quality control tester salaries in chicago, illinois

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This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Northbrook, Illinois job type: Contract salary: $39.00 - 45.90 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Project manages and executes tasks associated with the Change Control quality system following management guidance and oversight. Maintains & monitors the applicable change control system, associated databases to ensure that records are in a compliant state and generates metrics for routine reporting. Assures company compliance with global regulations, corporate standards and SOPs for Change Control and general quality systems. Supports additional Quality Assurance initiatives as requested. Executes tasks associated with all company quality systems as directed, with a focus on change control, as an individual contributor and updates related databases and/or tracking tools in a timely manner. Generates status reports as required and maintains relevant change control databases and/or project management plans.Is a subject matter expert (SME) for the global change control system and interfaces with local affiliate QA functions to integrate local change control activity with governing corporate change control(s). Acts a resource for affiliate QA with respect to change control system.Project Management of complex multi-faceted strategic change controls as it relates to business objectives and assurance of change control implementation for all globally impacted stakeholders.Initiates, evaluates, assesses and tracks change controls utilizing effective project management skills and tools to monitor global action items / deliverables to target due dates. Ensures compliant and timely implementation of changes.Utilizes technical skills and quality assurance experience to identify areas of concern in both electronic and paper-based change control quality systems, as well as specific project deliverables. Evaluates and assesses risks to facilitate timely notification to management and provides proposals for resolution.Coordinates the collection and tabulation of metrics related to the change control quality system as directed by management. Monitors system for positive and adverse trends.Assures global company adherence and compliance with corporate policies, SOPs and global regulatory standards. Identifies issues and initiates corrective and/or preventive actions as required.Supports any additional quality activities related to the performance of gap assessments and/or resolution of any identified risks as requested.Effectively communicates with departmental and global cross-functional teams to support and facilitate change control project deliverables.Responsible for the storage and maintenance of quality-controlled documentation related to change control activity.Executes tasks associated with general quality systems, and more specifically, the company global change control quality system. Project manages any assigned change control related activity and deliverables to completion in partnership with global company quality assurance affiliates and external business partners as applicable. Assists, develops and manages timelines to maintain compliance to company project timelines, SOPs, standards and global regulatory requirements.This role reports to the QA Commercial Quality Representative of either Latin America or Russia as applicable. Works closely with other areas such as Regulatory Affairs, PV, Legal, Commercial, Supply Chain, Market Access, Global Project Management and Product and Project Management.  qualifications: Required Must be fluent in Spanish with strong technical writing and speaking skills in English.Strong TrackWise skills.Minimum BA/BS with minimum 5 years of industry experience with a minimum of 3 years QA / QC experience and 2 years of project management.Knowledge of global GMPs and other industry regulationsStrong, effective communication and interpersonal skills with an emphasis on cultural awareness.Ethical, results-oriented professional with attention to detail.Individual contributor with understanding and commitment to team success and efficiently executes assigned tasks per management direction.Confident & professional representation of the company to external stakeholders including international health care professionals.Requires strong project management skills and ability to execute change control responsibilities. Preferred: GMP manufacturing and/or Commercial affiliate experience  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. 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.

Are you looking to join a company that can provide great stability and an amazing work culture? Do you have data entry experience and the desire to work with one of the largest global law firms? If so, our client is seeing a Litigation Support Technician to work in their downtown Chicago office. The position offers tremendous opportunity for growth. Apply now!salary: $26.5 - $31.25 per yearshift: Firstwork hours: 9 AM - 5 PMeducation: BachelorResponsibilities Work with the eDiscovery Operations Manager and other members of the Operations and Project Management team to evaluate Litigation & Practice Support department data archiving and deletion procedures Be department interface with Record department on department data lifecycle issues Accurately maintain lists of data to be deleted or archived Run commands to copy, QC data copies, and delete data Assist in duplication, creation, tracking and destruction of media Other projects as assigned SkillsLitigation supportTechnical SupportData Entry (2 years of experience is required)Microsoft Office (5 years of experience is required)OrganizationMulti-taskingQualificationsYears of experience: 2 yearsExperience level: Entry LevelRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. 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: Seeking an experienced senior level Medical Writer. The ideal candidate should have 3+ years of regulatory writing experience.   location: Northbrook, Illinois job type: Permanent salary: $150,000 - 165,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: May include but not limited to the following: Under minimal supervision, writes and edits clinical study reports, protocols, informed consent forms, and other clinical and regulatory documents including Investigator Brochures and annual reports.Assists with the preparation of briefing documents, INDs, and other major submissions (BLAs, MAAs) as needed.Leads the process of critical review of clinical regulatory documents and incorporates multiple reviews into successive drafts.Provides QC support for clinical regulatory documents as needed (cross-checking data and verifying content from source documents).Reviews case report forms, statistical analysis plans, and data tables and listings for content and format.Participates in clinical project team meetings.Ensures the quality of clinical regulatory documents by maintaining and promoting familiarity with ICH, GCP, and other standards.  qualifications: ? Education: Requires an advanced degree in a scientific discipline or a bachelor's degree with equivalent work experience. Experience: 3+ years experience writing/editing clinical regulatory documents including clinical study reportsPharmaceutical industry experience and background in biologics a plus Special Skills: Excellent writing, editing, attention to detail and verbal communication skillsAbility to critically analyze and synthesize complex scientific information from a broad range of scientific disciplines and clinical therapeutic areasProficiency in Microsoft WordFamiliarity with CTD, ICH, GCP and other standardsAbility to manage/prioritize multiple projects from conception to completion, working in a fast-paced environment  skills: GCP (Good Clinical 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.