Freelance Document Submission Staff

Role & responsibilitiesManage and oversee all production documentation activities for API manufacturing, ensuring compliance with GMP and regulatory standards.Prepare, review, and maintain batch records, SOPs, and production reports, ensuring accuracy and completeness.Coordinate with production, quality, and regulatory teams to ensure smooth documentation...

Regulatory Affairs, Chemistry, Manufacturing and Controls (RA CMC) facilitates product development and global registration by developing and executing regulatory strategies and managing effective regulatory agency interactions for product manufacturing and quality programs throughout product lifecycle. Amgens CMC submission execution team, Regulatory...

Job DescriptionMinimum 2 years of experience in medical transcription and scribing is required.We are looking for a Clinical Documentation Specialist. The ideal candidate will be responsible for creating accurate medical transcription documents from audio recordings, interpreting medical jargon, ensuring documentation quality, and supporting healthcare...

Sr. Associate Regulatory Affairs Career CategoryRegulatory Job Description Job Description: Amgen is a leading human therapeutics company in the biotechnology industry. For more than 40 years, the company has tapped the power of scientific discovery and innovation to advance the practice of medicine. As a Fortune 500 company serving millions of...

Career CategoryRegulatoryJob Description Job Description:Amgen is a leading human therapeutics company in the biotechnology industry.  For more than 40 years, the company has tapped the power of scientific discovery and innovation to advance the practice of medicine.  As a Fortune 500 company serving millions of patients, Amgen continues to be an...

We're Hiring: Green Building Documentation Specialist (2–4 yrs) Looking for a detail-oriented and motivated professional to join our team and support sustainability & certification projects inhashtagRealEstate. Role: Manage and compile documentation for IGBC, GRIHA, LEED, WELL certifications. Collaborate with project teams, consultants & certifying...

Job title: Trainee Junior specialist- Electronic Documentation SpecialistLocation: HyderabadOpella is the self-care challenger with the purest and third-largest portfolio in the Over-The-Counter (OTC) & Vitamins, Minerals & Supplements (VMS) market globally.  Our mission is to bring health in people's hands by making self-care as simple as it should be. For...

What you will doIn this vital role you will Prepare and oversee the preparation of regulatory submission documents that comply with global regulatory standardsWrite or oversee the writing of clinical study reports and Investigator Brochures for products in all phases of clinical development (phase 1 through 4)Write CTD sections including the Summary of...

The Documentation Specialist will be responsible for creating, managing, and maintaining technical documentation related to performance engineering and other non-functional testing processes and systems. This role ensures that all documentation complies with industry regulations, company standards, and supports internal teams by providing clear, accessible...

Freelance Opportunity: On-Premise Infrastructure Setup (Software + Networking)We are looking for an experienced System Administrator / DevOps Engineer to help design, configure, and document a small-scale on-premise compute infrastructure. The goal is to establish a secure, modular, and reliable system for multi-user computational workloads and collaborative...