Biocon Biologics Released Job Openings On 04/03/2022.Biocon Biologics is a globally recognized, innovation-led organization that is enabling access to high quality, advanced therapies for diseases that are chronic, where medical needs are largely unmet and treatment costs are high.
Vacancy Details:
Biocon Biologics Recruiting B.Pharma,M.sc,B.Tech Candidates with 00 – 15 Years of Experience for DEPUTY MANAGER/SENIOR EXECUTIVE/EXECUTIVE/TERRITORY BUSINESS MANAGER/SENIOR SCIENTIST/ASSOCIATE Position.
Important Details :
- Location :India
- No of Vacancies:Not Disclosed by Recruiter
- Details of Salary: Not Disclosed by Recruiter
- Opening date for online Application:04/03/2022
- Mode of application :Online
- How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps
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Job Description/Skills Required
TERRITORY BUSINESS MANAGER
Required Education Qualification:Â MBA
Required Experience:Â 4 – 6 years
EXECUTIVE
Shift execution for downstream operations.
Educational Qualifications
Required Education Qualification:Â B.Tech
Required Experience:Â 0 – 3 years
ASSOCIATE SCIENTIFIC MANAGER I
The candidate will work in biosimilar monoclonal antibody based bioassay development. , qualification and transfer to QC.
The following technical / functional skills are required for this position
1. Use of flow cytometry
2. Cell based and cell free assays
3. SPR techniques
4. Handling of primary and immortalized cells
5. Statistical analysis using software like Graph Pad Prism 7, PLA 3.0, softmax Pro, JMP-SAS.
Key Responsibilities
The candidate will design, perform, analyze and troubleshoot experiments for bioassay development for Biologics product development with minimal help.
• The candidate will be involved in intellectual contribution in developing bioassays for multiple type of diseases
• He/She will be managing junior level scientists and take quality systems and laboratory related responsibilities
SENIOR EXECUTIVE
- Responsible for preparation of marketing applications and post approval variation (life cycle management) applications for biosimilar products.
- Plan and author development of high quality regulatory documents, including briefing documents, CTAs, IND / IMPD, MAA / BLA, post-approval variation applications and responses to questions for products in compliance with approved filing plans, timelines, and regulatory requirements
- Active participation in implementation of regulatory strategies for registrations of biosimilar products in ICH regions
- Coordination of activities and deliverables provided by other cross-functional teams to support the development, approval, and post approval life cycle management of biosimilar products
- Collaboration with partners to develop and execute global regulatory activities
- Partner with regulatory team members to research and communicate relevant regulatory information regarding biosimilar products
- Active involvement in identifying process needs to meet internal challenges
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