We use cookies. Find out more about it here. By continuing to browse this site you are agreeing to our use of cookies.
#alert
Back to search results
New

Senior Technician 1, Quality Control

Antares Pharma
tuition reimbursement, 401(k)
United States, Minnesota, Hopkins
12500 Whitewater Drive (Show on map)
Sep 12, 2025

Save time and apply through your LinkedIn account. Click the Apply with LinkedIn button and your LinkedIn profile will be imported into our site.

In order to move forward, you will need to create an account. Your password must be eight characters long, contain at least one special character, one capital letter and a number.

We look forward to discovering your talents.

Welcome to an inspired career.

At Halozyme, we are reinventing the patient experience and building the future of drug delivery. We are passionate about the important work we do and constantly strive to do more. We embrace transformation and work hard to innovate for the future. We do this together, as One Team - we rise by lifting others up and believe in the power of working together for the collective win. That's why we need you-to help us make a significant impact by taking on increasingly complex challenges, leaping beyond the status quo, advancing our mission and making our One Team culture thrive.

How you will make an impact

The Senior Technician 1, Quality Control will provide an independent review of materials and documentation, supplied by both internal manufacturing and external suppliers, to determine material acceptability. This position will also assist Quality Engineers with data gathering/analysis and QMS maintenance.

In this role, you'll have the opportunity to:

  • Perform lot release testing, record data on data sheets and summarize, analyze, and perform basic statistical analysis on results when required.
  • Perform receiving inspection activities on incoming materials which can include confirming specifications, performing visual examination and taking variable measurements, and rejecting and returning unacceptable materials.
  • Provide independent, secondary peer review of fellow Technician's work.
  • Assemble sample product as needed for testing purposes.
  • Document inspection results by completing reports, logs, and inputting data into databases.
  • Monitor incoming product quality and report observations upward to Quality Engineering and/or Quality Management.
  • Maintain measurement equipment in an operable state by following setup procedure and monitoring calibration status.
  • Ability to identify when NCRs/Deviations have occurred and report upward.
  • Participate in Quality System Improvements through the CAPA process as a CAPA contributor.
  • Think critically and proactively suggest activities for continuous improvement as opportunities arise during the course of daily work. Propose procedures modifications as appropriate.
  • Collaborate with engineers regarding lot release and related issues.
  • Collaborate with engineers on developing new and modifying existing lab procedures/methods for inspecting and evaluating product.
  • Facilitate data and information collection for use in monthly/quarterly/annual performance metrics.
  • Develop and lead training exercises commensurate with area(s) of functional expertise.
  • Support internal and external audit activities as assigned by manager.
  • Support Internal Manufacturing activities.
  • Provide leadership/mentorship to other members of the QC team, including training of new team members during onboarding.
  • Comply with all applicable company policies and procedures and maintain current training on these records.
  • Work inside a laboratory environment. Ensure cleanliness of QC areas and properly handle materials.
  • Other activities as assigned by departmental management.

To succeed in this role, you'll need:

  • 2-4 years of experience working in a quality control role with ISO and GMP systems requirements with a high school education (an equivalent combination of experience and education may be considered)
  • Problem-solver with the ability to exercise sound judgment under challenging circumstances.
  • Excellent communication skills with the ability to effectively promote intra-and inter-organizational cooperation.
  • Ability to interface with technical services, R&D, manufacturing, and regulatory affairs to accomplish required tasks.
  • Ability to communicate with co-workers and all levels of management in a professional manner.
  • Familiarity with Microsoft Excel and/or other spreadsheet/database software for compilation/trending of data.
  • Familiarity with Minitab preferred.
  • Knowledge of GxP, 21CFR, ISO, QSR and other applicable Regulations, Standards, Directives and Guidance
  • Possess strong character with self-confidence and integrity necessary to ensure that the patient safety and customer satisfaction are always of utmost importance.
  • Strong background in a manufacturing and operations environment
  • Sound technical background and the ability to educate stakeholders, management and customers pertaining to quality assurance/control principles and techniques.
  • Ability to interface with internal customers at all levels and 3rd-party partners.
  • Technical, equipment, software knowledge necessary

In return, we offer you:

  • Full and comprehensive benefit program, including an Employee Stock Purchase Program and 401(k) matching.
  • Opportunities to grow in a culture that prioritizes learning, development and progression through in-house programs and tuition reimbursement.
  • A collaborative, innovative team that works as one to amplify your impact-on your career, the work you do and patients' lives.

The most likely base pay range for this position is $48K - $80K per year. Several factors, such as experience, tenure, skills, and particular business needs, will determine an individual's exact level of compensation. Base salary is only one element of employee compensation at Halozyme. Total compensation could include bonuses, sales incentives, and equity awards.

Halozyme, Inc. is an Equal Employment Opportunity (EEO) employer. It is the policy of the Company to provide equal employment opportunities to all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information.

Accessibility and Reasonable Accommodations:

Halozyme is committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans during our application process. If you need assistance or accommodation due to a disability, contact Human Resources at hrbox@halozyme.com.

To view all our open positions, please visit our career page. Additionally, our benefit offerings can be found here.

Applied = 0

(web-759df7d4f5-7gbf2)