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Director, Quality Management

Amneal · Piscataway, NJ

Apply on Amneal ↗
Level
Director+
Team
Quality
Base pay
$200k–$245k
Degree
Required
Experience asked
15+ years
Industry
Pharma & life sciences
Posted
Today

The role in 30 seconds

A director-level quality role at Amneal (pharma & life sciences) in Piscataway, NJ. In addition, Amneal offers a short-term incentive opportunity, such as a bonus or performance-based award as well as a long-term incentive award, such as restricted stock units, with this position within the first 12 months.

They ask for
15+ years · degree required
Tools it names
FDA / GMP, Internal audits
Base pay
$200k–$245k

Read from the posting. The full description is below.

From the plant jobs report · week of November 9, 2026

Quality Engineer roles in New Jersey: typical posted base $114k–$155k. This one lists $200k–$245k.

Median of the low and high ends of 13 live postings that list pay, out of 23 quality engineer openings in New Jersey, read from manufacturers' own careers sites.

New Jersey plant jobs report →Pay by team and state →What moves pay →

How this role compares

Against 22 other live quality postings in New Jersey.

Base pay
About 73% above similar roles

Typical $110k–$147k, from 11 postings that list pay.

Experience asked
More than usual (15+ vs 8+)

Similar roles usually ask 8+ years.

Skills these teams ask for most

  • Root cause 70%
  • Six Sigma 39%
  • Supplier quality 35%
  • New product launch 30%
  • AS9100 30%
  • ✓ Internal audits 26%

✓ = this posting asks for it too. % = share of similar postings that mention it.

It asks for 15+ years. If you're close, apply anyway: requirements are a wish list. Talk to someone doing this work there first.

At a glance

Promotion path mentioned

Pulled from the posting text. If it's not listed here, the posting didn't say.

How to get in at this plant

Five moves over a week or two. The first one takes ten minutes.

  1. 1

    Pick 2–3 people on the Quality team at Amneal

    Engineers who joined in the last year or two reply the most. Use the team search on this page to find them.

  2. 2

    Send a short, curious note

    One real question about their work. No favors yet. Each person gets a different note, written for this role.

  3. 3

    Turn a reply into a short call

    Questions worth asking about this team:

    • What does a normal week look like on your team?
    • Which standards drive the work here: ISO 13485, IATF 16949, AS9100?
    • How much of the job is customer complaints versus prevention?
    • How did you land the job? What stood out in your interviews?
  4. 4

    Apply with someone vouching for you

    If the call went well, ask whether they’d pass your résumé to the hiring manager. Send your résumé link, apply that day, and let them know.

  5. 5

    Bring proof to the interview

    One page of before-and-after numbers from projects you led: scrap, OEE, cycle time, cost. Plant managers hire on results.

This plant: Amneal in Piscataway

5 other open roles at this site.

Full description from AmnealAs posted on their careers site.Show

Essential Functions

  • ◆Lead network wide regulatory commitments monitoring and implementation of associated corrective and preventive actions (CAPAs). Identify compliance risks and implement corrective and preventive actions.
  • ◆Support external audits and inspections from regulatory agencies. Co-ordinate with site leaders in addressing inspection findings including draft response.
  • ◆Implement quality system compliance intelligence enabling proactive monitoring of changes in the worldwide drug, biologics, device regulations and guidance.
  • ◆Review of changes in regulations, gap assessment, development of action plan, and implementation. Interpret and communicate regulatory

requirements

to internal stakeholders.

  • ✓Participate in internal audits to ensure compliance with GMP, GCP, GLP, and other applicable standards. Identify potential non-compliances and suggest mitigation.
  • ✓Analyze current industry compliance trends and Amneal sites’ compliance ratings to establish compliance risks.

This position requires 30-40% travel both domestic and international.

Education

  • ✓Bachelors Degree (BA/BS) Chemistry, biology, Pharmacy, engineering or other technical fields - Required
  • ✓Master Degree (MS/MA) Chemistry, biology, Pharmacy, engineering or other technical fields - Preferred

Experience

  • ✓15 years or more in QA, QC, Compliance in pharmaceutical manufacturing company
  • ✓5 years or more in Working experience with USFDA
Show full description ↓

Description

The Director, Quality Management is responsible for standardization and proactive compliance of Amneal's Quality Management System (QMS) with the worldwide drug, biologics and combination products regulations and standards. This role is responsible for compliance monitoring, compliance risk identification, quality plan for new requirements, site inspection readiness, and regulatory authority (FDA, …) inspection support.

Specialized Knowledge

  • •Extensive experience in regulatory quality systems and compliance strategy.
  • •Leadership of global compliance programs and teams.
  • •Strong background in interacting with regulatory agencies.
  • •Proficient level knowledge of international regulation and standards (e.g., ICH, FDA, EMA).
  • •Strong attention to detail and organizational 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.

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