
Global Pharmaceutical Compliance Expert
2 weeks ago
We are seeking a skilled Regulatory Affairs Specialist to manage the submission and approval process for various pharmaceutical applications on a global scale.
- Manage Manufacturing License Application (MLA) submissions
- Oversee the Technical/Site application process
The ideal candidate will possess strong analytical and problem-solving skills, with the ability to work effectively in a fast-paced environment. Strong communication and project management skills are also essential.
Responsibilities:- Ensure compliance with regulatory requirements for pharmaceutical product development, approval, and marketing
- Collaborate with cross-functional teams to identify and mitigate risks associated with regulatory submissions
- Develop and implement strategies to improve regulatory processes and workflows
- Bachelor's degree in a related field (e.g., life sciences, law)
- Minimum 5 years of experience in regulatory affairs or a related field
- Proven track record of success in managing regulatory submissions and approvals
- Excellent analytical, problem-solving, and communication skills
Our company offers a competitive salary and benefits package, including health insurance, retirement plan, and paid time off.
About Us:Our company is a leading provider of consulting services to the pharmaceutical industry. We are committed to delivering high-quality solutions that meet the needs of our clients.
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