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Quality Control Pharma Jobs in Ohio (NOW HIRING)

Rottendorf Pharma GmbH

$91.34 - $125.60/hr

Du stellst die termingerechte Bearbeitung und Freigabe der Analytik in deinem Verantwortungsbereich sicher und unterstützt bei Bedarf andere QC-Bereiche. * Du bearbeitest Abweichungen, Complaints ...

Centor

Quality Lab Technician PPP NA

Millersburg, OH

$24.35/hr

... pharma, biotech and cosmetic industries. The company offers a comprehensive portfolio of ... Area of responsibility Quality Control: * Perform visual and dimensional inspections (microscope ...

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Quality Control Pharma information

Is quality control pharma a good career?

Quality Control Pharma involves testing and inspecting pharmaceutical products to ensure they meet safety and quality standards. It offers stable employment, opportunities for advancement, and requires attention to detail, knowledge of laboratory techniques, and often certifications such as GMP training.

What are the key skills and qualifications needed to thrive as a quality control professional in the pharmaceutical industry?

To thrive as a Quality Control professional in pharma, you need a strong background in chemistry, biology, or a related science, along with knowledge of Good Manufacturing Practices (GMP) and relevant regulations. Familiarity with laboratory instruments (e.g., HPLC, GC), LIMS software, and quality assurance certifications such as ASQ or ISO standards is typically required. Attention to detail, analytical thinking, and effective communication help professionals excel in ensuring product quality and regulatory compliance. These skills ensure that pharmaceutical products are consistently safe, effective, and compliant with industry standards.

What is quality control in the pharmaceutical industry?

Quality Control (QC) in the pharmaceutical industry refers to the processes and procedures used to ensure that pharmaceutical products meet required standards of quality, safety, and efficacy. QC professionals test raw materials, in-process samples, and finished products using various analytical techniques to verify that they comply with regulatory specifications. The goal is to detect and prevent defects, ensuring that only products that pass rigorous standards are released to the market. QC is essential for maintaining public health and regulatory compliance in the pharmaceutical sector.

What is the role of quality control in pharma?

The role of quality control in pharma involves testing and inspecting raw materials, in-process samples, and finished products to ensure they meet safety, efficacy, and quality standards. QC professionals use analytical techniques and follow Good Manufacturing Practices (GMP) to identify and prevent defects, supporting regulatory compliance and product consistency.

What is the difference between Quality Control Pharma vs Quality Assurance Pharma?

AspectQuality Control PharmaQuality Assurance Pharma
Primary FocusTesting and inspecting raw materials, in-process, and finished products for complianceDeveloping and maintaining quality systems and processes to prevent defects
CertificationsGMP, GLP, relevant laboratory certificationsGMP, ISO 9001, quality management system certifications
Work EnvironmentLaboratories, testing facilitiesQuality departments, documentation, audits
Common Employer RolesPharmaceutical companies, contract labsPharmaceutical companies, regulatory agencies

While both roles aim to ensure product quality, Quality Control Pharma focuses on testing and inspection, whereas Quality Assurance Pharma emphasizes establishing systems and processes to prevent issues. Understanding these differences helps in choosing the right career path or job focus within the pharmaceutical industry.

What are some of the common challenges faced by quality control professionals in the pharmaceutical industry?

Quality Control professionals in pharma often face challenges such as staying updated with evolving regulatory standards, managing tight timelines for product release, and ensuring accuracy in complex analytical testing. They must also coordinate closely with production and R&D teams to address any discrepancies or deviations quickly. Maintaining meticulous documentation and effectively handling audits are essential parts of the role, making attention to detail and strong communication skills particularly important.
What are popular job titles related to Quality Control Pharma jobs in Ohio? For Quality Control Pharma jobs in Ohio, the most frequently searched job titles are:
What job categories do people searching Quality Control Pharma jobs in Ohio look for? The top searched job categories for Quality Control Pharma jobs in Ohio are:
What cities in Ohio are hiring for Quality Control Pharma jobs? Cities in Ohio with the most Quality Control Pharma job openings:
Quality Control Pharma jobs near you
Infographic showing various Quality Control Pharma 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.

Quality Control Microbiology Technician

STAQ Pharma

Columbus, OH • On-site

$23.75 - $31.25/hr

Other

Posted 19 days ago

Job description

Quality Control Microbiology Technician 1

Quality Control Microbiology Technician 1 will provide clean room support for batch production and ensuring procedure adherence during filling of product. Utilize appropriate controlled documents and assist in quality control deviations/investigations.

Responsibilities
  • Ensure clean rooms and associated areas meet the required cleanliness standards as per company procedures.
  • Adhere to strict gowning and personal hygiene practices to prevent contamination and maintain integrity of the clean room environment.
  • Perform gowning qualification training for individuals from all departments who must enter ISO 7 classified areas.
  • Monitor and maintain clean room equipment such as viable and non-viable samplers to ensure optimal performance and compliance with established standards.
  • Perform and lead routine environmental monitoring activity in ISO 7 Classified Areas.
  • Work with production to resolve Quality issues and ensure documentation is complete.
  • Perform routine and non-routine viable, non-viable and surface environmental monitoring in all classified areas of the facility.
  • Incubation and enumeration of samples related to environmental monitoring processes. Train new personnel on enumeration activities.
  • Evaluate organisms by colony morphology and perform subculturing. Train new personnel on colony morphology assessment and subculturing activities.
  • Perform and/or verify gram stain testing morphology results.
  • Continuous improvement activities for environmental monitoring program.
  • Provide quality control and microbiology support for operations.
  • Collect, submit and manage microbiological samples to third party testing laboratories.
  • Assist with QC Microbiologists (and other investigators) with investigations as they relate to environmental monitoring or other quality control deviations.
  • Assist QC Microbiologists with data trending and data reporting as they relate to environmental monitoring or other data-generating processes.
  • Perform routine testing or cleaning associated with the BioSafety Cabinet. Lead and train new personnel on the cleaning procedures and testing procedures carried out in the BioSafety Cabinet.
  • Assist in process, procedural, equipment issues via experimentation or revision of procedures.
  • Other duties as assigned.
Required Skills/Abilities (examples)
  • Experience with cGMP aseptic manufacturing environment.
  • Strong attention to detail.
  • Comfortable in a fast-paced, small company environment and able to adjust workload based upon changing priorities.
  • Preferred previous pharmaceutical experience.
  • Proficient in using Microsoft Word, Excel, PowerPoint, Outlook.
  • Familiarity with 21 CFR Part 11/210/211
Education and Experience
  • Associate or Bachelor's degree in Microbiology, Biology, or related life sciences.
  • Experience in microbiology or quality control preferred.
  • Experience in a cGMP or cleanroom setting preferred.
Physical Requirements
  • Prolonged periods of sitting at a desk or laboratory bench and working on a computer.
  • Must be able to lift up to 15 pounds at times.

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