O2h Discovery- Video Requirement Drive for Chemistry -R&D On 10th July’ 2021
•Responsible to perform routine synthesis. (mg to gram scale ) & work independently under the guidance of the leader.
•Independently support the scientific team with instrumentation and equipment operation and maintenance.
•Able to understand & interpret various instruments like NMR, Mass, HPLC.
•Instrument purification like Combiflash, big columns, column packing. Deciding the mobile phase for purification.
•Independently handling all types of glassware assembly arrangement, reaction reagent charging, maintaining temperature, nitrogen, etc.
•Should be able to understand the written instruction from the scientist including patents and reprints where procedure highlighted by scientists.
•To train and support the team members.
•Meticulous Documentation & proper data management.
•To maintain the record book of the work done like purification or reaction.
•Based on shortlisting we will share an interview call letter to the candidates.
•Minimum of 1 year to 6 years of experience working into the relevant industry.
•Strong organizational, project management and problem-solving skills with impeccable
•Exceptional interpersonal skills.
•Friendly and professional demeanor.
•Ability to write repots and prepare spreadsheets and presentations.
•Excellent organizational skills write an ability to think proactively and prioritize work.
•Proactive, highly motivated with a ”can-do” attitude.
•Strong and accurate attention to detail.
For More Details and Apply for this position, Please visit –https://lnkd.in/eG-uQUA
Mr. Shiv Kumar is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 14 years of rich experience in pharmaceutical field.
During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube