Global Quality Starting Material Maintenance Expert Associate

Stada Pharma Services India Private Limited; Navi Mumbai; Hybrid; INR 600,000 - 1,200,000; Full time

Benefits offered by this job

Competitive salary & benefits

Global exposure

Multicultural work environment

Continuous learning

Job summary

Stada Pharma Services India Private Limited in Navi Mumbai seeks a detail-oriented QA professional to support GMP documentation management and quality system processes. The role includes change control, qualification activities, and regulatory-file preparation to drive improvements across sites.

Ideal candidates hold a science degree with strong English (B2+) and advanced MS Office skills. You will work in a fast-paced environment and collaborate across functions to ensure regulatory alignment

Qualifications

• University degree in pharmacy, biology, chemistry or comparable course of study.
• English language – B2 mandatory, C1 level advantage
• Advanced knowledge of MS Office

Responsibilities

• Active participation in Quality system processes, such as GMP documentation management, change control, qualification and requalification activities and others
• Maintaining and compiling GMP documentation such as specifications, analytical procedures, risk assessments, different reports, questionnaires and other
• Evaluating GMP documentation in line with the applicable GMP guidelines and files approved by regulatory authorities
• Ensure ongoing abidance by industry regulatory and quality requirements
• Drive improvements in Quality Documentation and processes
• Inspect data to detect areas for improvement
• Presenting results and monthly key performance numbers
• Worldwide communication with Group-owned production sites and contract manufacturers
• Performing other tasks at the order of direct superior

Skills

GMP knowledge

MS Office

Communication skills

Analytical skills

Adaptability

Cross-functional teamwork

Technical writing

Education

University degree in pharmacy/biology/chemistry

Tools

MS Office

Job description

Job Responsibilities:

• Active participation in Quality system processes, such as GMP documentation management, change control, qualification and requalification activities and others;
• Maintaining and compiling GMP documentation such as specifications, analytical procedures, risk assessments, different reports, questionnaires and other;
• Evaluating GMP documentation in line with the applicable GMP guidelines and files approved by regulatory authorities;
• Ensure ongoing abidance by industry regulatory and quality requirements;
• Drive improvements in Quality Documentation and processes;
• Inspect data to detect areas for improvement;
• Presenting results and monthly key performance numbers
• Worldwide communication with Group-owned production sites and contract manufacturers
• Performing other tasks at the order of direct superior

Key Competencies Required:

• Other required professional knowledge, skills and experience
• University degree in pharmacy, biology, chemistry or comparable course of study
• English language – B2 mandatory, C1 level advantage
• Advanced level of knowledge of MS Office package
• Good communication and negotiation skills, Fast learner and easily adaptable to changes
• Ability to work in a fast-paced, dynamic environment
• Ability to understand and discuss complex topics, technical writing skills
• Team-oriented, precise, analytical, responsible, independent
• Ability to work in cross functional teams

We Offer

• Competitive salary & benefits
• Opportunities for global exposure and professional development
• Supportive, collaborative, and multicultural work environment
• Continuous learning through international trainings and industry events