GHS Report

Technical Author

Role Title : Technical Author
Reports to Role (Title) : Turkey Toxicology Team Member
Location : Turkey
Scope :

Technical writer in Turkish with experience in at least two of the following areas: chemistry, biology, ecotoxicology, toxicology. Turkish citizenship and excellent fluency in both English and Turkish is required.

Position Details

Global Product Compliance (GPC) specializes in Global Regulatory Compliance Solutions across sectors globally. SSS Europe (renamed GPC Europe w.e.f 6th May 2020), a familiar name in chemical regulatory and compliance services now formally belongs under the umbrella of GPC Holding Sweden. Since 2008, we have emerged as one of the leading names among Global Regulatory Compliance service providers with Representation services in Europe, Asia and Middle East for respective chemical regulations. Today, our Turkish branch (Global Regulatory Compliance Danışmanlık Ltd. Şti.) serves more than 300 companies globally for Turkey’s chemical regulatory compliance.


Technical Writer with an MSc degree in a scientific field

Desired profile:

Technical writer with experience in at least two of the following areas: chemistry, biology, ecotoxicology, toxicology.

Understanding of Chemical Risk / Safety Assessment is desirable.

Experience with the Regulatory Compliance would be an advantage.

Good writing skills is a must.

Good attention to details is a must

Fluency in written and spoken English is a must.

Native level of Turkish is required.

Turkish citizenship is required.

Job Description / Responsibilities:

GPC specializes also in KKDIK(Kimyasalların Kaydı, Değerlendirmesi, İzni ve Kısıtlanması) regulation and KKDIK requires substances imported or manufactured yearly above 1 tone to be registered. For registration, registrants have to submit physicochemical, ecotoxicological, toxicological data depending on the tonnage of the registration dossier.

Therefore, the work involves desktop research and analysis of technical literature, review & summarization of scientific literature in context of toxicological impacts of chemicals, management and monitoring of pre-clinical studies with CROs (GLP Labs); interpretation of pre-clinical study results, and summarization of them. It is good to mention you have read and understood the description clearly in your application. The work requires outstanding technical knowledge of both languages as well as fluent communication skills with team members from different countries.

Please apply for this position with CV and cover letter. Both needs to be in English.