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$
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I will provide regulatory affairs, rims and pharma documentation support
Seema J
About this gig
I provide professional regulatory affairs and pharma compliance support backed by 9+ years of experience in pharmaceutical and healthcare projects.
My services include RIMS data enrichment and QC (Veeva Vault), regulatory documentation review, compliance assessment, certification coverage, audit support, and tender bid coordination. I have hands-on experience supporting regulated and semi-regulated markets, including ROW and ASEAN regions.
I work closely with clients to ensure accurate regulatory data, timely delivery, and high-quality documentation while maintaining compliance with GMP, GLP, and global regulatory requirements.
Whether you need help with regulatory data management, audits, certifications, or documentation, I deliver reliable, detail-oriented, and confidential support tailored to your project needs.
Please contact me before placing an order to confirm scope and timelines.
Get to know Seema J
Seema J
REGULATORY AFFAIRS LEAD
- FromIndia
- Member sinceJan 2026
- Avg. response time1 hour
Languages
English
Regulatory Affairs Specialist with 9 years of experience in the pharmaceutical industry, including with a proven track record of supporting global regulatory submissions, tender bid processes, and compliance for both regulated and semi-regulated markets. Adept in leveraging key regulatory tools and platforms such as Veeva Vault, REDS, ORION, CAST, Amplexor, and Darius System to drive submission accuracy and streamline documentation workflows. Demonstrated expertise in: Regulatory planning, authoring, and quality assurance of dossiers, Data collation and quality control.
Other Regulatory Compliance Consulting Services I Offer
FAQ
Q1. What industries do you support?
I support pharmaceutical, biotech, healthcare, and life sciences companies, including generic and branded manufacturers.
Q2. What regulatory services do you provide?
I provide regulatory affairs support, RIMS data enrichment and QC (Veeva Vault), compliance assessment, regulatory documentation review, audit support, certification coverage, and tender bid coordination.
Q3. Which regulatory tools do you work with?
I have hands-on experience with Veeva Vault, CAST, REDS, ORION, Amplexor, and Darius systems.
Q4. Do you support global markets?
Yes. I have experience working with regulated and semi-regulated markets, including ROW, ASEAN, and other international regions.
Q5. Will my data and documents be kept confidential?
Absolutely. All client data, regulatory information, and documents are handled with strict confidentiality.
Q6. What do you deliver at the end of the project?
Depending on the package, you will receive reviewed or enriched data, compliance outputs, and a summary document or report.
Q7. Should I contact you before placing an order?
Yes, I strongly recommend contacting me first to confirm scope, timelines, and package suitability.
