Summer Internship - Regulatory Affairs, Labeling

Hikma Pharmaceuticals USA Inc. • Columbus, OH

1d • $19 • Onsite

About The Position

We are committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds. We are seeking a talented and motivated College Summer Intern for our Regulatory Affairs team at our Columbus, Ohio site. As an Intern, you will earn practical experience as a fully integrated member of our team and participate in meaningful projects that will add value to our organization. In this role, you will provide support to the various Regulatory Affairs groups.

Requirements

• This internship will work 1st Shift hours.
• Regular and predictable onsite attendance and punctuality.
• Must be an Undergraduate, Graduate, or Professional Student in good academic standing.
• Must have completed 12 credit hours within a related major and/or other related coursework.
• Desired competencies include strong communication skills, taking initiative, detail oriented, and good teammate.
• Strong analytical and problem-solving skills (Business & Technical Knowledge)
• Ability to work independently and manage multiple tasks simultaneously.
• Highly motivated and inquisitive with a strong desire to learn.
• Organization skills to manage multiple tasks with strong attention to details.
• Planning and Organizational skills.
• Proficient usage of Microsoft Office applications.
• Strong mathematical, analytical, and problem-solving abilities.
• A positive, self-starting, can-do attitude, and a willingness to jump in to support the team.
• Excellent verbal and written communication skills, ability to communicate in a clear and persuasive manner, and attention to detail.
• Must be legally authorized to work in the United States without restriction, no sponsorship offered at this time.
• Must be willing to submit to a background investigation, including verification of your past employment, criminal history, and educational background.
• Must be willing to take a drug test.
• Must be 18 years of age or older.

Responsibilities

• Evaluates RLD updates and applies necessary revisions to company labeling.
• Works closely with regulatory team to provide regular updates on tasks.
• Assist in updating the comprehensive product list.
• Inputs meta data for products into the RIM system.
• Drafts annual reports for inactive products.
• Prepare redlines for artwork updates.
• Assist the Regulatory Affairs labeling team with daily tasks.
• Perform an audit of the current drug listings on DailyMed to ensure compliance.
• Other duties as assigned.

What This Job Offers

• Career Level: Intern
• Education Level: No Education Listed
• Number of Employees: 5,001-10,000 employees