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Temporary Quality Assurance Biotech Jobs (NOW HIRING)

Document audit findings and communicate performance gaps or training needs promptly and professionally. * Assist with onboarding and training of temporary QA employees provided through staffing ...

As a Temporary Quality Assurance Specialist working remotely in the United States, youll be a part of bringing humanity to business. #experienceTTEC Our employees have spoken. Our purpose, team, and ...

... new temporary QA staff employed through the temporary agencies. · Partners and collaborates with other team members to suggest new practices in training and facilitation methods. · Observes ...

... new temporary QA staff employed through the temporary agencies. · Partners and collaborates with other team members to suggest new practices in training and facilitation methods. · Observes ...

... new temporary QA staff employed through the temporary agencies. · Partners and collaborates with other team members to suggest new practices in training and facilitation methods. · Observes ...

As a Temporary Quality Assurance Specialist working remotely in the United States, you'll be a part of bringing humanity to business. #experienceTTEC Our employees have spoken. Our purpose, team, and ...

QA Associate

Irvine, CA

$85K - $115K/yr

PSC Biotech provides the life sciences with essential services to ensure that health care products ... Your Role We are seeking a QA Associate to support calibration and maintenance activities within a ...

Our client is a leading biotechnology company that combines technological expertise with world ... Temporary Position Work Type: Onsite Summary The QA Engineer is responsible for ensuring the timely ...

Who is CorDx? CorDx a multi-national biotech organization focused on pushing the limits of ... We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the ...

Who is CorDx CorDx a multi-national biotech organization focused on pushing the limits of ... We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the ...

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Temporary Quality Assurance Biotech information

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$12

$29

$62

How much do temporary quality assurance biotech jobs pay per hour?

As of Jul 27, 2026, the average hourly pay for temporary quality assurance biotech in the United States is $29.29, according to ZipRecruiter salary data. Most workers in this role earn between $18.75 and $34.38 per hour, depending on experience, location, and employer.

What is the difference between Temporary Quality Assurance Biotech vs Temporary Quality Control Biotech?

AspectTemporary Quality Assurance BiotechTemporary Quality Control Biotech
CertificationsGMP, GLP, QA certificationsGMP, GLP, QC certifications
Work EnvironmentDocumentation review, audits, complianceTesting, lab analysis, sample testing
Employer & Industry UsagePharmaceutical, biotech companies, manufacturingLaboratories, manufacturing, biotech firms

Temporary Quality Assurance Biotech focuses on ensuring compliance, documentation, and audit readiness, while Temporary Quality Control Biotech emphasizes testing, analyzing samples, and product quality verification. Both roles are essential in biotech manufacturing but differ in daily tasks and focus areas.

What are the key skills and qualifications needed to thrive as a Temporary Quality Assurance Biotech, and why are they important?

To thrive as a Temporary Quality Assurance Biotech, you need a background in biological sciences or a related field, strong attention to detail, and an understanding of regulatory standards like GMP or GLP. Familiarity with laboratory information management systems (LIMS), quality management software, and relevant certifications such as ASQ are highly beneficial. Excellent organizational skills, clear communication, and the ability to work well in a team help ensure seamless compliance and reporting. These skills and qualities are crucial to maintaining product quality, regulatory compliance, and efficient operations in a biotech environment.

What are Temporary Quality Assurance Biotech jobs?

Temporary Quality Assurance Biotech jobs involve short-term roles in biotechnology companies where professionals ensure that products and processes meet established quality standards and regulatory requirements. These positions typically focus on tasks such as monitoring laboratory practices, conducting audits, reviewing documentation, and supporting compliance efforts. Individuals in these roles help maintain product safety and efficacy by identifying issues and implementing corrective actions. Temporary QA positions are often used to support peak workloads, special projects, or to cover employee absences.

What are some typical challenges faced by Temporary Quality Assurance professionals in biotech companies, and how can they overcome them?

Temporary Quality Assurance (QA) professionals in biotech often encounter challenges such as quickly adapting to new protocols, integrating into established teams, and rapidly learning complex regulatory requirements. Since their assignments are time-bound, it's crucial to familiarize themselves with company-specific quality systems and documentation processes early on. Proactively seeking guidance from permanent team members and leveraging available training resources can help temporary QA staff contribute effectively and ensure compliance with industry standards.
What cities are hiring for Temporary Quality Assurance Biotech jobs? Cities with the most Temporary Quality Assurance Biotech job openings:
What are the most commonly searched types of Quality Assurance Biotech jobs? The most popular types of Quality Assurance Biotech jobs are:
What states have the most Temporary Quality Assurance Biotech jobs? States with the most job openings for Temporary Quality Assurance Biotech jobs include:
Temporary - Quality Assurance Technician

Temporary - Quality Assurance Technician

Trulieve

Quincy, FL

Other

PTO

Posted 13 days ago


Trulieve rating

5.3

Company rating: 5.3 out of 10

Based on 54 frontline employees who took The Breakroom Quiz

30th of 33 rated cannabis dispensaries


Job description

If you have an interest in being part of one of the fastest growing industries in the nation in you may consider wanting to work for Trulieve! If you have a desire to help others in need through your efforts, this may be the role for you! 

At Trulieve, we strive to bring our patients the relief they need in a product they can trust. Our plants are hand-grown in an environment specially designed to reduce unwanted chemicals and pests, keeping the process as natural as possible at every turn.

Our products are designed to alleviate seizures, severe and persistent muscle spasms, pain, nausea, loss of appetite, and other symptoms associated with serious medical conditions such as cancer.

Our specially trained staff works hand-in-hand with physicians to provide the right products and the correct dosage to ensure patients get the compassionate care they need.

To learn more about our company, please visit our website; 

https://www.trulieve.com

Requisition ID:  20287 

Remote Work Available: No 

Job Title: Temporary - Quality Assurance Technician - Processing

Department: Quality Assurance

Reports to: QA Supervisor or Team Lead

FLSA Status: Non-Exempt/ Hourly 

Location: Quincy, FL

POSITION SUMMARY 

The Temporary - Quality Assurance Technician - Processing is responsible for conducting visual scans of products to assure the quality and safety profiles of products intended for consumers meet specifications. QA Techs will be responsible for tracking the weight of each sample and keeping track of what cultivar is currently being worked on. Additionally, QA Techs will be required to safely handle and separate any adulterated product that is found during scans and escalate quality issues to the QA Lead and/or QA Supervisor.

ESSENTIAL DUTIES AND RESPONSIBILITIES 

  • Conduct visual inspections of cannabis and cannabis products for organic and inorganic adulterants and defects
  • Audits various applications to products to ensure SOP specifications and/or requirements are met
  • Document inspection results by completing reports and logs and inputting data into quality database QMS
  • Notify supervisor of any incidences of recurring equipment malfunctions and corrective actions taken along with any affected material or supplies noted
  • Maintain a safe and healthy work environment by following departmental standard operating procedures (SOPs), adhering to cGMP SOPs, and complying with legal regulations
  • Maintains and ensures that proper Personal Protective Equipment (PPE) is utilized and changed out regularly, or as needed
  • Communicate quality and/or compliance concerns with urgency to QA Supervisor or Team Lead
  • Identify possible areas for improvement in the quality control process
  • Keeps work area safe, clean, and organized
  • Performs other duties as requested

MINIMUM QUALIFICATIONS 

  • Must be able to pass a Level 2 background screening
  • Must be at least 21 years of age (State Law)
  • High School Diploma or GED required
  • Detail Oriented
  • Coachable and willing to learn
  • Ability to work in a fast-paced environment
  • Ability to focus and avoid distractions while working with little to no supervision
  • Comfortable operating digital scales, general
  • Basic computer knowledge - Microsoft Office
  • Basic math and reading comprehension
  • Organizational skills
  • Must be and remain compliant with all legal or company regulations for working in the cannabis industry
  • Knowledge of GMP requirements and HACCP
  • Conducts scale verifications as needed
  • Basic understanding of Trulieve ERP i.e., SAP

PHYSICAL REQUIREMENTS

  • Must be able to push, pull, move, and/or lift a minimum of 40lbs to a minimum height of 5 feet and able to push, pull, move, and/or carry such weight a minimum distance of 50 feet, with or without mechanical assistance.
  • Must be able to work seated/standing as appropriate at workstations for extended periods of time, maintain body equilibrium while climbing ladders, stairways, stopping, kneeling, crouching, and reaching, and use hands/fingers to hold, grasp, turn, pick, pinch frequently/constantly to complete tasks
  • Must be able to handle organic matter daily, able to wear PPE as appropriate (eye, face, hand, arm, head, foot, body, fall protection), and able to be exposed to hot, cold, wet, humid, or windy conditions while wearing PPE (95 degrees or greater)
  • Must have visual acuity with/without job aids to perform activities such as reading, viewing a computer terminal, visual inspection involving small parts/details. Clarity of vision at 20 ft or more in day and night/dark conditions
  • Must be able to speak and communicate verbally at conversation levels with co-workers, vendors, etc. (Moderate noise)

WORK SCHEDULE

  • 40+ hours weekly with flexible hours depending on department needs. Must be available to work occasional evenings, weekends, and holidays.

Equal Opportunity Employer l Trulieve Supports a Drug Free Workplace

Salary will be commensurate with experience.   A comprehensive benefits package including paid time off is offered with this position. 

Trulieve provides equal employment opportunities to all employees and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, pregnancy or any other characteristic protected by federal, state or local laws.


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