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...
medONE Pharma Solutions
Requires Clinical Process Associate
medONE is seeking a motivated and detail-oriented Clinical Process Associate to contribute to the success of company's clinical trials. If you're passionate about advancing medical research and thrive in a fast-paced environment, and want to hear from you!
As a Clinical Process Associate, you will play a crucial role in supporting the efficient and accurate execution of clinical trials.
You will be responsible for a variety of administrative and operational tasks, ensuring compliance with regulatory guidelines and internal SOPs.
Responsibilities:
-Assist with the preparation, review, and maintenance of clinical trial documentation (e.g., study protocols, informed consent forms, regulatory submissions).
- Maintain and update clinical trial databases and tracking systems.
-Coordinate and track the shipment and receipt of clinical trial supplies.
-Assist with the scheduling and coordination of site visits and meetings.
-Support the preparation of study-related reports and presentations.
-Ensure adherence to Good Clinical Practice (GCP) guidelines and company SOPs..
-Communicate effectively with internal and external stakeholders.
-Assist with the management of Investigator Site Files (ISFs) and Trial Master Files (TMFs).
-Assist with the preparation of audit and inspection readiness activities.
Qualifications:
-Bachelor's degree in a life science or related field.
-Minimum of 1 year of experience in a clinical research setting.
-Strong understanding of GCP guidelines and regulatory requirements.
-Excellent organizational and time management skills.
-Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
-Strong attention to detail and accuracy.
-Excellent communication and interpersonal skills.
-Ability to work independently and as part of a team.
-Experience with electronic data capture (EDC) systems (preferred).
Benefits:
-Opportunities for professional growth and development.
-Collaborative and supportive work environment.
-Chance to contribute to cutting-edge medical research.
Mail your resumes to: rashioffice54@gmail.com/jobs@moplindia.com
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