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Manufacturing Compliance Specialist

Nitto Denko Corp.
Posted 7 days ago, valid for 20 days
Location

Milford, MA, US

Salary

$77,500 - $94,000 per year

Contract type

Full Time

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Sonic Summary

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  • The Manufacturing Compliance Specialist role focuses on supporting compliance investigations and corrective actions within the Manufacturing group.
  • Candidates are required to have a BS in a technical discipline and 3-5 years of experience in a cGMP pharmaceutical manufacturing environment.
  • Key responsibilities include facilitating compliance investigations, supporting the revision of manufacturing SOPs, and conducting audits of quality and safety compliance systems.
  • The position also involves providing training for manufacturing staff and offering technical writing support for quality investigations.
  • The annual salary for this position ranges from $77,500.00 to $94,000.00.

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.




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