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Quality Control Research Associate Jobs in Detroit, MI

Quality Control Tech

Wayne, MI Β· On-site

$17 - $21.75/hr

High school diploma or equivalent required; technical certification or associate degree in quality control, manufacturing, or related field preferred. * Basic understanding of quality control ...

Quality Control Tech

Wayne, MI Β· On-site

$17 - $21.75/hr

High school diploma or equivalent required; technical certification or associate degree in quality control, manufacturing, or related field preferred. * Basic understanding of quality control ...

Our mission is to make research possible. That starts by employing a talented and highly qualified ... Currently, we are looking to add a GMP QC Chemist I to the team: Responsibilities and Duties:

Our mission is to make research possible. That starts by employing a talented and highly qualified ... Currently, we are looking to add a GMP QC Chemist I to the team: Responsibilities and Duties

Clinical Research Associate - Oncology - Detroit, MI ICON is a global healthcare intelligence and ... Resolve data queries and drive timely, high-quality data entry * Document site progress and ...

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Quality Control Research Associate information

See Detroit, MI salary details

$11

$25

$37

How much do quality control research associate jobs pay per hour?

As of Sep 15, 2026, the average hourly pay for quality control research associate in Detroit, MI is $25.21, according to ZipRecruiter salary data. Most workers in this role earn between $18.32 and $30.72 per hour, depending on experience, location, and employer.

What does a quality control research associate do?

A Quality Control Research Associate is responsible for ensuring that products, materials, and processes meet established quality standards in industries like pharmaceuticals, biotechnology, and manufacturing. They perform laboratory tests, analyze data, and document results to verify the safety, efficacy, and consistency of products. These professionals also help identify areas for process improvement and may assist in developing new testing protocols. Their work is essential for maintaining compliance with regulatory requirements and ensuring that only high-quality products reach the market.

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

To thrive as a Quality Control Research Associate, you need a strong background in biology or chemistry, experience with laboratory techniques, and typically a bachelor's degree in a related scientific discipline. Familiarity with analytical instruments such as HPLC, GC, and proficiency in data analysis software, as well as knowledge of industry regulations like GMP, are often required. Attention to detail, critical thinking, and effective communication are vital soft skills for ensuring accuracy and collaborating with team members. These competencies are essential to maintain product quality, comply with regulatory standards, and support the reliability of research outcomes.

What are some common challenges faced by quality control research associates, and how can they be addressed?

Quality Control Research Associates often encounter challenges such as managing tight deadlines while ensuring precise and accurate results, adapting to evolving testing protocols, and troubleshooting unexpected data inconsistencies. To address these challenges, it’s helpful to develop strong organizational skills, maintain clear documentation, and collaborate closely with both laboratory and cross-functional teams. Continuous learning and proactive communication can also help resolve issues quickly and uphold rigorous quality standards.

Is a Quality Control Research Associate a good career?

A Quality Control Research Associate is a valuable role in industries such as pharmaceuticals, manufacturing, and food production, focusing on ensuring product quality and compliance with standards. The position often requires attention to detail, knowledge of testing methods, and familiarity with regulatory guidelines, offering opportunities for career growth and specialization. It can be a stable career with potential advancement into supervisory or analytical roles.

Quality Control Chemist I

Riverview, MI β€’ On-site

Other

Posted 4 days ago


Job description

Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia. This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation. Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide.

For more details, please visit : www.piramalpharmasolutions.com

Job Title

Quality Control Chemist I

Job Description

Piramal Pharma Solutions’ HPAPI Research and Manufacturing facility (Ash Stevens, LLC), located in Riverview, Michigan, is seeking a qualified Quality Control Chemist I to join our Quality Control team. The Quality Control Chemist is responsible for providing analytical chemistry support for the facility.

Key Responsibilities
  • Support manufacturing operations through the testing of raw materials and starting materials as required to meet production timelines.
  • Perform cleaning verifications on multi-use equipment using approved methods.
  • Test reference standards and stability samples.
  • Document sample preparation, equipment set-up, and test results in laboratory notebooks or other appropriate test record forms.
  • Verify data with second quality team member as required.
  • Maintain all records as required to maintain compliance.
  • As required, test intermediates and final products to meet production timelines/client requirements.
  • Assist in the revision of documentation as required.
  • Participate in quality unit projects, including but not limited to supplier certification, methods development, methods validation and training of both quality unit members as appropriate.
  • Provide support in the maintenance and calibration of laboratory analytical instrumentation.
  • Assist in the maintenance of the QC laboratory through routine housekeeping, as well as keeping personal bench area and desk organized.
  • As required, perform routine testing on the water system (DI, ice, potable, and QC water), and prepare reports as needed.
Education/Experience

Bachelor’s degree in Chemistry or Biochemistry or equivalent. One (1) year of experience in pharmaceutical quality control or equivalent is preferred Familiarity with analytical testing and instrumentation.

Job Competencies

Excellent organizational and planning skills. Strong written, verbal, and interpersonal communication skills. High attention to detail. Demonstrated strong analytical skills, and the ability to work independently against multiple deadlines.

Job Conditions

The physical demands and work environment described here are representative of those that must be met by a team member to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Physical Demands

Frequent lifting, bending, stooping, squatting, pushing and pulling can be expected. Long periods of standing and walking can be expected in this position. This position may require long periods of sitting, typing, computer entry or looking at a computer.

Work Environment

Piramal Pharma Solutions is engaged in the business of pharmaceutical research and contract pharmaceutical manufacturing. As such, all PPS staff work in or nearby either chemical/pharmaceutical research or chemical/pharmaceutical manufacturing equipment and processes. Potential limited exposure to hazardous chemicals. Personal protective equipment including safety glasses, lab coats, gloves, specialized clothing including laboratory uniform and appropriate shoes may be required in areas associated with this position.

Company Overview

Piramal Pharma Limited, offers a portfolio of differentiated products and services through its 17 global development and manufacturing facilities and a global distribution network in over 100 countries. PPL includes Piramal Pharma Solutions (PPS), an integrated Contract Development and Manufacturing Organization; Piramal Critical Care (PCC), a Complex Hospital Generics business; and the India Consumer Healthcare business, selling over-the- counter products. In addition, one of PPL’s associate companies, AbbVie Therapeutics India Private Limited is a JV with AbbVie Inc. and has emerged as one of the market leaders in the ophthalmology therapy area. Further, PPL has a minority investment in Yapan Bio Private Limited. In October 2020, PPL received a 20% strategic growth investment from the Carlyle Group.

Equal Employment Opportunity

PPL provides equal employment opportunities to all employees and applicants for employment.

It prohibits discrimination and harassment based on race, color, age, sex, religion, national origin or ethnicity, disability status, genetics, protected veteran status, sexual orientation, gender identity, or expression, or any other characteristic protected by applicable law.

Our employment decisions are based on merit considering qualifications, skills, performance, and achievements.

Equal employment opportunity applies to all terms and conditions of employment, including recruitment, selection, training, social programs, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions.

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