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Quality Control Analyst Trainee Jobs in Arizona (NOW HIRING)

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Quality Control Inspector

Phoenix, AZ · On-site

$18.50 - $22/hr

We are seeking a Quality Control Inspector to join our team! Inspector will perform daily in ... Strong analytical and critical thinking skills * Excellent written and verbal communication skills

Develops and implements QC plan, ensuring environmental plan compliance, performance monitoring, analysis and reporting. * Advises the Project Manager on quality control, safety and environmental ...

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Quality Control Inspector

Phoenix, AZ · On-site

$18.50 - $22/hr

We are seeking a Quality Control Inspector to join our team! Inspector will perform daily in ... Strong analytical and critical thinking skills * Excellent written and verbal communication skills

Quality Control Technician

Phoenix, AZ · On-site

$17.75 - $22.75/hr

Monitoring and analyzing quality performance during the procedure. Ensuring that workflows ... Experience working as a QC technician for a construction contractor at TSMC's Arizona factory is a ...

Quality Control Technician

Phoenix, AZ

$17.75 - $22.75/hr

Monitoring and analyzing quality performance during the procedure. * Ensuring that workflows ... Experience working as a QC technician for a construction contractor at TSMC's Arizona factory is a ...

Quality Control Manager

Tucson, AZ · On-site

$90K - $1M/yr

Review Activity Hazard Analyses (AHAs) for constructability and quality-related requirements prior ... Complete and upload QC Reports, inspection records, deficiency logs, photos, and submittals using ...

... analysis of raw material, in-process and finished goods test results. ● Responsible for generating compliant QC documentation as part of the Device History Record required for releasing items into ...

Provide analytical support to Rapid Technology Application platform by releasing precise and ... control system. * Perform quality inspections on raw materials and finish good materials.

Provide analytical support to Rapid Technology Application platform by releasing precise and ... control system. * Perform quality inspections on raw materials and finish good materials.

Develops and implements QC plan, ensuring environmental plan compliance, performance monitoring, analysis and reporting. * Advises the Project Manager on quality control, safety and environmental ...

Provide analytical support to Rapid Technology Application platform by releasing precise and ... control system. * Perform quality inspections on raw materials and finish good materials.

Develops and implements QC plan, ensuring environmental plan compliance, performance monitoring, analysis and reporting. * Advises the Project Manager on quality control, safety and environmental ...

Develops and implements QC plan, ensuring environmental plan compliance, performance monitoring, analysis and reporting. * Advises the Project Manager on quality control, safety and environmental ...

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Quality Control Analyst Trainee information

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

AspectQuality Control Analyst TraineeQuality Control Analyst
CredentialsTypically requires a high school diploma or associate degree; on-the-job training providedUsually requires a bachelor's degree in life sciences, chemistry, or related field; may need certifications
Work EnvironmentEntry-level, supervised laboratory or manufacturing settingMore independent role in laboratory or production environment, performing routine testing
ResponsibilitiesAssisting with testing, learning procedures, gaining experiencePerforming quality tests, analyzing data, ensuring compliance

In summary, a Quality Control Analyst Trainee is an entry-level position focused on learning and assisting in quality control tasks, while a Quality Control Analyst is a more experienced role responsible for conducting tests and ensuring product quality independently.

What are some common challenges faced by Quality Control Analyst Trainees during their initial training period?

Quality Control Analyst Trainees often encounter challenges such as learning to interpret complex data, understanding regulatory standards, and adapting to the fast-paced lab environment. New trainees may also need time to become proficient with specialized laboratory equipment and software used for quality testing. Collaborating with experienced analysts and seeking feedback can help overcome these obstacles, while structured training programs and mentorship are typically provided to support the learning curve.

Is QC analyst a stressful job?

A Quality Control Analyst Trainee role can be stressful due to the need for precision, attention to detail, and strict adherence to quality standards. The job often involves repetitive tasks, strict deadlines, and the responsibility of ensuring product safety, which can contribute to work-related stress.

What is a QC analyst salary?

A Quality Control (QC) Analyst trainee typically earns an entry-level salary that ranges from $40,000 to $55,000 annually, depending on location and industry. As they gain experience and certifications, salaries can increase, and roles may include responsibilities such as testing, data analysis, and compliance with quality standards.

What does a Quality Control Analyst Trainee do?

A Quality Control Analyst Trainee assists in testing and inspecting products or materials to ensure they meet established standards of quality. They typically work under the supervision of experienced analysts, learning how to conduct laboratory tests, interpret data, and document findings. Their responsibilities may also include calibrating equipment, preparing samples, and helping to maintain a clean and safe work environment. This role is essential for ensuring products are safe, effective, and compliant with regulations.

What is a quality control trainee?

A quality control trainee is an entry-level position where individuals learn to inspect and test products or processes to ensure they meet quality standards. The role often involves training in quality assurance procedures, using testing tools, and following safety protocols under supervision.

How to become a QC analyst?

To become a Quality Control Analyst, candidates typically need a bachelor's degree in a relevant field such as chemistry, biology, or engineering. Gaining experience with laboratory techniques, quality assurance processes, and tools like GMP or ISO standards is beneficial, and some roles may require certifications like CQE or Six Sigma. Strong attention to detail and analytical skills are essential for success in this role.

What are the key skills and qualifications needed to thrive as a Quality Control Analyst Trainee, and why are they important?

To thrive as a Quality Control Analyst Trainee, you need a solid background in chemistry or biology, attention to detail, and at least a bachelor's degree in a related field. Familiarity with laboratory equipment, analytical instruments like HPLC or GC, and knowledge of quality management systems such as GMP are typically required. Strong problem-solving skills, effective communication, and the ability to work both independently and as part of a team make candidates stand out. These skills and qualities ensure accurate testing, regulatory compliance, and contribute to maintaining high product quality standards.
What are the most commonly searched types of Quality Control Analyst jobs in Arizona? The most popular types of Quality Control Analyst jobs in Arizona are:
What are popular job titles related to Quality Control Analyst Trainee jobs in Arizona? For Quality Control Analyst Trainee jobs in Arizona, the most frequently searched job titles are:
What job categories do people searching Quality Control Analyst Trainee jobs in Arizona look for? The top searched job categories for Quality Control Analyst Trainee jobs in Arizona are:
What cities in Arizona are hiring for Quality Control Analyst Trainee jobs? Cities in Arizona with the most Quality Control Analyst Trainee job openings:

Quality Control Specialist (Day Shift)

Hims and Hers Health, Inc.

Gilbert, AZ • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 20 days ago


Job description

Hims & Hers is the leading health and wellness platform, on a mission to help the world feel great through the power of better health. We are redefining healthcare by putting the customer first and delivering access to care that is affordable, accessible, and personal, from diagnosis to treatment to delivery. No two people are the same, so we provide access to personalized care designed for results. By normalizing health & wellness challenges and innovating on their solutions, we're making better health outcomes easier to achieve.
Hims & Hers is a public company, traded on the NYSE under the ticker symbol "HIMS." To learn more about the brand and offerings, you can visit hims.com/about and hims.com/how-it-works . For information on the company's outstanding benefits, culture, and its talent-first flexible/remote work approach, see below and visit www.hims.com/careers-professionals.
About the Role:
Hims & Hers is seeking an experienced Quality Control Specialist to join our Quality Unit located in Gilbert, Arizona. The position of Quality Specialist will focus on driving continuous improvement efforts that benefit and delight the Hims customer. We are looking for a highly motivated individual to help support and report to the Quality Control Manager. The Quality Specialist role is responsible for the inspecting and/or testing of product(s) before, during and after manufacturing process(es) to ensure products align with company and regulatory standards, as well as other processes necessary to quality operations. The position performs and leads activities "on the floor" in support of dispositioning product and/or raw materials while ensuring compliance with Quality Assurance (QA) policies and procedures, USP, SOPs, and where applicable cGMP. Assist with relevant environmental monitoring programs.
Day Shift Position: 6:30am to 05:00pm (Sun-Wed or Wed-Sat)
You Will:
  • Perform in process and post production quality checks, including testing, assessing products in the compounding suites ("shop floor") to ensure product acceptability.
  • Perform line clearance, where applicable.
  • Perform AQLs during the visual inspection process
  • Provide reports and trending data to QA management
  • Support departments in reporting, handling and escalation of investigations
  • Support external manufacturer non-conformance investigations to improve Quality processes.
  • Manage product retain samples.
  • Support change control system to provide improvement solutions
  • Support quality processes in the pharmacy - including inspections, pH meters and scale checks, non-conformance/deviation/complaint investigations, implement corrective action activities, training activities, etc.
  • Document & review of records: SOP generation, batch record review, COA acceptance, USP monographs, etc.
  • Recommend training needs, provide reports to QC Manager and Lead Pharmacist to ensure compliance with quality standards
  • Assist with incoming raw material inspections, as needed per the guidelines for collection, testing, and reporting quality data.
  • Assist with drafting SOPs and protocols to follow internal global policies, USP and other applicable regulatory guidelines
  • Ensures compliance with USP <795>, USP <797>, USP <800> and cGMP cleaning standards
  • Assist in audit activities with all appropriate third party audits & internal audits as required to ensure compliance.
  • Assist with the management of samples to be tested with contract laboratories.

You Have:
  • B.S. in chemistry, microbiology, biology, quality management, engineering, or related discipline preferred
  • 1-3 years experience in the area of quality assurance/control, process/quality engineering, and/or product formulation
  • A Pharmacy Technician license or willingness to obtain one within the first six months of employment (we cover costs and will help you obtain your trainee hours).
  • Experience within a 503b outsourcing facility or experience in cGMP or regulated environment with knowledge of FDA 21CFR 210 and 211, a plus
  • Aseptic processing experience and knowledge of ISO 14644
  • Working knowledge of USP-NF standards <795>, <797>, <800> including monographs
  • Ability to manage multiple tasks simultaneously, with strong time management and organizational skills.
  • Excellent interpersonal skills, communication skills and technical writing
  • Solid understanding of product testing including understanding best practices for testing product against defined specifications
  • Ability to multi-task and work independently. Highly motivated self-starter.
  • Solid computer skills with Word, Excel, PowerPoint, and Google platform applications.
  • Excellent skills in decision making, data collection and analysis, organizing and planning.
  • Working knowledge and application of statistical analysis including probability and trend analysis
  • Knowledge and experience in documentation and facility auditing
  • Some travel may be required

Our Benefits (there are more, but here are some highlights):
  • Competitive salary & equity compensation for full-time roles
  • Unlimited PTO, company holidays, and quarterly mental health days
  • Comprehensive health benefits including medical, dental & vision, and parental leave
  • Employee Stock Purchase Program (ESPP)
  • 401 (k) benefits with employer matching contribution

Conditions of Employment:
  • This position will require working with Hazardous Drugs (HD) and would require that Personal Protective Equipment (PPE) be worn for the length of working with these drugs. These items would include gloves, respiratory protection, gown, and other items as required.
  • This position requires medical approval to wear respiratory protection in the form of negative or positive pressure respirators, including N95, full face respirator, SCBA, or Powered Air Purifying Respirator (PAPR).
  • Physical exertion required. Including, but not limited to, walking up to 50% of the time, standing up to 100% of the time, squatting and bending up to 20% of the time and lifting up to 80% of the time for up to a twelve hour shift. Must be able to lift up to 50lbs.
  • Due to the risk of reproductive capability in handling or compounding certain Hazardous Drugs (HD) associates must be willing to confirm that they understand the potential risks (teratogenicity, carcinogenicity and reproductive effects) of handling hazardous drugs.

We are committed to building a workforce that reflects diverse perspectives and prioritizes ethics, wellness, and a strong sense of belonging. If you're excited about this role, we encourage you to apply-even if you're not sure if your background or experience is a perfect match.
Hims considers all qualified applicants for employment, including applicants with arrest or conviction records, in accordance with the San Francisco Fair Chance Ordinance, the Los Angeles County Fair Chance Ordinance, the California Fair Chance Act, and any similar state or local fair chance laws.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Hims & Hers is committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans in our job application procedures. If you need assistance or an accommodation due to a disability, please contact us at accommodations@forhims.com and describe the needed accommodation. Your privacy is important to us, and any information you share will only be used for the legitimate purpose of considering your request for accommodation. Hims & Hers gives consideration to all qualified applicants without regard to any protected status, including disability. Please do not send resumes to this email address.
To learn more about how we collect, use, retain, and disclose Personal Information, please visit our Global Candidate Privacy Statement.