Manufacturing Compliance Specialist

Nitto Denko Corp.

$77K — $94K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • BS in a technical discipline (Chemistry, Biology, Engineering preferred)
  • 3-5 years of experience in cGMP pharmaceutical manufacturing
  • Proficient in technical writing and communication
  • Experience leading cross-functional teams
  • Lean/SS certification preferred
  • Familiar with Microsoft applications and Excel graphing tools
  • Experience with root cause analysis.

Responsibilities

  • Facilitate and document compliance investigations to identify root causes
  • Support project teams in creating and updating SOPs and batch records
  • Conduct audits of quality and safety compliance systems
  • Enhance department performance through visual management tools
  • Train manufacturing staff on quality and safety compliance
  • Provide technical writing support for quality investigations

Benefits

  • Supportive manufacturing compliance culture
  • Opportunity to influence and lead cross-functional teams
  • Engagement with safety and quality across operations
  • Scope for continuous learning in compliance-related areas
  • Professional growth in a regulated environment
Full Job Description
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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