For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel passionate about.
Job Summary
Primarily responsible for reviewing and approving GMP laboratory data and reports supporting microbiological studies for Celsis ATP Bioluminescence and other Microbial Solutions products. This on-site position will be co-located with laboratory personnel at the Charleston site for fostering a collaborative working relationship with laboratory peers. This position will actively integrate with the Quality and Regulatory Affairs leadership to support upholding a high-quality standard in laboratory data. As a peer and mentor to laboratory staff, this position may also assist with daily tasks of maintaining supply materials, laboratory tidiness activities, and will be continually trained on laboratory processes to maintain understanding during quality review duties.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
• Is capable of understanding and applying requirements related to Alternative Microbiological Method Validation.
• Is a 100% on site position at this time for fostering a collaborative working relationship with laboratory peers.
• Understands and routinely applies Good Manufacturing Practices (GMP) towards reviewing laboratory data.
• Serves as a final Quality approver on Microbial Applications Lab reports.
• Serves as a Quality approver and collaborative resource for laboratory investigations.
• Has an ongoing understanding of various regulatory regulations as applicable to products tested in the Celsis laboratory.
• Maintain records compliance by adhering to regulatory guidelines set forth by the company and varying agencies.
• Assists with laboratory maintenance activities as appropriate.
• Perform all other related duties as assigned.
Job Qualifications
• Education: Bachelor's Degree in a Biological or Chemistry Sciences discipline.
• Experience: At least 2 years working in a GMP-regulated environment.
• Certifications/Licensures: None
• Must be comfortable working collaboratively or individually
• High standards for integrity and quality of work performed
The pay range for this position is $65,000 to $80,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.
About Microbial Solutions
Our Microbial Solutions business group has a comprehensive portfolio of endotoxin testing, microbial detection and microbial identification products and services is unlike any other, and has been purposefully designed to meet the complex and ever-changing needs of the industry. We help clients to ensure product safety and quality with easy-to-use yet robust testing solutions that satisfy regulatory requirements, support critical decision making and improve operational efficiencies.
About Charles River
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
With over 20,000 employees within 110 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. And in 2019, revenue increased to $2.62 billion.
At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 80% of the drugs approved by the FDA in the last five years.
We're committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.
Equal Employment Opportunity
Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin, veteran or disability status.
It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_**********. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
For more information, please visit ***************
$65k-80k yearly Easy Apply 7d ago
Looking for a job?
Let Zippia find it for you.
Clinical Care Reviewer
Integrated Resources 4.5
Interviewer job in North Charleston, SC
A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
Job Description
Duration: 3 Months (Contract to Hire)
Responsibilities:
• Under the direction of the unit Supervisor, the
Clinical Care Reviewer
is responsible for completing medical necessity reviews.
• Using clinical knowledge and nursing experience, the nurse reviews provider requests for inpatient and outpatient services, working closely with members and providers to collect all information necessary to perform a thorough medical necessity review. It is within the nurse's discretion to pending requests for additional information and/or request clarification.
• The nurse will use his/her professional judgment to evaluate the request to ensure that appropriate services are approved and recognize care coordination opportunities and refer those cases as needed.
•The nurse will apply medical health benefit policy and medical management guidelines to authorize services and appropriately identify and refer requests to the Medical Director when guidelines are not met.
• The nurse will maintain current knowledge and understanding of the laws, regulations, and policies that pertain to the organizational unit's business and uses clinical judgment in their application.
Qualifications
Required Skills & Experience:
• Current, unrestricted
SC Registered Nurse license.
• 3+ years' experience in critical care or ER within an acute care environment.
•
2+ years' experience in utilization management
, preferably within managed care.
• Comfortable utilizing MS Office products, including Excel, Word, and Outlook.
Additional Information
Kind Regards
Harry Chaudhary
Clinical Recruiter
Integrated Resources, Inc.
IT Life Sciences Allied Healthcare CRO
Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I
Direct# 732-429-1869
(BOARD) # 732-549-2030 - Ext - 207
Email id - www.irionline.com
$47k-72k yearly est. 1d ago
New Home Quality Reviewer
2M Quality 3.5
Interviewer job in Anderson, SC
This is a part time, 1099 position.
Job duties include:
Looking at newly built homes from a customer's perspective to identify defects in workmanship, quality, completeness, consistency, and professionalism. (Reviews take on average 1 to 1.5 hours to complete) Each review is meant to evaluate the quality of the finished construction.
Driving to construction sites and conducting quality reviews on the day it is scheduled. Work may be started anytime during the day between 8 am to 3:30 pm. Reports are submitted on site electronically upon completion of review and no later than 5PM.
Entering review results online using your own tablet while on the job site. Training will be provided on how to enter a Quality Review Report in the report database.
Reviewers are not required to walk on roofs or in attics.
No tools, lights or ladders are used in the review.
Residential construction experience is preferred but not required.
Required equipment:
Tablet (Cellular enabled from 2020 model or newer)
Blue painter's tape
Hard hat (Required to be worn while on the job site.)
Access to email while out in the field either though a tablet or phone
Preferred background experience:
General Contractor/Superintendent/Project Manager
Familiar with punch list writing or general QC/QA principles.
Home Renovation or Remodeling
Familiar with fit and finish reviews or warranty walk through with homeowners
Ideal candidates will be:
Detail oriented - able to be thorough and consistent
Able to recognize defects in a home from a buyer's viewpoint.
Reliable - work must be completed on the scheduled day between 8am - 5pm
Principled - able to work unsupervised while providing thoroughness and consistency in each home
Able to connect to the internet via Wi-Fi
Have experience working with a mobile device and familiar on how to solve minor technical issues that could occur while out in the field.
Able to drive to sites around the area. (Drive time is not compensated). Management will group work orders whenever possible minimizing drive time between stops.
This is a part-time position. Reviewers must be available 4-5 days Monday thru Friday to work partial and sometimes full days. Days off must be given to the scheduler a week or more in advance (except in the case of emergencies).
Compensation: Paid per review completed.
Pay rate ranges from $75-$90 per new review.
Introductory period lasts for 30 -60 days, and pay is $65-$75 per review during that timeframe.
There is a $10/house raise when introductory period ends.
**No phone calls please**
$40k-53k yearly est. 4d ago
Clinical Reviewer, Occupational Therapy
Evolent 4.6
Interviewer job in Columbia, SC
**Your Future Evolves Here** Evolent partners with health plans and providers to achieve better outcomes for people with most complex and costly health conditions. Working across specialties and primary care, we seek to connect the pieces of fragmented health care system and ensure people get the same level of care and compassion we would want for our loved ones.
Evolent employees enjoy work/life balance, the flexibility to suit their work to their lives, and autonomy they need to get things done. We believe that people do their best work when they're supported to live their best lives, and when they feel welcome to bring their whole selves to work. That's one reason why diversity and inclusion are core to our business.
Join Evolent for the mission. Stay for the culture.
**What You'll Be Doing:**
As an Occupational Therapist, Clinical Reviewer you will be a key member of the utilization management team. We can offer you a meaningful way to make a difference in patients lives, in a non-clinical environment. You can enjoy better work- life balance on a team that values collaboration and continuous learning while providing better health outcomes.
Collaboration Opportunities:
+ Routinely interacts with leadership and management staff, Physicians, and and other CR's whenever input is needed or required.
Job Summary
Functions in a clinical review capacity to evaluate all cases, which do not pass the authorization approval process at first call while promoting a supportive team approach with call center staff. Initial clinical reviewers are supported by Physician clinical review staff (MDs) in the utilization management determination process.
Job Description
+ Reviews charts and analyzes clinical record documentation in order to approve services that meet clinical review criteria.
+ Conducts ongoing activities which monitor established quality of care standards in the participating provider network and for other clinical staff.
+ Conducts regular audits, as assigned, to ensure guidelines are applied appropriately.
+ In states where required, refers all cases that an approval cannot be rendered to the Physician Clinical Reviewer. In States where allowed, will make denial determinations as a specific case warrants.
+ Converses with medical office staff in order to obtain additional pertinent clinical history/information; notifies of approvals and denials, giving clinical rationale.
+ Provides optimum customer service through professional/accurate communication while maintaining NCQA and health plans required timeframes.
+ Documents all communication with medical office staff and/or treating provider.
+ Practices and maintains the principles of utilization management by adhering to policies and procedures.
+ Participates in on-going training programs to ensure quality performance in compliance with applicable standards and regulations.
**The Experience You'll Need (Required):**
+ Current, unrestricted state licensure as a Occupational Therapist
+ A occupational therapist must hold a state license in occupational therapy and hold an occupational therapy degree from an accredited education program and pass the national certification examination.
+ 5+ years clinical experience is preferred
+ Strong interpersonal and communication skills.
+ Strong clinical, communication, and organizational skills
+ Energetic and curious with a passion for quality and value in health care
+ Computer Proficiency
+ Not under current exclusion or sanction by any state or federal health care program, including Medicare or Medicaid, and is not identified as an "excluded person" by the Office of Inspector General of the Department of Health and Human Services or the General Service Administration (GSA), or reprimanded or sanctioned by Medicare.
+ No history of disciplinary or legal action by a state medical board
To ensure a secure hiring process we have implemented several identity verification steps, including submission of a government issued photo ID. We conduct identity verification during interviews, and final interviews may require onsite attendance. All candidates must complete a comprehensive background check, in-person I-9 verification, and may be subject to drug screening prior to employment. The use of artificial intelligence tools during interviews is prohibited and monitored. Misrepresentation will result in immediate disqualification from consideration.
**Technical Requirements:**
We require that all employees have the following technical capability at their home: High speed internet over 10 Mbps and, specifically for all call center employees, the ability to plug in directly to the home internet router. These at-home technical requirements are subject to change with any scheduled re-opening of our office locations.
**Evolent is an equal opportunity employer and considers all qualified applicants equally without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.** **If you need reasonable accommodation to access the information provided on this website, please contact** ************************** **for further assistance.**
The expected base salary/wage range for this position is $. This position is also eligible for a bonus component that would be dependent on pre-defined performance factors. As part of our total compensation package, Evolent is proud to offer comprehensive benefits (including health insurance benefits) to qualifying employees. All compensation determinations are based on the skills and experience required for the position and commensurate with experience of selected individuals, which may vary above and below the stated amounts.
Don't see the dream job you are looking for? Drop off your contact information and resume and we will reach out to you if we find the perfect fit!
$44k-56k yearly est. 5d ago
Appraisal Reviewer
Lima One Capital 3.9
Interviewer job in Greenville, SC
Reporting directly to the Appraisal Supervisor, this person facilitates all value-related disputes and ensures compliance of company, industry, and regulatory agency standards during the appraisal process. This role is responsible for functioning as an appraisal subject matter expert to ensure Lima One Capital, industry, and regulatory appraisal standards & requirements are met. They will perform reviews and evaluations of all appraisals completed to ensure compliance with regulatory guidelines. Determine levels of appraisal quality and deficiencies to govern Lima One Capital's list of ineligible appraisers and/or reporting to state appraisal licensing boards.
Duties and Responsibilities:
Review standard appraisals and any additional provided documents for consistency. Ensure appraisal conforms to company, industry and other regulatory agency standards.
Ensure the appraisal review includes a thorough analysis of the appraisal report for reasonable assumptions, appropriate technical analysis, current market conditions, and ensures compliance with USPAP and Lime One Capital guidelines.
Provide evidence of review with relevant comments regarding validity of conclusions, adequacy of due diligence, etc. Also, provide an in-depth analysis of the appraisal that will help underwriters make sound judgment decisions regarding the collateral aspect of the loan and ultimately limit collateral risk.
Respond to valuation questions and disseminate valuation guidelines and requirements with internal/external customers.
Maintain thorough and up-to-date knowledge of the Uniform Standards of Professional Appraisal Practice, the Appraiser Independence Requirements (AIR) and company valuation guidelines that are pertinent to the appraisal review process.
Confirm AIR compliance and evaluate subsequent revised appraisal reports.
Maintain a good working relationship with the Appraisal Management Companies and panel appraisers while monitoring appraisal orders, value dispute requests, and status inquiries.
Perform analysis and review of appraisals utilized for Lima One Capital securitization projects.
Process escalated requests from lending business units or underwriting, for appraisal reviews for lending business units, and underwriting on complex property types.
Track all completed services to assist in the creation of monthly business reviews when necessary.
Triage value reconsideration requests for compliance and relevancy and review all subsequent revised appraisals.
Other duties may be assigned.
Requirements
Equivalent Education Level Required: State Certified Appraiser license required
Required Experience, Knowledge, Skills and Competencies:
Minimum of 5+ years' experience in real estate appraisals
Real estate appraisal experience in both traditional and/or investment bank environments.
Knowledge of principles, practices, methods and techniques of real estate appraisal.
Ability to recognize and interpret real estate sales/rental data and market trends.
Ability to utilize data resources and internet services to evaluate appraisal value conclusions.
Time management skills - ability to manage multiple priorities and clients at the same time.
Ability to assess the stability of a property's value and/or income, relative to its market.
Ability to think autonomously while exhibiting initiative and sound judgment to address issues relating to the appraisal and make appropriate recommendations as they relate to risk.
Excellent analytical and communication skills, including written and oral.
Work independently in a fast-paced environment while collaborating within a team setting.
Preferred Experience, Knowledge:
Real estate review experience
Experience as an in-house review appraiser within the mortgage industry
National real estate valuation experience
What We Offer:
Industry Leading Benefits:
Medical, Dental and Vision Insurance
Life Insurance, Short-Term Disability, and Long-Term Disability
Hospitalization and Accidental Insurance
Flexible Spending Accounts - Health and Dependent Care
Health Savings Account
Safe Harbor 401K with company match
Growing Families Support (including paid parental leave, infertility support and assistance, childcare reimbursement, and elder care)
Pet Insurance
Work Life Balance: 12 paid time off days and 5 sick days, in addition to 12 paid holidays - that's about a month of time to rest, relax, and recharge every year.
Career Development: We prioritize the growth and success of our team members. You'll benefit from continuous learning opportunities, dedicated mentorship, and the chance to refine your skills and advance your career.
New Headquarters: Join us in our brand new, thoughtfully designed office in the heart of Downtown Greenville (parking is paid for!)
Why Lima One?
At Lima One Capital we're relentlessly focused on a simple but powerful goal: to be the nation's premier lender for real estate investors. Inspired by that vision, every member of our team is driven by our mission to create opportunities for our customers and employees by educating, empowering, and financing real estate investors who are building, improving, and stabilizing their neighborhoods and communities nationwide.
Loans Funded: $10+ billion in loans funded, 30k loans closed since 2010
Geography: 46 states + D.C. where we revitalize neighborhoods
Employees: ~300 employees with competitive benefits and perks
Stability: Backed by the immense resources of MFA Financial, a publicly traded mortgage REIT with 25 years of proven success
Veteran Founded: Founded by 2 US Marine Corps veterans, we proudly approach every deal and decision with grit, determination, boldness, and integrity
Recognized by the Inc.5000 as one of America's fastest growing companies, Lima One specializes in providing real estate investors with financing for their rental, fix-and-flip, and new construction projects. The company is distinguished as one of South Carolina's Best Places to Work and Top Workplaces. Lima One is headquartered in downtown Greenville, South Carolina. Learn more about us at limaone.com.
Lima One Capital does not sponsor H1B Visas. To be considered for employment, a candidate must be authorized to work in the United States for any employer and not require sponsorship, now or in the future.
Notice to Third Party Recruiters and Agencies
Lima One Capital does not accept unsolicited resumes or candidate submissions from recruiters or employment agencies. In the absence of a fully executed agreement for a specified position, Lima One Capital has no obligation to pay any referral compensation or recruiter fee. In the event a recruiter or agency submits a resume or candidate without an agreement, Lima One Capital explicitly reserves the right to pursue and hire those candidate(s) without any financial obligation to the recruiter or agency. Any unsolicited resumes, referrals, or candidate submissions, including those communicated to a member of the Human Resources team or a hiring manager, shall be deemed the property of Lima One Capital. If you or your agency would like to be considered as a future recruiting partner, please email ********************** (Subject: Agency Partner Request).
$37k-55k yearly est. Easy Apply 36d ago
Batch Record Reviewer
Nephron Pharmaceuticals 4.3
Interviewer job in West Columbia, SC
Apply Description
Job Purpose:
The purpose of the Batch Record Review (BRR) role is to ensure that all manufacturing and packaging processes comply with regulatory standards, company policies, and quality requirements before product release. This role plays a critical part in maintaining product integrity, patient safety, and regulatory compliance by verifying that production records are complete, accurate, and meet Current Good Manufacturing Practices (cGMP) and other industry regulations (e.g., FDA, ISO).
By meticulously reviewing batch documentation, identifying deviations, and ensuring corrective actions are taken, the BRR role helps prevent product defects, recalls, and compliance issues, ultimately safeguarding public health and maintaining company credibility.
Essential Duties and Responsibilities:
Oversee status of batches through disposition/release process and remove barriers, communicate escalations as appropriate.
Performs final batch disposition of finished drug product and combination product batches, to ensure high quality medicine (cGMP Compliance) is released within expected metrics to ensure timely release to market.
Performs review checklist to verify all requirements have been performed and meet requirements.
Collaborates within Manufacturing to resolve batch record discrepancies or errors as it relates to Good Documentation Practices (GDP).
Review documentation for manufacturing activities associated with commercial, development, and engineering execution in accordance with good documentation practices, including but not limited to executed batch records, master batch records, and product specific documents.
Independently executes batch record review for completeness, accuracy and cGMP compliance.
Support the evaluation and lot disposition of drug product. Critically review various documentation types to ensure completeness, accuracy and compliance including but not limited to test methods, method validation protocols and reports and Standard Operating Procedures (SOPs).
Contributes to process improvement of batch records and associated processes (e.g. turnaround times) to ensure all Quality Assurance (QA) batch disposition deadlines are met.
Responsible for the review and approval of cGMP documentation against SOPs in order to ensure compliance in Manufacturing processes.
Raise deviations as needed in order to capture potential impacts to product quality.
Communicate significant quality risks that may impact product suitability or regulatory compliance in a timely manner to Executive Management.
Work with colleagues to instill a sense of ownership and commitment to quality.
Provide technical support to the leadership team in the decision-making process.
Supplemental Functions:
· Performs and maintains archiving of all batch documentation to include copying, scanning, and filing.
Revise or review standard operating procedures and submit procedural changes as needed to meet local, Global and Regulatory requirements.
Keep abreast of industry developments, forthcoming regulations, guidance, best practices, etc for all Scientific Areas.
Performs and assists with additional work duties or responsibilities as assigned or apparent.
Job Specifications and Qualifications:
Knowledge & Skills:
Comprehensive knowledge of quality system requirements such as US FDA, cGMP, GCP, EMA, and ICH guidelines and has a proven track record of successfully implementing these requirements to ensure patient safety and compliance with FDA and other applicable health authorities' requirements.
Competent in Microsoft Word and Excel.
Knowledgeable in Adobe Acrobat (PDF) advanced features and workflows.
Familiar with document management software, including SharePoint.
Excellent written and oral communication skills.
Team player and must be able to interact with all departments.
Ability to work independently and be dependable.
Technical writing skills required.
Strong attention to detail.
Specific expertise, skills, and knowledge within Quality Assurance gained through education and experience.
The ability and willingness to change direction and focus to meet shifting organizational and business demands.
The ability to create and contribute to an environment that values people, encourages trust, teamwork, and open communication, and provides participation, learning, feedback and recognition.
The ability to effectively manage one self, demonstrates integrity, be productive under pressure, and achieve development goals.
The ability to manage a multitude of resources and to be accurate and current with data and information.
Education/Experience:
BS degree preferred with at least 1 year of experience in a regulated cGMP Environment. In lieu of degree, at least 4 years of equivalent experience in pharma manufacturing operations considered and strong background in GDP.
Working Conditions / Physical Requirements:
This position requires bending, typing, lifting (up to 40 1bs.), vision (20/20). Standing (10%), sitting (80%) and walking (10%) throughout the facility.
$36k-49k yearly est. 21d ago
Quality Reviewer
Lexington Medical Center 4.7
Interviewer job in West Columbia, SC
Radiation Oncology Full Time Day Shift Between the hours 0700AM-500PM Sign-On Bonus: 0 Lexington Health is a comprehensive network of care that includes six community medical and urgent care centers, nearly 80 physician practices, more than 9,000 health care professionals and Lexington Medical Center, a 607-bed teaching hospital in West Columbia, South Carolina. It was selected by Modern Healthcare as one of the Best Places to Work in Healthcare and was first in the state to achieve Magnet with Distinction status for excellence in nursing care. Consistently ranked as best in the Columbia Metro area by U.S. News & World Report, Lexington Health delivers more than 4,000 babies each year, performs more than 34,000 surgeries annually and is the region's third largest employer.
Lexington Health also includes an accredited Cancer Center of Excellence, the state's first HeartCARE Center, the largest skilled nursing facility in the Carolinas, and an Alzheimer's care center. Its postgraduate medical education programs include family medicine and transitional year residencies, as well as an informatics fellowship.
Job Summary
Reporting to the Director/Medical Director, the Quality Reviewer carries out audits for chart QA and charges on all Radiation Medicine patients. The reviewer ensures accounts are prepared for final billing in an accurate and timely manner with Corporate Compliance. The Reviewer manages and reports departmental data for statistical trending and evaluation of services and implements reports for specific Departmental needs. The Reviewer monitors and facilitates patient satisfaction, recommending enhanced services and improved processes. The Reviewer ensures Departmental compliance with HIPAA policies and regulations.
Minimum Qualifications
Minimum Education: Bachelor's Degree in Health Care or Management Field
Minimum Years of Experience: 5 Years previous experience as a Registered Therapist
Substitutable Education & Experience: None.
Required Certifications/Licensure: ARRT in Radiation Therapy;
Current SC License.
Required Training: Computer literate;
Knowledge of billing.
Essential Functions
* Quality Services/Patient Care/QI:
* Promotes a quality environment conducive to exceptional Radiation Oncology services.
* Monitors and assesses environment of care specific to patient satisfaction. Makes recommendations for enhanced services and processes.
* Works with the Director and staff to minimize or eliminate barriers to quality care.
* Audits and reviews Radiation Oncology charts on a weekly basis for accuracy and thoroughness in charting, documentation, and charging.
* Serves on the Department's CQI Committee.
* Demonstrates competence to provide developmentally appropriate care/treatment for the following patient populations: Adolescent (13 years through 17 years), Adult (18 years to 65 years), Geriatric (Over 65 years).
* Material Resources:
* Makes recommendations to Management for tools and resources needed to enhance patient satisfaction and services.
Duties & Responsibilities
* Data Management/Reporting:
* Generates and Reports monthly and yearly statistical data for Accounting, LMC Administration, and DHEC.
* Tracks and trends statistical data for Director/internal Departmental review.
* Implements ARIA reports and custom EPIC reports for staff and physicians for the purpose of enhancing workflow and assessing volume and referral trends.
* Discharges all HRON accounts which are no longer active.
* Reviews all charts upon initiation and completion and properly ICD codes them for efficient and accurate final billing.
* Maintains up-to-date chargemaster, staying current with latest CPT rules and reimbursement issues.
* Performs all other duties as assigned.
We are committed to offering quality, cost-effective benefits choices for our employees and their families:
* Day ONE medical, dental and life insurance benefits
* Health care and dependent care flexible spending accounts (FSAs)
* Employees are eligible for enrollment into the 403(b) match plan day one. LHI matches dollar for dollar up to 6%.
* Employer paid life insurance - equal to 1x salary
* Employee may elect supplemental life insurance with low cost premiums up to 3x salary
* Adoption assistance
* LHI provides its full-time employees employer paid short-term disability and long-term disability coverage after 90 days of eligible employment
* Tuition reimbursement
* Student loan forgiveness
Equal Opportunity Employer
It is the policy of Lexington Health to provide equal opportunity of employment for all individuals, and to remain compliant with applicable state and federal laws and regulations. Lexington Health strives to provide a discrimination-free environment, and to recruit, select, on-board, and employ all employees without regard to race, color, religion, sex, age, disability, national origin, veteran status, or pregnancy, childbirth, or related medical conditions, including but not limited to, lactation. Lexington Health endeavors to upgrade and promote employees from within the hospital where possible and consistent with the employee's desires and abilities and the hospital's needs.
$43k-54k yearly est. 3d ago
Quality Technical Reviewer - Celsis
Charles River Laboratories 4.3
Interviewer job in Charleston, SC
For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel passionate about.
**Job Summary**
Primarily responsible for reviewing and approving GMP laboratory data and reports supporting microbiological studies for Celsis ATP Bioluminescence and other Microbial Solutions products. This on-site position will be co-located with laboratory personnel at the Charleston site for fostering a collaborative working relationship with laboratory peers. This position will actively integrate with the Quality and Regulatory Affairs leadership to support upholding a high-quality standard in laboratory data. As a peer and mentor to laboratory staff, this position may also assist with daily tasks of maintaining supply materials, laboratory tidiness activities, and will be continually trained on laboratory processes to maintain understanding during quality review duties.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
* Is capable of understanding and applying requirements related to Alternative Microbiological Method Validation.
* Is a 100% on site position at this time for fostering a collaborative working relationship with laboratory peers.
* Understands and routinely applies Good Manufacturing Practices (GMP) towards reviewing laboratory data.
* Serves as a final Quality approver on Microbial Applications Lab reports.
* Serves as a Quality approver and collaborative resource for laboratory investigations.
* Has an ongoing understanding of various regulatory regulations as applicable to products tested in the Celsis laboratory.
* Maintain records compliance by adhering to regulatory guidelines set forth by the company and varying agencies.
* Assists with laboratory maintenance activities as appropriate.
* Perform all other related duties as assigned.
**Job Qualifications**
* Education: Bachelor's Degree in a Biological or Chemistry Sciences discipline.
* Experience: At least 2 years working in a GMP-regulated environment.
* Certifications/Licensures: None
* Must be comfortable working collaboratively or individually
* High standards for integrity and quality of work performed
The pay range for this position is $65,000 to $80,000. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, and location.
**About Microbial Solutions**
Our Microbial Solutions business group has a comprehensive portfolio of endotoxin testing, microbial detection and microbial identification products and services is unlike any other, and has been purposefully designed to meet the complex and ever-changing needs of the industry. We help clients to ensure product safety and quality with easy-to-use yet robust testing solutions that satisfy regulatory requirements, support critical decision making and improve operational efficiencies.
**About Charles River**
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
With over 20,000 employees within 110 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. And in 2019, revenue increased to $2.62 billion.
At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 80% of the drugs approved by the FDA in the last five years.
We're committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.
**Equal Employment Opportunity**
Charles River Laboratories is an Equal Opportunity Employer - all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin, veteran or disability status.
It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_**********. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
For more information, please visit ***************
231011
$65k-80k yearly Easy Apply 12d ago
Clinical Care Reviewer
Integrated Resources 4.5
Interviewer job in North Charleston, SC
Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.
We've stayed true to our focus of finding qualified and experienced professionals in our specialty areas. Our partner-employers know that they can rely on us to find the right match between their needs and the abilities of our top-tier candidates. By continually exceeding their expectations, we have built successful ongoing partnerships that help us stay true to our commitments of performance and integrity.
Our team works hard to deliver a tailored approach for each and every client, critical in matching the right employers with the right candidates. We forge partnerships that are meant for the long term and align skills and cultures. At IRI, we know that our success is directly tied to our clients' success.
Job Description
Under the direction of the unit Supervisor, the Clinical Care Reviewer is responsible for completing medical necessity reviews. Using clinical knowledge and nursing experience, the nurse reviews provider requests for inpatient and outpatient services, working closely with members and providers to collect all information necessary to perform a thorough medical necessity review. It is within the nurse's discretion to pending requests for additional information and/or request clarification. The nurse will use his/her professional judgment to evaluate the request to ensure that appropriate services are approved and recognize care coordination opportunities and refer those cases as needed. The nurse will apply medical health benefit policy and medical management guidelines to authorize services and appropriately identify and refer requests to the Medical Director when guidelines are not met. The nurse will maintain current knowledge and understanding of the laws, regulations, and policies that pertain to the organizational unit's business and uses clinical judgment in their application.
Qualifications
• Current, unrestricted SC Registered Nurse license.
• 3+ years' experience in critical care or ER within an acute care environment.
• 2+ years' experience in utilization management, preferably within managed care.
• Comfortable utilizing MS Office products, including Excel, Word, and Outlook.
Additional Information
Thanks
Warm Regards
Kavita
732 - 662 - 5619
$47k-72k yearly est. 1d ago
New Home Quality Reviewer
2M Quality 3.5
Interviewer job in Oak Grove, SC
This is a part time, 1099 position.
Job duties include:
Looking at newly built homes from a customer's perspective to identify defects in workmanship, quality, completeness, consistency, and professionalism. (Reviews take on average 1 to 1.5 hours to complete) Each review is meant to evaluate the quality of the finished construction.
Driving to construction sites and conducting quality reviews on the day it is scheduled. Work may be started anytime during the day between 8 am to 3:30 pm. Reports are submitted on site electronically upon completion of review and no later than 5PM.
Entering review results online using your own tablet while on the job site. Training will be provided on how to enter a Quality Review Report in the report database.
Reviewers are not required to walk on roofs or in attics.
No tools, lights or ladders are used in the review.
Residential construction experience is preferred but not required.
Required equipment:
Tablet (Cellular enabled from 2020 model or newer)
Blue painter's tape
Hard hat (Required to be worn while on the job site.)
Access to email while out in the field either though a tablet or phone
Preferred background experience:
General Contractor/Superintendent/Project Manager
Familiar with punch list writing or general QC/QA principles.
Home Renovation or Remodeling
Familiar with fit and finish reviews or warranty walk through with homeowners
Ideal candidates will be:
Detail oriented - able to be thorough and consistent
Able to recognize defects in a home from a buyer's viewpoint.
Reliable - work must be completed on the scheduled day between 8am - 5pm
Principled - able to work unsupervised while providing thoroughness and consistency in each home
Able to connect to the internet via Wi-Fi
Have experience working with a mobile device and familiar on how to solve minor technical issues that could occur while out in the field.
Able to drive to sites around the area. (Drive time is not compensated). Management will group work orders whenever possible minimizing drive time between stops.
This is a part-time position. Reviewers must be available 4-5 days Monday thru Friday to work partial and sometimes full days. Days off must be given to the scheduler a week or more in advance (except in the case of emergencies).
Compensation: Paid per review completed.
Pay rate ranges from $75-$90 per new review.
Introductory period lasts for 30 -60 days, and pay is $65-$75 per review during that timeframe.
There is a $10/house raise when introductory period ends.
**No phone calls please**
$39k-53k yearly est. 4d ago
Clinical Care Reviewer
Integrated Resources 4.5
Interviewer job in North Charleston, SC
A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
Job Description
Duration: 3 Months (Contract to Hire)
Responsibilities:
• Under the direction of the unit Supervisor, the Clinical Care Reviewer is responsible for completing medical necessity reviews.
• Using clinical knowledge and nursing experience, the nurse reviews provider requests for inpatient and outpatient services, working closely with members and providers to collect all information necessary to perform a thorough medical necessity review. It is within the nurse's discretion to pending requests for additional information and/or request clarification.
• The nurse will use his/her professional judgment to evaluate the request to ensure that appropriate services are approved and recognize care coordination opportunities and refer those cases as needed.
•The nurse will apply medical health benefit policy and medical management guidelines to authorize services and appropriately identify and refer requests to the Medical Director when guidelines are not met.
• The nurse will maintain current knowledge and understanding of the laws, regulations, and policies that pertain to the organizational unit's business and uses clinical judgment in their application.
Qualifications
Required Skills & Experience:
• Current, unrestricted SC Registered Nurse license.
• 3+ years' experience in critical care or ER within an acute care environment.
• 2+ years' experience in utilization management, preferably within managed care.
• Comfortable utilizing MS Office products, including Excel, Word, and Outlook.
Additional Information
Kind Regards
Harry Chaudhary
Clinical Recruiter
Integrated Resources, Inc.
IT Life Sciences Allied Healthcare CRO
Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I
Direct# 732-429-1869
(BOARD) # 732-549-2030 - Ext - 207
Email id - www.irionline.com
$47k-72k yearly est. 60d+ ago
Clinical Care Reviewer
Integrated Resources 4.5
Interviewer job in North Charleston, SC
Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.
We've stayed true to our focus of finding qualified and experienced professionals in our specialty areas. Our partner-employers know that they can rely on us to find the right match between their needs and the abilities of our top-tier candidates. By continually exceeding their expectations, we have built successful ongoing partnerships that help us stay true to our commitments of performance and integrity.
Our team works hard to deliver a tailored approach for each and every client, critical in matching the right employers with the right candidates. We forge partnerships that are meant for the long term and align skills and cultures. At IRI, we know that our success is directly tied to our clients' success.
Job Description
Under the direction of the unit Supervisor, the Clinical Care Reviewer is responsible for completing medical necessity reviews. Using clinical knowledge and nursing experience, the nurse reviews provider requests for inpatient and outpatient services, working closely with members and providers to collect all information necessary to perform a thorough medical necessity review. It is within the nurse's discretion to pending requests for additional information and/or request clarification. The nurse will use his/her professional judgment to evaluate the request to ensure that appropriate services are approved and recognize care coordination opportunities and refer those cases as needed. The nurse will apply medical health benefit policy and medical management guidelines to authorize services and appropriately identify and refer requests to the Medical Director when guidelines are not met. The nurse will maintain current knowledge and understanding of the laws, regulations, and policies that pertain to the organizational unit's business and uses clinical judgment in their application.
Qualifications
• Current, unrestricted SC Registered Nurse license.
• 3+ years' experience in critical care or ER within an acute care environment.
• 2+ years' experience in utilization management, preferably within managed care.
• Comfortable utilizing MS Office products, including Excel, Word, and Outlook.
Additional Information
Thanks
Warm Regards
Kavita
732 - 662 - 5619