. Must have hands-on experience and knowledge of chromatographic methods of analysis (HPLC, GC, TLC, AA). Familiarity with cGMP and Federal regulations.HPLC experience is a must, GMP experience is a bonus skills: HPLC, 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.

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