Top 19 Remote oncology Jobs in Aurora Il

Manager Quality Assurance
Versiti, Inc. —Aurora, IL
- $100,000 a year
- Full-time
- Microsoft Excel
- 6 years
- Bachelor's degree
- Paid holidays
- Disability insurance
23h
Trust Operations & Consent Manager
Atrium Health —Oak Brook, IL
- $51.05 - $76.60 an hour
- Full-time
- Remote
- Marketing
- 3 years
- Bachelor's degree
- Paid parental leave
- Disability insurance
Cancer & Tumor Registrar II
UChicago Medicine AdventHealth Hinsdale —Woodridge, IL
- $22.68 - $42.19 an hour
- Full-time
- Anatomy knowledge
- 5 years
- Databases
- Paid parental leave
- Disability insurance
Specialty Account Representative - Chicago - North
Pharmacosmos Therapeutics Inc —Chicago, IL
- $150,000 - $164,000 a year
- Full-time
- Remote
- Bachelor of Science
- Mid-level
- 3 years
Quick Apply
Oncology Concierge Pharmacy Technician
Onco360 —Woodridge, IL
- From $24 an hour
- Full-time
- Basic math
- High school diploma or GED
- Analysis skills
- Paid holidays
- Disability insurance
Quick Apply
Cancer Registry Coordinator
UChicago Medicine AdventHealth Hinsdale —Hinsdale, IL
- $23.32 - $43.37 an hour
- Full-time
- 5 years
- Research
- Senior level
- Paid parental leave
- Disability insurance
Compliance Auditor
Onco360 —Woodridge, IL
- From $60,000 a year
- Urgently hiring
- Microsoft Outlook
- Writing skills
- Basic math
Quick Apply
Regional Sales Director - Midwest
Pharmacosmos Therapeutics Inc —Chicago, IL
- $186,000 - $217,000 a year
- Full-time
- Remote
- 5 years
- Bachelor of Science
- Analysis skills
Quick Apply
RN Clinical Team Director - Hospice
AccentCare, Inc. —Burr Ridge, IL
- $100,000 - $112,000 a year
- Full-time
- CPR Certification
- Nursing
- Surgery
- Health savings account
- Paid holidays
Quick Apply
5d
Board Certified Rheumatologist for Part Time Disability File Reviews
Brown & Brown Absence Services Group —United States
- $225 - $2,200 a week
- Contract
- Remote
- Psychiatry
- Internal Medicine
- Clinic experience
- Disability insurance
Quick Apply
Clinician (Oncology / Hematology) - AI Trainer
micro1 —United States
- $160 - $200 an hour
- Contract
- Remote
- 5 years
- BC/BE
- No experience needed
- Flexible schedule
11d
CIBMTR Program Manager
Registry Partners —United States
- From $35 an hour
- Weekends as needed
- Remote
- 5 years
- Supervising experience
- Senior level
- Health insurance
- Dental insurance
Quick Apply

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Manager Quality Assurance

Versiti, Inc. -
Aurora, IL

Apply Now

Job Details

Full-time
$100,000 a year
23 hours ago

Benefits

Paid holidays
Disability insurance
Health insurance
Dental insurance
Paid time off
Vision insurance
401(k) matching
Employee discount
Life insurance

Qualifications

Microsoft Excel
Copy machines
Production risk assessment
Bachelor's degree
Data-driven problem-solving
Quality control experience within pharmaceutical industry
Productivity software
Pharmaceutical manufacturing facility experience

Full Job Description

Overview:

Versiti is a fusion of donors, scientific curiosity, and precision medicine that recognize the gifts of blood and life are precious. We are home to the world-renowned Blood Research Institute, we enable life saving gifts from our donors, and provide the science behind the medicine through our diagnostic laboratories. Versiti brings together outstanding minds with unparalleled experience in transfusion medicine, transplantation, stem cells and cellular therapies, oncology and genomics, diagnostic lab services, and medical and scientific expertise. This combination of skill and knowledge results in improved patient outcomes, higher quality services and reduced cost of care for hospitals, blood centers, hospital systems, research and educational institutions, and other health care providers. At Versiti, we are passionate about improving the lives of patients and helping our healthcare partners thrive.

Position Summary:

This position must be independent from production associated activities in order to meet the cGMP definition of an independent Quality Unit and function in review, approval and release tasks as defined by the cGMP regulations. Responsible for establishing and implementing effective Quality systems to meet or exceed cGMP requirements. Ensures the activities and controls used to determine the accuracy and reliability of the establishment's personnel, equipment, reagents, operations and release or rejection of final product in the manufacturing of biomaterial products including their testing Collaborates with Center management to ensure compliance with all applicable regulations, laws, guidelines, standards and Company policies, and that the Center is "inspection ready" at all times Ensures all staff are trained and competently performing their duties as evidenced by the auditing of the program Leads investigations to determine root causes, corrective/preventative actions and appropriate review of resulting effectiveness checks Proactively facilitates communication and interdepartmental coordination resolving quality issues and to host audits, both internal and external.

Total Rewards Package:

Compensation

The target salary for this position is $100,000 annually.

The target salary is based on internal averages. Versiti sets salary ranges aligned to local markets in which the job is performed. Compensation decisions take into account internal salary averages and differentiation based on education, experience, skills, and performance. Specific salary and benefits information is shared at the time of the phone screening based on your location and qualifications.

Benefits
Versiti provides a comprehensive benefits package based on your job classification. Full-time regular employes are eligible for Medical, Dental, and Vision Plans, Paid Time Off (PTO) and Holidays, Short- and Long-term disability, life insurance, 7% match dollar for dollar 401(k), voluntary programs, discount programs, others.

Responsibilities:

Ensure center is “inspection ready” at all times by managing adherence to Standard Operating Procedures (SOPs), the organization’s QMS, compliance policies, utilizing sound Quality principles, self-inspection learnings, non-conformity discovery and appropriate remediation. Prepare regular reports to Management and corporate quality management as to the state of quality and systems at the Center.
Function as the responsible Quality Assurance reviewer to approve or reject final products before shipping, batch records, quarantine releases, rework, destruction and associated documentation such as Certificates of Analyses.
Manage site Quality Assurance program including but not limited to calibration management, monitoring of compliance to defined processes (e.g. sampling, competency checks, Key Performance Indicators (KPIs), trending and analysis of those KPIs, root cause and failure mode impact assessment and change management.
Working knowledge of the change management process and appropriately raise ideas for consideration for change locally and upward to quality and Center management.
Receive and provide feedback to staff on observations leading to improved adherence to cGMP regulations. Report concerns or deficiencies to Center personnel and/or Center management immediately. Review operations staff’s RCA, corrective actions and effectiveness checks to resolve audit observations and other non-compliance issues of deficiencies.
Lead and function as the key Quality representative for site supplier, customer and regulatory audits. Lead Center’s review of findings, coordination of Corrective and Preventive Actions (CAPA), if needed and successful closure of audits in a timely fashion. Utilize quality tools and applications to facilitate understanding of issues and documentation.
Conduct routine audits of internal procedures and documentation, as necessary.
Adhere to all HR policies and practices through fair and equitable treatment of all employees. Communicate effectively with HR to ensure HR compliance and ensure Center management is doing the same.
Comply with all Federal, State and local regulatory laws, standards and guidelines.
Maintain confidentiality of all personnel, contributor and Center information.
Monitor CAPA’s and effectiveness checks to ensure issues are resolved.
Performs other duties as assigned
Complies with all policies and standards

Qualifications:

Education

Bachelor's Degree required

Experience

7-9 years Minimum of six years QA oversight of biological manufacturing operations, utilizing a risk-based approach to biologic material manufacturing, required
Working knowledge and experience practicing under a QMS preferred
Two or more years performing as a responsible cGMP Quality sign off for a regulated product preferred
Working knowledge of 21 CFR 210, 211 and 820 preferred
Demonstrated ability to work with remote resources across multiple sites preferred

Knowledge, Skills and Abilities

Experience with batch record review, results outside of specifications, and CAPA investigations
Experienced with both Quality and production related documentation, line clearances, and status control of raw materials and finish product, approval of C of A’s, quarantine and release of in-process and finished goods.
Internal and external audit experience, preferred lead audit support
Strong understanding of FDA regulations as they apply to blood products or pharmaceuticals.
Positive, enthusiastic, and customer service oriented interpersonal skills
Ability to work as part of a high performing team and collaborate effectively with staff at all levels and establish highly functional relationships within and outside the company.
Excellent technical writing and verbal communication skills.
Domestic travel (~10%) as needed.
Strong oral, written and listening skills.
Ability to assess priorities and successfully manage workload to timelines.
Ability to define problems, collect data, establish facts, and draw valid conclusions.
Understanding of basic scientific/technical concepts and ability to analyze moderate to complex data and glean basic information from the data.
Previous experience with electronic quality systems such as for document control, training, and change control preferred..

Tools and Technology

Personal Computer (desk top, lap top, tablet) required
General office equipment (computer, printer, fax, copy machine) required
Microsoft Suite (Word, Excel, PowerPoint) required

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Refine Your Search

remote oncology jobs in aurora il

Manager Quality Assurance

Trust Operations & Consent Manager

Cancer & Tumor Registrar II

Specialty Account Representative - Chicago - North

Oncology Concierge Pharmacy Technician

Cancer Registry Coordinator

Compliance Auditor

Regional Sales Director - Midwest

RN Clinical Team Director - Hospice

Board Certified Rheumatologist for Part Time Disability File Reviews

Clinician (Oncology / Hematology) - AI Trainer

CIBMTR Program Manager

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