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Quality Control Stability Jobs in Michigan (NOW HIRING)

Cayman

QC Chemist, GMP

Ann Arbor, MI · On-site

Perform analytical testing to support method validation, transfer, verification, stability studies ... Experience: 2-5 years of relevant GMP QC laboratory experience with modern analytical ...

Technique, Inc.

Quality Manager

Jackson, MI · On-site

MSA & SPC - Apply MSA (Gage R&R, bias, linearity, stability) and SPC (Cpk/Ppk) to drive process control. * Welding & Fabrication Quality - Apply familiarity with AWS compliance; WPS/PQR/WPQ ...

Technique Inc

Quality Manager

Jackson, MI · On-site

MSA & SPC - Apply MSA (Gage R&R, bias, linearity, stability) and SPC (Cpk/Ppk) to drive process control. * Welding & Fabrication Quality - Apply familiarity with AWS compliance; WPS/PQR/WPQ ...

CEDENT

Chemist (Ferndale, MI)

Ferndale, MI · On-site

Carry out routine day-to-day quality control testing of Water, Raw Materials, Bulk, Finished Products and Stability samples in the Quality Control Laboratory. Perform routine chemical testing by such ...

Cedent

Chemist (Ferndale, MI)

Ferndale, MI · On-site

Carry out routine day-to-day quality control testing of Water, Raw Materials, Bulk, Finished Products and Stability samples in the Quality Control Laboratory. Perform routine chemical testing by such ...

CEDENT

Chemist

Ferndale, MI · On-site

Carry out routine day-to-day quality control testing of Water, Raw Materials, Bulk, Finished Products and Stability samples in the Quality Control Laboratory. Perform routine chemical testing by such ...

TOWER LABORATORIES LTD.

Chemist- 1st shift

Montague, MI · On-site

... QC unit as a whole. ESSENTIAL FUNCTIONS: * Perform raw material, in-process, finished product, and stability sample testing using instrumental analytical, wet chemicals, and physical analytical ...

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Quality Control Stability information

What is the difference between Quality Control Stability vs Quality Control Inspector?

AspectQuality Control StabilityQuality Control Inspector
CertificationsOften requires certifications like Six Sigma, ISO auditor, or quality management certificationsTypically requires quality inspection certifications or training
Work EnvironmentFocuses on maintaining process stability in manufacturing or production settingsPerforms inspections on products or materials on the production line
Employer & Industry UsageUsed in manufacturing, aerospace, automotive, and industries emphasizing process consistencyCommon in manufacturing, food production, and assembly lines

Quality Control Stability involves ensuring that manufacturing processes remain consistent over time, emphasizing process control and reduction of variability. In contrast, a Quality Control Inspector primarily conducts inspections to verify product quality at various stages. Both roles are essential in quality management but focus on different aspects of quality assurance.

What are some common challenges faced in a Quality Control Stability role, and how can they be addressed?

Professionals in Quality Control Stability often encounter challenges such as managing tight timelines for stability testing, interpreting ambiguous results, and ensuring compliance with evolving regulatory requirements. Effective communication with cross-functional teams—such as R&D, production, and regulatory affairs—is essential to address discrepancies and maintain data integrity. Staying organized, maintaining thorough documentation, and keeping up to date with industry guidelines help mitigate these challenges and ensure smooth workflow.

What are the key skills and qualifications needed to thrive as a Quality Control Stability specialist, and why are they important?

To thrive as a Quality Control Stability specialist, you need a solid background in chemistry or related sciences, experience with stability testing, and typically a bachelor’s degree in a scientific field. Familiarity with laboratory instruments (such as HPLC, GC), stability management systems, and knowledge of regulatory guidelines like ICH are essential. Attention to detail, problem-solving, and strong organizational skills help ensure accurate data analysis and effective reporting. These abilities are crucial for maintaining compliance, product safety, and reliability in pharmaceutical or biotech environments.

What is a Quality Control Stability role?

A Quality Control Stability role involves monitoring and evaluating the stability of pharmaceutical products, ensuring they maintain their quality, safety, and efficacy throughout their shelf life. Professionals in this position design and execute stability studies, analyze the results, and document findings according to regulatory requirements. They play a crucial part in ensuring compliance with industry standards and supporting product development and release. This role typically requires expertise in analytical testing, regulatory guidelines, and laboratory practices.
What are popular job titles related to Quality Control Stability jobs in Michigan? For Quality Control Stability jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Quality Control Stability jobs in Michigan look for? The top searched job categories for Quality Control Stability jobs in Michigan are:
What cities in Michigan are hiring for Quality Control Stability jobs? Cities in Michigan with the most Quality Control Stability job openings:
Quality Control Stability jobs near you
Infographic showing various Quality Control Stability job openings in Michigan as of June 2026, with employment types broken down into 90% Full Time, and 10% Contract. Highlights an 100% In-person job distribution.

Quality Control Chemist

Piramal Pharma Limited

Riverview, MI • On-site

Full-time

Posted 25 days ago

Job description

Be the First to Apply

Division

Piramal Pharma Solutions

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

Job Description

Piramal Pharma Solutions' HPAPI Research and Manufacturing facility (PPL Pharma Solutions Riverview LCC), located in Riverview, Michigan, is seeking a qualified Quality Control Chemist II to join our Quality Control team. The Quality Control Chemist II is responsible for providing analytical chemistry support for the facility.

Key responsibilities.

  • Perform testing on intermediates and final products to meet production/client timelines.

  • Support manufacturing operations through the testing of raw materials and starting materials as required to meet production timelines.

  • 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.

  • Assist in the preparation of new and revised documentation as required.

  • 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.

  • Act as the primary QC contact for the Production team and/or Program Manager for any given project or synthetic step.

  • Provide necessary training and guidance to newer employees on GMP issues and analytical issues.

  • EDUCATION/EXPERIENCE.

    • Bachelor's degree in Chemistry or Biochemistry or equivalent.

    • Minimum five (5) years of experience in pharmaceutical quality control in a cGMP environment.

    • Hands on thorough knowledge of analytical testing and instrumentation specifically HPLC, GC, Residual Solvents, KF, solid state testing.

    • Familiarity with GMP requirements/regulations.

  • 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

Apply