QA, QC, ADL, R&D

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πŸ›‘οΈ Verified Career Listing Directly reviewed and cross-referenced with hiring sources.

AMI Lifescience

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πŸŽ“ Pharma
πŸ“ Ankleshwar
πŸ’Ό Fresher
βœ” Verified Job
Email Application
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AMI Lifesciences is hiring candidates across multiple technical functions within the pharmaceutical API manufacturing and R&D ecosystem. The opportunities include Production, QC, ADL, and R&D Synthesis, with eligibility ranging from 2026 freshers to professionals with 2–8 years of relevant experience. Candidates with qualifications including B.Tech Chemical Engineering, M.Sc Organic Chemistry, M.Sc Analytical Chemistry, M.Pharm, and Ph.D Chemistry can explore the relevant positions. The roles offer exposure to API manufacturing, analytical development, quality control, process development, CDMO projects, peptides, and oncology APIs. Candidates interested in developing their careers in the pharmaceutical and life sciences industry are encouraged to attend the walk-in interview.

Job Overview

Particulars Details
Position QA, QC, ADL, R&D
Company AMI Lifescience
Location Ankleshwar
Job Type Full-Time
Experience Fresher
Category / Department Pharma
Application Mode Email

🏒 About AMI Lifescience

AMI Lifesciences is a rapidly growing Indian pharmaceutical company focused on the development and manufacturing of Active Pharmaceutical Ingredients (APIs). The organization provides opportunities across manufacturing, analytical, quality, and research functions, supporting professionals who want to develop careers within the pharmaceutical industry.

Company Mission
The company’s work is centered on delivering high-quality pharmaceutical API solutions while maintaining strong standards across manufacturing, research, analytical development, and quality operations.

Company Vision
AMI Lifesciences aims to contribute to the pharmaceutical industry through strong technical capabilities, innovation, quality-focused processes, and the development of advanced API solutions.

Core Values
πŸ”Ή Quality and compliance
πŸ”Ή Scientific excellence
πŸ”Ή Innovation and continuous improvement
πŸ”Ή Operational discipline
πŸ”Ή Collaboration and teamwork
πŸ”Ή Commitment to pharmaceutical standards

What Makes Them Different
The organization offers opportunities across multiple specialized areas of the API value chain, from production and quality control to analytical development and advanced R&D synthesis. Its exposure to areas such as CDMO projects, peptides, oncology APIs, process development, and technology transfer provides professionals with opportunities to build specialized technical expertise.

Leadership / Company Philosophy
The company’s professional environment emphasizes technical capability, quality-focused operations, regulatory compliance, and continuous development across pharmaceutical manufacturing and R&D functions.

πŸ“
Office Location

πŸ“ AMI Lifesciences
Work Locations: Karakhadi

πŸ’‘ Editor's Note / Preparation Tip

πŸ“„ Resume Preparation Tips

1️⃣ Clearly mention your educational qualification and graduation year, especially if you are a 2026 pass-out.
2️⃣ Highlight relevant technical skills such as HPLC, GC, Method Development, Method Validation, API Synthesis, or Process Development.
3️⃣ Mention hands-on experience with relevant instruments and analytical techniques, including NMR, IR, and Mass Spectrometry where applicable.
4️⃣ Showcase experience with cGMP, GLP, ICH guidelines, GMP documentation, BMRs, SOPs, and validation protocols.
5️⃣ For experienced candidates, quantify your contributions to process optimization, technology transfer, API production, or analytical development.

🎯 Interview Preparation

1️⃣ Revise fundamental concepts related to your target department: Production, QC, ADL, or R&D Synthesis.
2️⃣ Prepare to explain your practical knowledge of HPLC, GC, analytical method development, and method validation if applying for QC or ADL.
3️⃣ For R&D roles, revise organic synthesis, reaction mechanisms, process development, API synthesis, and characterization techniques.
4️⃣ Understand key concepts related to cGMP, GLP, ICH guidelines, SOPs, BMRs, stability studies, and regulatory compliance.
5️⃣ Be prepared to discuss your academic projects, industrial training, research work, or previous professional experience in detail.

πŸ’‘ Professional Tips

1️⃣ Select the department that best matches your qualification, technical expertise, and career goals.
2️⃣ Carry multiple copies of your updated resume and organize all required documents before attending the walk-in.
3️⃣ Research API manufacturing, CDMO, and pharmaceutical industry trends before the interview.
4️⃣ Be ready to explain how you ensure data integrity, documentation accuracy, and compliance in laboratory or manufacturing environments.
5️⃣ Demonstrate a strong understanding of safety, quality, teamwork, and continuous improvement, as these are critical in pharmaceutical operations.

πŸ“ Job Description

πŸš€ Walk-In Interview | Freshers & Experienced Professionals | AMI Lifesciences

Looking to build your career in the pharmaceutical API industry? πŸ§ͺπŸ’Š AMI Lifesciences, one of India’s rapidly growing API manufacturing companies, is conducting a Walk-In Interview Drive for opportunities across Production, Quality Control (QC), Analytical Development Laboratory (ADL), and R&D Synthesis.

The company is inviting applications from 2026 pass-out freshers as well as experienced professionals with up to 8 years of experience, depending on the department. If you have a background in Chemical Engineering, Organic Chemistry, Analytical Chemistry, Pharmacy, or Chemistry, this could be an excellent opportunity to take the next step in your pharma career! πŸš€


Position Details

Company: AMI Lifesciences
Job Type: Walk-In Interview
Departments: Production, Quality Control (QC), Analytical Development Laboratory (ADL), R&D Synthesis
Work Locations: Karakhadi & Ankleshwar, Gujarat
Experience: Freshers to 8 Years
Interview Date: 24 July 2026 (Friday)
Interview Time: 09:30 AM – 03:30 PM
Interview Venue: Productivity House, 4th Floor, BPC Road, Alkapuri, Vadodara, Gujarat – 390007
Application Mode: Walk-In Interview / Email Application

Preferred Skills

⭐ Experience in API manufacturing and bulk drug production
⭐ Hands-on knowledge of HPLC and GC
⭐ Experience with analytical method development and validation
⭐ Understanding of cGMP and GLP practices
⭐ Knowledge of ICH guidelines and regulatory documentation
⭐ Experience in API synthesis and process development
⭐ Exposure to CDMO, peptide, or oncology projects
⭐ Experience with technology transfer and process optimization
⭐ Knowledge of characterization techniques such as NMR, IR, and Mass Spectrometry

Detailed Job Description / Responsibilities

1️⃣ Production | Karakhadi & Ankleshwar

β€’ Execute API production operations according to established processes and procedures.
β€’ Support batch start-up activities and production operations.
β€’ Monitor manufacturing processes and ensure smooth batch execution.
β€’ Perform calibration checks of balances and relevant equipment.
β€’ Follow cGMP requirements throughout production activities.
β€’ Maintain accurate production documentation and batch records.
β€’ Ensure compliance with established safety, quality, and operational procedures.

2️⃣ Analytical Development Laboratory (ADL) | Karakhadi

β€’ Conduct HPLC method development and optimization activities.
β€’ Perform analytical method validation in accordance with ICH guidelines.
β€’ Prepare analytical specifications and Methods of Analysis (MOA).
β€’ Maintain analytical documentation and laboratory records.
β€’ Follow GLP and applicable quality requirements.
β€’ Support instrument calibration and qualification activities.
β€’ Contribute to analytical development and laboratory process improvements.

3️⃣ Quality Control (QC) | Karakhadi & Ankleshwar

β€’ Perform analytical testing using HPLC and GC techniques.
β€’ Conduct raw material testing as per approved procedures.
β€’ Perform finished product analysis and related quality assessments.
β€’ Support stability study activities and documentation.
β€’ Maintain and monitor laboratory instrument calibration.
β€’ Follow GMP documentation and quality control procedures.
β€’ Ensure compliance with applicable regulatory and quality requirements.

4️⃣ R&D Synthesis – CDMO, Peptides & Oncology | Karakhadi

β€’ Perform API synthesis and support process development activities.
β€’ Work on CDMO projects involving pharmaceutical development.
β€’ Contribute to peptide synthesis and oncology API projects.
β€’ Support technology transfer and scale-up activities.
β€’ Characterize compounds using NMR, IR, and Mass Spectrometry.
β€’ Prepare and maintain DMF-related documentation.
β€’ Support process optimization and improvement initiatives.
β€’ Collaborate on research and development activities related to API synthesis.

Candidate Requirements

πŸŽ“ B.Tech Chemical Engineering: Production – 2026 Pass-outs / Freshers
πŸŽ“ M.Sc Organic Chemistry: QC, ADL, and R&D Synthesis
πŸŽ“ M.Sc Analytical Chemistry: QC and ADL
πŸŽ“ M.Pharm: QC and ADL
πŸŽ“ Ph.D Chemistry: R&D Synthesis
πŸ’Ό Freshers: 2026 Pass-outs for Production and QC
πŸ’Ό ADL: Freshers to 8 Years
πŸ’Ό R&D Synthesis: 2–8 Years
πŸ§ͺ Relevant knowledge or experience in pharmaceutical API manufacturing, analytical development, quality control, or R&D synthesis will be beneficial.

Why Join AMI Lifesciences?

🌟 Build a career in the growing pharmaceutical API industry
πŸ§ͺ Gain exposure to API manufacturing and pharmaceutical R&D
πŸ”¬ Work with analytical development and quality control processes
πŸ’Š Explore opportunities in CDMO, peptide, and oncology API projects
πŸ“š Develop expertise in cGMP, GLP, ICH, and regulatory practices
πŸš€ Gain practical exposure to process development and technology transfer
πŸ§‘β€πŸ”¬ Opportunities available for both freshers and experienced professionals
🌐 Work across specialized functions within the pharmaceutical value chain

How to Apply

🚨 Walk-In Interview:
πŸ“… Date: 24 July 2026 (Friday)
⏰ Time: 09:30 AM – 03:30 PM
πŸ“ Venue: Productivity House, 4th Floor, BPC Road, Alkapuri, Vadodara, Gujarat – 39000

πŸ“© Unable to attend the walk-in?
Send your updated resume to: careers@amilifesciences.com


πŸ“Œ Documents to Carry: Updated Resume | Educational Certificates | Experience Certificates (if applicable) | Latest 3 Months Salary Slips | Current CTC Details | Salary Breakup | Passport Size Photograph | Identity Proof

Know someone who would be a great fit? Tag them or share this opportunity with your network! πŸš€


πŸ’‘ Required Qualifications & Skills

βœ“ ️ API Manufacturing and Bulk Drug Production βœ“ ️ cGMP Compliance βœ“ ️ GLP Documentation βœ“ ️ HPLC Analysis βœ“ ️ Gas Chromatography (GC) βœ“ ️ Analytical Method Development βœ“ ️ Method Optimization βœ“ ️ Method Validation βœ“ ️ Knowledge of ICH Guidelines βœ“ ️ SOP Preparation βœ“ ️ Batch Manufacturing Records (BMR) βœ“ ️ Validation Protocols βœ“ ️ Stability Studies βœ“ ️ API Synthesis βœ“ ️ Process Development βœ“ ️ CDMO Projects βœ“ ️ Peptide Synthesis βœ“ ️ Oncology APIs βœ“ ️ Technology Transfer βœ“ ️ NMR, IR Spectroscopy, and Mass Spectrometry

πŸš€ Career Guidance & Interview Insights

To help you succeed, we've compiled original preparation guides, resume keywords, and growth analytics for this category of role.

Joining as a QA, QC, ADL, R&D offers a fantastic opportunity to work at the forefront of technological innovation. You will be exposed to modern software development lifecycles, collaborate with cross-functional product teams, and design scalable architectures that directly impact end-users. The continuous learning curve in tech ensures that your programming, debugging, and system engineering skills remain highly marketable and sharp.

Expected Career Progression Roadmap:

The career roadmap in technology is highly rewarding. Typical progression starts as a Junior Software Engineer, moving to Associate Developer and then Senior Software Engineer (3-6 years). From there, professionals choose between an individual contributor trackβ€”becoming a Tech Lead, Staff Engineer, and Principal Architectβ€”or a management track, advancing to Engineering Manager, Director of Engineering, and Chief Technology Officer (CTO).

Expected Technical & Behavioral Questions:

  • Q1: How do you optimize database query performance?
    Answer Tip: Talk about indexing strategies, query execution plan analysis, avoiding N+1 queries, and implementing caching layers (like Redis).
  • Q2: Explain the differences between Microservices and Monolithic architecture.
    Answer Tip: Highlight scaling advantages, loose coupling, independent deployments, network latency considerations, and data consistency challenges in microservices.
  • Q3: How do you handle merge conflicts in Git?
    Answer Tip: Explain checking out the local branch, pulling the latest main branch, running git merge, opening the conflicted files to resolve blocks manually, and committing the resolved merge.
πŸ’‘ Pro-Tip: Before your interview, research the company's recent news, product launches, and Glassdoor work reviews. Prepare 2-3 thoughtful questions for the interviewer regarding team dynamics and success metrics for this role.

To pass automated ATS (Applicant Tracking System) screening and catch the recruiter's eye, tailor your resume with the following tips:

  • Keywords to include: Software Engineering, SDLC, OOP, CI/CD Pipelines, SQL databases, Agile, Unit Testing, Code Review, Cloud Architectures (AWS/Azure).
  • Format: Use a clean, single-column resume format. Avoid graphics, text boxes, or tables which can scramble ATS parser outputs.
  • Quantify Results: Instead of writing 'wrote code', write 'Developed a caching system that reduced server response times by 35%.'
Estimated Market Compensation in India:

Estimated compensation for this role type in India is β‚Ή3,50,000 - β‚Ή6,00,000 per annum (Freshers/Entry level). The actual salary package offered depends on factors such as company size, work mode (remote or on-site), individual technical proficiency, and negotiations during final HR rounds.

Suggested Professional Certifications:

Highly recommended certifications include: AWS Certified Solutions Architect, Microsoft Certified: Azure Fundamentals, Certified Kubernetes Administrator (CKA), Oracle Certified Professional Java SE, or tech-stack specific achievements (e.g. Meta Front-End Developer certification).

Frequently Asked Questions

1️⃣ Where will the walk-in interview be conducted?
The interview will be held at Productivity House, 4th Floor, BPC Road, Alkapuri, Vadodara, Gujarat – 390007.

2️⃣ What is the interview date and timing?
The walk-in interview is scheduled for 24 July 2026 (Friday), from 09:30 AM to 03:30 PM.

3️⃣ Are freshers eligible?
Yes. 2026 pass-out freshers are eligible for specific Production and QC opportunities. ADL also considers candidates from fresher level up to 8 years of experience.

4️⃣ What experience is required for R&D Synthesis?
The R&D Synthesis opportunity requires candidates with 2–8 years of experience and relevant expertise in areas such as API synthesis, process development, CDMO, peptides, or oncology APIs.

5️⃣ What if I cannot attend the walk-in interview?
Candidates unable to attend can send their updated resumes to careers@amilifesciences.com.

6️⃣ What documents should candidates carry?
Candidates should carry their updated resume, educational certificates, experience certificates if applicable, latest 3 months’ salary slips, current CTC details, salary breakup, passport-size photograph, and identity proof.

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