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job summary: Randstad is the #1 HR Solutions Company in the World and we are sourcing for a QC Sr Scientist in the Northern Suburbs of Chicago, IL. The ideal candidate will perform testing of raw materials, in process samples, finished products, stability samples and cleaning samples in support of release of materials. Additionally, this position will support other activities associated with laboratory operation and will review data for compliance, review policy and procedure documents as necessary to meet cGMP regulations and applicable guidelines. This is a direct hire position and can start immediately.   location: Waukegan, Illinois job type: Permanent salary: $80,000 - 90,000 per year work hours: 7 to 3 education: Bachelors   responsibilities: JOB SUMMARY Individual will perform testing of raw materials, in process samples, finished products, stability samples and cleaning samples in support of release of materials. Additionally, this position will support other activities associated with laboratory operation and will review data for compliance, review policy and procedure documents as necessary to meet cGMP regulations and applicable guidelines. Perform training of other scientists on complex and/or specialized analytical techniques. Act as a resource for instrument troubleshooting and guidance to other scientists. Must be able to work in a complex, fast paced environment with an ability to prioritize. Responsibilities Conducts daily activities in accordance with the company Cardinal RulesPerform testing of raw materials, in process samples, finished products, stability samples and cleaning samples in support of release of materials while striving to adhere to assigned due dates. Assess and prioritize workload with minimal Management supervision.Provide project support through testing requests, compilation of data, feedback on analysis approach and reporting of findings to supervisor and / or project lead including issues/abnormal observations while striving to adhere to assigned due dates.Perform technical and compliance review of complex analytical tests.Execution of testing protocols without deviation.Willingness to work on Safebridge Category I-III compounds.Perform training of other scientists on complex and/or specialized analytical techniques.Requires full understanding of multiple instruments including functionality and the ability to troubleshoot issues. Review of instrument qualification packets.Authoring of templated technical documents.Maintain analytical equipment (periodic calibration and maintenance) in accordance with PI policies and procedures.Maintain files as directed.Perform data entry into spreadsheets and proprietary computer systems.Operate following company policies and procedures to meet cGMP regulations and ICH guidelines.Maintain documentation in an accurate, clear and concise manner in accordance to company policies and procedures.Maintain a clean, safe and orderly workplace, following all applicable EHS policies and procedures.  qualifications: ??Qualifications Bachelor's degree (BS) in Chemistry related fieldFour (4)+ years of experience in a GMP analytical laboratoryAccurate Documentation and Observation skillsWorking knowledge of the cGMP regulations preferredWorking knowledge of safe handling practices of dangerous chemicalsComputer skills (spreadsheet, database and word processing window based programs)Hands-on experience with the operation and maintenance of analytical instrumentation preferred. (HPLC or GC using Empower, ICP-MS)Excellent Communication skills Physical Requirements Must have good hearing and sight - adequate for safety programs in a pharmaceutical manufacturing plantMust be able to sit and/or stand for extended periodsAbility to work effectively under pressure to meet deadlinesFrequent sitting, standing, walking, climbing of stairs, use of computer monitor screen, talking, writing, listeningMust be able to lift 25 lbs. or occasionally lift up to 35 lbs.Ability to wear proper safety equipment when working in the laboratory or plant  skills: Quality control, HPLC, SOP, Pharmacology, Data Analysis, Analytical Chemistry, Chemistry, Chromatography, GLP (Good Laboratory Practice), Protein Purification, Data Analysis Software, 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.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility). Applications accepted on ongoing basis until filled.

job summary: Randstad is the #1 HR Services Company in the World and we are sourcing for a QC Scientist in the Northern Suburbs of Chicago, IL. The ideal candidate will be will perform testing of raw materials, in process samples, finished products, stability samples and cleaning samples in support of release of materials. Additionally, this position will support other activities associated with laboratory operation and will review data for compliance, review policy and procedure documents as necessary to meet cGMP regulations and applicable guidelines. Perform training of other scientists on standard analytical techniques. Must be able to work in a complex, fast paced environment with an ability to prioritize. This is a contract position and can start immediately.   location: Waukegan, Illinois job type: Temporary salary: $28 - 30 per hour work hours: 7 to 3 education: Bachelors   responsibilities: ESSENTIAL DUTIES AND RESPONSIBILITIES: Conducts daily activities in accordance within the clients rules and regulationsPerform testing of raw materials, in process samples, finished products, stability samples and cleaning samples in support of release of materials while striving to adhere to assigned due dates.Provide project support through defined testing requests, compilation of data and reporting of findings to supervisor and / or project lead including issues/abnormal observations while striving to adhere to assigned due dates.Perform technical and compliance review of complex analytical tests.Execution of testing protocols without deviation.Willingness to work on Safebridge Category I-III compounds.Perform training of other scientists on standard analytical techniques.Requires full understanding of at least one instrument including functionality and the ability to troubleshoot issues.Maintain analytical equipment (periodic calibration and maintenance) in accordance with PI policies and procedures.Maintain files as directed.Perform data entry into spreadsheets and proprietary computer systems.Operate following clients policies and procedures to meet cGMP regulations and ICH guidelines.Maintain documentation in an accurate, clear and concise manner in accordance to company policies and procedures. Maintain a clean, safe and orderly workplace, following all applicable EHS policies and procedures.  qualifications: QUALIFICATIONS: BS degree in chemistry or biology or related field2+ years of experience in a GMP analytical laboratoryAccurate Documentation and Observation skillsWorking knowledge of the cGMP regulations preferredWorking knowledge of safe handling practices of dangerous chemicalsComputer skills (spreadsheet, database and word processing window based programs)Hands-on experience with the operation and maintenance of analytical instrumentation preferred. (Polarimetry, pH and conductivity meters, Automatic titrators, TOC, HPLC or GC using Empower)Excellent Communication skills PHYSICAL REQUIREMENTS: Must have good hearing and sight - adequate for safety programs in a pharmaceutical manufacturing plant Must be able to sit and/or stand for extended periods Ability to work effectively under pressure to meet deadlines Frequent sitting, standing, walking, climbing of stairs, use of computer monitor screen, talking, writing, listening Must be able to lift 25 lbs. or occasionally lift up to 35 lbs. Ability to wear proper safety equipment when working in the laboratory or plant  skills: Quality control, SOP, Quality Assurance, Biology, Chemistry, GLP (Good Laboratory Practice), GMP (Good Manufacturing Practice), LIMS (Laboratory Information Management System, MRP (Material Requirements Planning) 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.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility). Applications accepted on ongoing basis until filled.

job summary: Randstad is the #1 HR Solutions Company in the World and we are sourcing for a QC Sr Scientist in the Northern Suburbs of Chicago, IL. The ideal candidate will perform testing of raw materials, in process samples, finished products, stability samples and cleaning samples in support of release of materials. Additionally, this position will support other activities associated with laboratory operation and will review data for compliance, review policy and procedure documents as necessary to meet cGMP regulations and applicable guidelines. This is a direct hire position and can start immediately.   location: Waukegan, Illinois job type: Permanent salary: $80,000 - 90,000 per year work hours: 7 to 3 education: Bachelors   responsibilities: ? JOB SUMMARY Individual will perform testing of raw materials, in process samples, finished products, stability samples and cleaning samples in support of release of materials. Additionally, this position will support other activities associated with laboratory operation and will review data for compliance, review policy and procedure documents as necessary to meet cGMP regulations and applicable guidelines. Perform training of other scientists on complex and/or specialized analytical techniques. Act as a resource for instrument troubleshooting and guidance to other scientists. Must be able to work in a complex, fast paced environment with an ability to prioritize. Responsibilities Conducts daily activities in accordance with the company Cardinal RulesPerform testing of raw materials, in process samples, finished products, stability samples and cleaning samples in support of release of materials while striving to adhere to assigned due dates. Assess and prioritize workload with minimal Management supervision.Provide project support through testing requests, compilation of data, feedback on analysis approach and reporting of findings to supervisor and / or project lead including issues/abnormal observations while striving to adhere to assigned due dates.Perform technical and compliance review of complex analytical tests.Execution of testing protocols without deviation.Willingness to work on Safebridge Category I-III compounds.Perform training of other scientists on complex and/or specialized analytical techniques.Requires full understanding of multiple instruments including functionality and the ability to troubleshoot issues. Review of instrument qualification packets.Authoring of templated technical documents.Maintain analytical equipment (periodic calibration and maintenance) in accordance with PI policies and procedures.Maintain files as directed.Perform data entry into spreadsheets and proprietary computer systems.Operate following company policies and procedures to meet cGMP regulations and ICH guidelines.Maintain documentation in an accurate, clear and concise manner in accordance to company policies and procedures.Maintain a clean, safe and orderly workplace, following all applicable EHS policies and procedures.  qualifications: ??Qualifications Bachelor's degree (BS) in Chemistry related fieldFour (4)+ years of experience in a GMP analytical laboratoryAccurate Documentation and Observation skillsWorking knowledge of the cGMP regulations preferredWorking knowledge of safe handling practices of dangerous chemicalsComputer skills (spreadsheet, database and word processing window based programs)Hands-on experience with the operation and maintenance of analytical instrumentation preferred. (HPLC or GC using Empower, ICP-MS)Excellent Communication skills Physical Requirements Must have good hearing and sight - adequate for safety programs in a pharmaceutical manufacturing plantMust be able to sit and/or stand for extended periodsAbility to work effectively under pressure to meet deadlinesFrequent sitting, standing, walking, climbing of stairs, use of computer monitor screen, talking, writing, listeningMust be able to lift 25 lbs. or occasionally lift up to 35 lbs.Ability to wear proper safety equipment when working in the laboratory or plant  skills: Quality control, HPLC, SOP, Pharmacology, Data Analysis, Analytical Chemistry, Chemistry, Chromatography, GLP (Good Laboratory Practice), Protein Purification, Data Analysis Software, 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.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility). Applications accepted on ongoing basis until filled.