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Qc Specialist In Biotech Jobs (NOW HIRING)

Jetpack Shipping

Quality Control Specialist

Akron, OH · On-site

Summary: A Quality Control Specialist in the dietary supplement industry is responsible for ... ensuring that all products meet established standards of quality and safety before they reach ...

Lonza

Quality Control Specialist

Portsmouth, NH · On-site

Quality Control Specialist Location: Portsmouth, NH (On-site) At Lonza, a leading contract ... Minimum of 3+ years of experience in a GMP, pharmaceutical, biotechnology, environmental ...

Operations Manager

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Quality Control (QC) Specialist

Huntley, IL · On-site

$20 - $23/hr

Quality Control (QC) Specialist - Huntley, IL $20.00 - $23.00/Hourly Position Summary: We are ... The QC Inspector will play a vital role in upholding our commitment to integrity customer ...

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System One

Quality Control Specialist

Miami, FL · On-site

$48K/yr

Quality Control Specialist Location: Miami, Florida Type: Direct Hire Compensation: $48,006.40 Work ... Experience in quality assurance, compliance monitoring, or process improvement preferred.

System One

Quality Control Specialist

Miami, FL · On-site

$48K/yr

Quality Control Specialist Location: Miami, Florida Type: Direct Hire Compensation: $48,006.40 Work ... Experience in quality assurance, compliance monitoring, or process improvement preferred.

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Qc Specialist In Biotech information

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$12

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$49

How much do qc specialist in biotech jobs pay per hour?

As of Jul 25, 2026, the average hourly pay for qc specialist in biotech in the United States is $28.64, according to ZipRecruiter salary data. Most workers in this role earn between $19.95 and $35.58 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a QC Specialist in Biotech, and why are they important?

To thrive as a QC Specialist in Biotech, you need a solid background in biological sciences, analytical techniques, and quality assurance processes, often supported by a relevant bachelor's degree. Familiarity with laboratory information management systems (LIMS), regulatory guidelines (such as GMP), and analytical instruments like HPLC and PCR is typically required. Strong attention to detail, problem-solving skills, and effective communication set outstanding candidates apart in this role. These skills ensure accurate testing, regulatory compliance, and reliable product quality in a highly regulated environment.

What is the difference between Qc Specialist In Biotech vs Quality Control Analyst?

AspectQc Specialist In BiotechQuality Control Analyst
CredentialsBachelor's in Life Sciences or related field, certifications like ASQBachelor's in Chemistry, Biology, or related field, certifications often similar
Work EnvironmentBiotech labs, manufacturing facilities, regulated environmentsLaboratories, manufacturing sites, quality assurance settings
Employer & Industry UsageBiotech companies, pharmaceutical firms, biotech manufacturingPharmaceutical companies, biotech firms, contract labs
Common Search & ComparisonYesYes

The main difference between a Qc Specialist In Biotech and a Quality Control Analyst lies in their specific industry focus. Qc Specialists In Biotech typically work within biotech companies focusing on biotech-specific products and regulations, while Quality Control Analysts may work across various industries including pharmaceuticals and manufacturing. Both roles require similar credentials and work environments, but their industry applications and specific responsibilities differ slightly.

What does a QC Specialist in biotech do?

A QC (Quality Control) Specialist in biotech is responsible for ensuring that products, materials, and processes meet established quality standards and regulatory requirements. They perform laboratory tests, analyze data, document results, and help troubleshoot any issues related to product quality. QC Specialists also assist with maintaining compliance with Good Manufacturing Practices (GMP) and may participate in audits or inspections. Their work helps ensure the safety, efficacy, and consistency of biotech products such as pharmaceuticals or biologics.

What are some common challenges faced by a QC Specialist in the biotech industry, and how can they be addressed?

QC Specialists in biotech often encounter challenges such as keeping up with evolving regulatory standards, troubleshooting complex analytical instruments, and managing tight timelines for product release. Staying current with industry regulations and regularly participating in training can help address compliance issues. Building strong cross-functional relationships with R&D, manufacturing, and regulatory teams also facilitates smoother communication and problem-solving when unexpected issues arise. Proactively documenting processes and maintaining meticulous records further supports efficiency and audit readiness.
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Qc Specialist In Biotech jobs near you
Infographic showing various Qc Specialist In Biotech job openings in the United States as of July 2026, with employment types broken down into 41% Locum Tenens, 1% As Needed, 50% Full Time, 1% Part Time, 4% Contract, and 3% Summer. Highlights an 82% Physical, 3% Hybrid, and 15% Remote job distribution, with an average salary of $59,574 per year, or $28.6 per hour.
Quality Control Specialist

Quality Control Specialist

Jetpack Shipping

Akron, OH • On-site

Full-time

Posted 15 days ago

Job description

JetPack Shipping is a leader in private label fulfillment. It is our mission to provide effortless on-demand private label products while fixating on providing a transparent customer experience. We drive operational excellence into our processes and capabilities while continuously creating growth for our employees, partners, and consumers. We are always on the lookout for like minded individuals to add to our ever growing staff.

Summary:

A Quality Control Specialist in the dietary supplement industry is responsible for ensuring that all products meet established standards of quality and safety before they reach consumers. This role involves developing, implementing, and monitoring quality control processes and procedures. Key responsibilities include conducting inspections and tests on raw materials, in-process products, and finished goods, maintaining detailed records of quality checks, and identifying areas for improvement. The specialist collaborates with production and compliance teams to ensure adherence to regulatory requirements, such as those set by the FDA and GMP regulations. Strong analytical skills, attention to detail, and knowledge of industry standards are essential for success in this position. We are hiring for 1st and 2nd Shift.

Responsibilities:

A Quality Control Specialist in the dietary supplement industry is responsible for ensuring that products meet specific standards of quality and safety before they reach consumers. This involves overseeing the entire production process, from raw material selection to finished product testing, to ensure compliance with regulatory requirements and company standards. Their role is critical in safeguarding consumer health and maintaining brand reputation by preventing the distribution of substandard or unsafe products.

Quality Control & Auditing:

  • Conduct routine inspections of raw materials, in-process production, and finished goods.
  • Perform line checks and verification of manufacturing and packaging processes.
  • Audit batch records and verify compliance with Good Manufacturing Practices(GMP).

Production Process Monitoring:

  • Verify that manufacturing processes comply with Good Manufacturing Practices (GMPs).
  • Monitor critical control points to prevent deviations from batch standards.
  • Ensure proper calibration and maintenance of equipment.

In-Process Testing:

  • Conduct tests at various stages of manufacturing to ensure composition and quality.
  • Check for uniformity and consistency in capsule or tablet weight, dissolution, and disintegration.

Finished Product Testing:

  • Perform thorough testing of the final product for active ingredient potency and purity.
  • Ensure compliance with product specifications, including label claims.
  • Test for microbial contamination and other potential safety hazards.

Document and Record Keeping:

  • Maintain accurate and detailed records of inspections, tests, and audits.
  • Ensure traceability of all materials and products through comprehensive documentation.

Root Cause Analysis and Corrective Actions:

  • Investigate quality issues or product failures to determine root causes.
  • Implement corrective and preventive actions to avoid recurrence.

Continuous Improvement:

  • Identify areas for process improvement to enhance product quality and efficiency.
  • Foster a culture of quality and safety awareness within the organization.

By focusing on these areas, a Quality Control Specialist can help ensure that dietary supplements are safe, effective, and of high quality, thereby protecting consumer health and maintaining regulatory compliance.

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