Ajanta Pharma Hiring QA Officer

- B.Pharm/M.Sc QA Officer Vacancy – Ajanta Pharma Paithan
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Location & Contact
- Why Join Ajanta Pharma?
- Frequently Asked Questions (FAQs)
- Ajanta Pharma Jobs Table
B.Pharm/M.Sc QA Officer Vacancy – Ajanta Pharma Paithan
B.Pharm/M.Sc QA Officer openings at US FDA-approved Ajanta Pharma facility, Paithan. 3–4 yrs experience. Apply before 27/10/2025!
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 M.Sc 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.
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.
Job Role & Responsibilities
Department: Quality Assurance (QA)
Designation: Officer – QA
Experience: 3–4 years
Educational Qualification: B.Pharm / M.Sc
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:
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Maintain and update all training records, matrices, and attendance sheets accurately.
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Coordinate and execute GMP and job-specific training sessions for employees.
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Manage cross-departmental coordination to ensure smooth training execution and planning.
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Conduct induction training for new joiners to align them with company standards.
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Provide support in training applications (TRIMS) for tracking and reporting.
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Monitor training effectiveness and provide feedback for continuous improvement.
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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.
Eligibility / Qualifications
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Education: B.Pharm or M.Sc in Pharmaceutical Sciences or related fields
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Experience: 3–4 years in OSD formulation QA at US FDA-approved facilities
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Skills Required:
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Hands-on experience in training management and TRIMS applications
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Knowledge of GMP, OSD formulation processes, and QA practices
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Strong cross-functional communication and coordination skills
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Ability to plan and execute induction and ongoing training sessions
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Relevant Courses: B.Pharm, M.Sc Pharmaceutical Sciences, Industrial Pharmacy, Regulatory Affairs, QA & QC Practices, OSD Formulation Management
Location & Contact
Location:
Ajanta Pharma Limited
B-4/5/6, MIDC Area, Paithan, Dist. Chhatrapati Sambhajinagar, Maharashtra – 431148
Application Process:
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Submit your resume/CV to: cv.ptn@ajantapharma.com
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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!
Why Join Ajanta Pharma?
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Work in a US FDA-approved OSD formulation facility, ensuring international quality compliance.
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Gain exposure to cutting-edge QA practices, GMP standards, and training management tools.
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Collaborate with experienced QA professionals and cross-functional teams.
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Opportunities for professional growth, skill development, and career progression.
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Be part of a Great Place to Work certified organization.
Frequently Asked Questions (FAQs)
Q1: Who is eligible for the QA Officer position?
A: Candidates with a B.Pharm or M.Sc 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.
Ajanta Pharma Jobs Table
Category | Details |
---|---|
Company | Ajanta Pharma Limited |
Vacancies | Officer – Quality Assurance |
Required Education | B.Pharm, M.Sc Pharmaceutical Sciences |
Experience | 3–4 years in OSD formulation QA |
Location | Paithan, Dist. Chhatrapati Sambhajinagar, Maharashtra |
Application Deadline | 27/10/2025 |

To apply for this job email your details to cv.ptn@ajantapharma.com