Role Overview:

As an Engineering Manager in the Life Sciences domain, you will spearhead the design, development, and delivery of high-stakes software solutions that power critical pharmaceutical and clinical operations. You will act as the bridge between complex technical engineering teams and non-technical business stakeholders, ensuring that our digital products not only meet rigorous performance standards but also adhere to the stringent regulatory frameworks governing the industry. By fostering a culture of technical excellence and compliance-first thinking, you will directly influence the efficiency of clinical data management and the safety of patient-centric applications, ultimately accelerating the time-to-market for life-saving innovations. You will be based in our Hyderabad office, collaborating with cross-functional global teams to drive digital transformation in a highly regulated environment.

Key Responsibilities:

- Lead and mentor high-performing engineering teams through the full SDLC, ensuring the timely delivery of robust, scalable, and compliant software products.

- Oversee Computer System Validation (CSV) and ensure all software releases strictly comply with 21 CFR Part 11, HIPAA, and GXP standards to mitigate regulatory and operational risks.

- Collaborate with Product Management to translate complex business requirements into actionable technical roadmaps that align with long-term organizational goals.

- Implement and refine Agile methodologies to enhance team productivity, transparency, and responsiveness to changing market demands.

- Manage end-to-end project lifecycles, including resource allocation, risk management, and stakeholder reporting, to ensure projects are delivered within scope and budget.

- Drive a culture of Software Quality Assurance by integrating automated testing and rigorous code reviews into the development pipeline to maintain the highest standards of system integrity.

Required Skillset:

- Demonstrated expertise in Engineering Management with 8 - 12 years of experience, specifically within the Life Sciences or Pharmaceutical software domain.

- Proven ability to navigate complex regulatory landscapes, including deep knowledge of GXP, 21 CFR Part 11, and HIPAA compliance protocols.

- Strong proficiency in managing the full SDLC and Agile project management, with a track record of delivering enterprise-grade software solutions.

- Exceptional communication skills, with the ability to articulate technical challenges and strategic vision to executive leadership and cross-functional teams.

- A Bachelor's or Master's degree in Computer Science, Engineering, or a related field, complemented by a proactive approach to problem-solving in a hybrid work environment.

- Demonstrated leadership in fostering collaborative team environments, mentoring junior engineers, and driving continuous improvement in software quality and delivery processes.