Jobs at Sage Grey Technologies Limited

Summary

• The Video Editor will be a key member of the Marketing & Growth team, responsible for conceptualizing, editing, and optimizing video assets across all company channels including social media, website, YouTube, paid advertising, events, and internal communications.

Responsibilities

• Edit and produce high-quality short-form and long-form videos from raw footage.
• Create trending, platform-optimized content (Instagram Reels, TikTok, YouTube Shorts, LinkedIn, etc.).
• Apply motion graphics, animations, text overlays, transitions, color grading, and sound design.
• Add subtitles/captions in English and any required local languages.
• Ensure 100% adherence to brand guidelines and visual identity.
• Optimize videos for different platforms (aspect ratio, length, resolution, file size).
• Work closely with Digital Marketing Officer, social media/Community Manager, and Graphic Designers on campaign deliverables.
• Shoot occasional simple videos or BTS footage when required.
• Maintain organized project files and asset library.
• Stay updated with video trends, editing techniques, and platform best practices.
• Support live events and real-time video editing when needed.

Deliverables

• Weekly content as scheduled in the marketing calendar.
• Campaign videos, product explainers, testimonials, ads, and event highlights.
• Multiple versions of videos for different platforms.
• Proper archiving and handover of all project files.

Qualifications

• Interested candidates should possess a Bachelor’s Degree with 2 - 3 years experience.

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Job Summary

• Adverse Drug Reaction (ADR) Monitoring: Collect, assess, document, and report adverse drug reactions and other safety-related information associated with pharmaceutical products.
• Case Processing and Safety Reporting: Review individual case safety reports (ICSRs), ensure accurate data entry, and submit reports to regulatory authorities within required timelines.
• Drug Safety Surveillance: Monitor safety signals, analyze trends in drug-related risks, and contribute to risk-benefit evaluations for medicines.
• Regulatory Compliance Ensure pharmacovigilance activities comply with local and international regulations and guidelines such as those from the World Health Organization, U.S. Food and Drug Administration, or European Medicines Agency.
• Preparation of Safety Documentation: Assist in preparing periodic safety update reports (PSURs), risk management plans (RMPs), standard operating procedures (SOPs), and other pharmacovigilance documents.

Requirements

• Candidates should possess an HND / B.Sc Degree with 1 - 2 years work experience.