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Quality Engineer Associate Jobs in Jenison, MI (NOW HIRING)

West Pharmaceutical Services

Technician, Quality

Walker, MI · On-site

$17.25 - $23.25/hr

... Engineering Change Requests (ECR's). * Assist in the design & drawing reviews and make ... The associate may lift and/or move up to 25 pounds and occasionally lift and/or move more than 55 ...

West Pharmaceutical Services

Technician, Quality

Walker, MI · On-site

$17.25 - $23.25/hr

... Engineering Change Requests (ECR's). * Assist in the design & drawing reviews and make ... The associate may lift and/or move up to 25 pounds and occasionally lift and/or move more than 55 ...

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Quality Engineer Associate information

See Jenison, MI salary details

$15

$29

$43

How much do quality engineer associate jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for quality engineer associate in Jenison, MI is $29.41, according to ZipRecruiter salary data. Most workers in this role earn between $23.46 and $33.89 per hour, depending on experience, location, and employer.

What does a quality engineer associate do?

A Quality Engineer Associate supports the quality assurance and control processes within manufacturing or production environments. Their responsibilities typically include inspecting products, monitoring production processes, assisting with quality audits, and helping to implement quality standards and procedures. They work closely with senior quality engineers and production teams to identify defects, resolve quality issues, and ensure that products meet required specifications. This entry-level role is a great starting point for a career in quality engineering, as it provides hands-on experience with quality systems and tools.

What are some common challenges a quality engineer associate might face in their daily work?

Quality Engineer Associates often encounter challenges such as balancing multiple projects with tight deadlines, interpreting complex product specifications, and effectively communicating quality standards to cross-functional teams. They may also need to troubleshoot unexpected production issues and adapt quickly to new processes or technologies. Developing strong analytical and problem-solving skills, as well as building collaborative relationships with manufacturing, engineering, and quality assurance teams, can help overcome these challenges.

What are the key skills and qualifications needed to thrive as a quality engineer associate, and why are they important?

To thrive as a Quality Engineer Associate, you need a solid understanding of quality control principles, data analysis, and basic engineering concepts, usually supported by a bachelor’s degree in engineering or a related field. Familiarity with tools such as statistical process control (SPC), Six Sigma methodologies, and quality management systems (QMS) is often required, and certifications like ASQ CQE can be beneficial. Strong attention to detail, problem-solving abilities, and effective communication skills help you collaborate across teams and address quality issues proactively. These skills are vital for ensuring product reliability, compliance with standards, and continuous improvement in manufacturing or service processes.

What is the difference between Quality Engineer Associate vs Quality Technician?

AspectQuality Engineer AssociateQuality Technician
CredentialsTypically requires a bachelor's degree in engineering or related field; certifications like ASQ CQE are a plusUsually requires a high school diploma or associate degree; certifications like CQI or CQT are common
Work EnvironmentInvolves analysis, process improvement, and collaboration with engineering teamsFocuses on inspection, testing, and data collection on the production floor
Employer & Industry UsageUsed across manufacturing, aerospace, automotive, and electronics industriesCommonly employed in manufacturing and production settings

The Quality Engineer Associate and Quality Technician roles share a focus on quality assurance but differ mainly in responsibilities and required education. The associate typically engages in process analysis and improvement, while the technician concentrates on testing and inspection tasks. Both roles are vital in maintaining product quality within manufacturing industries.

Are quality engineer associates paid well?

Quality engineer associates typically earn competitive salaries that vary based on experience, location, and industry. Entry-level positions may start lower, but with skills in quality management tools and certifications, salaries can increase significantly over time.

Is a Quality Engineer Associate an entry level job?

A Quality Engineer Associate is typically considered an entry-level position in quality assurance and engineering. It often requires basic knowledge of quality tools, inspection processes, and sometimes certifications like Six Sigma Green Belt, making it suitable for those starting their careers in quality roles.

What cities near Jenison, MI are hiring for Quality Engineer Associate jobs?

Cities near Jenison, MI with the most Quality Engineer Associate job openings:

Quality Engineer Associate jobs near you
Infographic showing various Quality Engineer Associate job openings in Jenison, MI as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 18% Part Time, 3% Contract, and 2% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $61,175 per year, or $29.4 per hour.

Technician, Quality

West Pharmaceutical Services

Walker, MI • On-site

$17.25 - $23.25/hr

Full-time

Re-posted 16 days ago

Key responsibilities

  • Performs receiving, start-up, in-process, and final inspections of materials and products.

  • Reviews and approves production records, composes reports, and maintains documentation related to quality control.

  • Operates automated inspection equipment and performs analytical testing on various materials.

West Pharmaceutical Services rating

8.5

Company rating: 8.5 out of 10

Based on 32 frontline employees who took The Breakroom Quiz

13th of 122 rated packaging manufacturers

Job description

At West, we're a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West's indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?
There's no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.
We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.
Job Summary
Performs receiving inspections, start-up inspections, in-process and final inspections. Completes documentation & reviews production records. Performs analytical testing on various materials. Troubleshoots and solves technical problems. Programs and operates automated inspection equipment. Prepares shipping documentation & documentation audits.
Essential Duties and Responsibilities
  • Inspects and release incoming materials. May perform analytical testing, evaluates, records and reports on the chemical and physical properties of various substances and materials to determine product release approval status.
  • Review and approve Batch Production Records from each job.
  • Compose Non-Conformance Report (NCR) Deviations, Document Change Notices (DCN), Out of Specification (OOS), Work Instructions, Incoming Quality Control (IQC) forms and Engineering Change Requests (ECR's).
  • Assist in the design & drawing reviews and make recommendations for improvements, clarification, and correctness as needed.
  • Assists shift personnel with quality issues and/or measurement techniques.
  • Input incoming lots into expiration/retest database.
  • Maintain expiration/retest date database for incoming materials. Review retest dates and arrange for testing of materials for retest. Review expiration dates and arrange for disposal of expiring materials.
  • Conforms with and abides by all regulations, policies, work procedures, instruction, and all safety rules.
  • Provides a "Customer Service" attitude when interacting with internal and external customers while accomplishing work, production, and achieving quality standards.
  • Maintains a clean, orderly, and safe workstation and environment at all times.
  • Other duties as assigned

Education
  • High School or equivalent

Work Experience
  • Less than 3 years of experience.

Preferred Knowledge, Skills and Abilities
  • Knowledge and experience with FDA and ISO Quality Systems to include SPC and calibrations systems.
  • Proficiency with PC and Microsoft Office; Knowledge of QMS Master Control, MeasureLink and other Quality systems is preferred.
  • Experience with ISO 9000 standards and GMP's
  • Must be able to prioritize and perform position responsibilities accurately and meet required deadlines.
  • Strong attention to detail; Strong problem identification/analysis and solving skills with hands-on approach.
  • Excellent verbal and written communication skills; Maintain an organized and clean quality Lab.
  • Ability to multi-task and prioritize in a fast-paced environment; Ability to interface with all personnel levels.
  • Motivated self-starter with ability to work independently on multiple assignments in a team environment.

Travel Requirements
None: No travel required
Physical Requirements
  • While performing the duties of this job, the associate frequently is required to sit, walk, stand, balance, stoop, kneel, or crouch to support production needs. The associate may lift and/or move up to 25 pounds and occasionally lift and/or move more than 55 pounds.

Shift
Shift 2- Every other Saturday, Sunday, Monday, Tuesday (5:45PM to 6:00AM)
West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status. If you have a special need that requires accommodation in order to apply to West, please send an email to Apply.Accommodation@westpharma.com. Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening.

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