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Required Drug Substance (Viral Vaccine Experience)- Upstream /Downstream Processing of viral vaccines

Job Opportunity - Drug Substance (Viral Vaccine Experience) Bharat Biotech is looking for skilled professionals with hands-on experience in Drug Substance manufacturing for Viral Vaccines. Details are provided below  1. Location: Hyderabad 2. Experience: 2-6 Years 3. Key Skills & Experience Required a. Experience in Upstream /Downstream Processing of viral vaccines b. Operation and handling of bioreactors, fermenters, centrifuges, chromatography systems, filtration units c.  Knowledge of cell culture techniques (mammalian/avian cell lines)  d. Familiarity with aseptic techniques, GMP documentation, batch records e. Understanding of process optimization, scale-up, and technology transfer f. Exposure to in-process testing, troubleshooting, and equipment cleaning/sterilization g. Ability to work in a regulated, fast-paced manufacturing environment 4. How to Apply Interested candidates can share their updated CV to kiran4978@bharatbiotech.com Mention subject line as: Appl...
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Require Clinical Research Coordinators (CRC) at Cytenet Life Sciences For Multiple Locations

Hiring: Clinical Research Coordinators (CRC) at  Cytenet Life Sciences 

Details are provided Below

Number of Vacancies: 03 (one each in Mumbai, Pune, and Jaipur)

Key Responsibilities:
1. Coordinate and oversee the day-to-day operations of clinical trials.
2. Assist PI in recruiting, screening, and enrolling study participants.
3. Assist PI in obtaining informed consent from study participants.
4. Schedule and conduct participant visits and follow-ups.
5. Collect and record accurate data in accordance with the study protocol.
6. Ensure compliance with study protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements.
7. Maintain study documentation and ensure data integrity.
8. Assist in preparing EC dossier for EC submission.
9. Communicate effectively with study CRO, sponsors, investigators, EC and other stakeholders.
10 Monitor study progress and report any issues or deviations from the protocol to the study sponsor or principal investigator.
11. Participate in site visits, audits, and inspections as required.
12. Provide regular updates and reports to the clinical research team and management.

Qualifications & Experience:
1. Master's/Bachelor's degree in life sciences, healthcare, or a related field.
2. Previous experience in clinical research or a related field is preferred
(0.5-1.5 years).
3. Knowledge of GCP, ICH guidelines, and regulatory requirements.
4. Strong organizational and time-management skills.
5. Excellent communication and interpersonal skills.
6. Attention to detail and ability to maintain accurate records.
7. Proficiency in Microsoft Office and clinical trial management software.

Working Conditions:
1. Full-time position.
2. Based in Mumbai, Pune, or Jaipur, with potential travel to clinical sites.
3. Participation in ongoing training and development programs.

How to Apply:
Submit your resume and cover letter to info@cytenet.org. 
Be sure to include city name (Mumbai, Pune, or Jaipur) in the subject line of your email.

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