---
title: Manufacturing Compliance Specialist
description: Nitto Denko Corporation is hiring for the Manufacturing Compliance Specialist
  role in Milford, MA. See the full description and apply.
type: job
url: https://www.foundrole.com/jobs/manufacturing-compliance-specialist-at-nitto-denko-corporation-01a13ef4-3eea-7949-bcbc-3b02442f80ab
date: 2026-11-01T03:15:12Z
og_description: Join Nitto Denko Corporation as Manufacturing Compliance Specialist in Milford,
  MA. Pays $77.5K–$94K per year.
og_image: https://www.foundrole.com/og/2ha9xo.png
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  - label: Home
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---

| | |
|---|---|
| **Company** | Nitto Denko Corporation |
| **Location** | Milford, MA |
| **Salary** | $77.5K/yr - $94K/yr |
| **Posted** | Oct 31, 2026 |

## Is this job real?

**Ghost job check:** B · Low risk. Probably a real opening.

## Visa sponsorship

- **H-1B:** Nitto Denko Corporation sponsors H-1B visas. It filed 3 H-1B petitions (FY2025 Q4 – FY2026 Q3).
- **E-Verify:** No E-Verify enrollment on record for Nitto Denko Corporation.

## Pay for similar jobs

Most similar jobs pay $90,000 – $162,000 a year (median $113,000).

## Description

## **About this opportunity :**

The Manufacturing Compliance Specialist position is responsible for supporting all compliance (Quality and Safety) investigations and corrective actions, as well as the origination and revision of quality documentation in support of the Manufacturing group. This person will work with Manufacturing managers, supervisors, and leads to assure the growth and maintenance of a quality and safety compliance culture.

**Key Responsibilities:**

- Facilitate, document, and review compliance related investigations to ensure root causes are identified, corrective actions implemented, and the effectiveness of these corrective actions fulfill regulatory and business requirements.
- Support project team with originating and revising manufacturing related SOPs and batch records.
- Supports audits of all quality and safety compliance systems including safety analysis/risk assessment, 5S, training, documentation, and general manufacturing operations to assure continual compliance.
- Would support on time performance within the department using visual management tools.
- Support training opportunities for manufacturing staff in the areas of quality and safety compliance.
- Provide technical writing support for quality investigations and assure standards for investigational reporting are met.

**Required Skills/Abilities:**

- A BS in a technical discipline is required, Chemistry, Biology, Engineering preferred.
- 3-5 years of experience in a cGMP pharmaceutical manufacturing environment with demonstrate experience writing investigations and other quality documents.
- Experience leading departmental and cross-functional teams through effective peer-to-peer influence is strongly recommended.
- Lean/SS certification is preferred.
- Must have strong technical writing and communication skills.
- Experience leading root cause analysis is strongly recommended.
- Must be experienced with standard Microsoft business applications and proficient with Excel graphing tools. Knowledge of statistical software tools is preferred.

The annualized salary range for this role is $77,500.00 - $94,000.00.
## Skills

- Safety Regulations Compliance
- Peer-To-Peer
- Influencing
- Batch Record Review
- Plant Operations
- Investigation
- Safety Analysis
- Statistical Software
- Microsoft Dynamics 365
- Microsoft Excel
- Graphing
- Risk Management
- Statistical Analysis
- Root Cause Analysis
- Technical Writing
- Pharmaceutical Manufacturing
- Corrective And Preventive Action (Capa)
- Standard Operating Procedures (Sop)
- Communication
- Writing
- Business Requirements

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