Job Opening: Apprentice Trainee - Microbiologist (API Industry) Details are Provided below 1. Company: Asence Pharma Pvt 2. Department: Quality Control -Microbiology 3. Location: Ranoli, Vadodara 4. Role Overview: Company is looking for a dedicated and enthusiastic Apprentice Trainee - Microbiologist to join their Quality Control Microbiology team. This role offers a great opportunity to gain hands-on experience in microbial analysis, environmental monitoring, and aseptic techniques in an API manufacturing environment. 5. Eligibility: B.Sc. / M.Sc. in Microbiology or Biotechnology 6. Key Responsibilities: -Perform environmental monitoring (EM) of cleanrooms -Carry out microbiological testing of raw materials, water, and finished products -Maintain proper documentation as per GMP guidelines -Assist in validation and sterility assurance activities -Adhere to safety and quality procedures 7. How to Apply: Send your updated resume to hr@asence.com with the subj...
Aurigene Oncology Requires Research Associate/ Scientist - Cell and Gene Therapy ( Manufacturing)
Details are provided below
1. Post - Research Associate/ Scientist - Cell and Gene Therapy ( Manufacturing)
2. Qualification- M. Sc. ( Specialization in any Life Sciences)
3. Experience- 2 to 13 Years
4. Mandatory Skills- Candidate should be from vaccine or biosimilar background, experience in Upstream Manufacturing, handling Mammalian Cell Culture, QMS.
5. Roles and Responsibilities
a. Responsible for optimization of CAR cells Manufacturing processes using normal human or patient derived primary blood components following ethical practices and QMS as per GMP guidelines.
b. Actively engage in the manufacture of CAR - T cell Therapy products by diligently prioritizing the lab functions to meet critical deadlines
c. Establish and carefully execute transductions by viral vector and non viral vector based approaches, activation and expansion of immune cells ( T cells , NK cells etc ) isolated from Clinical specimens without compromising sterility and Quality parameters as per the guidelines and defined criteria by maintaining highest standards and assist in technical transfer and core R and D activities.
d. To review and document SOPs , Protocols and reports pertaining to the program requirements.
e. Work with vendors to evaluate raw materials and consumables for compatibility with the manufacturing processes.
f. Prepare for and participate in the compliance monitoring inspections/regulatory agency interactions.
6. How to Apply- Interested Candidates may share their resume to gayathiri_n@aurigene.com
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