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Laboratory Specialist– Pharma
About IMCD
IMCD is a leading global distributor and formulator of specialty chemicals and ingredients. An entrepreneurial group founded IMCD in 1995 in the Netherlands. Our vision to transform the distribution industry by continuously adding value to the supply chain through expertise and innovation is what still drives us today. Today, we have operations in over 50 countries, where we successfully combine local knowledge with global expertise to obtain sustainable results. IMCD is a strong, innovative business partner and accelerator of solutions for suppliers and producers of consumer, industrial and durable goods in diverse business sectors. Our commercial excellence and solid operations structure facilitate healthy growth.
We are looking for an experienced Laboratory Specialist for our soon-to-be-opened Pharma Technical Centre in Istanbul-Ümraniye, which will serve as the EMEA Technical Centre.
Job Description
The Laboratory Specialist will be responsible for conducting analytical tests, ensuring laboratory compliance with Good Laboratory Practices (GLP), and supporting technical service activities within the Pharma Technical Centre (PTC). This role involves working closely with the Laboratory Manager and internal stakeholders to deliver high-quality analytical results and technical support to customers and suppliers.
Key Responsibilities
Analytical Testing and Reporting
Perform analytical tests (e.g., HPLC, dissolution, pH, viscosity, etc.) according to established methods and procedures.
Ensure accuracy, repeatability, and reliability of test results.
Document all analytical results following IMCD’s quality and data integrity standards.
Support troubleshooting and data interpretation activities in coordination with senior technical staff.
Laboratory Operations
Maintain laboratory equipment and ensure calibration and preventive maintenance are performed on time.
Manage sample handling, inventory, and lab consumables.
Follow all safety and quality protocols in line with IMCD’s Good Laboratory Practices (GLP).
Collaboration and Support
Work closely with the Laboratory Manager and sales teams to support customer projects and supplier requests.
Participate in internal projects related to method validation, analytical support, or product evaluation.
Continuous Improvement
Support the implementation of Electronic Laboratory Notebook (ELN) tools and other digital systems.
Contribute to continuous improvement initiatives in laboratory processes and safety practices.
Competencies
Attention to Detail
Analytical Thinking
Communication and Teamwork
Quality and Laboratory Management
Time Management
Continuous Improvement Mindset
Required Education and Experience
Bachelor’s or Master’s degree in Chemistry, Pharmaceutical Sciences, or related field.
Minimum 3 years of analytical laboratory experience in the pharmaceutical or related industry.
Hands-on experience with analytical instruments (e.g., HPLC, UV, dissolution, etc.).
Strong knowledge of laboratory safety and GLP principles.
Good command of English (both written and spoken).
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