Forward Deployed Engineer, Life Sciences AI

About the role

We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations to be future-ready. We offer accelerated, global growth opportunities for talent that is bold, industrious and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship and is guided by passion, innovation, collaboration and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out www.careers.indegene.com

What if we told you that you can move to an exciting role in an entrepreneurial organization without the usual risks associated with it?

We understand that you are looking for growth and variety in your career at this point and we would love for you to join us in our journey and grow with us. At Indegene, our roles come with the excitement you require at this stage of your career with the reliability you seek. We hire the best and trust them from day 1 to deliver global impact, handle teams and be responsible for the outcomes while our leaders support and mentor you.

We are a profitable rapidly growing global organization and are scouting for the best talent for this phase of growth. With us, you are at the intersection of two of the most exciting industries of healthcare and technology. We offer global opportunities with fast-track careers while you work with a team that is fueled by purpose. The combination of these will lead to a truly differentiated experience for you.

If this excites you, then apply below.

Forward Deployed Engineer, Life Sciences AI

Role summary

You sit with the client, not behind a ticket queue. You take our AI agents into a pharma brand team, medical affairs group or regulatory function and get them running in a validated, audit-ready state. You debug in environments we do not own, translate brand and compliance needs into working agents, and carry the lessons back to product.

What you own

End-to-end delivery of AI agent deployments for 2 to 4 biopharma accounts, from discovery through go-live and handover.

Integration into the client commercial and medical stack: Veeva CRM and Vault, Salesforce, IQVIA and other patient and sales data feeds, MDM, SSO and SCIM.

Compliance-aware build: FDA 21 CFR Part 11 and EU Annex 11 expectations, GxP validation documentation, full audit trails, PII and PHI handling.

Field debugging on live client data and infrastructure, then shipping the fix, config change or upstream patch.

Reusable assets: deployment runbooks, validation templates, connector patterns and reference architectures.

The client voice into product: quantify the gap, file it, argue the roadmap case.

A week in the life

Monday: an agent summarising medical information requests returns wrong citations against Veeva Vault, so you trace it to a stale index. Tuesday: the client validation lead needs evidence for the audit trail before Thursday. Wednesday: you re-architect the IQVIA data feed for their scale and run a joint session with their IT. Thursday: go-live to one brand team, gated and reversible. Friday: handover, validation pack signed off, one product gap filed.

Must have

10+ years in customer-facing technical delivery: FDE, solutions engineering, data engineering or technical consulting.

Production Python or TypeScript, strong SQL, and comfort reading unfamiliar schemas under time pressure.

Hands-on with pharma commercial or clinical data: Veeva CRM or Vault, Salesforce, IQVIA, patient support or real-world data.

GxP and validation awareness: computer system validation, audit trails, change control, data integrity.

Cloud and networking: IAM, VPC, Docker, Kubernetes basics, Terraform.

LLM and agent fluency: agent configuration, retrieval pipelines, prompt evaluation, token and cost control.

Executive-grade communication: you can explain a root cause to a brand lead and a validation lead in the same meeting.

Good to have

MLR review workflow experience across commercial content and promotional material.

Regulatory or medical affairs exposure: submissions, labelling, pharmacovigilance safety data.

Privacy regime depth: HIPAA, GDPR, India DPDP Act.

Air-gapped or on-premise installation experience.

Life sciences or consulting background with a global biopharma client base.

Qualifications

Bachelor’s or Master’s in engineering, computer science, life sciences or a related field.

Proven record of shipping something into production that you did not fully control.

Willingness to travel up to 50% to client sites.

Right to work in the location you are hired for.

What this role is not

Not inbound support. You are engaged before the ticket exists.

Not quota-carrying sales. You are measured on deployments that hold.

Not a pure backend product seat. You work where client and product meet.

If you have taken AI or data capabilities into a regulated pharma environment and made them stick, this is your role.

EQUAL OPPORTUNITY

Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, candidate’s merit and qualification.

We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.