42 Government Regulations jobs in Kenya

Company Description

Welcome to Techwise Managed Services Limited – your partner in secure, innovative, and successful business operations. As a leading Managed Service Provider (MSP), we deliver cutting-edge IT and security solutions that drive efficiency, protection, and business growth. Our certified professionals ensure seamless operations, robust security, and scalable technology to keep you ahead in the digital age. With a customer-centric approach and 24/7 support, we empower businesses with technology solutions that enhance performance, resilience, and success.

Job Responsibilities

* Working with Windows Server

* Working with Active Directory Domain Controllers (Design, Deploy and Migration/Upgrade AD's)

* Backup and recovery of AD / Exchange, maintenance, performance, and security monitoring.

* Managing DNS, DHCP, IIS, DFS, RAS, VPN

* Group Policy Administration

* Working with Server Hardware/Software issues and providing Remote support (Phone, Email and Chat)

* Working with Printers and Scanners

* Working with End User support (Desktop Support)

* Working with Windows 8, Windows 10 & MAC Desktop environment

* Working with Monitoring System and Antivirus software Management.

* Monitor and respond quickly and effectively to requests received through the IT helpdesk

* Working with Cluster and Load Balance technologies

* Working with VMWare ESX / vSphere & Microsoft HyperV

* Participate in meetings and conference calls related to support Proactively identify process improvements and Handling customer escalations.

* Working with SAN / NAS devices

*Create and update documentation for IT administrators and personnel

* Perform other tasks as assigned.

Recommended Software Skills for this position (installing, configuring, and troubleshooting)

* Microsoft Server 2012 R2, 2016 & 2019

* Microsoft Active Directory

* VMWare ESX / ESXi

* Microsoft Office applications, Outlook, Excel, Word, Visio

* Office 365 Administration

* Good Understanding on Cloud Technologies (Azure/AWS)

Required Skills

* Strong Knowledge and Remote Support

* TCP/IP network routing, communications ports (port-forwarding), and configuring hardware firewall rules

* Must have had lead role in design and implementation of Active Directory systems

*3-5years of Experience as a System Administrator

* Strong written communication and documentation skills

* Domain-name registration and modification, authoritative DNS host changes

* DNS record types, modifying records and migrating domains and/or DNS hosts

* Configuring and troubleshooting network printing and scanning via TCP/IP

* Understanding and developing strategies for data protection via data backups and business-continuance planning for disaster-recovery situations

* Working with technical-support services to develop solutions to problems with various products' support departments, including ISPs and hardware & software manufacturers

* Ability to learn new technologies and run training secession.

* Must have reliable transportation, Internet access from home and be on call for issues after hours.

* Willing to work in 24*7 Shift

* Strong Analytical Skills

* Strong Communication Skills

* Must have exp to work with US/UK clients

*Willing to work in Night shifts

Company Description

Welcome to Techwise Managed Services Limited – your partner in secure, innovative, and successful business operations. As a leading Managed Service Provider (MSP), we deliver cutting-edge IT and security solutions that drive efficiency, protection, and business growth. Our certified professionals ensure seamless operations, robust security, and scalable technology to keep you ahead in the digital age. With a customer-centric approach and 24/7 support, we empower businesses with technology solutions that enhance performance, resilience, and success.

Role Description

This is a full-time, on-site role as a Digital Marketing Officer located in Nairobi County, Kenya. As the Digital Marketing Officer, you will be responsible for developing and implementing digital marketing strategies to improve brand awareness and increase sales. You will also work with the marketing team to create and manage content for digital platforms, analyze customer data to improve marketing campaigns, and manage social media channels.

Responsibilities

· Assist in the formulation of strategies to build a lasting digital connection with consumers

· Plan and monitor the ongoing company presence on social media (Twitter, Facebook etc.)

· Launch optimized online adverts through Google Adwords, Facebook etc. to increase company and brand awareness

· Be actively involved in SEO efforts (keyword, image optimization etc.)

· Prepare online newsletters and promotional emails and organize their distribution through various channels

· Provide creative ideas for content marketing and update website

· Collaborate with designers to improve user experience

· Measure performance of digital marketing efforts using a variety of Web analytics tools (Google Analytics, WebTrends etc.)

· Acquire insight in online marketing trends and keep strategies up-to-date

· Maintain partnerships with media agencies and vendors

Requirements

· Proven experience as Digital Marketing Executive or similar role

· Excellent understanding of digital marketing concepts and best practices

· Experience with B2C social media, Google Adwords and email campaigns and SEO/SEM like
SEMrush
.

· Working knowledge of ad serving tools (e.g., DART, Atlas)
and marketing automation platforms (e.g., Mailchimp, Klaviyo, HubSpot

· Perfect knowledge of web analytics tools (e.g. Google Analytics, NetInsight, WebTrends etc.)

· Skills and experience in creative content writing

· Analytical mindset and critical thinking

· Excellent communication and interpersonal skills

. Bachelors Degree in Business, Marketing or Related

. 3-5 years of Experience in Digital Marketing

Company Description

At COREVIX, we are committed to redefining the aesthetics industry across East Africa by enhancing access to the world's finest beauty and wellness innovations. Through a network of premium medical spas and a portfolio of high-quality consumables, we deliver cutting-edge treatments, advanced technology, and expert-driven solutions. Guided by excellence, innovation, and a customer-centric approach, we strive to inspire confidence, transform lives, and shape the future of aesthetics in the region.

Role Description

This is a full-time on-site role for a Regulatory Affairs Specialist located in Nairobi County, Kenya. The Regulatory Affairs Specialist will be responsible for preparing and submitting regulatory documents, ensuring compliance with regulatory requirements, managing regulatory submissions, and staying up-to-date with regulatory affairs. The Specialist will also liaise with different departments to ensure all regulatory documentation is accurate and meets relevant standards.

Qualifications

• Experience with Regulatory Documentation and Regulatory Submissions
• Knowledge of Regulatory Compliance, Regulatory Requirements, and Regulatory Affairs
• Strong attention to detail and excellent organizational skills
• Ability to work collaboratively and communicate effectively with cross-functional teams
• Bachelor's degree in a relevant field such as Life Sciences, Pharmacy, or Chemistry
• At least 2 years of experience in regulatory affairs or a related field
• Proficiency with regulatory software and data management systems
• Fluency in English and Swahili would be an advantage

• Prepare, review, and submit regulatory dossiers for new product registrations and variations.
• Monitor and interpret evolving regulatory requirements in relevant markets.
• Liaise with regulatory agencies to facilitate product approvals and address inquiries.
• Develop and maintain regulatory strategies for product lifecycle management.
• Ensure compliance with local and international pharmaceutical regulations, including Good Manufacturing Practices (GMP) and Good Clinical Practices (GCP).
• Collaborate with R&D, Quality Assurance, and Marketing departments to ensure regulatory requirements are integrated into product development and commercialization processes.
• Provide regulatory guidance and support to cross-functional teams.
• Maintain accurate and up-to-date regulatory documentation and databases.
• Conduct regulatory assessments for new product development projects and line extensions.
• Manage post-approval regulatory activities, including annual reports and labeling updates.
• Participate in regulatory inspections and audits.

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science discipline. A Master's degree is a plus.
• Minimum of 4 years of experience in regulatory affairs within the pharmaceutical industry.
• Solid understanding of pharmaceutical regulatory frameworks in key markets (e.g., KEBS, EMA, FDA).
• Experience in preparing and submitting Common Technical Document (CTD) modules.
• Excellent knowledge of drug development processes and product lifecycle management.
• Strong analytical, problem-solving, and critical thinking skills.
• Exceptional written and verbal communication skills, with the ability to clearly articulate complex regulatory information.
• Proficiency in regulatory information management systems.
• Ability to work independently and collaboratively in a team environment.
• High level of accuracy and meticulous attention to detail.
• Adaptability to changing regulatory landscapes and business priorities.

• Develop and implement regulatory strategies for new product registrations and post-approval changes.
• Prepare, review, and submit high-quality regulatory dossiers to health authorities in accordance with applicable guidelines (e.g., ICH, WHO).
• Serve as the primary point of contact for regulatory agencies, responding to queries and facilitating communication.
• Monitor changes in the regulatory landscape and assess their impact on the company's products and strategies.
• Ensure compliance with all relevant pharmaceutical regulations, guidelines, and company policies.
• Collaborate closely with cross-functional teams, including R&D, quality assurance, manufacturing, and marketing, to ensure alignment on regulatory matters.
• Manage the regulatory review and approval process for labeling, promotional materials, and advertising.
• Provide regulatory guidance and training to internal stakeholders.
• Maintain regulatory documentation and databases.
• Participate in regulatory intelligence activities and competitor analysis.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field.
• Minimum of 6 years of experience in pharmaceutical regulatory affairs.
• Proven experience in preparing and submitting regulatory dossiers for various types of medicinal products.
• In-depth knowledge of global pharmaceutical regulations and guidelines.
• Excellent understanding of drug development processes and lifecycle management.
• Strong analytical and problem-solving skills.
• Exceptional written and verbal communication skills, with meticulous attention to detail.
• Ability to work independently, manage multiple priorities, and meet tight deadlines in a remote setting.
• Proficiency in regulatory information management systems is a plus.
• Must be legally authorized to work in Kenya.

• Develop and implement global regulatory strategies for product development and lifecycle management.
• Manage the preparation, review, and submission of regulatory filings (e.g., INDs, NDAs, MAAs, variations) to health authorities worldwide.
• Serve as the primary regulatory contact for assigned projects, providing expert guidance and strategic input to cross-functional teams.
• Interpret and apply complex global regulatory requirements, guidelines, and policies.
• Conduct regulatory intelligence activities to monitor changes in the regulatory landscape and assess their impact.
• Lead regulatory agency interactions, including pre-submission meetings and responses to agency queries.
• Ensure compliance with all relevant regulations, including GMP, GCP, and GLP.
• Review and approve labeling, promotional materials, and other regulated product information.
• Develop and maintain strong relationships with key health authorities and external stakeholders.
• Mentor and guide junior regulatory affairs professionals.

• Bachelor's degree in Pharmacy, Life Sciences, or a related scientific discipline. Advanced degree (M.S., Ph.D., Pharm.D.) is highly preferred.
• 8+ years of progressive experience in pharmaceutical regulatory affairs.
• Demonstrated success in preparing and submitting major regulatory filings (e.g., NDAs, MAAs) and achieving approvals.
• In-depth knowledge of global regulatory requirements (e.g., FDA, EMA, ICH guidelines).
• Strong understanding of drug development processes, from preclinical through commercialization.
• Excellent analytical, strategic thinking, and problem-solving skills.
• Exceptional written and verbal communication and presentation skills, with the ability to clearly articulate complex regulatory issues.
• Proven ability to manage multiple projects simultaneously and work effectively under pressure.
• Strong leadership and team collaboration skills, with experience working in a remote environment.
• Detail-oriented with a high level of accuracy and compliance.