Regulatory affairs Specialist @ Saraca Solutions

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Regulatory affairs Specialist

Saraca Solutions
8 - 12 years
Hyderabad
27 days ago
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Job Description

Good understanding for regulations and policies issued by India, US FDA and EU, and ability to interpret international regulatory requirements.
Excellent written, organizational, and communication skills is required, and have a flexible

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RA role in medical device,US FDA,EU
Bachelor degree in Medical,Mechanical,Electric Life Science/other healthcare related majors
8yrs exp for RA role in medical device/pharmaceutical industry

Job Classification

Industry: Engineering & Construction
Functional Area / Department: Legal & Regulatory
Role Category: Corporate Affairs
Role: Regulatory Affairs Compliance
Employement Type: Full time

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Company: Saraca Solutions
Location(s): Hyderabad

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Keyskills: pharmaceutical usfda regulatory ra regulatory affairs ectd fda drug safety anda documentation ent pharmacovigilance regulatory requirements ich ctd clinical research quality assurance qms regulations drug regulatory affairs clinical trials

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Your name (*)

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Preferred City (* max. 2 w/comma)

Designation / Expected Role

Current / Recent Company (*)

Experience (*)

Expected Salary (*)

Desired Industry (*):

Functional area / Department (*):

Enter Skills (key skills, subjects, technologies & roles to use in search)

Write briefly about yourself, your experience and education (*)

Attach ResumeMax 2.38 MB (RTF, PDF, DOC, DOCX formats only parsed)

Please, check the file size and type.

Add social media [ + ]

Create password

I agree with website service terms and conditions

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Saraca Solutions

SARACA is a global IT consulting and services company with Fortune 500 customers. 95% of our customers are from USA with 99% recurring business. We have expertise in software development and testing with core focus on niche technologies

Regulatory affairs Specialist @ Saraca Solutions

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