Regulatory Affairs Intern

Job Description

JOB DESCRIPTION

• Gives support for the preparation of all regulatory and GMP files,
• Responsible for translation and filing of the related parts of the regulatory and GMP submission dossiers,
• Gives support to RA senior specialists & specialists and RA manager on her/his daily regulatory tasks with regard to filing, achieving, tracking, documenting, etc.
• Gives support to the daily business activities of the units. 

QUALIFICATIONS

• 4th/5th years students or graduates from Pharmacy Faculties,
• Able to work full-time during summer,
• Good command of written and spoken English is preferred,
• Good command of MS Office applications,
• Self-motivated with good communication skills,
• Willingness to work with high result orientation,
• Ability to multi-task and work in a fast-paced environment,
• Strong in analytical and interpersonal skills.

Current Employees apply HERE

Current Contingent Workers apply HERE

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Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company.  No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. 

Employee Status:

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Shift:

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Hazardous Material(s):

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