We are hiring!!!!! Qualification: M.Sc. in life-science (Biotechnology and Microbiology Preferred). Experience: - 1 to 3 years of experience in Pharmacology and Toxicology (In-Vitro) with OECD GLP , NABL (ISO/IEC 17025:2017). >> Job description: Responsible for Cytotoxicity and Genotoxicity studies and their maintenance. Validated AMES and Cytotoxicity assays for medical devices according to ISO standards, ensuring accuracy and reliability in toxicological testing methodologies To act as a Study Director for in vitro studies as per the requirements of OECD GLP principle and ISO 17025. Should have performed Invivo Micronucleus assay, Ames assay & Chromosomal aberration. Authored comprehensive Standard Operating Procedures (SOPs) for laboratory activities Skills: Assays: AMES- bacterial reverse mutation assay, In vitro and In vivo micronucleus test and biochemistry parameters In vitro and In vivo Chromosome aberration test, Local Lymph Node Assay, Cell Gene Mutation assay Primary Cell lines handled. >> Benefits: Large campus with leave facilities like Casual Leave, Privilege leave, Sick leave School/college fees deduction for employee's staff Yearly Annual Health Check Up Report. Gym facility Hostel and Canteen facility. Employee engagement activities, tours and training and much more. Job Types: Full-time, Permanent Pay: ₹15,000.00 - ₹63,078.48 per month Benefits: Food provided Leave encashment Paid sick time Paid time off Schedule: Morning shift Work Location: In person
Ribosome Research Center is Preclinical Contract Research Organization is hiring, apply today...... Department: Quality Assurance Location - Surat Qualification: M.Sc. in life-science or M. Pharm (Pharmacology Toxicology / Quality Assurance). Experience: 4 to 8 years of experience in OECD GLP & NABL (ISO/IEC 17025:2017) Employee having experience in Toxicology department (study personnel or study director) with OECD GLP experience can also apply. ~ Interested candidate can share cv on 74349 36627 or on hrd@ribosomeresearch.com ~ No. of vacancy: 01 Job description: Should possess experience of QAU as per OECD GLP and NABL (ISO/IEC 17025:2017). Plan and perform study based, process based, facility based inspection. Review of SOP, Change control, Deviation, CAPA etc. Review of computerized system validation documents as per regulatory requirements e.g. 21CFR part 11. Perform vendor audit. Managed regulatory inspections like NGCMA, CDSCO, NABL. Effective in verbal and written communication skills. ~ Interested candidate can share cv on 74349 36627 or on hrd@ribosomeresearch.com ~ Benefits: Girls and Boys Hostel PL,CL and SL Job Type: Full-time Pay: ₹20,000.00 - ₹60,000.00 per year Benefits: Flexible schedule Food provided Health insurance Internet reimbursement Leave encashment Paid time off Provident Fund Schedule: Day shift Morning shift Work Location: In person
We are hiring urgent hiring Assistant Business Manager and Manager for our CRO ⏬⏬⏬⏬ ⟹ Company name: Ribosome Research Center ⟹ Location: Kim Surat Qualification - MBA (Marketing), Immediate joiners preferred Experience: 4 to 10 years working as BDE in Preclinical Research Center (GLP Certified) Salary: No bar for the right candidate. Job description: 1. Developing strategic market positioning and creating market space. 2. Generate new leads as per contract research services & create effective market campaigns in Pre clinical R & D, Pharma R & D, drug testing, toxicology, analytical testing etc. 3. Managing key global strategies and working with research team to develop services of Contract Research Organisation aligning to the needs of OECD GLP compliances along with managing existing businesses and creating long term business opportunities. ---Interested applicants can share cv on 74349 36627 or on [email protected] Salary: Upto 12 LPA Job Type: Full-time Pay: ₹30,000.00 - ₹150,000.00 per month Benefits: Flexible schedule Food provided Health insurance Internet reimbursement Leave encashment Paid time off Provident Fund Schedule: Day shift Morning shift Supplemental Pay: Commission pay Performance bonus Yearly bonus Work Location: In person
We are hiring urgent hiring Assistant Business Manager and Manager for our CRO ⏬⏬⏬⏬ ⟹ Company name: Ribosome Research Center ⟹ Location: Kim Surat Qualification - MBA (Marketing), Immediate joiners preferred Experience: 4 to 10 years working as BDE in Preclinical Research Center (GLP Certified) Salary: No bar for the right candidate. Job description: 1. Developing strategic market positioning and creating market space. 2. Generate new leads as per contract research services & create effective market campaigns in Pre clinical R & D, Pharma R & D, drug testing, toxicology, analytical testing etc. 3. Managing key global strategies and working with research team to develop services of Contract Research Organisation aligning to the needs of OECD GLP compliances along with managing existing businesses and creating long term business opportunities. ---Interested applicants can share cv on 74349 36627 or on hrd@ribosomeresearch.com---- Salary: Upto 12 LPA Job Type: Full-time Pay: ₹30,000.00 - ₹150,000.00 per month Benefits: Flexible schedule Food provided Health insurance Internet reimbursement Leave encashment Paid time off Provident Fund Schedule: Day shift Morning shift Supplemental Pay: Commission pay Performance bonus Yearly bonus Work Location: In person
Job Description: You will be responsible for Cytotoxicity and Genotoxicity studies and their maintenance, including validated AMES and Cytotoxicity assays for medical devices according to ISO standards, ensuring accuracy and reliability in toxicological testing methodologies. You will act as a Study Director for in vitro studies as per the requirements of OECD GLP principle and ISO 17025. Additionally, you should have experience in performing Invivo Micronucleus assay, Ames assay, and Chromosomal aberration. You will be expected to author comprehensive Standard Operating Procedures (SOPs) for laboratory activities. Key Responsibilities: - Conduct Cytotoxicity and Genotoxicity studies - Perform validated AMES and Cytotoxicity assays for medical devices - Act as a Study Director for in vitro studies following OECD GLP and ISO 17025 requirements - Perform Invivo Micronucleus assay, Ames assay, and Chromosomal aberration - Author Standard Operating Procedures (SOPs) for laboratory activities Qualifications Required: - M.Sc. in life-science (Biotechnology and Microbiology Preferred) - 3 to 15 years of experience in Pharmacology and Toxicology (In-Vitro) with OECD GLP, NABL (ISO/IEC 17025:2017) Additional Company Details: The company offers a large campus with leave facilities like Casual Leave, Privilege leave, Sick leave, school/college fees deduction for employee's staff, Yearly Annual Health Check Up Report, Gym facility, Hostel and Canteen facility, Employee engagement activities, tours, training, and more. Work Type: Full-time Benefits: - Flexible schedule - Food provided - Health insurance - Internet reimbursement - Leave encashment - Paid time off - Provident Fund Schedule: - Day shift - Morning shift Performance bonus Work Location: In person,