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Specialist - Ms&T

Novartis
Novartis
2-6 years
Not Disclosed
Hyderabad, India
10 March 6, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Specialist – MS&T (Manufacturing Science & Technology)

Location: Hyderabad, India
Company: Novartis Healthcare Private Limited
Job ID: REQ-10072856
Department: Technical Operations – Production / Manufacturing
Employment Type: Full-Time
Work Mode: Onsite
Experience Required: Minimum 6 years in MS&T, Quality Assurance, Regulatory, or Biologics Manufacturing

Job Overview
Novartis is seeking a skilled Specialist – Manufacturing Science & Technology (MS&T) to support the Radio Ligand Therapy (RLT) platform by managing deviations, investigations, and quality system activities across manufacturing sites. This role plays a critical part in ensuring regulatory compliance, driving root cause investigations, and implementing effective Corrective and Preventive Actions (CAPA).

The specialist will collaborate closely with cross-functional teams including Production, Quality Assurance, Engineering, and site leadership to support quality management processes and continuous improvement initiatives in a cGMP-regulated environment.

Key Responsibilities

Deviation and Investigation Management

  • Manage deviation records within the 1QEM system using the Novartis quality management framework.

  • Lead and participate in investigations related to deviations, complaints, and Out-of-Expectation (OOX) events.

  • Conduct detailed root cause investigations using tools such as Fishbone diagrams, 5 Whys, process mapping, and timeline analysis.

  • Ensure timely communication and coordination with site stakeholders and cross-functional teams.

Quality Management System (QMS) Support

  • Support QMS activities including Change Controls, CAPA implementation, effectiveness checks, and risk assessments.

  • Track key metrics related to change control documentation including compliance, timelines, and quality performance.

  • Participate in periodic QMS reviews and contribute to continuous improvement initiatives.

Documentation and Compliance

  • Develop and maintain high-quality documentation related to deviation management and investigation processes.

  • Support preparation and review of GxP documents such as SOPs, procedures, and trend reports.

  • Ensure compliance with cGMP standards, internal quality policies, and global regulatory requirements.

Cross-Functional Collaboration

  • Work closely with Production, Engineering, and Quality teams to resolve process issues.

  • Facilitate deviation review meetings and translate investigation outcomes into actionable documentation.

  • Provide technical expertise for process-related challenges within manufacturing operations.

Audit and Inspection Readiness

  • Maintain inspection readiness across assigned areas.

  • Support Health Authority audits and ensure compliance with quality and regulatory standards.

  • Ensure adherence to environmental, health, and safety policies within operational processes.

Required Qualifications

Education

  • Bachelor’s degree in Pharmacy, Pharmaceutical Technology, Chemical Engineering, Biotechnology, Biomedical Engineering, Chemistry, or a related life science field.

  • Advanced degree such as M.Tech, M.Sc., or equivalent is preferred.

Experience

  • Minimum 6 years of experience in MS&T, Quality Assurance, Regulatory Affairs, or Biologics manufacturing.

  • At least 2 years of direct experience in MS&T or manufacturing operations.

  • Strong experience in deviation handling, root cause investigation, and CAPA management.

  • Familiarity with regulatory guidance related to validation, product filing, and post-approval changes.

Technical Skills

  • Strong knowledge of cGMP and Good Documentation Practices (GDP).

  • Expertise in deviation management, RCA, CAPA, and change control systems.

  • Experience with risk assessments and quality management frameworks.

  • Understanding of drug substance manufacturing processes and process control strategies.

  • Experience using statistical tools such as Minitab or Statistica for basic data analysis and interpretation.

  • Knowledge of technology transfer, complaints handling, and OOX management.

Professional Skills

  • Excellent analytical and problem-solving abilities.

  • Strong communication, presentation, and technical report writing skills.

  • Ability to work effectively with cross-functional teams in a regulated pharmaceutical environment.

  • Good project management and data analytics capabilities.

Why Join Novartis
At Novartis, innovation and collaboration drive breakthrough solutions that improve patient outcomes worldwide. Employees work in an inclusive and dynamic environment focused on scientific advancement, professional development, and meaningful impact on global healthcare.

Equal Opportunity Statement
Novartis is committed to building an inclusive workplace and welcomes applications from individuals of diverse backgrounds. Reasonable accommodations are available for applicants with disabilities during the recruitment process.