Amgis Hiring QC, ADL, QA & Warehouse
- Company Overview
- Job Role & Responsibilities
- Quality Control (QC)
- QC – ADL (Analytical Development Laboratory)
- Quality Assurance (QA)
- Warehouse Department
- Eligibility / Qualifications
- Location & Work Environment
- Application Process
- Why API Industry Experience Adds High Career Value
- Frequently Asked Questions (FAQs)
- 1. Is API experience mandatory?
- 2. Are freshers eligible?
- 3. What is the job location?
- 4. What departments are hiring?
- 5. How do I apply?
- Job Summary
BSc MSc Pharma API Jobs Panoli Ankleshwar
QC, ADL, QA & Warehouse vacancies (1–7 yrs) at Amgis Lifescience Ltd., Panoli Ankleshwar. API industry experience required.
Amgis Lifescience Ltd. is inviting experienced professionals from the Pharmaceutical API and Intermediate manufacturing industry to join its growing operations at Panoli, Ankleshwar. The company has announced multiple openings across Quality Control (QC), Analytical Development Laboratory (ADL), Quality Assurance (QA), and Warehouse departments.
If you are searching for API manufacturing jobs in Ankleshwar, pharmaceutical QC vacancies in Gujarat, ADL analyst careers, QA executive roles in API plants, or warehouse jobs in pharma industry, this opportunity offers hands-on exposure in a compliance-driven manufacturing environment.
Company Overview
Amgis Lifescience Ltd. operates in the Active Pharmaceutical Ingredient (API) and pharmaceutical intermediate segment, supporting regulated and semi-regulated markets. API manufacturing is one of the most compliance-intensive sectors within the pharmaceutical industry, requiring strict adherence to GMP guidelines, documentation control, and regulatory audit readiness.
Companies operating in API clusters like Panoli and Ankleshwar play a critical role in the global pharmaceutical supply chain. Professionals working in such facilities gain strong exposure to:
- GMP-compliant API manufacturing systems
- Analytical method validation and development
- Quality Management Systems (QMS)
- Regulatory documentation and audit preparation
- Warehouse control and material traceability
Experience in API manufacturing significantly strengthens long-term career growth in pharmaceutical quality, regulatory, and technical operations.
Job Role & Responsibilities
Amgis Lifescience Ltd. is hiring for the following departments:
Quality Control (QC)
Experience: 2–4 Years
Industry Background: Pharma API / Intermediate Mandatory
Key Responsibilities:
- Performing routine analysis of raw materials, intermediates, and finished APIs
- Handling analytical instruments such as HPLC, GC, UV, and related equipment
- Maintaining laboratory documentation as per GMP and ALCOA principles
- Supporting OOS, OOT, and deviation investigations
- Ensuring compliance with regulatory standards and audit requirements
QC professionals ensure product quality and data integrity before release for commercial supply.
QC – ADL (Analytical Development Laboratory)
Experience: 3–4 Years
Mandatory Requirement: ADL Knowledge
Key Responsibilities:
- Method development and validation for API and intermediates
- Preparing analytical protocols and validation reports
- Supporting technology transfer from R&D to commercial production
- Troubleshooting analytical challenges during scale-up batches
- Ensuring documentation compliance with regulatory expectations
ADL roles require strong technical understanding of analytical chemistry and regulatory documentation practices.
Quality Assurance (QA)
Experience: 4–7 Years
Industry Background: Pharma API / Intermediate Mandatory
Key Responsibilities:
- Managing QMS activities including change control, deviation, and CAPA
- Reviewing batch manufacturing records and analytical reports
- Supporting internal and external regulatory audits
- Ensuring compliance with GMP and data integrity guidelines
- Handling documentation review and validation processes
QA professionals are responsible for maintaining overall plant compliance and ensuring readiness for regulatory inspections.
Warehouse Department
Experience: 1–3 Years
Industry Background: Pharma API / Intermediate Mandatory
Key Responsibilities:
- Managing receipt, storage, and dispatch of API raw materials and intermediates
- Maintaining inventory records and ERP documentation
- Ensuring material traceability and GMP compliance
- Coordinating with production and QA teams
- Supporting audit requirements related to material management
Warehouse professionals play a critical role in maintaining supply chain integrity and regulatory compliance.
Eligibility / Qualifications
Educational Qualifications (comma-separated):
B.Sc Chemistry, M.Sc Chemistry, B.Pharm, M.Pharm, Any Graduate (Warehouse – with pharma API experience)
Experience Requirements:
- 1–7 years depending on department
- Mandatory experience in Pharmaceutical API or Intermediate manufacturing
- Hands-on exposure to GMP-compliant environments
Core Competencies:
- Knowledge of GMP and regulatory requirements
- Strong documentation and audit readiness skills
- Analytical and problem-solving abilities
- Understanding of API manufacturing processes
Candidates without API industry background may not be considered.
Location & Work Environment
Location: Panoli, Ankleshwar, Gujarat
Ankleshwar and Panoli are among India’s major API manufacturing hubs. Working in this cluster provides exposure to export-oriented production, regulatory audits, and high-volume API operations.
Compensation will be based on experience, technical skills, and current CTC.
Application Process
Interested candidates are requested to share their updated resume at:
Email: hrd@amgislifescience.com
Contact/WhatsApp: 8141104608
Application Tips:
- Clearly mention API industry experience in your CV.
- Highlight analytical instrumentation exposure (for QC/ADL roles).
- Mention QMS and audit experience (for QA role).
- Include current CTC and notice period.
Shortlisted candidates will be contacted for further selection rounds.
Why API Industry Experience Adds High Career Value
The API manufacturing sector operates under strict global regulatory frameworks. Professionals trained in API quality control, analytical development, and quality assurance develop advanced compliance and technical expertise.
Career advantages include:
- Strong demand for GMP-trained professionals
- Opportunities in regulated export markets
- Higher salary growth with compliance expertise
- Transition pathways into regulatory affairs and validation roles
Building a career in API manufacturing offers long-term stability and global employability.
Frequently Asked Questions (FAQs)
1. Is API experience mandatory?
Yes. Pharma API or Intermediate manufacturing background is required.
2. Are freshers eligible?
No. Relevant industry experience is mandatory.
3. What is the job location?
Panoli, Ankleshwar, Gujarat.
4. What departments are hiring?
QC, QC-ADL, QA, and Warehouse.
5. How do I apply?
Send your resume to hrd@amgislifescience.com or contact via WhatsApp at 8141104608.
Job Summary
| Company | Amgis Lifescience Ltd. |
|---|---|
| Vacancies | QC Executive; QC-ADL Analyst; QA Executive; Warehouse Executive |
| Required Education | B.Sc, M.Sc, B.Pharm, M.Pharm, Graduate (with API experience) |
| Experience | 1–7 Years (API/Intermediate Industry Mandatory) |

To apply for this job email your details to hrd@amgislifescience.com