PKS Integration Operations Manager

Novartis India; Hyderabad; On-site; INR 2,400,000 - 4,200,000; Full time

Job summary

Novartis in Hyderabad seeks an Integration Operational Manager to drive M&A and asset integrations across non-GxP and GxP environments. You will coordinate with PKS Experts, SMEs and the Integration Lead to manage studies inventories, reference substances, and data transfers, ensuring compliant operational execution.

The role emphasizes scientific deep dives, gap analyses, contract/invoice reviews, and timely communication with the line manager to integrate acquired assets into PKS.

Qualifications

• PhD with 3+ years industry experience or MSc with 6+ years.
• Experience in bioanalytical science in a GCP-regulated environment preferred.
• Strong knowledge of GxP, FDA and ICH guidelines related to sample management.

Responsibilities

• Guide PKS subteam on the integration process.
• Review documents (BioA, ADME, etc.).
• Prepare FDA tabulated summaries; highlight gaps.
• Manage inventories of studies, samples, reagents and raw data.

Skills

Project management

GxP understanding

GCP familiarity

Biochemistry/Pharma knowledge

Education

PhD in biochemistry/chemistry/pharmaceutical sciences

Master's degree +6 years industry experience

Job description

Summary

As an Integration Operational Manager working across non-GxP and GxP environments, you will support the integration of M&A activities and asset acquisitions across all modalities. You will work closely with a dedicated team, including PKS Expert and its SMEs (BA, ADME, …) and a BR Line Function Integration Lead, to drive key operational activities. These include facilitating scientific deep dives and gap analyses, managing inventories of studies, study samples, reference substances, critical reagents, e-data, and raw data archives, and supporting the review of business partners, contracts, and invoices. Under the supervision of the PKS Integration Ops Lead, you will manage several M&A and asset integrations in parallel while maintaining clear and consistent communication with your line manager. This role is critical to ensuring the seamless integration of acquired assets into the Novartis BioMedical Research PharmacoKinetic Sciences (PKS) department.

Summary

As an Integration Operational Manager working across non-GxP and GxP environments, you will support the integration of M&A activities and asset acquisitions across all modalities. You will work closely with a dedicated team, including PKS Expert and its SMEs (BA, ADME, …) and a BR Line Function Integration Lead, to drive key operational activities. These include facilitating scientific deep dives and gap analyses, managing inventories of studies, study samples, reference substances, critical reagents, e-data, and raw data archives, and supporting the review of business partners, contracts, and invoices. Under the supervision of the PKS Integration Ops Lead, you will manage several M&A and asset integrations in parallel while maintaining clear and consistent communication with your line manager. This role is critical to ensuring the seamless integration of acquired assets into the Novartis BioMedical Research PharmacoKinetic Sciences (PKS) department.

Key Responsibilities

• Guide and support the PKS subteam on the integration process
• Review of relevant documents ( BioA, ADME etc… )
• Bioanalytical reports (MVR, TKR, BDR, IG, analytical plans).
• Prepare the "FDA" tabulated summaries and highlight missing validation steps and gaps
• Work on the inventories of studies, study samples, drug, reference substances and critical reagents, work closely with the BA SME to provide recommendations on what needs to be transferred to Novartis. Get a clear understanding about the nature, volume and current location of the raw data.
• Contribute to data transfer to Novartis repositories
• Contribute to Source Data Verification
• Liaise with Biomedical Research integration office representative
• Liaise with Procurement, IT, Legal and other LF related to M&A

Essential Requirements

• PhD with at least 3 years of industry experience, or a master’s degree with at least 6 years of industry experience, in biochemistry, chemistry, pharmaceutical sciences, or a related field. Project management experience or skills are preferred; an MBA is an asset.
• Prior experience as a bioanalytical scientist in a GCP-regulated environment is preferred.
• Strong understanding of GxP guidelines, FDA regulations, and ICH guidance related to sample management, laboratory documentation, and lab operations.
• Familiarity with general PK sciences, including ADME, PK, and bioanalysis, is a plus.
• Strong communication and organizational skills, with the ability to work independently and collaboratively across multiple projects while meeting timelines.
• Willingness to take on additional responsibilities as needed, with the flexibility to adapt to changing priorities and strategies.

Why Novartis:

Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Benefits and Rewards:

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