Candidate must complete initial training course provided by LC Housekeeping prior to working in regulated environments at Abbott Lake County site.
Must be able to complete accurate and legible written records in compliance with Good Manufacturing Practices when documenting work performed, (room attestations, work orders, cleaning logs) auditable by regulatory agencies.
Must be able to operate a computer to complete required compliance/technical training, to download daily work instructions to handheld computer and document work performed, then sync back into the CMMS for GMP review and archiving.
High School diploma or equivalent is required,
Must be able to read and comprehend written information to include Corporate Quality Documents, Cross Divisional Operating Procedures &, Safety Guidelines, Departmental Basic Operating Procedures &, Safety Guidelines and Operating Instructions.
Requires adherence to quality and regulatory requirements (as referenced in GMP's, SOP's, DEA, OSHA, DEP and Abbott standards).

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Front Desk Associate

Bears Fit

Vernon Hills, IL 60061

Remote Part Time Data Entry Clerk -$1400 weekly

The Job Place

Vernon Hills, IL

$1,400/wk

RemoteNo Experience

Data Entry Specialist - Remote / Entry Level

Easy Recruiter

Vernon Hills, IL

RemoteHealth InsuranceRetirement Benefit

New, Posted 10 hours ago

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Quality Associate II

Vantive

Deerfield, IL 60015

$80,000-$90,000/yr

~ 18 min OnsiteFlexible ScheduleChildcare AssistanceEducation AssistanceHealth InsurancePaid Time OffRetirement Benefit

Bachelor's Degree required (preferably in science, engineering or equivalent field)
Minimum of 3 years of experience in Quality, or related field in the medical products/pharmaceutical industry
Solid understanding of FDA Regulations, Health Canada requirements and Application of Good Distribution Practices
Experience preferred for the following: distribution and warehousing in US and Canada, Quality Management Systems, FDA and Health Canada regulations, supplier quality
Oversight of distribution/warehouse-related external suppliers.
Responsible for compliance with FDA and Health Canada requirements, ISO standards and Vantive QMSby applying rigorous quality standards, including Standard Operating Procedures (SOPs) and Current Good Manufacturing Practices (cGMP).
Responsible to ensure compliance with Regulatory, Corporate and Local Quality requirements and for providing Quality oversight of Vantive US and Canada warehousing and distribution operations, including internal warehouse site QA activities, internal renal fleet drivers, external warehousing partners (i.e., 3PL providers, wholesalers, freight forwarders and consolidation/ deconsolidation centers), and external transportation providers.
Must be proficient with Microsoft Office and other data collection/analysis programs (e.g. Minitab)
Education and/or Experience: Minimum of 3 years of experience in Quality, or related field in the medical products/pharmaceutical industry
Able to manage multiple projects and/or responsibilities simultaneously
Must have basic English written and oral communication skills adequate to connect with other team members
Act as a key partner with US and Canada Vantive Operations (including Supply Chain, Logistics and Fulfillment) to manage Quality requirements and oversight of all 3PL activities.

SmartExplore AI is experimental.