QA Inspector

Noven

Miami, FLOn-siteFull time
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Location
Miami, FL
Work style
On-site
Job type
Full time
Posted
Oct 11
8 days ago
Career path

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About the company

Noven

Pharmaceuticals · 201 to 500 employees

Noven on LinkedIn

What you'll do

  • Inspect and approve rooms, lines, equipment, components, in-process items, and finished products; perform sampling and testing.
  • Monitor manufacturing compliance, document and review records, report deviations, and perform QA transactions.

What you need

  • Requires a high school diploma or equivalent, basic computer and math skills, and the ability to read, write, communicate, and follow instructions in English.
  • Must be able to stand for more than one hour at a time and occasionally lift and carry up to 50 pounds.
  • Education: a high school diploma

Key skills

Basic computer skillsBasic math skillsread, write, communicatefollow instructions

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See full description on company page, apply now

Read the full posting here
QA Inspector Job Locations US-FL-Miami Job ID 2026-2702 # of Openings 1 Type Full Time Regular Category Quality FLSA Status Non-Exempt Work Shift 1st Shift Overview Perform Quality Assurance tasks such as sampling, inspections, and tests designed to ensure manufactured products are in compliance with internal SOP’s, Safety initiatives, Company policies, FDA and DEA regulations. Document all work performed, ensuring accuracy and thoroughness. Inform management of any deviations from established standards/procedures. Responsibilities Inspect and approve rooms, lines and equipment prior to use by manufacturing and R&D personnel. Approve components for in-process operations. Monitor manufacturing areas for compliance with internal SOPs, cGMPs and FDA/DEA regulations. Document all work activity in appropriate batch records, forms, and logs to ensure accuracy and compliance. Sample in-process items, and finished products. Perform required inspections and testing of in-process items and finished products. Process and distribute samples to different departments. Review records for cGMP compliance for accuracy and thoroughness. Inform management of problems, failures and deviations from established internal and regulatory standards. Apply disposition sticker to components and in-process materials. Issue QA Alerts whenever any questionable component, in-process material or product is identified at any stage of production or storage. Perform swab and Rodac Plate sampling as required. Perform transactions in JD Edwards when required. Qualifications Competencies: Education / Experience: High school diploma or equivalent. Basic computer skills required. Basic math skills required (i.e., calculating %, addition, subtraction, multiplication, division). Ability to read, write, communicate and follow instructions (verbal and written) in English is required. Judgment / Decision Making: Duties performed within a framework of departmental or functional protocol requiring a minimal degree of original thinking. Work Environment: Majority of time spent at manufacturing plants with exposure to machines with moving parts airborne products, chemicals, muscular strain and noise. Carelessness could result in minor injury. May handle or work with laminates and units containing a Class II Controlled Substance. Ability to work second and third shift, if required. Ability to work Saturday and/or Sunday, if required. Physical Demands: Regularly required to stand for more than one hour at a time; occasionally lifts and carries objects weighing up to 50 pounds. Visual acuity and manual dexterity required to proofread documents and operate computer. Options Apply for this job online Apply Share Email this job to a friend Refer Sorry the Share function is not working properly at this moment. Please refresh the page and try again later. Share on your newsfeed Noven Pharmaceuticals, Inc is an E-Verify employer. Application FAQs Software Powered by ICIMS www.icims.com

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