The Stallion Laboratories Regulatory Affairs Openings and hiring is started now. Interested candidates may send their resumes now to the email address provided below.
About Company:
Stallion Laboratories began its journey in 1988 as a private pharmaceutical formulation manufacturer. Over the years, it has built a remarkable reputation for handling specialized products in formulations. The company boasts a production facility approved by WHO GMP and maintains stringent quality control qualifications adhering to GLP standards. The key to its success stems from a strong belief in fostering creativity and an unwavering commitment to maintaining top-notch work quality.
Stallion Laboratories Regulatory Affairs Openings— Overview:
| Company Name | Stallion Laboratories |
| Post | Sr. Manager / AGM |
| Department | Regulatory Affairs |
| Location | Corporate Office |
| Markets | US, EU, UK, Canada, China, Australia. |
| Salary | Salary is no bar for potential leaders. |
| Last Date | 20th January, 2024 |
| Company Website | stallion labs |
Job Description
Find the required role for the Stallion Laboratories Regulatory Affairs Openings as follows:
- Having good experience in handling the entire regulatory product lifecycle in listed regulated markets.
- Providing White Paper Strategy to CFTs throughout life cycle starting from development, execution, filing to approval followed by commercial launch.
- Make sure that documents like ANDA, ANDS, IDL, and Dossier are made and filed very well and according to all the current rules, which include but are not limited to original filing, deficiency handling, post-approval variation /supplements filing.
- Keeping everyone up to date with all the current rules and giving knowledge about how rules work in our organization.
- Expertise in providing Regulatory strategic solutions based on experience with different regulated Agencies to come out of the box thinking.
- Having good experience working with different clients and other partners on shared projects.
- Being very good at managing projects, coordination, communication, and interpersonal skills.
- Having a sound understanding of Regulatory impact assessment on business continuity and contingency perspective.
- Providing tactical and strategic decisions on managing critical changes during commercial evel to ensure regulatory compliance is maintained.
- Exposure to participating in Regulated Audits is preferred
- Guiding APD, P&D, Sourcing, QA, QC, Mfg, and Other teams on current regulatory requirements and providing technical knowledge on immediate implementation aspects.
- Conducting periodic regulatory and technical training throughout the organization.
How to Send a Resume?
Job Location: 8th Floor, Devpath, B/H Super Mall, Near Lai Bungalow, Navrangpura, Ahmedabad, Gujarat 380009
Please send your CV to: [email protected] and specify the subject line with Dept. Name.