ACKJOBS Job Portal Logo

ACK JOBS

India’s Trusted Job Portal for Pharma, Chemical, Engineering, Construction & Corporate Jobs

Assistant Manager QA Validation

Aristo Pharmaceuticals Pvt Ltd

Majitar, Rangpo, Sikkim

Department: Quality Assurance

Experience: 5-10 Years

Industry: Pharmaceutical

Education: BPharm

Job Description

Assistant Manager QA Validation at Aristo Pharmaceuticals Pvt Ltd

Aristo Pharmaceuticals Pvt Ltd is currently hiring for the position of Assistant Manager QA Validation in the Quality Assurance department within the Pharmaceutical industry.

Roles & Responsibilities

Aristo Pharmaceuticals Pvt Ltd is inviting applications for the position of Assistant Manager – QA Validation at its pharmaceutical manufacturing facility located in Majitar, Rangpo, Sikkim. This full-time opportunity is suitable for B.Pharm qualified professionals with 5 to 10 years of experience in pharmaceutical quality assurance and validation activities. The selected candidate will be responsible for managing validation programs, reviewing qualification documents, ensuring regulatory compliance, and supporting continuous improvement initiatives within manufacturing operations. Candidates should possess strong knowledge of equipment qualification, process validation, cleaning validation, documentation control, and GMP compliance requirements. This role offers an excellent opportunity to work with a reputed pharmaceutical organization while contributing to product quality, regulatory readiness, and operational excellence. Professionals seeking growth in pharmaceutical validation and quality assurance are encouraged to apply.

Location

Majitar, Rangpo, Sikkim, India

Employment Type

Full-time

Experience Required

5 to 10 years

Educational Qualification

B.Pharm

Key Responsibilities

  • Manage process, equipment, and cleaning validation activities.
  • Review qualification protocols and validation reports.
  • Ensure compliance with GMP and regulatory guidelines.
  • Coordinate validation schedules across departments.
  • Support audit and inspection readiness initiatives.
  • Review change control and quality documentation.
  • Monitor validation status and compliance metrics.
  • Participate in risk assessments and quality improvement programs.
  • Coordinate with production, engineering, and QC teams.
  • Provide guidance on validation-related quality requirements.

Required Skills & Competencies

  • Strong knowledge of pharmaceutical validation systems.
  • Experience in equipment and process qualification.
  • Understanding of GMP and regulatory compliance.
  • Technical documentation and report review expertise.
  • Analytical and problem-solving abilities.
  • Audit preparedness and compliance management skills.
  • Excellent communication and coordination capabilities.
  • Attention to detail and accuracy.
  • Knowledge of risk management principles.
  • Leadership and team collaboration skills.

Why Join Aristo Pharmaceuticals Pvt Ltd?

Aristo Pharmaceuticals Pvt Ltd offers employees the opportunity to work in a quality-focused pharmaceutical environment supported by modern manufacturing facilities and robust compliance systems. The company encourages professional development, continuous learning, and long-term career growth while maintaining high standards of quality and innovation.

How to Apply

Register on our portal to apply for this opportunity and stay updated with the latest job openings. Existing users can directly log in to continue their application and explore more opportunities.

Check our website - www.ackjobs.com - regularly for the latest job market updates. Join our WhatsApp and social media groups through the website.

WhatsApp Group
Join now & get instant job alerts!
Join