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Quality Control Stability Analyst Jobs in Ohio (NOW HIRING)

RESILIENCE

Senior Analyst, QC Microbiology

West Chester, OH · On-site

$22.75 - $30.50/hr

For more information, please visit www.resilience.com Position Summary The Senior Analyst, QC Microbiology performs and documents microbiological testing on raw materials, in-process and finished ...

Astrix Inc

QC Associate Scientist

Concord, OH · On-site

$75K - $80K/yr

... analytical chemistry principles and laboratory safety practices. * education and experience. * Demonstrated experience working in cGMP/GLP environments, including QC or stability testing.

Olon USA LLC

Associate Scientist, QC

Painesville, OH · On-site

Inspect and perform complex chemical analyses on raw materials, in-process samples, and finished ... control or stability, and interaction with quality assurance is required. Specific Skills and ...

M&R Ready Mix, Inc.

Quality Control Technician

Stony Ridge, OH · On-site

$17.75 - $22.75/hr

Shared success that creates stability for our employees and quality products for our customers ... Analyze testing data and prepare reports related to quality and production performance * Assist in ...

Hycom, Inc.

Be Seen First

Quality Control Manager

Barberton, OH · On-site

$90K - $100K/yr

The QCM is responsible for all departmental activities and maintaining quality control processes, analyzing the results and giving feedback and guidance to the production team. S/he will develop ...

LeafHome

Quality Control Specialist

Fairfield, OH · On-site

The Quality Control Field Specialist is responsible for overseeing and continuously improving ... Strong analytical and documentation skills. Proficiency with CRM, inspection tools, and reporting ...

LeafHome

Quality Control Specialist

Fairfield, OH

$60K - $65K/yr

The Quality Control Field Specialist is responsible for overseeing and continuously improving ... Strong analytical and documentation skills. Proficiency with CRM, inspection tools, and reporting ...

LeafHome

Quality Control Specialist

Fairfield, OH · On-site

$60K - $65K/yr

The Quality Control Field Specialist is responsible for overseeing and continuously improving ... Strong analytical and documentation skills. Proficiency with CRM, inspection tools, and reporting ...

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Quality Control Stability Analyst information

What is a quality control stability analyst?

Quality Control Stability Analysts are professionals responsible for testing and evaluating the stability of pharmaceutical products over time. They design, conduct, and interpret experiments to ensure products maintain their safety, potency, and quality throughout their shelf life. Their work is crucial for regulatory compliance, as they document and report stability data according to industry standards and guidelines. These analysts often work in laboratory environments and collaborate closely with quality assurance and manufacturing teams.

What are the key skills and qualifications needed to thrive as a quality control stability analyst?

To thrive as a Quality Control Stability Analyst, you need a solid background in chemistry or related sciences, familiarity with Good Laboratory Practices (GLP), and often a relevant bachelor's degree. Experience with laboratory instrumentation such as HPLC, GC, and LIMS, along with knowledge of regulatory guidelines like ICH and FDA, is typically required. Attention to detail, strong organizational skills, and effective communication are critical soft skills in this role. These competencies ensure accurate data analysis, compliance with regulations, and reliable stability testing to maintain product quality and safety.

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

AspectQuality Control Stability AnalystQuality Control Analyst
CertificationsGMP, GLP, relevant laboratory certificationsGMP, GLP, relevant laboratory certifications
Work EnvironmentPharmaceutical, biotech labs focusing on stability testingManufacturing labs, quality testing environments
Job FocusMonitoring product stability over time, data analysis for stability programsPerforming routine quality tests, raw material and finished product testing

The main difference is that a Quality Control Stability Analyst specializes in stability testing and data analysis related to product shelf life, while a Quality Control Analyst performs general quality testing. Both roles require similar certifications and work in related environments, but their focus areas differ within the quality assurance process.

How much does a quality control stability analyst earn?

A quality control stability analyst typically earns between $50,000 and $80,000 annually, depending on experience, location, and industry. Entry-level positions may start lower, while experienced analysts with certifications can earn higher salaries. Compensation often includes benefits such as health insurance and paid time off.

What are some typical challenges faced by quality control stability analysts, and how can they be addressed?

Quality Control Stability Analysts often face challenges such as managing multiple projects with tight timelines, accurately interpreting stability data, and ensuring compliance with stringent regulatory requirements. Balancing the need for meticulous documentation with the fast-paced nature of product development can also be demanding. To address these challenges, analysts benefit from strong organizational skills, effective communication with cross-functional teams (like R&D and production), and ongoing training on evolving industry standards and regulatory guidelines.
What are popular job titles related to Quality Control Stability Analyst jobs in Ohio? For Quality Control Stability Analyst jobs in Ohio, the most frequently searched job titles are:
What job categories do people searching Quality Control Stability Analyst jobs in Ohio look for? The top searched job categories for Quality Control Stability Analyst jobs in Ohio are:
What cities in Ohio are hiring for Quality Control Stability Analyst jobs? Cities in Ohio with the most Quality Control Stability Analyst job openings:
Quality Control Stability Analyst jobs near you
Infographic showing various Quality Control Stability Analyst job openings in Ohio as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 11% Part Time, 6% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution.

Senior Analyst, QC Microbiology

RESILIENCE

West Chester, OH • On-site

$22.75 - $30.50/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 12 days ago

Job description

A career at Resilience is more than just a job - it's an opportunity to change the future.
Resilience is a technology-focused biomanufacturing company that's changing the way medicine is made. We're building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need.
For more information, please visit www.resilience.com
Position Summary
The Senior Analyst, QC Microbiology performs and documents microbiological testing on raw materials, in-process and finished products, and environmental samples. The role ensures GMP compliance through timely review of laboratory data and documentation, communicates findings, and supports corrections. This position also authors SOPs and serves as a subject matter expert for the EDMS system.
Position Responsibilities
  • Evaluates data trends and authors reports associated with trends.
  • Leads and/or actively participates in investigations involving manufacturing process areas, related to QC processes or data, such as sampling, deviations potentially affecting QC results, investigational sampling, and testing.
  • Provides and follows up on ideas for continuous improvements in laboratory processes.
  • Maintains and troubleshoots testing equipment.
  • Completes required training and trains QC employees in GMP, SHE, QC methods and processes. As well as, good aseptic techniques, and instrumentation based on expertise.
  • Actively support and/or lead the implementation of compendial changes for raw materials, in-process or finished products tests in accordance with applicable Pharmacopoeias such as USP/NF, European Pharmacopeia, British, and Japanese Pharmacopeia.
  • Troubleshoots methods and processes.
  • May serve as an expert in a specific area of laboratory equipment, process, or system.
  • Serve as a subject manner expert during regulatory inspections including potential demonstrations and inspection room discussions.
  • Demonstrates expertise on authoring Quality records (Deviations, CAPAs, and Change Controls).
  • Answer and guide others in documentation, compliance, and other process questions.
  • Gather, organize, and communicate operational information to others.
  • Facilitate communication between management and non-management and team meetings.
  • Provide leadership, development, and mentoring for others.
  • Provide support in coordinating activities in the laboratory.
  • Identify temporary and permanent fixes to address issues.
  • Coordinate with representatives from other departments.
  • Attend team meetings to discuss progress, initiatives, and/or other matters.
  • Collect, record, report and trend metrics when applicable.
  • Wear gowning, sterile garments, and PPE (Personal Protective Equipment) as required by specific activities.
  • Consult cross-functionally as an SME (Subject Matter Expert) on systems and/or processes within a functional area.
  • Perform logbook reviews.
  • Lead process improvement activities and teams to meet strategic goals.
  • Use MAXIMO and/or CMMS (Computerized Maintenance Management System) to manage logistics.
  • Alert supervisor or manager when problems occur outside of SOPs (Standard Operating Procedures).
  • Perform regular audits of SOPs (Standard Operating Procedures) and/or work instructions.
  • Review and approve documentation needed for qualification of equipment and processes.
  • Attend and facilitate inter-departmental meetings to discuss matters involving the coordination of multiple departments when necessary.
  • Interact with other departments to implement corrective/preventative actions.
  • Review and approve quality records as a SME when required.
  • Provide "off shift" support (i.e., night shift support if you normally workday shift).
  • Coordinate qualification activities.
  • Assess and implement improvements in productivity, waste generation, quality and cost.
  • Recommend compliance resolutions to management.

Hours (Day Shift):
  • Sunday - Wednesday
  • 10 hour shift

Minimum Qualifications
  • Prior experience in a regulated GMP environment.
  • Working knowledge of cGXP requirements and a strong familiarity with production operations.
  • Excellent attention to details and problem-solving skills.

Preferred Qualifications
  • Bachelor's degree in a Science subject (Microbiology, or closely related subjects)
  • 5 years QC Microbiology laboratory experience.
  • High level knowledge and competence with a specific piece of laboratory equipment, or a QC/QA process or system.
  • Prior experience supporting microbiological testing in a sterile pharmaceutical operation environment.

This position may also include the following conditions:
  • This role is primarily non-sedentary. May include but not limited to standing, walking, repetitive motion, and chemical usage.
  • All employees are expected to adhere to the Quality Management System established in the Quality Manual, Quality Policy, Standard Operating Procedures, Current Good Manufacturing Practices, and any other applicable regulations and standards to the duties within their role.
  • The items described here are representative of those that must be met successfully to perform the essential functions of this job.
  • The work schedule listed reflects the employee's expected schedule at the time of hire. The Company reserves the right to modify work schedules at any time, with or without notice, based on business needs, operational requirements, or other considerations. Nothing in this description creates a guarantee of specific hours, days, or shift assignments.

Sponsorship or support for work authorization, including visas, is not available for this position.
Resilience is an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, physical or mental disability, genetic information, or characteristic, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state, and local laws. Requests for reasonable accommodation can be made at any stage of the recruitment process.
Resilience offers employees a robust total rewards program including an annual cash bonus program, a 401(k) plan with a generous company match and our benefits package which is thoughtfully designed to support our employees with great healthcare (including medical, dental and vision), family building benefits, life and disability insurance, paid vacation, paid holidays, other paid leaves of absence, tuition reimbursement and support for caregiving needs. Our target base pay hiring range for this position is $75,000.00 - $116,250.00 per year. Actual base pay is dependent upon a number of factors, including but not limited to, the candidate's geographical location, relevant experience, qualifications, skills and knowledge. Excited about Resilience? We encourage you to apply and start a conversation with one of our recruiters.

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