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...
Job Opening: Microbiologist (8-12 Years) – Pharmaceutical Industry
Company is seeking a highly skilled and experienced Microbiologist with 8-12 years of experience in the pharmaceutical industry to join our team. If you have a strong background in microbiological testing, quality control, and regulatory compliance, inviting you to apply for this exciting opportunity.
Details are provided below
1. Position: Team Leader/Assistant Manager2. Experience: 8-12 Years
3. Industry: Pharmaceutical C.R.O.
4. Location: Bommasandra industrial area phase 4 Bangalore.
5. Job Type: Full-Time
6. Key Responsibilities:
- Conduct microbiological testing and analysis of raw materials, in-process materials, and finished products to ensure compliance with industry standards.
- Perform environmental monitoring, microbial identification, and validation of cleaning processes.
- Supervise microbiology laboratory operations, including training and mentoring junior team members.
- Develop and implement microbiological protocols, procedures, and investigations in compliance with GMP (Good Manufacturing Practice) guidelines.
- Ensure compliance with regulatory requirements, including FDA, EMA, and other relevant standards.
- Collaborate with quality assurance and other departments to investigate microbial contamination issues and implement corrective actions.
- Prepare detailed reports and documentation for audits, inspections, and regulatory submissions.
- Oversee the validation and calibration of microbiological equipment and ensure proper maintenance.
- Manage microbiological data analysis and ensure accurate record-keeping of test results.
Master’s degree in Microbiology.
8. Experience-
- 8-12 years of experience in microbiology within the pharmaceutical industry.
- In-depth knowledge of microbiological techniques, laboratory practices, and regulatory requirements.
- Strong understanding of GMP, GLP (Good Laboratory Practice), and industry-specific standards.
- Proven ability to lead teams and manage projects in a laboratory setting.
- Excellent communication, organizational, and problem-solving skills.
- Ability to work under pressure and meet deadlines while ensuring the highest standards of quality.
Please send your resume to hrd@stabicon.com
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