AMI Lifesciences Walk-In Interview 2025: AMI Lifesciences, a prominent pharmaceutical company specializing in Active Pharmaceutical Ingredients (APIs), is holding a Walk-In Interview on 19th September 2025 for Quality Control and Quality Assurance positions. The company is known for its commitment to quality, compliance, and innovation in pharmaceutical manufacturing. If you are looking to build a career in API production, this is a golden opportunity to work with a globally reputed firm near Vadodara.
About AMI Lifesciences
AMI Lifesciences has established itself as a leader in manufacturing and delivering high-quality APIs for healthcare worldwide. Focusing on regulatory excellence, technological innovation, and continuous process improvements, AMI ensures its products and services meet stringent global standards. The company encourages talented professionals to join its mission of advancing pharmaceutical manufacturing using cutting-edge technology and quality processes.
Walk-In Interview Details
- Date: 19th September 2025 (Friday)
- Time: 10:00 AM to 3:00 PM
- Location: Karakhadi (Near Vadodara), Gujarat
Eligible candidates can directly attend the walk-in session with their updated resumes and relevant documents.
Also Apply: KLM Laboratories Pvt Ltd Hiring 2025 | Officer – Production Job | Vadodara, Gujarat
Job Positions & Eligibility
1. Quality Control
- Qualification: M.Sc. in Organic Chemistry, Analytical Chemistry, or M. Pharm
- Experience: 2 to 5 years in the API industry
- Key Responsibilities:
- Conduct HPLC (High-Performance Liquid Chromatography), GC (Gas Chromatography), and wet chemical analyses to ensure product compliance.
- Analyze raw materials, intermediates, and finished products according to quality standards.
- Prepare SOPs following regulatory requirements.
- Maintain GLP documentation and audit-ready records.
- Use multiple laboratory software platforms for testing and reporting.
2. Quality Assurance
- Qualification: M.Sc. in Organic Chemistry or M. Pharm
- Experience: 4 to 12 years in the API industry
- Key Responsibilities:
- Ensure cGMP and regulatory compliance across quality assurance operations.
- Manage activities like AQA, IPQA, batch release, deviations, CAPA, and change control.
- Review analytical data adhering to ALCOA+ principles for data integrity.
- Conduct in-process quality checks, on-floor QA, and maintain accurate documentation.
- Oversee qualification, maintenance, and calibration reviews.
- Prepare regulatory-compliant documents.
- Lead automation, digitalization, and continuous improvement initiatives.
Important Notes for Candidates
- AMI Lifesciences does not charge any application, training, or testing fees.
- Candidates unable to attend the walk-in interview may send their profiles via email to: careers@amilifesciences.com
Why Work at AMI Lifesciences?
Joining AMI Lifesciences means becoming part of a company dedicated to pharmaceutical excellence and innovation. Employees gain exposure to advanced analytical technologies, regulatory environments, and continuous improvement processes that are benchmarks in the industry. With a focus on career development and a collaborative work culture, AMI offers a fulfilling professional journey in the pharmaceutical sector.