Top 7 Quality auditor Jobs in Lafayette, In

Quality Assurance Auditor III
INOTIV INC —West Lafayette, IN
- Full-time
- Bachelor of Science
- Bachelor's degree
- Senior level
- Paid parental leave
- Disability insurance
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Quality Assurance Auditor (SYO)
Subaru of America —Lafayette, IN
- $28.46 - $33.65 an hour
- Overtime
- ASE Certification
- Mid-level
- High school diploma or GED
- Profit sharing
- Health insurance
Auditor - Crawfordsville
THE CLOSURE SYSTEMS COMPANIES INC —Crawfordsville, IN
- Writing skills
- High school diploma or GED
- Communication skills
- On-the-job training
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Roaming Auditor
thyssenkrupp Supply Chain Services NA, Inc. —Lafayette, IN
- Overtime
- Computer literacy
- English
- Mid-level
- Paid holidays
- Health insurance
2d

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Quality Assurance Auditor (SYO)
Subaru of America —Lafayette, IN
Associates degree from an accredited college or university or ASE certification (ASE G1 or similar certifications) preferred.
$28.46 - $33.65 an hour

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Quality Assurance Auditor/Inspector
Sam Dong —Delaware, OH
Read and interpret blueprints, specifications, and technical drawings. Reasonable accommodations will be considered in accordance with applicable federal, state…
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Lead Director, SOX/SOC1 Audit Governance & Quality Controls
CVS Health —Columbus, OH
Bachelor’s degree in business, finance, accounting, healthcare administration, or a related field; advanced degree preferred.
$100,000 - $231,540 a year
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quality auditor jobs near lafayette, in

Quality Assurance Auditor III

INOTIV INC -
West Lafayette, IN

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Job Details

Full-time

Benefits

Paid parental leave
Disability insurance
Health insurance
Dental insurance
401(k)
Paid time off
Parental leave

Qualifications

EPA
GLP
Defect resolution root cause analysis
Laboratory equipment performance testing and validation
Safety protocol adherence
Audit report preparation
Procedural guides
Standard Operating Procedures (SOPs) implementation
Bachelor of Science
Preventive action implementation
Laboratory instrument validation
Direct client contact
Process improvement
Quality control preventive actions
Corrective and preventive actions (CAPA)
FDA 21 CFR Part 11
Quality control audit
Quality reports
Audit Reporting
Laboratory staff training
Quality assurance audits
Policy & process development
Vendor performance evaluation
Bachelor's degree
Quality risk management
Compliance training programs
Quality assurance standard operating procedures
Team training
Data Security (Data management)
Laboratory standard operating procedures

Full Job Description

Corporate

Demonstrate Inotiv Core Values

Follow all Standard Operating Procedures (SOPs) and other applicable laboratory or company policies and procedures

Maintain confidential information

General

Interact with clients, other employees, and the community in a professional manner

Support and participate in company initiatives as directed

Maintain thorough knowledge of facility SOPs, policies, study protocols, etc.

Adhere to all safety regulations and procedures

Provide assistance or support to other Inotiv QA team members as necessary

Perform other duties as assigned

Specific

Demonstrate solid understanding of application and interpretation of FDA and EPA GLPs as well as applicable international regulations

Keep abreast of new rules, guidance and industry standards in order to improve laboratory compliance

Conduct audits of designated studies and facilities to assess compliance with protocols, SOPs, methods and relevant regulations (audits may include direct observation of study conduct and/or laboratory processes, review of protocols, study data and reports, or review of facility records and SOPs as well as subcontractor contributions)

Prepare an audit report and submit all findings to Study Director/Principal Investigator and management promptly

Issue accurate quality assurance statements for inclusion in final reports

Demonstrate solid knowledge of electronic data collection systems used in data generation, including proper use, reporting, audit trails, security/Part 11 compliance, data correction, and QC

Input and/or update information in the Master Schedule program as required by GLP regulations and SOPs

Actively participate in managing quality program to ensure compliance with regulatory requirements and serve as a resource for staff on regulatory topics.

Support and/or participate in quality assurance inspections from existing or potential clients and regulatory agencies. Assist with managing responses including provision of corrective and preventive actions as assigned.

Conduct site- specific and corporate quality training for new hires and other employees, as assigned.

Champion the development of standard Quality policies, procedures, job aids and training documents.

Support investigation and CAPA activities to ensure elimination or mitigation of quality issues and risks. Apply problem solving methodology including root cause analysis to situations where data suggest process is not operating effectively or variability exceeds expectations.

Participate in or lead subcontractor and/or vendor evaluations

Participate in equipment and software validation efforts.

Serve as a resource to represent the QA team on regulatory topics (e.g, at study initiation meetings), as requested

Participate in departmental business, process or general regulatory projects, as assigned

Perform other duties as assigned.

Education and Experience

B.S. in chemistry or life sciences or Bachelor’s degree or higher in a related field and

Three to five years of experience in a GLP preferably with 1-3 or more years of auditing experience, or

Equivalent combination of education and regulatory, quality, compliance and/or industry experience.

RQAP-GLP certification preferred.

This position could be offered at different levels for candidates who qualify with a combination of advanced levels of education and/or years of experience. The salary range will adjust along with the level of the role to match the person’s relevant experience and/or education level.

Inotiv is a growing contemporary drug discovery and development company where we “Play to Win” in an industry rich with opportunity. Together, we face challenges and together we win in the delivery of world-class drug discovery and development solutions that impact the health and well-being of people all over the world. There’s an opportunity for everyone at all phases of a career, each individual’s unique skill set has an impact on the work we conduct. If you have the talent and desire to impact the quality of people’s lives, we have the career opportunities to make it happen. Join us in embracing research and science to impact the health and well-being of people all over the world.

Salary will be commensurate with experience and responsibilities. Benefits include health and dental coverage, short- and long-term disability, paid time off, paid parental leave, 401K, and more!

Inotiv is an Equal Opportunity Employer. It is our policy to provide a fair and equal employment opportunity to all persons, regardless of age, race, color, religion, sex, gender, gender identity, gender expression, sexual orientation, genetic information, disability, national origin, veteran status, or any other basis prohibited by law. This policy governs all aspects of employment, including selection, job assignment, compensation, discipline, termination and access to benefits and training.

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quality auditor jobs in lafayette, in

Quality Assurance Auditor III

Quality Assurance Auditor (SYO)

Auditor - Crawfordsville

Roaming Auditor

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