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Takeda Pharmaceutical
LEXINGTON, MA | Full Time
$129k-171k (estimate)
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Integrated Resources Inc
Lexington, MA | Full Time
$141k-187k (estimate)
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Integrated Resources Inc
Lexington, MA | Full Time
$141k-187k (estimate)
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Integrated Resources Inc
Lexington, MA | Full Time
$141k-187k (estimate)
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Manager Regulatory Affairs-CMC
$141k-187k (estimate)
Full Time 3 Months Ago
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Integrated Resources Inc is Hiring a Manager Regulatory Affairs-CMC Near Lexington, MA

Company DescriptionIntegrated 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.Job DescriptionJob Title: Manager Regulatory Affairs-CMCLocation: Lexington, MA Duration: 4 months (Possibility of extension) Business Function: R&D Department Name: Global Regulatory Affairs Primary Role:Under the general direction of the CMC Regulatory Affairs team, develop a Core Dossier for Module 2.3 and Module 3 CTD sections for a marketed product, and leverage the Core Dossier documents to support Marketing Authorization Applications for international regions. Manage preparation of Core Dossier and CMC components for international marketing applications in a timely manner to meet corporate objectives.Responsibilities:50% of the time develops global CMC Core Dossier for Module 2.3 and Module 3 CTD sections50% of the time prepares CMC components of new Marketing Authorization Applications for international countries EDUCATION & EXPERIENCE Requirements:Bachelor’s degree in pharmacy, biochemistry, chemistry, biology or related pharmaceutical field.Minimum of 5 years of related experience within a pharmaceutical company, CRO or similar organization and with minimum of 2 years International/Global CMC regulatory experience in biologics/small molecule drug development and registration activities.Key Skills and Competencies:Knowledgeable in ICH guidelines, Latin American CMC and core dossier requirementEnsures timely delivery of high quality regulatory submissionsMust be highly organized, committed to excellence, and possess both determination and attention to detail. Additional InformationWe do have referral bonus of $500 per candidate, if you refer any of your friends or colleague who are looking out for the same job.Thanks & Regards,Seema ChawhanClinical RecruiterIntegrated Resources, Inc.IT Life Sciences Allied Healthcare CROCertified MBE |GSA - Schedule 66 I GSA - Schedule 621IDIRECT # - 732-844-8724LinkedIn: https://in.linkedin.com/in/seemachawhanGold Seal JCAHO Certified ™ for Health Care Staffing“INC 5000’s FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)

Job Summary

JOB TYPE

Full Time

SALARY

$141k-187k (estimate)

POST DATE

03/17/2024

EXPIRATION DATE

06/12/2024

HEADQUARTERS

BONITA SPRINGS, FL

SIZE

50 - 100

FOUNDED

2014

REVENUE

$10M - $50M

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