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Weekend Quality Control Specialist Jobs (NOW HIRING)

Intellectt INC

Quality Control Specialist

El Paso, TX · On-site

Quality Control Specialist Location : El Paso, Texas. If you are currently exploring new opportunities, please share your updated resume with me at laxmiprasanna@intellectt.com Role: Quality Control ...

Jetpack Shipping

Quality Control Specialist

Akron, OH · On-site

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 ...

Jetpack Shipping

Quality Control Specialist

Akron, OH · On-site

$18 - $19/hr

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 ...

Planet 13

Quality Control Specialist

Jacksonville, FL · On-site

$18/hr

The Quality Control Specialist is responsible for supporting quality assurance activities ... Must be flexible and able to work long hours and weekends as required * Able to adapt in a quick ...

SpectronRx

QC Specialist

Indianapolis, IN

$29 - $34/hr

Quality Control Specialist COMPANY OVERVIEW SpectronRx is a growing Contract Development and Manufacturing Organization (CDMO) based in Indianapolis, Indiana, and production locations in South Bend ...

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Weekend Quality Control Specialist information

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How much do weekend quality control specialist jobs pay per hour?

As of Aug 5, 2026, the average hourly pay for weekend quality control specialist 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 does a Weekend Quality Control Specialist do?

A Weekend Quality Control Specialist is responsible for inspecting products, services, or processes during weekend shifts to ensure they meet quality standards. They may perform tests, document findings, and collaborate with teams to address issues, often using quality management tools and following safety protocols.

What is the difference between Weekend Quality Control Specialist vs Weekend Quality Assurance Technician?

AspectWeekend Quality Control SpecialistWeekend Quality Assurance Technician
CertificationsISO, Six Sigma, or industry-specific quality control certificationsISO, Six Sigma, or industry-specific QA certifications
Work EnvironmentManufacturing, production, or food processing facilitiesManufacturing, production, or service industries
Job FocusInspecting products for defects, ensuring complianceDeveloping and implementing quality standards, process improvements
Common UsageQuality inspection roles during weekendsQuality process monitoring and improvement roles during weekends

The Weekend Quality Control Specialist primarily focuses on inspecting products and ensuring compliance during weekend shifts, while the Weekend Quality Assurance Technician emphasizes developing quality standards and improving processes. Both roles require similar certifications and work in comparable environments, but their core responsibilities differ in scope and focus.

What cities are hiring for Weekend Quality Control Specialist jobs? Cities with the most Weekend Quality Control Specialist job openings:
What are the most commonly searched types of Quality Control Specialist jobs? The most popular types of Quality Control Specialist jobs are:
What states have the most Weekend Quality Control Specialist jobs? States with the most job openings for Weekend Quality Control Specialist jobs include:
Weekend Quality Control Specialist jobs near you

Quality Control Specialist (Weekend)

WuXi Biologics

Cranbury, NJ • On-site

$60K - $96K/yr

Full-time, Other

Posted 26 days ago

Job description

Job Title - Quality Control Specialist (Weekend)
Work Location - Cranbury, NJ
Job Summary:
The QC specialist (Weekend Shift) is responsible for the quality and on-time testing/collection of samples, EM (Environmental sampling), Water and Gas system sampling (when required) with raw material sampling to the various testing sections. This role will also ensure QC deliverables to internal departments and external clients are accurate and consistent. Demonstrates strong oral and written communication skills and actively contributes to training, report generation and GMP documentation.
Job Responsibilities:
  • Adhere to GMP sampling (Clean rooms, WFI, gas) and testing, follow laboratory procedures according to and in compliance with cGMP guidelines and internal SOPs.
  • Able to follow and conduct EM sampling in cleanroom areas in/between the various building sites in Cranbury or other US sites (when needed).
  • Able to support sample receiving, transporting needs in/between the various building sites in Cranbury or other US sites (when needed).
  • Perform micro related testing including but not limit to bioburden, pH, growth promotion, endotoxin, conductivity, TOC, nitrate, plate readings, plate transferring etc (when required).
  • Receive required samples, perform testing, report results independently and in a timely manner (when required).
  • Able to input data and generate EM data trend charts and reports.
  • Able to initiate investigation/excursions when having OOS/OOL/Atypical results.
  • Able to perform reagents/consumables inventory management (LIMS receiving, disposal etc) to ensure consistent QC Micro operation needs.
  • Operate according to the experimental or sampling plan and deliver results, testing/sampling method/SOP's
  • Record and organize experimental data in accordance with "Good Document Management Practices" to ensure data integrity.
  • Ensure compliance to training, preparation, documentation and general lab maintenance requirements for Industry Standards and/or Regulations.
  • Assist in preparing SOP, protocols, final reports, investigations, and deviations as needed.
  • Assist in investigating any Out-of-Specification results and laboratory deviations, conducting root cause analysis, and implementing CAPA.
  • Assist in preparing or executing validation documents to support new materials, process changes and qualifications.
  • Maintains laboratory notebooks and worksheets for QC tasks as required.
  • Work for weekend shift (Wed to Mon, or Thur to Tue)
  • Support night shift work when required by supervisor (when needed)
  • Any other duties assigned by the supervisor (when applicable).

Job Qualifications:
Education and Experience:
  • High school certificate or above degree and/or advanced Graduate degree in Chemistry, Microbiology, Biochemistry or equivalent field.
  • High school certificate: 2 years and above working experience is preferred
  • Bachelor's degree: 1 year and above working experience is preferred
  • Master's degree: no requirement

Technical Skills / Knowledge:
  • Candidate must possess willingness to learn analytical and QC operations of pharmaceutical industry, understand current regulations and industry trends of biologics product development, characterization and manufacturing testing requirement including cGMP, ICH, EMA, FDA, and other global compendia regulations and guidance.
  • Basic familiarity with analytical instruments and methodologies, such as TOC, conductivity meter is preferred but not mandatory.
  • Basic experience with software and information systems (e.g. Empower, TrackWise, Master Control, LES, lab notebook and preferably LIMS). Ability to adapt between strategic and tactical thinking/planning and manage multiple priorities to achieve department and site objectives.
  • Ability to understand technical data

Problem Solving:
  • Basic experience in planning and ability to solve simple QC technical and operation problems.
  • Be able to raise issues immediately to supervisor and work with supervisor when in doubt.

Communication Skills:
  • Proficiency in English is required. Good communications skills (verbal, written, and presentation skills).
  • Effectively exchange information or discuss clearly framed issues or ideas with colleagues.

The anticipated salary range for this position is $60,200 to $96,300
Job description does not intend to list all the duties and responsibilities assigned to this position. Employee holding this position would be required to perform other job-related duties/responsibilities based on their expertise and company business needs.
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

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