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Visual Inspection Production Technician Jobs (NOW HIRING)

AOI

Inspection Shift Engineer (7am-7pm)

Sugar Land, TX · On-site

$66K - $85K/yr

Main tasks include visual inspection production line training for variety of product families ... Technical training for operators and technicians * Regularly and effectively communicate status of ...

Evonik

Visual Inspection Operator

Birmingham, AL · On-site

$16.50 - $21.50/hr

Perform manual visual inspection of the final product. Involves individually manipulating each unit in the lot to inspect against a detailed criteria to pass or reject the unit. * Carry out finished ...

American-Trim

$16/hr

Production Requisition Number : APPLI002264 * Posted : September 8, 2026 * Full-Time * On-site ... This is a light manufacturing position involving hands-on assembly, visual quality inspection and ...

New

Curaleaf

Production Technician

Hammonton, NJ · On-site

$16.50 - $20.50/hr

Title: Production Technician Pay Rate: $ 17.00 per hour Location: Hammonton, NJ Job Type ... Conduct in-process and final quality checks, including testing, visual inspections, and precise ...

Curaleaf

Production Technician

Chambersburg, PA · On-site

$17.25 - $21.50/hr

Production Technician Pay Rate: $ 17.00 to $ 17.50 per hour Location: Chambersburg, PA Job Type ... Conduct in-process and final quality checks, including testing, visual inspections, and precise ...

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Visual Inspection Production Technician information

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How much do visual inspection production technician jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for visual inspection production technician in the United States is $19.23, according to ZipRecruiter salary data. Most workers in this role earn between $16.59 and $20.67 per hour, depending on experience, location, and employer.

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For Visual Inspection Production Technician jobs, the most frequently searched job titles are:

Production Technician I - ILP 1st Shift

Sugar Land, TX • On-site

QuVa Pharma
Pharmaceutical and Medicine Manufacturing • 1 - 5K employees
Learn more about QuVa Pharmaexternal

$15.50 - $19.50/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 23 hours ago

QuVa Pharma rating

7.7

Company rating: 7.7 out of 10

Based on 10 frontline employees who took The Breakroom Quiz

Job description

Our Production Technician I - ILP plays a vital role within our organization. Once you complete our training, your responsibilities will include supporting execution of product visual inspection, labeling and packaging (ILP) operations at the Quva facility in accordance with established processes and procedures. At Quva, you will be an essential part of a mission-driven organization dedicated to expanding critical access to quality, affordable medication and data insights while promoting a culture of innovation, collaboration, and continuous improvement. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US.
This is a full-time role for our 1st shift, working Monday through Friday from 6:00 AM to 2:30 PM CST. This is a set, consistent schedule with minimum overtime requirements and based on site in our Sugar Land location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws.
Watch this video to learn more
What the Production Technician I - ILP Does Each Day:
  • Assists preparation of inspection and packaging room materials supplies
  • Conducts labeling and the processing of production materials as required
  • Daily/ Bi-Weekly/Monthly cleaning of room and equipment and fills out appropriate preventative maintenance forms and checklists in accordance with SOP's
  • Conduct and complete line and room clearances as per established procedures
  • Completes necessary documents for accountability and traceability of products following Good Documentation Practices (GDPs); comply with cGMPs, and company ISO standards
  • Complies with 503B guidelines; cGMPs, standard operating procedures and company policies
  • Performs equipment calibration checks and troubleshoots production equipment as needed
  • Completes documentation of activities in accordance with established procedures
  • Immediately notifies production management of deviations to established processes or procedures
  • Assists other areas as needed (cleaning; non-sterile filling; kitting and preparation operations, etc.)
  • Primary, secondary, and tertiary labeling of products
  • Secondary and final packaging of product
  • Requires visual inspection of product
  • Maintains inspection ready environment and supports internal / external audits

Our Most Successful Production Technician I - ILP:
  • Promotes active listening with team members; Contributes appropriately to conversations; Strong verbal and written communication skills with the ability to work effectively with other departments within the organization and with people at all levels of the organization
  • Understands how various issues affect each other and the outcome of projects; Improves upon existing approaches by seeking opportunities to creatively transform; mechanical aptitude a plus
  • Effectively and productively engages with others and establishes trust, credibility, and confidence with others
  • Listens to internal customers, ensures commitments are met, sets appropriate internal customer expectations
  • Has working knowledge of cGMPs and regulatory requirements as well as all applicable SOPs
  • Follows policies and procedures; completes administrative tasks correctly and on time
  • Approaches others in a tactful manner; reacts well under pressure; treats others with respect and consideration regardless of their status or position; accepts responsibility for own actions; follows through on commitments
  • Has strong attention to detail
  • Is flexible and can adapt to support multiple production areas and shifts as needed

Minimum Requirements for this Role:
  • High school Diploma or GED from recognized institution or organization required
  • Will be required to undergo a color perception exam and must be able to produce a passing test result
  • Will be required to undergo a vision exam and must be able to produce 20/20 vision with or without correction
  • Able to successfully complete a drug and background check
  • 18+ years of age
  • Must be currently authorized to work in the United States on a full-time basis; Quva will not sponsor applicants for work visas

Any of the Following Will Give You an Edge:
  • Pharmaceutical experience

Benefits of Working at Quva:
  • Set, full-time, consistent work schedule
  • Comprehensive health and wellness benefits including medical, dental and vision
  • 401k retirement program with company match
  • 17 paid days off plus 8 paid holidays per year
  • Occasional weekend and overtime opportunities with advance notice
  • National, industry-leading high growth company with future career advancement opportunities

About Quva:
Quva is a national, industry-leading provider of compounded injectable medicines and software solutions that help power the business of hospital and health-system pharmacy. Quva Pharma produces and distributes injectable medicines required by health care providers and critical to patient care. Quva BrightStream partners with health-systems to analyze large amounts of data and through AI and machine learning, develops software solutions that turns the data into insights that are used to better run their pharmacy operation. Quva's overall product and technology offerings help health-systems achieve greater value and deliver the highest-quality patient care.
Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is "at will."
California Consumer Privacy Act (CCPA) Notice for Applicants and Employees
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.

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