Exciting pharma jobs alert! Aarti Pharmalabs Ltd. is conducting a walk-in interview on 17th April 2026 for Production jobs, QA jobs, and QC jobs in API manufacturing. Explore pharmaceutical careers in India with a USFDA-compliant leader. Apply now for roles offering competitive salaries and growth opportunities.
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About the Company
Aarti Pharmalabs Ltd. is a leading Indian manufacturer of Active Pharmaceutical Ingredients (APIs), pharmaceutical intermediates, New Chemical Entities (NCEs), and xanthine derivatives. With six state-of-the-art manufacturing facilities and two R&D centers, the company delivers high-quality drug substances for clinical and commercial phases.
Its plants hold prestigious accreditations including USFDA, EU GMP, EDQM, and others, enabling strong global presence across regulated markets like the USA, Europe, and Japan.
Committed to innovation, regulatory excellence, backward integration, and sustainable practices, Aarti Pharmalabs continues to expand as a trusted CDMO partner for innovator pharma and biotech companies worldwide.
Job Details
- Company Name: Aarti Pharmalabs Ltd.
- Experience: 2–10 years (varies by role)
- Qualification: B.Sc./M.Sc./B.E./B.Tech (Chemical), B.Pharm/M.Pharm, B.Sc. (Microbiology)
- Location: Tarapur, Palghar, Maharashtra (Unit-V, MIDC Tarapur)
- Work Type: On-site
Job Description
Aarti Pharmalabs Ltd. is actively hiring experienced professionals to strengthen its API & Bulk Drug manufacturing team at Unit-V, Tarapur. The company seeks candidates with backgrounds from reputed firms accredited by USFDA, EDQM, TGA, or ANVISA for roles in production, quality assurance, and quality control.
These opportunities focus on GMP-compliant operations in a regulated environment, supporting high-quality API production for global markets.
Production Officer / Executive / Sr. Executive (07 Openings)
- Department: Production (Manufacturing Plant & Powder Processing Area)
- Market: API / Bulk Drug Manufacturing
- Role: Shift In-charge and operational roles in batch manufacturing
- Experience: 5–10 years in API manufacturing
- Education/Qualification: B.Sc./M.Sc./B.E./B.Tech (Chemical)
Quality Assurance (QMS) (04 Openings)
- Department: Quality Assurance
- Market: API Manufacturing
- Role: QMS documentation and compliance management
- Experience: 2–5 years in API
- Education/Qualification: B.Pharm/M.Pharm/M.Sc.
Quality Control (Microbiology) (01 Opening)
- Department: Quality Control – Microbiology
- Market: API Manufacturing
- Role: Microbiological testing and regulatory compliance
- Experience: 2–5 years
- Education/Qualification: B.Sc. (Microbiology)/M.Sc.
Quality Control (04 Openings)
- Department: Quality Control
- Market: API Manufacturing
- Role: Laboratory testing and stability studies
- Experience: 2–5 years
- Education/Qualification: B.Sc./M.Sc.
Skills/Qualifications
- Strong hands-on experience in API manufacturing equipment (reactors, centrifuges, dryers)
- Thorough knowledge of GMP documentation, batch operations, and shift handling
- Expertise in QMS elements: APQR, CpK, Change Control, Deviation, OOS, Incident Management, and SOP preparation/review
- Deep understanding of USFDA and WHO guidelines (mandatory for Microbiology role)
- Experience in laboratory testing, stability studies, method validation, and regulatory audit handling
- Preferred background from USFDA/EDQM/TGA/ANVISA accredited companies
Key Responsibilities
- Handle batch operations and manage shifts in manufacturing and powder processing areas
- Perform GMP documentation and maintain compliance records
- Manage change control, deviations, OOS, and incidents effectively
- Conduct microbiological testing and ensure regulatory adherence
- Execute laboratory testing, stability studies, and method validation
- Prepare, review, and control SOPs and related QMS documents
- Support audit readiness and regulatory compliance activities
Benefits/Perks
- Competitive salary with no upper bar for outstanding candidates
- Excellent career growth opportunities in a rapidly expanding organization
- Exposure to global regulatory standards and international projects
- Collaborative work culture focused on innovation and excellence
- Learning and development in cutting-edge API manufacturing and CDMO services
For more pharma jobs across India, explore opportunities on Pharma Recruiter.
How to Apply
Interested candidates can send their updated CV to akshata.patil@aartipharmalabs.com. Mention the position applied for in the subject line. Shortlisted candidates will be invited for the walk-in interview.
Strong CTA: Don’t miss this chance to build your pharmaceutical career with a reputed API manufacturer. Apply today!
Walk-in Interview Details
- Date: Friday, 17th April 2026
- Time: 10:00 AM – 4:00 PM
- Venue: Aarti Pharmalabs Ltd., Unit-V, Plot No. L-28/29, MIDC Tarapur, Palghar-401506
- Contact: Tel: +91 8855010262 | Email: akshata.patil@aartipharmalabs.com
Why You Should Join
Joining Aarti Pharmalabs means becoming part of a forward-thinking organization recognized for quality, compliance, and innovation in the API sector. The company offers long-term career stability, continuous learning through advanced R&D, and a culture that values excellence and sustainability.
With strong regulatory track record and global client base, professionals here gain valuable exposure while contributing to a healthier tomorrow.
FAQs
Q1: What is the eligibility for Production roles at Aarti Pharmalabs?
A: Candidates need 5–10 years of API manufacturing experience with B.Sc./M.Sc./B.E./B.Tech (Chemical) qualification. Background from regulated plants is preferred.
Q2: How can I apply for these QA/QC pharma jobs?
A: Email your CV to akshata.patil@aartipharmalabs.com or attend the walk-in interview on 17th April 2026 at the Tarapur venue.
Q3: Is prior USFDA experience mandatory?
A: It is highly preferred, especially for Microbiology and QMS roles. Thorough knowledge of USFDA/WHO guidelines is mandatory for QC (Micro).
Q4: What salary can I expect?
A: Salary ranges from Rs. 4.0–8.0 LPA for Production roles (no bar for exceptional candidates). Compensation for QA/QC roles is competitive based on experience.
Q5: Are these on-site positions?Q5: Are these on-site positions?
A: Yes, all roles are on-site at the Tarapur manufacturing facility.
