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Project Manager - Quality Systems

Collabera Technologies - North Chicago, IL

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Job Description

Description Home Search Jobs Job Description Project Manager - Quality SystemsContract: North Chicago, Illinois, USSalary Range: 60.00 - 65.00 | Per HourJob Code: 367994End Date: 2026-04-04 Days Left: 16 days, 3 hours leftApplyTo Discuss more about this job opportunity, please reach out to Deepak Arya (LinkedIn URL - /in/deepak-arya-8a79aa22a/ ), email your updated resume at Email - deepak.arya@ . Thank you!Pay Range: $60 to $65 an hour (Negotiable base on the experience) Position Details: Client Industry: PharmaceuticalContract Duration: 06 months (Possibilities of Extension)Description:The project Manager, Quality Systems is responsible for supporting and maintaining compliant quality systems within a regulated manufacturing environment. This role ensures that product, process, and system quality activities meet regulatory requirements and internal quality standards. The position works cross-functionally to implement quality strategies, maintain documentation systems, and support continuous improvement initiatives. The role helps ensure compliance across the product lifecycle, from raw material inspection through final product shipment. The individual will also translate quality strategy into operational actions to support business and regulatory objectives.Must Haves Bachelor's degree in Life Sciences or a related scientific field 8 or more years of experience in Quality within a regulated manufacturing environment Experience writing and managing Quality System procedures, SOPs, and process documentation Experience with Supplier Quality or Supplier Controls Experience supporting pharmaceutical or medical device manufacturing Strong written and verbal communication skills Knowledge of regulatory compliance and quality standards in manufacturing environments Day to Day Provide Quality Assurance support for manufacturing operations and quality system activities Ensure compliance of products, processes, and systems with internal standards and regulatory requirements Support and maintain quality system processes including document control, training, validation, and labeling Review and maintain quality documentation including procedures, records, and compliance reports Collaborate with cross-functional teams to implement quality initiatives and resolve quality issues Support quality strategy implementation and translate strategic goals into operational actions Monitor quality activities from raw material inspection through final product release and shipment Ensure quality processes align with corporate policies and applicable regulatory guidelines Plusses ASQ Certification (such as CQE or CQA) Experience supporting biologics, cosmetics, or combination products Experience with quality intelligence or quality data analysis Prior experience supporting validation programs or quality training programs. Benefits:The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, (paid time , paid sick and safe time , hours of paid vacation time, weeks of paid parental leave, paid holidays annually - AS Applicable)Job Requirement Quality Systems Pharmaceutical SOPs Documentation Reach Out to a Recruiter Recruiter Email PhoneDeepak Arya deepak.arya@ Apply Now

Created: 2026-04-02

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