Job Details

ID #44740929
State Massachusetts
City Norton
Job type Contract
Salary USD US$60 - US$67 per hour + competitive, health benefits, 401K US60 - US67 per hour + competitive health benefits 401K
Source Real Staffing
Showed 2022-08-10
Date 2022-08-10
Deadline 2022-10-09
Category Et cetera
Create resume

Manufacturing Compliance Specialist

Massachusetts, Norton, 02766 Norton USA

Vacancy expired!

Summary of Key Responsibilities: Develop, implement, and manage strong GMP systems for manufacturing operations with adherence to quality standards and applicable guidelines and regulations Partner with technical leadership and cross-functional partners such as Manufacturing, Quality, Engineering, Validation, and Facilities to implement product, process, and raw material improvements. Provide support for Norton manufacturing operations, investigations, continuous improvement projects, and program lifecycle management Drive continuous improvement and operational excellence culture thru self-detecting and self-correcting processes and systems. Ensures timely completion of manufacturing documentation and/or quality systems to achieve disposition requirements. Support training, documentation, change controls, deviation and CAPA activities. Organize and lead ad hoc cross functional teams to manage investigations and implementation of changes Experienced with root cause analysis methodology/tools. Ensure high levels of communication with team, support resources and management regarding issue identification and resolution. Supports the generation, review, and approval of various manufacturing documentation, including procedures, protocols and reports, quality systems, and investigations. Acts as manufacturing subject matter expert for assessments for change controls, validation protocols, and document changes. Provides support to Manufacturing program documentation, including training requirements and methodology, safety requirements, and cost savings initiatives.

Requirements: At least 4 years' experience in a GMP Facilities environment within the biotech or pharmaceutical industries Highly Knowledgeable of quality systems and cGMP regulations Must have excellent interpersonal and customer service skills Excellent written and oral communication skills

EOE Statement: Specialist Staffing Group is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

To find out more about Real please visit

Vacancy expired!

Subscribe Report job