Vrabotuvanje.com - R&D Scientist - Purification and Isolation of Active Pharmaceutical Ingredients (APIs) - Росоман - Синцеритас АД Скопје
Сподели
Tweet
Сподели
Испрати на пријател

R&D Scientist - Purification and Isolation of Active Pharmaceutical Ingredients (APIs)

Росоман

Рок за пријавување:

  • Синцеритас АД Скопје
  • Адреса: Ул.Никола Кљусев бр.11, 1000 Скопје

R&D Scientist - Purification and Isolation of Active Pharmaceutical Ingredients (APIs)

At SINCERITAS, we cultivate and process pharmaceutical-grade cannabis into medicinal products to improve patient health and provide relief. Offering cutting-edge solutions for numerous medical needs, we strive to meet every client’s unique requests by tailor-making each product.
 
We are a team of experienced science professionals that use industry-standard practices in agricultural and pharmaceutical techniques to manufacture high-quality medicinal cannabis products consistently and reliably. Our products are developed to retain all of the plant’s essential components and ensure a maximum medicinal effect, particularly in patients with rare and difficult-to-treat conditions.
 
Through ongoing scientific research and development, we aim to unlock the full therapeutic potential of cannabis, opening the doors to new and revolutionary medical treatments.
 
Sinceritas is made up of talented diverse team of over 60 employees who deliver innovative solutions that add value across a variety of Business Service functions. Our company culture is build on three pillars: Science.Progress.Trust
 
SINCERITAS offers premium workspace at our facility in Rosoman and administrative office in Skopje. 
 
As an R&D Scientist specializing in the purification and isolation of Active Pharmaceutical Ingredients (APIs), you will play a crucial role in the research and development process of pharmaceutical compounds. Your primary responsibility will be to develop, optimize, and implement purification and isolation techniques to ensure the production of high-quality APIs for pharmaceutical applications.

 
Key Responsibilities:
  • Conduct in-depth literature reviews to stay abreast of the latest advancements in purification and isolation techniques.
  • Design and execute experiments to develop novel methods for the purification and isolation of APIs.
  • Collaborate with cross-functional teams to integrate purification processes into the overall drug development strategy.
  • Optimize existing purification processes to improve efficiency, yield, and purity of APIs.
  • Scale-up laboratory processes for potential transfer to manufacturing, ensuring scalability and reproducibility.
  • Utilize a variety of analytical techniques, such as HPLC, GC and mass spectrometry, to characterize and assess the quality of isolated APIs.
  • Collaborate with analytical scientists to develop and implement methods for real-time monitoring of purification processes.
  • Develop and implement quality control measures to ensure the consistent production of APIs meeting regulatory and quality standards.
  • Investigate and address any deviations or discrepancies in the purification process.
  • Maintain detailed and accurate records of experimental procedures, results, and conclusions.
  • Prepare technical reports and documentation for internal and external stakeholders.
  • Stay informed about regulatory guidelines and ensure that all purification and isolation processes comply with relevant regulatory requirements.
  • Ph.D. in Chemistry, Pharmaceutical Sciences, or a related field with a focus on organic synthesis and purification.
  • Proven experience in the purification and isolation of pharmaceutical compounds, preferably with a background in API development.
  • Strong knowledge of chromatography, crystallization, and other purification techniques.
  • Familiarity with analytical techniques used in pharmaceutical research.
  • Excellent problem-solving skills and ability to troubleshoot and optimize processes.
  • Effective communication and collaboration skills.
Preferred Skills:
  • Experience with process scale-up and technology transfer to manufacturing.
  • Familiarity with Good Manufacturing Practices (GMP) and regulatory requirements.
  • Ability to work independently and as part of a multidisciplinary team.
  • Strong project management skills.
What we offer:

By investing in new development capabilities, state-of-the-art manufacturing facility, and partnerships we have the opportunity to shape the future of SINCERITAS and give more patients access to affordable, high-quality medicines - sustainably. Our dynamism and entrepreneurial spirit are driven by an open, collaborative culture, supported by our talented and ambitious colleagues who, in return for the use of their skills, experience an agile and collegial environment with impactful, flexible careers in which diversity is welcome and personal development is encouraged!

In addition to a basic salary in line with market, we offer:

1. Organized transport from Skopje to Rosoman

2. Provided meal for all the employees who are performing their job in Rosoman

3. Collective insurance for all the employees

Additional information: Candidates who meet the above conditions can send their CVs via Fast Apply.

Брза апликација
Испрати на пријател Принтај

СПОРЕДЕТЕ ЈА ВАШАТА ПЛАТА

Просечната плата во категоријата
Фармација и Биотехнологија изнесува 36.814 MKD.

Дознај ја платата за посакуваната позиција според твоите квалификации!

Започни

Vrabotuvanje.com.mk користи колачиња (анг. cookies) за да ви овозможи подобро корисничко искуство. Повеќе информации можете да прочитате овде