Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Specialist - Ms&T

Novartis
Novartis
2-6+ years
Not Disclosed
Hyderabad, India
10 March 13, 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)

Company: Novartis Healthcare Private Limited
Location: Hyderabad, India
Business Unit: Production / Manufacturing
Functional Area: Technical Operations
Job Type: Full-Time
Employment Type: Regular
Job ID: REQ-10072856

Experience Required
Minimum 6+ years of experience in Manufacturing Science & Technology (MS&T), Quality Assurance, Regulatory Affairs, or biologics manufacturing within the pharmaceutical or biotechnology industry. At least 2 years of experience in MS&T or manufacturing operations is preferred.

Education
Bachelor’s degree in Pharmacy, Pharmaceutical Technology, Chemical Engineering, Biomedical Engineering, Biotechnology, Chemistry, or related life sciences disciplines. Advanced qualifications such as M.Tech, M.Sc., or equivalent postgraduate education are considered advantageous.

Job Overview
Novartis is seeking a Specialist – MS&T to support deviation management, investigation processes, and quality management activities within the Radio Ligand Therapy (RLT) platform. The role involves collaborating with cross-functional operations teams to manage deviations, perform root cause investigations, and implement corrective and preventive actions in accordance with global quality standards.

The position plays a critical role in ensuring compliance with cGMP regulations, improving manufacturing processes, and maintaining inspection readiness across the site.

Key Responsibilities
Manage deviations within the 1QEM system in alignment with the Novartis quality management framework for assigned sites.
Conduct root cause investigations using established methodologies such as Fishbone diagrams, 5 Whys analysis, timeline analysis, and process mapping.
Collaborate with cross-functional teams including Production, Quality Assurance, Engineering, and site leadership to resolve quality events and investigations.
Coordinate with site stakeholders and ensure timely communication regarding investigation progress and outcomes.
Facilitate deviation review meetings and translate key discussions into clear and actionable documentation.
Track and report metrics related to change control documentation including timeliness, compliance, and quality performance indicators.
Develop, revise, and maintain high-quality documentation associated with deviation management processes while ensuring alignment with cGMP standards and regulatory requirements.
Support quality management system activities including Change Control, CAPA management, effectiveness checks, risk assessments, and OOX (Out-of-Expectation) events.
Participate in periodic quality management reviews to identify process improvements and quality enhancements.
Provide technical expertise to resolve process-specific challenges while ensuring compliance with internal procedures, safety standards, and regulatory guidelines.
Maintain inspection readiness for the assigned area of responsibility.
Support development and review of GxP documentation including SOPs, working procedures, and quality trend reports.
Assist in regulatory inspections and health authority audits by ensuring compliance with Quality Management System standards.
Follow all workplace safety, environmental protection, and operational procedures as required.
Complete assigned objectives and key performance indicators while supporting operational priorities and ad hoc business requirements.

Required Skills and Competencies
Strong knowledge of cGMP regulations and Good Documentation Practices.
Expertise in deviation handling, root cause analysis, and CAPA management.
Experience with change control management, risk assessments, and effectiveness checks.
Understanding of drug substance manufacturing processes and process control principles.
Knowledge of complaint handling and OOX investigation processes.
Experience in technology transfer and process improvement initiatives.
Strong report writing, documentation, and data interpretation skills.
Ability to manage cross-functional projects and support operational improvement initiatives.

Technical Skills
Familiarity with statistical tools such as Minitab or Statistica for basic statistical analysis and data interpretation.
Knowledge of validation requirements, product filing processes, and post-approval regulatory changes.
Ability to perform risk assessments and gap analysis for manufacturing processes.

Professional Skills
Strong communication and presentation skills.
Excellent analytical and problem-solving capabilities.
Ability to collaborate with multidisciplinary teams and stakeholders.
Strong attention to detail and commitment to quality standards.

Equal Opportunity Employer
Novartis is committed to building a diverse and inclusive workplace. The company provides equal employment opportunities to all qualified individuals regardless of race, gender, religion, disability, age, sexual orientation, gender identity, or any other protected characteristic under applicable law.