Qureos Mentor

EVA Pharma

<div>Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are committed to fostering a supportive and innovative environment for our team members.
Job Summary
We are seeking a passionate and talented Employee Experience Specialist to join our dynamic team. 
The ideal candidate will contribute to our mission of enhancing human health and well-being by ensuring an exceptional employee journey across all countries &mdash; from on-boarding to off-boarding &mdash; helping us maintain a positive, engaging, and high-performing workplace culture.
 
 
Key Responsibilities:<ul><li>
Design and implement initiatives that enhance the employee lifecycle across countries (on-boarding, retention and off-boarding).</li></ul>
<ul><li>Monitor and analyze employee satisfaction and engagement metrics, and propose continuous improvement strategies.</li></ul>
<ul><li>Support the planning and execution of culture-building activities and employee events.
</li></ul><ul><li>Create personalized on-boarding experiences to ensure smooth transitions for new hires.</li></ul><ul><li>
Develop and implement initiatives that promote diversity, equity, and inclusion.</li></ul><ul><li>
Ensure a positive off-boarding process and gather exit insights for continuous improvement.</li></ul> 

Requirements 
<ul><li>Bachelor&rsquo;s degree in Human Resources, Business Administration, Psychology, or a related field.</li></ul>
<ul><li>1-2 years of experience in on-boarding, or a similar HR role.</li></ul>
<ul><li>Strong interpersonal and communication skills, with a focus on empathy and problem-solving.</li></ul>
<ul><li>Demonstrated ability to handle sensitive employee matters with confidentiality and professionalism.</li></ul>
<ul><li>Experience using HR systems and engagement survey tools is a plus.</li></ul>
<ul><li>Creative thinker with a proactive and collaborative mindset.</li></ul> 

Benefits</div>

Employee Experience Specialist

<div>EVA Pharma is hiring Analytical Expert within R&amp;D Analytical Development. The role drives analytical method development, characterisation, validation, stability, and technology transfer across small molecules, Peptides, DPI, Gels, and Patches &mdash; while coaching and coordinating a team of analysts.
Key responsibiities:
Method Development &amp; Validation<ul><li>
Develop and optimise HPLC/UPLC and dissolution methods for DS and DP across Solids, Steriles, Peptides, DPI, Gels, and Patches</li><li>
Execute full ICH Q2(R1) method validation: specificity, linearity, accuracy, precision, robustness, LOD/LOQ</li><li>
Author validation reports and maintain lifecycle documentation</li></ul>
Characterisation &amp; Impurity Profiling<ul><li>
Lead physicochemical and solid-state characterisation of DS and DP</li><li>
Conduct impurity profiling and forced degradation studies per ICH Q3A/Q3B</li><li>
Characterise Gel and Patch products: rheology, release rate, drug migration, adhesion, and skin permeation</li><li>
Profile Peptide APIs: identity, purity, aggregation, and sequence confirmation</li><li>
Support DPI characterisation: APSD via NGI/ACI, fine particle fraction, and blend uniformity</li></ul>
Bioassay Support<ul><li>
Support development and qualification of bioassay methods for potency and biological activity</li><li>
Review and interpret bioassay data for batch release and stability</li></ul>
Stability Studies<ul><li>
Design and execute stability protocols per ICH Q1A&ndash;Q1F for DS and DP</li><li>
Manage sampling plans, testing schedules, and data interpretation</li><li>
Author shelf-life justification and stability summary reports for regulatory submissions</li></ul>
Dissolution Method Development<ul><li>
Develop biorelevant dissolution methods for solid, semi-solid (Gels), and transdermal (Patch) dosage forms</li><li>
Validate dissolution methods and establish acceptance criteria per ICH/Ph. Eur./USP</li></ul>
Tech Transfer to QC<ul><li>
Lead method transfer from R&amp;D to QC: protocols, acceptance criteria, and inter-lab comparison</li><li>
Train QC analysts on transferred methods and resolve technical discrepancies</li><li>
Ensure complete, audit-ready transfer documentation</li></ul>
Regulatory &amp; CMC Support<ul><li>
Contribute analytical sections to CTAs, MAAs, DMFs, and local dossiers</li><li>
Prepare validation reports, specifications, and analytical justifications</li><li>
Support regulatory queries and inspection readiness</li></ul>
Team Leadership &amp; Mentorship<ul><li>
Lead and coordinate a team of 3&ndash;6 analysts: priorities, workload, and delivery tracking</li><li>
Coach analysts through technical challenges, troubleshooting, and data interpretation</li><li>
Conduct regular feedback sessions and support individual development plans</li><li>
Foster scientific discipline, accuracy, and continuous improvement</li></ul> 

Requirements 
Education:
Master's or PhD in Pharmaceutical Sciences, Analytical Chemistry, or related field
Overall Experience:
 10&ndash;15 years in pharmaceutical analytical development (R&amp;D environment), 2&ndash;3 years leading or coordinating a small analytical team or project group
Technical skills:<ul><li>
HPLC/UPLC method development and validation &mdash; minimum 6&ndash;8 years hands-on</li><li>
Impurity profiling, forced degradation, and stability studies per ICH guidelines</li><li>
Dissolution method development for solid, semi-solid (Gel), and transdermal (Patch) dosage forms</li><li>
Gel and Patch characterisation: release rate, rheology, adhesion, permeation</li><li>
Peptide or DPI analytical characterisation</li><li>
Analytical method transfer to QC with formal transfer protocols</li><li>
Contribution to at least one regulatory dossier (CTA, MAA, or local registration)</li></ul></div>

Senior R&D Manager

<div>Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for Health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are committed to fostering a supportive and innovative environment for our team members.
Job Summary:
We are seeking a passionate and talented Graphic Designer to join our dynamic team.
The ideal candidate will contribute to our mission of enhancing human health and well-being, ensuring that we meet the highest standards of excellence in our industry. 
Key Responsibilities<ul><li>
Develop packaging artwork in line with brand guidelines, customer requirements, and regulatory standards.</li><li>
Prepare print-ready files and support quality checks before production.</li><li>
Collaborate with Marketing, Communications, and Commercial teams to translate business needs into visual designs.</li><li>
Maintain organized artwork files, databases, and documentation.</li><li>
Ensure timely delivery of multiple design tasks while maintaining accuracy and attention to detail.</li></ul> 

Requirements 
<ul><li>
Bachelor&rsquo;s degree in Graphic Design, Applied Arts, or a related field.</li><li>
0&ndash;2 years of experience (fresh graduates with strong portfolios are encouraged to apply).</li><li>
Proficiency in Adobe Creative Suite (Illustrator, Photoshop, InDesign).</li><li>
Basic understanding of layout, color, and printing processes.</li><li>
Strong attention to detail, creativity, and time management skills.</li><li>
Good command of English.</li></ul></div>

Graphic Designer

<div>Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for Health and well-being as a fundamental human right. Recognized and certified as a best place to work, we provide a dynamic and supportive work environment that encourages innovation and professional growth.
Job Summary:
We are looking for a skilled HSE Professional to Provides a safe and healthy industrial environment for employees, products, and the community by developing and managing effective HSE policies and strategies aligned with Eva Pharma's vision, while ensuring efficient team performance and successful implementation.
Key Responsibilities:<ul><li>
Facilitate implementation of HSE policies and programs while ensuring compliance with legal requirements and internal procedures.
</li><li>Oversee safety work permits before operations and monitor environmental measurements (noise, light, energy, etc.).
</li><li>Establish internal audits and self-inspection programs, follow up on findings, and implement corrective actions.
</li><li>Maintain and update emergency plans, conduct drills, and lead investigations of incidents to identify root causes and preventive actions.
</li><li>Train employees on HSE practices, manage PPE and first aid readiness, and ensure contractors comply with all HSE requirements.</li></ul> 

Requirements 
<ul><li>
Bachelor degree of Engineering, Science, or Pharmacy.</li></ul><ul><li>
4&ndash;6 years of experience in HSE management.
</li><li>Strong knowledge of HSE laws, regulations, and safety systems.
</li><li>Experience in risk assessment, audits, and incident investigation.</li><li>
Preferably in 10th of Ramadan Zone.</li></ul></div>

HSE Professional

<div>Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for Health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are committed to fostering a supportive and innovative environment for our team members. 
Job Summary
We are seeking a passionate and talented Medical Science Liaison to join our dynamic team.
The ideal candidate will contribute to our mission of enhancing human health and well-being, ensuring that we meet the highest standards of excellence in our industry.
Key Responsibilities<ul><li>
Ability to analyze, interpret, and synthesize complex clinical data, study design, and statistical analysis into actionable insights.</li><li>
Skills in mapping, segmenting, and conducting peer-to-peer discussions with Key Opinion Leaders (KOLs) and healthcare providers (HCPs).</li><li>
Proficiency in translating scientific information into engaging, scientifically accurate, and balanced presentations.</li></ul> 

Requirements 
<ul><li>
Medical degree or relevant scientific background in life sciences.</li><li>
 2-3 years of experience in the pharmaceutical industry or a related field, with minimum 1 year of experience in medical affairs; Cardiovascular, Diabetes or Obesity related experience is a plus.</li></ul></div>

Medical Science Liaison