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Home Based Program Cost Control Analyst Jobs in Illinois

Actalent

Product Cost Engineer

Peoria, IL

Ability to perform cost analysis, cost estimation, and cost control in a manufacturing context ... Work Environment This is an onsite role based in Peoria, Illinois, within a manufacturing-focused ...

Labor Solutions, LLC

Senior QC Analyst

Wheeling, IL · On-site

$25 - $33/hr

Senior QC Analyst Hourly * Part-Time or Full-Time * Flexible Schedule A premier Midwest ... Based in Wheeling, Illinois, we operate a cGMP-aligned processing facility with a focus on quality ...

Ferrero

Cost Accountant

Franklin Park, IL

$71K - $94K/yr

... cost control, budgeting, capital project analysis, and monthly closings while embedding financial ... Actual compensation will be determined based on experience, qualifications, and other job-related ...

Ferrero

Cost Accountant

Franklin Park, IL · On-site

$71K - $94K/yr

... cost control, budgeting, capital project analysis, and monthly closings while embedding financial ... Actual compensation will be determined based on experience, qualifications, and other job-related ...

Ferrero

Cost Accountant

Franklin Park, IL · On-site

$71K - $94K/yr

... cost control, budgeting, capital project analysis, and monthly closings while embedding financial ... Actual compensation will be determined based on experience, qualifications, and other job-related ...

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All JobsHome Based Program Cost Control Analyst JobsHome Based Program Cost Control Analyst Jobs in Illinois

Home Based Program Cost Control Analyst information

What is the difference between Home Based Program Cost Control Analyst vs Home Based Project Coordinator?

AspectHome Based Program Cost Control AnalystHome Based Project Coordinator
Primary FocusMonitoring and controlling project costs, budgeting, financial analysisManaging project schedules, coordinating tasks, communication
Required SkillsCost analysis, budgeting, financial reportingProject management, communication, organization
Work EnvironmentPrimarily financial and analytical tasks, remoteCoordination and communication, remote or onsite
Common CertificationsNone required but often preferred: CAP, CPCNone required but PMP or CAPM beneficial

The Home Based Program Cost Control Analyst primarily focuses on financial oversight, budgeting, and cost management within projects, ensuring expenses stay within budget. In contrast, the Home Based Project Coordinator handles project scheduling, task coordination, and communication to keep projects on track. Both roles often work remotely and may share similar certifications, but their core responsibilities differ significantly in scope and focus.

What does a home based program cost control analyst do?

A home-based program cost control analyst monitors and manages project budgets, tracks expenses, and analyzes financial data to ensure cost efficiency. They use tools like spreadsheets and project management software to identify cost overruns and support financial decision-making within the organization.

What are the most commonly searched types of Program Cost Control Analyst jobs in Illinois?

The most popular types of Program Cost Control Analyst jobs in Illinois are:

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For Home Based Program Cost Control Analyst jobs in Illinois, the most frequently searched job titles are:

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The top searched job categories for Home Based Program Cost Control Analyst jobs in Illinois are:

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Cities in Illinois with the most Home Based Program Cost Control Analyst job openings:

Home Based Program Cost Control Analyst jobs near you

Quality Control (QC) Analyst II

Kashiv BioSciences, LLC

Chicago, IL • On-site

$24.75 - $33.25/hr

Full-time

Re-posted 15 days ago

Job description

Description

Position Summary


The Quality Control Analyst II will be responsible for analytical testing and data verification supporting both late-stage clinical and commercial biosimilar products in cGMP-compliant laboratories and will also be expected to be engaged in continuous improvement initiatives to drive efficiency and effectiveness of Kashiv's Quality Systems. 


A strong background in protein chemistry will be essential to perform and troubleshoot techniques such as HPLC, SDS-PAGE, cell-based bioassays, capillary electrophoresis, SDS-PAGE, ELISA, and standard compendial assays. A demonstrated ability to collaborate across multiple departments to drive timely resolution of projects, laboratory investigations, and process improvements is required.


Essential Duties & Responsibilities

  • Analytical testing to support product in-process, release, and stability programs.
  • Strong knowledge of cGMP, Quality Systems, and ICH / regulatory guidance.
  • Conduct, compile, and/or review Out of Specification lab investigations, deviations, and corrective and preventative actions plans.
  • Work with cross-functional teams to advance projects, maintain equipment, and authoring of documents and reports.
  • Train other analysts to perform laboratory procedures and assays. Participate in internal assessments and audits as and when required.
  • Performs other functions as required or assigned
  • Complies with all company policies and standards

Requirements

Minimum Qualifications:


Education:

  • Bachelor's degree in biotechnology, biochemistry, chemistry, or related field with a minimum of 5 years of experience in a pharmaceutical/biotech QC laboratory. 
  • Alternatively, Master's degree in above areas with 3 years of experience in a pharmaceutical/biotech QC laboratory or PhD in above areas with a minimum of 2 years of experience. 

Preferred Qualifications: 


Experience:

  • Previous experience in a cGMP laboratory.
  • Strong background in protein chemistry and experience troubleshooting analytical results.
  • Demonstrated success at writing, revising, and complying with SOPs, protocols/reports, and QC methods.

Special Skills:

  • Demonstrated success working with techniques such as HPLC, SDS-PAGE, cell-based bioassays, capillary electrophoresis, SDS-PAGE, ELISA, and standard compendial assays. 
  • Previous experience supporting regulatory inspections (e.g. PAI).
  • Familiarity with preparing regulatory dossiers and data packages for interactions between Kashiv and regulatory agencies.

Work Environment & Physical Demands:

  • Some time spent in an office doing office work (reading, writing, reviewing, and editing documents).
  • Significant amount of time spent in the laboratory.
  • Must be able to work extended hours or weekend hours as requested.
  • Must be able to lift at least 25 lbs.
  • Ability to work under pressure and meet deadlines. 
  • High-paced environment structured to meet ambitious project goals
  • Some travel may be required

Supervisory Responsibility, if any: No


This position description is not a complete list of all responsibilities, duties, or skills required for the job and is subject to review and change at any time, with or without notice, in accordance with the needs of the organization.


Kashiv BioSciences, LLC provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, or genetics. In addition to federal law requirements, Kashiv BioSciences, LLC complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

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