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New · posted Oct 15

Amneal Pharmaceuticals · Pharmaceuticals

Supervisor, Quality Assurance

  • Piscataway, NJ
  • On-site
  • Full-time
  • Manager
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EmploymentFull-time
Deadline

Open until filled

The role

The Supervisor, Quality Assurance, schedules and coordinates daily priorities for incoming raw materials and labeling components, in-process testing, finished product sampling, in-process labeling and packaging operations, sampling and inspection activities on all work shifts.

What you need

3 ways to qualify

  1. Bachelor’s

    + 1 year of experience

    Bachelor’s Degree (BA/BS): Minimum 1 year of pharmaceutical/manufacturing experience, including 1+ year in a supervisory or lead role

  2. or

    Associate

    + 5 years of experience

    Associate Degree (AA/AS): Minimum 5 years of pharmaceutical/manufacturing experience, including 2+ years in a supervisory or lead role

  3. or

    High school

    + 3 years of experience

    High School Diploma or GED: Minimum 3 years of pharmaceutical/manufacturing experience, including 5+ years in a supervisory or lead role

    Specialized Knowledge

    • Knowledge of cGMPs.

    The annual salary for this position ranges from $90,000 to $105,000 annually. In addition, Amneal offers a short-term incentive opportunity, such as a bonus or performance-based award , with this position within the first 12 months. Amneal ranges reflect the Company’s good faith estimate of what Amneal reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, experience, geographic location and other relevant skills.

    At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement. We also promote employee well-being with programs that help you enjoy your career alongside life’s many other commitments and opportunities.

    What you'll do

    1. Responsible for scheduling and coordinating daily priorities for incoming raw material, in-process material, finished product and in-process packaging/labeling operations sampling and inspection activities.
    2. Trains, supervises and evaluates the performance of QA inspectors, QA Specialist and QA Auditors to assure compliance with Standard Operating Procedures (SOPs)/cGMP.
    3. Responsible for final product: Monitors all stages of QA in-process/packaging operations to ensure strict compliance with cGMP/SOPs.
    4. Assists management with the development of new and revised SOPs, executes validation & qualification studies, performs investigations and other assignments as required.
    5. Handles Change Controls, Deviations, Corrective Actions and Preventative Actions (CAPA) through effective quality management tools.
    6. Handles customer complaints to include retrieval of samples, performing applicable tests, preparation of reports and submission before due date.
    7. Monitors and ensures that batch records are audited per manufacturing/packaging/shipping requirements, when required.
    8. Conducts internal audits for compliance with SOP, cGMP & FDA requirements.
    1. Initiates, investigates and completes CAPA for all QA unplanned deviations under the guidance of QA Manager.
    2. Writes, reviews and revises SOPs as directed by QA Manager/Director.
    3. Plans, monitors and supervises cross training of all QA Inspectors.
    4. Monitors absences and prepares Kronos, HR requestions/data change forms for all shift personnel, whenever required.
    5. Reviews performance of all QA Inspectors in the shift as and when directed by HR.

    Pay and benefits

    $90,000 – $105,000 a year

    Employer provided
    How this compares
    • Short-term incentive/bonus opportunity

    • Health and insurance benefits

    • 401(k) matching contribution

    • Employee well-being programs

    Where you'll work

    Piscataway, NJOn-siteOpen in Maps (opens in a new tab)

    More jobs in Piscataway, NJ

    Job intelligence

    The context around this role

    Live data · October 15, 2026

    Salary intelligence

    How the pay compares

    This role's midpoint is 36% below the US median for Quality Assurance roles at this level.

    This roleEmployer provided

    $90,000 to $105,000 a year

    Manager roles in New Jersey6 roles publishing pay

    Middle half $127,125 to $161,875, median $143,750

    Manager roles in the US105 roles publishing pay

    Middle half $126,000 to $167,500, median $153,000
    Annual base pay
    Annual base payLowMedianHigh
    This role$90,000—$105,000
    New Jersey$127,125$143,750$161,875
    All US$126,000$153,000$167,500

    This role: Amneal Pharmaceuticals's own published range. Comparisons: the base pay employers published on open Quality Assurance roles at the same level on Regulatory Jobs, October 15, 2026. Nothing is estimated.

    Career trajectory

    Where this role sits in Quality Assurance

    The general path across 845 open Quality Assurance roles on Regulatory Jobs, with the titles they carry most. Not Amneal's own promotion track.

    1. Earlier

      Associate & Specialist

      Often: Quality Engineer · Quality Technician

      $79K median227 open
    2. One step back

      Senior & Principal

      Often: Quality Engineer · Senior Quality Engineer

      $123K median353 open
    3. This role

      Manager

      Often: Manager, Quality Assurance · Quality Manager

      $153K median136 open
    4. Next step

      Director

      Often: Director, Quality · Associate Director, Clinical Quality Assurance

      $209K median114 open
    5. Later

      VP & Executive

      Often: Vice President, Quality Assurance · AVP

      $302K median15 open

    Skills DNA

    What this role leans on

    How many of the posting's 20 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

    GMP and compliance: 6 linesLab testing and methods: 2 linesDocumentation and SOPs: 7 linesInvestigations and CAPA: 4 linesValidation and qualification: 1 lineRegulatory submissions: 3 linesQuality systems and risk: 1 lineCollaboration and leadership: 4 linesGMPLab testingDocumentationInvestigationsValidationSubmissionsQuality systemsTeamwork
    • Documentation and SOPs7
    • GMP and compliance6
    • Investigations and CAPA4
    • Collaboration and leadership4
    • Regulatory submissions3
    • Lab testing and methods2
    • Validation and qualification1
    • Quality systems and risk1

    Regulatory intelligence

    The rules behind this role

    Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.

    Company hiring pulse

    Amneal on Regulatory Jobs

    14
    Open roles
    10
    Distinct roles
    2
    Locations

    By discipline

    • Quality14 100%

    By level

    • Senior & Principal7 50%
    • Associate & Specialist4 29%
    • Manager2 14%
    See all 14 Amneal roles

    More roles at Amneal

    All 14 Amneal roles

    Similar Quality Assurance roles elsewhere

    Supervisor, Quality Assurance at Amneal

    Open until filled. $90K–$105K a year, employer provided.

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      Supervisor, Quality Assurance at Amneal Pharmaceuticals — Piscataway, NJ | Regulatory Jobs