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Internship Pharmaceutical Quality Engineer Jobs (NOW HIRING)

Quality Engineer

Vandalia, OH

$67K - $87K/yr

... internships or co-op roles, in manufacturing, product development, or quality engineering within a regulated industry such as medical device or pharmaceutical. * Hands-on experience with root cause ...

New

Manager, Quality Engineer

Miami, FL · On-site

$68K - $88K/yr

The Quality Engineer Manager will oversee Quality Engineers and Interns in their day to day tasks ... Experience in Tissue Banking, Pharmaceutical, Medical Device, or Biologics industry preferred.

New

Manager, Quality Engineer

Miami, FL · On-site

$68K - $88K/yr

The Quality Engineer Manager will oversee Quality Engineers and Interns in their day to day tasks ... Experience in Tissue Banking, Pharmaceutical, Medical Device, or Biologics industry preferred.

New

Quality Engineer

Cambridge, MA · On-site

$78K - $101K/yr

Medical Device / Pharmaceutical Job Summary We are seeking a highly motivated and detail-oriented Quality Engineer to support quality assurance and compliance activities within a GMP-regulated ...

Quality Engineer

Tysons Corner, VA

$72K - $93K/yr

The ideal candidate has 0-1 years of experience in quality engineering, software testing, internships, or academic projects; is eager to grow automation skills; and is curious about emerging tools ...

Quality Engineer

Newark, NJ · On-site

$75K - $97K/yr

Bachelor's Degree in Engineering, Pharmaceutical Sciences, Chemistry, Biology, Life Sciences, or a related technical discipline. * 3-5+ years of Quality Engineering, Quality Assurance, Validation, or ...

Job Title: Quality Engineer The Quality Engineer will maintain and improve quality systems ... Experience in regulated industries such as medical devices, aerospace, pharmaceuticals, or ...

Job Title: Quality Engineer The Quality Engineer will maintain and improve quality systems ... Experience in regulated industries such as medical devices, aerospace, pharmaceuticals, or ...

Quality Engineer

El Paso, TX · On-site

$65K - $84K/yr

Provide quality engineering support for manufacturing processes to ensure compliance with FDA ... Knowledge of FDA Quality System Regulation (21 CFR Part 820) and/or Pharmaceutical GMP requirements ...

Quality Engineer

El Paso, TX · On-site

$65K - $84K/yr

Provide quality engineering support for manufacturing processes to ensure compliance with FDA ... Knowledge of FDA Quality System Regulation (21 CFR Part 820) and/or Pharmaceutical GMP requirements ...

Quality Engineer

El Paso, TX · On-site

$65K - $84K/yr

Provide quality engineering support for manufacturing processes to ensure compliance with FDA ... Knowledge of FDA Quality System Regulation (21 CFR Part 820) and/or Pharmaceutical GMP requirements ...

Quality Engineer

El Paso, TX · On-site

$65K - $84K/yr

Provide quality engineering support for manufacturing processes to ensure compliance with FDA ... Knowledge of FDA Quality System Regulation (21 CFR Part 820) and/or Pharmaceutical GMP requirements ...

Quality Engineer

El Paso, TX · On-site

$65K - $84K/yr

Provide quality engineering support for manufacturing processes to ensure compliance with FDA ... Knowledge of FDA Quality System Regulation (21 CFR Part 820) and/or Pharmaceutical GMP requirements ...

Quality Engineer

El Paso, TX · On-site

$65K - $84K/yr

Provide quality engineering support for manufacturing processes to ensure compliance with FDA ... Knowledge of FDA Quality System Regulation (21 CFR Part 820) and/or Pharmaceutical GMP requirements ...

Quality Engineer

Tarboro, NC · On-site

$64K - $83K/yr

Position Summary Reporting to the Quality Manager, the Quality Engineer will support quality ... Internship, co-op, laboratory, research, or manufacturing experience is preferred but not required.

Quality Engineer

Ormond Beach, FL · On-site

$63K - $81K/yr

Quality Engineer · Department: Quality Engineering · Location: Ormond Beach, FL (USA) · ... Labs, Pharmaceutical Isolators, Biosafety Cabinets, Modular & Mobile Controlled Environments ...

EDUCATION/EXPERIENCE REQUIREMENTS * BS in an Engineering related field, with a minimum of 2 years of medical device or pharmaceutical Quality Engineering related experience. * Process and Material ...

EDUCATION/EXPERIENCE REQUIREMENTS * BS in an Engineering related field, with a minimum of 2 years of medical device or pharmaceutical Quality Engineering related experience. * Process and Material ...

Quality Engineer III

North Haven, CT

$71K - $92K/yr

... Pharmaceutical & IT services to a diverse set of customers across various industries around the ... Performs Quality Engineering functions in support of projects associated to product development ...

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Internship Pharmaceutical Quality Engineer information

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How much do internship pharmaceutical quality engineer jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for internship pharmaceutical quality engineer in the United States is $19.31, according to ZipRecruiter salary data. Most workers in this role earn between $16.11 and $20.91 per hour, depending on experience, location, and employer.

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What states have the most Internship Pharmaceutical Quality Engineer jobs?

States with the most job openings for Internship Pharmaceutical Quality Engineer jobs include:

$68K - $88K/yr

Full-time

Posted 2 days ago

New


Job description

Description

Job purpose

The Quality Engineer Manager will be responsible for developing, revising, and maintaining Quality processes, procedures, and metrics to support all functional areas at Vivex Biologics, Inc. This individual will be responsible for providing Quality guidance in process improvement and technology transfer efforts. The Quality Engineer Manager will oversee Quality Engineers and Interns in their day to day tasks as well as the timely completion of projects. This role will also be responsible for reviewing and approving process validation and equipment qualification (IQ, OQ, PQ protocols and reports. The Quality Engineer Manager is also expected to provide support to the Regulatory Affairs team by providing guidance with standards and regulations requirements for supplier qualifications, certifications and licensing, and audits.


Duties and responsibilities

  1. Manage Quality Assurance Engineers and Interns by managing schedules, assigning and prioritizing their workload, establishing due dates, and performing their performance reviews.
  2. Ensure company is in compliance with all internal policies and procedures and external federal, state, and governing body regulations and standards.
  3. Responsible for initiating and leading technical investigations, risk assessments (including FMEA, root cause analysis, and corrective and preventive actions related to non-conformances, deviations, and customer complaints.
  4. Work cross-functionally to provide quality and regulatory guidance to all functional areas in the organization.
  5. Participate in quality planning activities to evaluate existing and develop new measurement systems to evaluate and improve departmental output.
  6. Identify process improvement opportunities using Lean principles and lead the development and implementation of process improvements activities.
  7. Perform pre-validation assessments and review and approval of process validation and equipment qualification (IQ, OQ, PQ protocols and reports.
  8. Provide support to Regulatory Affairs in the completion of supplier qualifications and audits.
  9. Other duties as assigned.


Requirements

Qualifications

  1. A minimum of a Bachelor's degree in Engineering or a related technical discipline is required (e.g. Biology, Chemistry, etc..
  2. A minimum of 8 years of related Engineering or Quality experience is required.
  3. Experience in Tissue Banking, Pharmaceutical, Medical Device, or Biologics industry preferred.
  4. Experience with Non-Conformances, Deviations, Complaints and Corrective and Preventive Actions (CAPAs) required.
  5. Experience with Process Validations and Equipment Qualifications.
  6. Expert knowledge in the interpretation and application of FDA, AATB, and ISO standards and guidelines.
  7. American Society for Quality (ASQ) certification preferred.
  8. Certified Tissue Bank Specialist (CTBS) certification preferred.
  9. Must demonstrate effective oral, written, communication and presentation skills.


Working conditions

Must be willing to work weekends and evening hours as necessary. Must be willing to accommodate travel if necessary. The job may require work to be performed inside the controlled cleanroom manufacturing area where the engineer would be exposed to tissue processing.


Physical requirements

While performing the duties of this job, the employee is regularly required to sit for prolonged periods of time. The employee may occasionally be required to pull, lift and/or move objects weighing up to 30 pounds.


Direct reports


Quality Assurance Engineers and Interns