Exciting opportunities await as Aurigene Pharmaceutical Services, a leading CDMO in biologics, is expanding! We’re seeking talented professionals with 3 to 8 years of experience to join our innovative teams. If you’re passionate about advancing healthcare through cutting-edge biologics, this is your chance to make an impact!
Job Details
| Field | Details |
|---|---|
| Job Title | Upstream R&D, Downstream R&D, Formulations R&D, Cell Line Development, Upstream Manufacturing, Downstream Manufacturing, Quality Assurance |
| Company | Aurigene Pharmaceutical Services |
| Job Type | Full-Time |
| Location | Multiple locations (Hyderabad, Bengaluru, or other sites; to be confirmed) |
| Department | Biologics R&D, Manufacturing, Quality Assurance |
| Experience | 3–8 Years |
Job Description
Upstream R&D
- Qualifications: Relevant degree in biotechnology, biochemistry, or related fields
- Experience: 3–8 years in upstream process development for biologics
- Vacancies: Multiple
Responsibilities
- Develop and optimize cell culture processes for biologics production
- Conduct experiments to enhance yield and productivity
- Support scale-up activities for clinical and commercial manufacturing
Required Skills
- Expertise in bioreactor operations and cell culture techniques
- Knowledge of cGMP and bioprocess optimization
- Analytical and problem-solving skills
Downstream R&D
- Qualifications: Relevant degree in biotechnology, chemical engineering, or related fields
- Experience: 3–8 years in downstream process development
- Vacancies: Multiple
Responsibilities
- Design and optimize purification processes for biologics
- Perform chromatography, filtration, and ultrafiltration techniques
- Support technology transfer to manufacturing
Required Skills
- Proficiency in downstream purification technologies
- Understanding of cGMP and regulatory requirements
- Strong documentation and data analysis skills
Formulations R&D
- Qualifications: Relevant degree in pharmacy, chemistry, or related fields
- Experience: 3–8 years in biologics formulation development
- Vacancies: Multiple
Responsibilities
- Develop stable formulations for biologics (e.g., mAbs, proteins)
- Conduct stability and compatibility studies
- Support clinical supply manufacturing
Required Skills
- Expertise in biologics formulation and analytical methods
- Knowledge of regulatory guidelines (ICH)
- Innovative problem-solving abilities
Cell Line Development
- Qualifications: Relevant degree in biotechnology, molecular biology, or related fields
- Experience: 3–8 years in cell line engineering
- Vacancies: Multiple
Responsibilities
- Develop and optimize mammalian or microbial cell lines
- Perform genetic engineering and clone selection
- Ensure scalability for production
Required Skills
- Proficiency in molecular biology and cell culture
- Experience with CHO or E. coli systems
- Attention to detail and regulatory compliance
Upstream Manufacturing
- Qualifications: Relevant degree in biotechnology, engineering, or related fields
- Experience: 3–8 years in upstream manufacturing
- Vacancies: Multiple
Responsibilities
- Oversee bioreactor operations and production batches
- Ensure compliance with cGMP standards
- Troubleshoot process deviations
Required Skills
- Hands-on experience with large-scale bioprocessing
- Knowledge of cGMP and safety protocols
- Team leadership and coordination
Downstream Manufacturing
- Qualifications: Relevant degree in biotechnology, chemical engineering, or related fields
- Experience: 3–8 years in downstream manufacturing
- Vacancies: Multiple
Responsibilities
- Manage purification processes at scale
- Ensure quality and yield of biologics products
- Support regulatory audits
Required Skills
- Expertise in large-scale purification systems
- Strong understanding of cGMP and quality systems
- Problem-solving and process optimization skills
Quality Assurance
- Qualifications: Relevant degree in pharmacy, biotechnology, or related fields
- Experience: 3–8 years in QA for biologics
- Vacancies: Multiple
Responsibilities
- Ensure compliance with cGMP and regulatory standards
- Review batch records and conduct audits
- Manage deviation and CAPA processes
Required Skills
- Knowledge of cGMP, GLP, and regulatory guidelines
- Experience with QA documentation and audits
- Attention to detail and analytical mindset
Application Details
- Date: Apply by April 30, 2025
- Time: Open application (contact for interview scheduling)
- Contact: Email your updated CV to pranavgayal@aurigeneservices.com
- Website: Visit www.aurigeneservices.com for more details
Documents Required
- Updated Resume
- Photocopy of Educational Certificates
- Experience Certificates
- Aadhar Card Copy
Important Notes
- Eligibility: Candidates must have 3–8 years of experience in biologics-related roles
- Pre-Apply: Email your CV to be considered
- Joining Preference: Immediate joiners or short notice periods prioritized
How to Apply
- Email Application: Send your updated CV to pranavgayal@aurigeneservices.com with the subject “Application for [Department] – Aurigene Biologics – April 2025”.
- Pro Tip: Highlight your experience in upstream/downstream processes, cell line development, or QA in biologics in your CV!
- Application Deadline: Apply by April 30, 2025.
Don’t wait! Join Aurigene Pharmaceutical Services and be part of a growing biologics powerhouse today! 🚀🌍
Eligibility Reminder: Candidates must have 3–8 years of relevant experience in the specified biologics fields. Ensure your CV reflects your expertise.