Ajanta walk-in Quality Control, Production

BPharm 5+ Vacancies Ajanta Pharma Paithan Walk-in

Meta Description: B.Pharm, M.Pharm, B.Sc candidates apply for 5+ vacancies at Ajanta Pharma Paithan. Production & QC roles with 2–5 yrs experience.

URL Slug: ajanta-pharma-production-qc-osd

Ajanta Pharma Limited is conducting a walk-in interview for experienced professionals in Production and Quality Control at its USFDA-approved OSD formulation facility. This hiring drive targets candidates with hands-on experience in regulated pharmaceutical manufacturing environments.

If you are searching for pharma jobs in Maharashtra, OSD production jobs, QC analyst pharma roles, HPLC jobs in pharma industry, or high-paying GMP jobs in India, this opportunity offers strong career growth in a globally recognized pharmaceutical company.

Company Overview

Ajanta Pharma Limited is a leading specialty pharmaceutical company engaged in the development, manufacturing, and marketing of high-quality finished dosage formulations. With operations across 30+ countries and seven advanced manufacturing facilities in India, Ajanta is known for its strong regulatory compliance and innovation-driven approach.

The Paithan facility, approved by USFDA and other global agencies, focuses on Oral Solid Dosage (OSD) manufacturing, making it a critical hub for international pharmaceutical supply.

Working at Ajanta Pharma provides exposure to global regulatory standards, advanced manufacturing systems, and high-demand pharmaceutical technologies.

Job Role & Responsibilities

Production Officer / Sr. Officer (OSD Manufacturing)

• Handle granulation, compression, coating, pelletization, and capsule filling operations
• Manage packing activities including auto cartonator and track & trace systems
• Operate and monitor SCADA systems and electronic batch records (eBMR/eBPR)
• Ensure compliance with GMP guidelines and batch documentation

Quality Control Officer / Sr. Officer

• Perform analysis of finished products (FP), in-process samples (IP), and stability samples
• Conduct method validation and method transfer activities
• Operate analytical instruments such as HPLC and LIMS systems
• Ensure compliance with GLP, GMP, and regulatory standards

These roles are critical in maintaining product quality, regulatory compliance, and efficient pharmaceutical manufacturing.

Eligibility / Qualifications

Required Education:

• B.Pharm
• M.Pharm
• B.Sc (Chemistry)
• M.Sc (Chemistry)

Relevant Courses:

Pharmaceutics, Pharmaceutical Analysis, Organic Chemistry, Analytical Chemistry, Industrial Pharmacy, Chemistry

Experience Required:

• Production: 2–5 Years
• Quality Control: 3–5 Years

Skills Required:

• OSD manufacturing and packing operations
• HPLC analysis and analytical testing
• GMP, GLP, and documentation practices
• SCADA, e-Log, PAS-X systems (preferred)
• Experience in USFDA/MHRA approved plants

Location & Salary

• Job Location: Paithan, Chhatrapati Sambhajinagar (Aurangabad), Maharashtra

Salary:

• Competitive salary based on experience and industry standards
• Additional benefits as per company policy

Application Process

Candidates can attend the walk-in interview or apply via email.

Walk-in Details:

• Date: 10th May 2026 (Sunday)
• Time: 10:00 AM to 04:00 PM

Venue:

The Fern Kesarval Hotel & Spa
Verna Plateau, Kesarval, Cortalim
Goa – 403710

Documents to Carry:

• Updated Resume
• Current CTC Structure
• Last 3 Salary Slips
• Educational Certificates
• Employment Documents

Apply via Email:

• Email: cv.ptn@ajantapharma.com

Why Join Ajanta Pharma?

• Work in USFDA-approved OSD formulation facility
• Exposure to global pharmaceutical manufacturing standards
• Hands-on experience with advanced systems like SCADA and PAS-X
• Strong career growth in production and quality control domains
• Opportunity to contribute to global healthcare solutions

These roles directly support the production of high-quality medicines distributed across international markets.

FAQs

Who can apply for Ajanta Pharma roles?

Candidates with B.Pharm, M.Pharm, B.Sc, or M.Sc with relevant experience.

What experience is required?

2–5 years for production and 3–5 years for QC roles.

Is regulatory experience mandatory?

Yes, candidates must have experience in USFDA/MHRA-approved facilities.

What skills are important?

OSD manufacturing, HPLC analysis, GMP compliance, and documentation.

Can candidates apply online?

Yes, candidates can send their CV via email if unable to attend walk-in.

Final Thoughts

Ajanta Pharma offers a strong platform for professionals aiming to grow in regulated pharmaceutical manufacturing. With increasing global demand for compliant OSD production and analytical testing, these roles provide stability, growth, and exposure to international standards.

For candidates targeting high-growth pharma careers, especially in production and quality control, this opportunity delivers both technical advancement and long-term career value.

---

Company	Ajanta Pharma Limited
Vacancies	Production Officer, Sr Officer, QC Officer
Required Education	B.Pharm, M.Pharm, B.Sc, M.Sc
Experience	2–5 Years