Working at Etico
Etico Lifesciences is more than a CDMO; it is a center for scientific excellence. We foster an environment where technical rigor is balanced with an entrepreneurial spirit, allowing our team to solve complex pharmaceutical challenges for global markets.
Whether you are a seasoned scientist or a high-potential graduate, Etico offers the infrastructure and the mentorship required to build a distinguished career in pharmaceutical R&D.
Scientific Integrity
We uphold the highest standards of data integrity and ICH compliance.
Global Exposure
Direct exposure to US, EU, UK, and Australian regulatory markets.
Flat Hierarchy
Open access to leadership and collaborative cross-functional project teams.
Agile R&D
Speed-to-market driven by efficient decision-making and advanced lab tech.
Open Opportunities
Showing 6 PositionsSenior Scientist - Formulation Development
Lead the development of complex Oral Solid Dosages (OSD) and Controlled Release formulations. Manage projects from pre-formulation to pilot-scale tech transfer.
- Expertise in QbD (Quality by Design) principles.
- Experience with US/EU regulatory submissions.
Research Associate - Analytical Development
Execute method validation and stability management for niche generics. High proficiency in HPLC/UPLC and impurity profiling is essential.
- Proficiency in chromatographic software (Empower).
- Strong understanding of ICH stability guidelines.
Executive - R&D Quality Assurance
Review and audit R&D laboratory notebooks, validation protocols, and CMC documentation to ensure data integrity and USFDA compliance.
- Thorough knowledge of GLP and 21 CFR Part 11.
- Experience in auditing analytical data.
Executive - Business Development (CDMO)
Identify and cultivate partnerships with pharmaceutical companies in EU and GCC markets. Support project estimation and client relationship management.
- Strong communication and market research skills.
- Background in Life Sciences or Pharma Management.
Group Leader - Advanced Analytical Services
Oversee multiple analytical project teams. Accountable for method robustness, troubleshooting complex impurities, and final stability reporting for filings.
- Prior experience leading large analytical teams.
- Subject matter expert in LC-MS/MS and method validation.
Technician - Sterile Filling (Parenterals)
Operate sterile filling lines for oncology and non-oncology parenteral products. Ensure strict adherence to aseptic techniques and batch records.
- Experience in Grade A/B cleanroom environments.
- Knowledge of aseptic gowning and sterile procedures.
Benefits & Wellbeing
Mentorship
Work directly with HODs having 16+ years of global pharma experience.
Health Cover
Comprehensive medical insurance for employees and immediate family.
Facility
Work in a high-tech USFDA-registered facility with world-class instrumentation.
Can't find the right role?
We are always looking for driven scientific minds. Send your CV to [email protected]
General Application