Global Regulatory Affairs (CMC) Manager

A Few Words About Us
Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Client: Direct Client

Location: Lexington, MA

Job Title: Global Regulatory Affairs (CMC) Manager

Duration: 5 Months + (Possible Extension)

Summary 

Under the direction of the Director of Regulatory Affairs direct and manage Regulatory Affairs activities for developing global CMC strategies across product life cycles & execution in North America. Provide collaborative support for execution of global strategies to other regions (EU & International). Manage submissions and interactions with the FDA and Health Canada for CMC issues. Provide support to other HA interactions as required. 

Job Function and Description: 

• Provide regulatory support, guidance and expertise to internal groups such as product development, QA, QC and manufacturing teams to ensure that all applicable regulatory requirements are considered and appropriately incorporated into development programs and that products are developed and manufactured in compliance with appropriate regulations and guidelines so that they be studied and marketed as planned. 

• Manage preparation of US and Canada applications in a timely manner to meet corporate objectives. 

• Collaborate with EU & International regulatory colleagues to ensure global perspective and provide support in the preparation of EU and International regulatory documentation in a timely manner to meet corporate objectives. 

• Develop global CMC regulatory strategy and manage regulatory activities and timelines for one or more investigational and marketed products 

• Collaborate with EU & International regulatory colleagues in development of global CMC regulatory strategies. 

• Lead the preparation and filing of CMC sections of regulatory submissions and interactions with regulatory agencies. 

• Review and approve technical documentation including technology transfer protocols, validation protocols, technical reports, manufacturing and labeling information to assure conformance with regulations; and regulatory guidelines.

• Provide CMC regulatory guidance to project / product teams. 

• Manage regulatory assessment and guidance on product compliance topics including change controls, deviations, and GMP investigations.

Education & Experience:

• B.A. / B.A./ M.S. / Ph.D. in biochemistry, chemistry, biology or related pharmaceutical field. Minimum of 4 years experience in pharmaceutical product development including significant experience in CMC regulatory affairs with a strong biologics background or equivalent. 

• Experience in directing interactions with regulatory authorities desired.

• Knowledgeable in ICH and FDA guidelines relevant to CMC aspects of product development and maintenance. 

• Significant coordination with cross-functional teams internally and regulatory authorities externally.

Thanks!!!

Warm Regards,

Amrit Singh

Clinical Recruiter

Integrated Resources, Inc.

IT REHAB CLINICAL NURSING

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