Syngene Hiring Senior Research Associate

Senior Research Associate Openings | Syngene Bangalore

Apply for Senior Research Associate role at Syngene International, Bangalore. Qualification: Master’s in Life Sciences/Biotech, 3–6 years’ experience.

Syngene International Ltd., a globally recognized contract research, development, and manufacturing organization (CRDMO), is inviting applications for the position of Senior Research Associate at its Bangalore facility. This role is ideal for experienced professionals in bioprocess development, downstream processing, and biopharmaceutical research who are looking to grow their careers with a leading organization serving top pharma and biotech clients worldwide.

Company Overview

Syngene International (BSE: 539268, NSE: SYNGENE, ISIN: INE398R01022) is an integrated research-to-manufacturing solutions provider catering to pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical sectors. With over 4,500 scientists and a 1.9 million sq. ft. facility, Syngene delivers cutting-edge services in drug discovery, development, and manufacturing. The company has dedicated R&D centers for global leaders like Amgen, Baxter, Bristol-Myers Squibb, and Herbalife, and partnerships with multinationals such as GSK and Merck KGaA. Syngene’s focus on innovation, IP security, and regulatory compliance has made it a trusted partner for advancing healthcare and scientific research.

Job Role & Responsibilities

As a Senior Research Associate – Downstream Process Development, your role will include:

• Designing and executing laboratory experiments related to downstream process (DSP) development.
• Documenting experiments in laboratory notebooks and digital systems for regulatory compliance.
• Drafting experimental protocols and obtaining approval from team leads.
• Managing general lab maintenance and inventory to ensure smooth operations.
• Preparing detailed reports, protocols, and technology transfer documents.
• Supporting process scale-up and contributing to client-driven biopharma projects.

Eligibility / Qualifications

• Education: Master’s degree in Life Sciences, Chemical Engineering, Biotechnology, Biochemistry, or related fields.
• Experience: 3–6 years of hands-on experience in downstream process development (DSP) for biopharmaceuticals.
• Preferred Expertise:
  • Strong experience working with CHO cell lines.
  • Exposure to monoclonal antibodies, fusion proteins, and biologics.
  • Ability to draft and review technical documents for regulatory and client requirements.

Location & Salary

• Location: Bangalore, Karnataka, India
• Salary: Competitive and aligned with industry standards.

Application Process

Interested candidates who meet the eligibility requirements are encouraged to apply directly through Syngene’s official careers page:

Apply Here

Apply before 23rd August 2025 to secure your chance!

Why Join Syngene?

• Opportunity to work with a globally respected CRDMO serving top-tier pharma and biotech clients.
• Access to world-class infrastructure and advanced technologies.
• Be part of a diverse, innovation-driven team of 4,500+ scientists.
• Collaborative work culture with focus on continuous learning and growth.
• Equal opportunity employer committed to diversity and inclusion.

Frequently Asked Questions (FAQs)

Q1: What qualifications are required for this role?
Candidates must hold a Master’s in Life Sciences, Biotechnology, Biochemistry, or Chemical Engineering with 3–6 years of DSP experience.

Q2: What type of projects will I be working on?
You will be involved in downstream process development for biopharmaceuticals, including monoclonal antibodies and fusion proteins.

Q3: Is experience with CHO cell lines required?
Yes, prior experience with CHO cell-based processes is highly preferred.

Q4: Where is this job located?
The role is based at Syngene’s Bangalore facility, Karnataka.

Q5: How do I apply?
You can apply via the official Syngene careers page using the provided application link.

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