R&D Senior Formulation Development Specialist İş İlanı
İşveren Hakkında
QUALIFICATIONS AND JOB DESCRIPTION
Pharmactive Pharmaceuticals, established in 2010 with the understanding of "How Happy is the One Who Offers a Cure" is one of the largest generic pharmaceutical companies in our country and continues to bring hope to the patients in Turkey and throughout the world.
We believe that our team is the most valued resource for our success and we can build a better future together. We invite you to be a part of this team in Pharmactive R&D Directorate as R&D Senior Formulation Development Specialist.
Would you like to be a member of this team that is shaping the future?
QUALIFICATIONS AND SKILLS
· Bachelor’s degree in Chemistry, Chemical Engineering or Pharmacy
· At least 2-5 years of experience in new product formulation development studies within the scope of R&D in the pharmaceutical industry (Prefered)
· Full knowledge of GMP and GLP regulations
· Experience in developing products for EU and US markets and well-versed in EU and US regulations (Prefered)
· Full knowledge of and experience in the use of Lab Scale and pilot production equipment
· Experience in risk-based product evaluation
· Excellent command of English (Prefered)
· High proficiency in Microsoft Office applications
· Strong communications skills and good at teamwork
· Ambitious attitude for continious learning and development and for taking initiative
· Personal skills of innovative, solution oriented and result oriented team player
· Located in/ able to locate in Çorlu, Çerkezköy, Silivri, Büyükçekmece, Beylikdüzü (Prefered)
· No military obligation for male candidates
JOB DESCRIPTION
· Performing all formulation or formulation laboratory studies of products that are decided to be developed
· Completing trial and scale-up pilot production formulation studies
· Taking role in technology transfer process
· Accompanying the first commercial productions of the products
· Taking role in developing new products for domestic and international markets
· Carrying out product improvement works
· Preparation and implementation of related procedures within the department
· Following up laws and regulations, changes, dynamics and innovations in pharma industry locally and globally
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