Ajanta Pharma Hiring QA Officer

B Pharm/MSc QA Officer Vacancy – Ajanta Pharma Paithan

B Pharm/MSc QA Officer openings at US FDA-approved Ajanta Pharma facility, Paithan. 3–4 yrs experience. Apply before 27/10/2025!

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Ajanta Pharma Limited, a US FDA-approved pharmaceutical formulation company, invites qualified professionals to join its Quality Assurance (QA) team at its Paithan facility, Maharashtra. This role is ideal for B Pharm or MSc graduates with 3–4 years of experience in OSD (Oral Solid Dosage) formulation operations. Candidates will play a pivotal role in training, GMP compliance, and QA excellence, ensuring the organization continues to meet international regulatory standards.

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Company Overview

Ajanta Pharma Limited is a globally recognized pharmaceutical manufacturer, committed to delivering high-quality, patient-focused medicines. The company’s Paithan facility is US FDA-approved, reflecting strict adherence to international quality standards, regulatory compliance, and GMP practices.

Ajanta Pharma has been certified as a “Great Place to Work” (Feb 2024 – Feb 2025), highlighting its commitment to employee development, workplace excellence, and professional growth opportunities. The company fosters a culture of quality, accountability, and continuous improvement, making it an ideal workplace for QA professionals.

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Job Role & Responsibilities

Department: Quality Assurance (QA)
Designation: Officer – QA
Experience: 3–4 years
Educational Qualification: B Pharm / MSc

The selected candidate will be responsible for ensuring GMP compliance, training execution, and quality standards across the OSD formulation operations. The role combines training management, cross-department coordination, and regulatory adherence, contributing to the organization’s operational efficiency.

Key Responsibilities:

• Maintain and update all training records, matrices, and attendance sheets accurately.

• Coordinate and execute GMP and job-specific training sessions for employees.

• Manage cross-departmental coordination to ensure smooth training execution and planning.

• Conduct induction training for new joiners to align them with company standards.

• Provide support in training applications (TRIMS) for tracking and reporting.

• Monitor training effectiveness and provide feedback for continuous improvement.

• Support QA leadership in ensuring compliance with US FDA and GMP standards.

This role is critical for maintaining a robust training culture, ensuring that the workforce is well-equipped, compliant, and capable of upholding Ajanta Pharma’s quality standards.

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Eligibility / Qualifications

• Education: B Pharm or MSc in Pharmaceutical Sciences or related fields

• Experience: 3–4 years in OSD formulation QA at US FDA-approved facilities

• Skills Required:

  • Hands-on experience in training management and TRIMS applications

  • Knowledge of GMP, OSD formulation processes, and QA practices

  • Strong cross-functional communication and coordination skills

  • Ability to plan and execute induction and ongoing training sessions

Relevant Courses: B Pharm, MSc Pharmaceutical Sciences, Industrial Pharmacy, Regulatory Affairs, QA & QC Practices, OSD Formulation Management

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Location & Contact

Location:
Ajanta Pharma Limited
B-4/5/6, MIDC Area, Paithan, Dist. Chhatrapati Sambhajinagar, Maharashtra – 431148

Application Process:

• Submit your resume/CV to: cv.ptn@ajantapharma.com

• Ensure applications are sent before 27/10/2025, as this communication is valid until then.

CTA: Apply today to become part of a US FDA-approved facility and contribute to global pharmaceutical quality standards!

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Why Join Ajanta Pharma?

• Work in a US FDA-approved OSD formulation facility, ensuring international quality compliance.

• Gain exposure to cutting-edge QA practices, GMP standards, and training management tools.

• Collaborate with experienced QA professionals and cross-functional teams.

• Opportunities for professional growth, skill development, and career progression.

• Be part of a Great Place to Work certified organization.

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Frequently Asked Questions (FAQs)

Q1: Who is eligible for the QA Officer position?
A: Candidates with a B Pharm or MSc degree and 3–4 years of experience in QA at US FDA-approved OSD facilities are eligible.

Q2: Can freshers apply for this role?
A: No, only professionals with prior experience in OSD QA operations will be considered.

Q3: What are the primary responsibilities?
A: Responsibilities include training coordination, GMP compliance, TRIMS management, induction sessions, and cross-departmental QA support.

Q4: Where is the job location?
A: Paithan, Dist. Chhatrapati Sambhajinagar, Maharashtra.

Q5: How do I apply?
A: Email your CV to cv.ptn@ajantapharma.com before 27/10/2025.

Q6: What is the importance of TRIMS in this role?
A: TRIMS is used for tracking training, attendance, and compliance records, ensuring structured workforce development and audit readiness.

Q7: What growth opportunities exist for this role?
A: Career progression to Senior QA Officer, QA Executive, or QA Team Lead is possible with consistent performance.

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