386 Lifestyle Coach jobs in Kenya
Senior Wellness Coach & Lifestyle Consultant
Posted 18 days ago
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Responsibilities:
- Provide one-on-one and group coaching sessions to clients, focusing on physical health, nutrition, mental well-being, and stress management.
- Develop personalized wellness plans tailored to individual client needs, goals, and lifestyle.
- Educate clients on healthy eating habits, exercise routines, sleep hygiene, and mindfulness techniques.
- Monitor client progress, provide ongoing support, and adjust strategies as needed to ensure success.
- Conduct comprehensive wellness assessments and develop detailed action plans.
- Facilitate workshops and webinars on various wellness topics.
- Stay current with the latest research and trends in health, wellness, nutrition, and fitness.
- Maintain accurate and confidential client records.
- Foster a positive and motivating environment for clients, encouraging sustainable lifestyle changes.
- Collaborate with other wellness professionals and healthcare providers when necessary.
- Certification from a recognized coaching program (e.g., ICF ACC/PCC) and/or a degree in Nutrition, Health Sciences, Psychology, or a related field.
- Minimum of 5 years of experience in wellness coaching, health consulting, or a related role.
- In-depth knowledge of nutrition, fitness principles, stress management techniques, and behavioral change strategies.
- Proven ability to develop and implement effective, personalized wellness plans.
- Excellent active listening, empathy, and motivational skills.
- Strong communication and presentation abilities, suitable for remote client interactions.
- Proficiency in using virtual meeting platforms and wellness tracking apps.
- Ability to work independently, manage a client caseload, and maintain excellent organizational skills.
- Commitment to continuous professional development in the wellness field.
- Experience with corporate wellness programs is a plus.
Remote Holistic Wellness Coach & Lifestyle Consultant
Posted 10 days ago
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Qualifications:
- Certification from a reputable holistic health or wellness coaching program.
- Proven experience as a wellness coach, health coach, or lifestyle consultant.
- Strong knowledge of nutrition, fitness, stress management, mindfulness, and other areas of holistic well-being.
- Excellent communication, active listening, and motivational skills.
- Demonstrated ability to develop personalized wellness plans and provide effective coaching support.
- Experience with conducting virtual consultations and using online coaching platforms.
- Empathy, patience, and a genuine passion for helping others improve their health.
- Ability to work independently and manage client schedules effectively in a remote environment.
- Professionalism and commitment to maintaining client confidentiality.
- Knowledge of complementary and alternative therapies is a plus.
Senior Quality Control Analyst - Pharmaceutical Manufacturing
Posted 3 days ago
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Job Description
Responsibilities:
- Develop, validate, and implement analytical test methods for raw materials, in-process samples, and finished products.
- Perform quantitative and qualitative analysis using techniques such as HPLC, GC, spectroscopy, and wet chemistry.
- Review and interpret test results, ensuring compliance with pharmacopoeial standards (e.g., USP, BP, EP) and internal specifications.
- Investigate out-of-specification (OOS) results and out-of-trend (OOT) data, determining root causes and implementing corrective and preventive actions (CAPAs).
- Maintain accurate and complete laboratory records, adhering to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
- Calibrate and maintain laboratory equipment, ensuring proper functioning and calibration status.
- Participate in internal and external audits, providing necessary documentation and support.
- Contribute to the development and improvement of Standard Operating Procedures (SOPs) related to quality control.
- Train and mentor junior analysts on laboratory procedures and techniques.
- Stay updated on relevant regulatory guidelines and industry best practices in pharmaceutical quality control.
- Prepare technical reports and summaries of analytical findings.
Qualifications:
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biochemistry, or a related life science discipline.
- Minimum of 5 years of experience in a Quality Control laboratory within the pharmaceutical industry.
- Extensive hands-on experience with analytical instrumentation (HPLC, GC, UV-Vis, FTIR, etc.).
- Thorough knowledge of GMP, GLP, and relevant regulatory requirements (e.g., FDA, EMA).
- Proven experience in method validation, OOS/OOT investigations, and CAPA management.
- Strong understanding of pharmaceutical product development and manufacturing processes.
- Excellent analytical, problem-solving, and critical thinking skills.
- Meticulous attention to detail and a commitment to data integrity.
- Strong written and verbal communication skills.
- Ability to work independently and manage multiple tasks efficiently in a remote setting.
This is a fully remote position, offering the flexibility to work from your preferred location while contributing to critical pharmaceutical quality assurance. The operational context for this role is tied to the pharmaceutical landscape of Kitale, Trans-Nzoia, KE .
Remote Pharmaceutical Manufacturing Technician Apprentice
Posted 5 days ago
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Job Description
Program Highlights:
- Comprehensive remote training in pharmaceutical manufacturing.
- Exposure to GMP and quality control standards.
- Mentorship from industry experts.
- Development of practical skills in a virtual environment.
- Potential for career advancement.
- High school diploma or equivalent.
- Strong interest in science and manufacturing.
- Excellent learning aptitude and problem-solving skills.
- Reliable internet connection and a suitable remote workspace.
- Good communication and collaboration abilities.
- Must be eligible for apprenticeship programs.
Lead Automation Engineer - Pharmaceutical Manufacturing
Posted 18 days ago
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Job Description
Responsibilities:
- Lead the design, development, and implementation of automation solutions for pharmaceutical manufacturing processes.
- Develop and maintain automation control systems (PLC, SCADA, HMI) for new and existing equipment.
- Ensure all automation systems comply with GxP regulations, FDA, and other relevant industry standards.
- Perform root cause analysis for automation-related issues and implement corrective actions.
- Develop and execute validation protocols (IQ, OQ, PQ) for automation systems.
- Manage automation projects, including scope definition, budgeting, scheduling, and resource allocation.
- Mentor and provide technical guidance to junior automation engineers and technicians.
- Collaborate with engineering, operations, and quality assurance teams to identify automation opportunities and challenges.
- Stay updated on the latest automation technologies, software, and industry best practices.
- Develop and deliver training programs for operators and maintenance personnel on automation systems.
- A Bachelor's degree in Electrical Engineering, Chemical Engineering, Mechanical Engineering, or a related field.
- A Master's degree or Professional Engineering certification is a plus.
- Minimum of 8 years of experience in industrial automation, with at least 3 years in the pharmaceutical or regulated manufacturing industry.
- Proven experience with PLC programming (e.g., Siemens, Rockwell), SCADA systems, and HMIs.
- Strong understanding of GxP validation principles and their application to automation systems.
- Experience in project management methodologies.
- Excellent problem-solving, analytical, and critical thinking skills.
- Strong leadership and team collaboration abilities.
- Exceptional communication and interpersonal skills.
- Ability to work independently and manage complex projects in a remote setting.
- Proficiency in relevant automation software and simulation tools.
Lead Process Chemist - Pharmaceutical Manufacturing
Posted 18 days ago
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Job Description
The ideal candidate will possess a Master's or Ph.D. in Organic Chemistry, Chemical Engineering, or a closely related field, with a minimum of 7 years of progressive experience in process chemistry, preferably within the pharmaceutical or fine chemical industry. A strong understanding of synthetic organic chemistry, reaction kinetics, thermodynamics, and scale-up principles is essential. Experience with process hazard analysis, impurity profiling, and solid-state chemistry will be highly valued. Proficiency in common laboratory techniques and analytical instrumentation (HPLC, GC, NMR, Mass Spectrometry) is required. You should demonstrate exceptional problem-solving abilities, strong leadership qualities, and the capacity to manage multiple projects simultaneously. Excellent communication and interpersonal skills are vital for collaborating with internal stakeholders and external partners. You will be expected to stay abreast of the latest advancements in process chemistry and manufacturing technologies, and to foster a culture of continuous improvement within the team.
This role offers a unique opportunity to influence the development of life-saving medications and contribute to significant advancements in pharmaceutical manufacturing. You will work in a collaborative, research-driven environment, with the flexibility of a fully remote work arrangement. The **Nakuru, Nakuru, KE** location, while not requiring physical presence, aligns with our operational focus, and your remote contributions will be pivotal to our success. If you are a motivated and experienced chemist looking to take on a challenging leadership role with significant impact, we encourage you to apply.
Senior Quality Assurance Manager - Pharmaceutical Manufacturing
Posted 20 days ago
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Lead Process Engineer - Pharmaceutical Manufacturing
Posted 20 days ago
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Senior Operations Manager - Pharmaceutical Manufacturing
Posted 18 days ago
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Principal Process Engineer, Pharmaceutical Manufacturing
Posted 20 days ago
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Key Responsibilities:
- Lead the design, development, and optimization of chemical and pharmaceutical manufacturing processes.
- Develop and execute process validation strategies, ensuring compliance with GMP and regulatory requirements.
- Troubleshoot complex process issues, identify root causes, and implement effective solutions to minimize downtime and improve yield.
- Utilize process simulation and modeling tools to evaluate process alternatives and identify efficiency gains.
- Collaborate with R&D, quality assurance, and engineering teams to ensure seamless technology transfer from lab to commercial scale.
- Develop and implement process control strategies and advanced process analytical technology (PAT).
- Prepare detailed technical documentation, including process flow diagrams, P&IDs, equipment specifications, and validation reports.
- Mentor junior engineers and provide technical leadership on cross-functional project teams.
- Stay abreast of the latest advancements in pharmaceutical manufacturing technologies and regulatory guidelines.
- Conduct process hazard analyses (PHAs) and ensure the safety of all manufacturing operations.
- Ph.D. or Master's degree in Chemical Engineering, Biochemical Engineering, or a closely related field.
- A minimum of 8-10 years of progressive experience in process engineering within the pharmaceutical or biotechnology industry.
- Extensive experience with GMP manufacturing principles and regulatory requirements (FDA, EMA, etc.).
- Proven track record in process design, scale-up, validation, and troubleshooting.
- Expertise in process modeling and simulation software (e.g., Aspen Plus, SuperPro Designer).
- Strong understanding of unit operations relevant to pharmaceutical manufacturing.
- Exceptional analytical, problem-solving, and data interpretation skills.
- Excellent written and verbal communication skills, with the ability to present technical information effectively.
- Demonstrated leadership experience and ability to influence cross-functional teams.
- Ability to thrive in a fast-paced, dynamic, and remote work environment.