Top 3 Supplier quality engineer Jobs in Newburgh, In

Quality Auditor - Pharmaceutical
SQA Services —Evansville, IN
- $1,300 a day
- Contract
- 5 years
- Writing skills
- Residential
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1d
Quality Assurance Engineer
Philip Morris International U.S. —Owensboro, KY
- Full-time
- Mid-level
- SQL
- Bachelor's degree
- Health insurance
- Dental insurance
Quality Engineer
Dana Incorporated —Henderson, KY
- Mid-level
- Math
- Organizational skills
3d

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Quality Assurance Technician
Philip Morris International U.S. —Owensboro, KY
Computer literate, data entry, document control, and procedural implementation. Complete periodic technical product reports and report on product problems…
$53,600 - $67,000 a year
3d
Quality Assurance Inspector
Amcor —Evansville, IN
Communicate with employees from the prior shift. Complete the daily inspection reports. Gather samples of product from thermoformers. Minimum lifting of 25 lbs.
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3d

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Supplier Quality Engineer
Nifco America, Corp. —Canal Winchester, OH
ASQ or equivalent certification or training (CQE, LSS Belt, etc). IATF certification for Internal or Lead auditor with documentation available.
$70,000 - $88,000 a year
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Supplier Quality Engineer (Supplier Performance Agent)
Noramtec Consultants Americas —Ohio
Coordinate your own work travel plans by doing the reservation, follow up, expense claim and financial review. You have a minimum of ten (10) years experience.
From $35 an hour
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1d

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supplier quality engineer jobs near newburgh, in

Quality Auditor - Pharmaceutical

SQA Services -
Evansville, IN

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Job Details

Contract
$1,300 a day
1 day ago

Qualifications

Pharmaceutical regulatory compliance
Writing skills
Workplace dispute resolution
GMP
De-escalation techniques
Pharmaceutical company experience
Quality assurance experience within pharmaceutical industry
Biomedical regulatory compliance
FDA regulations
Pharmaceutical manufacturing facility experience

Full Job Description

For nearly 30 years, SQA Services has been a leading provider of managed supplier quality services, offering audits, assessments, remote surveillance, corrective actions, remediation, inspections, and engineering solutions to manufacturers across all industries. We deliver these services by deploying a network of highly skilled associates based throughout the United States and in over 90 countries worldwide, ensuring rapid on-site support at your supplier locations. Our associates are expert quality assurance professionals with extensive experience and local expertise, enabling us to represent our clients on-demand and with greater speed and efficiency than our competitors.

We’re hiring a Pharma Quality Auditor. This is a contract opportunity in which you will perform supplier quality audits at various suppliers in the Midwest. These audits are generally 1-2 days long. You are given the flexibility to accept or reject these assignments according to your own availability.

Key Responsibilities

Perform supplier audits at various sites within your region of residence
Assure quality in the supply chains of various clients within the pharmaceutical, medical device, cosmetics, biologics, and/or animal health industries
Coordinate, prepare, execute, and deliver supplier audits based on your own and the client schedule
Utilize your regulatory knowledge of various standards from ISO, CFR, FDA, etc…
Respond to the Content team in a timely manner regarding edits/questions to your audit report
Write audit reports in accordance with client specifications

Required Qualifications

5+ years of hands-on audit experience in pharmaceutical, medical device, and/or biologics industries
Has been the lead auditor in at least 10 audits
Direct audit experience to 21 CFR part 210/211, EU Vol 4, and Canada GMP
Strong communication and writing skills
Proven ability to deescalate workplace conflicts effectively
Ability to adapt to new technology and software.
Willingness to travel regionally

Preferred Qualifications

Direct audit experience to ISO 17025, ISO 15378, IPEC GDP, ICH Q7, ISO 13485, 21 CFR 100, and/or 21 CFR 507
ISO certifications are a plus but not mandatory

Pay Rate:

$1300 for a 1-day audit. Includes: Time spent preparing for the audit, traveling, performing the audit, writing the report, and responding to questions from our Content team of editors and the client until the report is finalized. Does not include: Following up on CAPA for any findings or reimbursement for travel expenses - expenses are reimbursed at cost with receipts per SQA travel policy. Note that SQA helps with the preparation of the audit and proofreads all audit reports.

Note: SQA is an Equal Opportunity Employer. Employment is based on merit and qualifications, and is not influenced by race, color, religion, gender, national origin, veteran status, disability, age, sexual orientation, gender identity, marital status, or any other legally protected status.

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We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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