Aristo Pharmaceutical Hiring– QA Officers / Senior Officers for OSD Manufacturing Unit | Apply Now

Aristo Pharmaceutical, one of India’s well-known pharmaceutical companies, has announced an exciting recruitment drive for experienced Quality Assurance (QA) professionals. The company is inviting applications for QA Officers and Senior Officers for its OSD (Oral Solid Dosage) Manufacturing Unit located in Sikkim.

Candidates with experience in OSD formulation manufacturing and a strong understanding of cGMP, documentation, and quality systems are encouraged to apply.

Job Overview

Particulars Details

Company Name

Aristo Pharmaceutical

Job Role

QA Officer / Senior Officer

Department

Quality Assurance (QA)

Manufacturing Unit

OSD Manufacturing

Qualification

M.Sc / B.Pharm

Experience

2–6 Years

Job Location

Sikkim

Employment Type

Full-Time

About Aristo Pharmaceutical

Aristo Pharmaceutical is a trusted pharmaceutical company recognized for delivering high-quality healthcare products. With advanced manufacturing facilities and strict compliance with international quality standards, Aristo offers excellent career growth opportunities for pharmaceutical professionals.

Vacancy Details

Position Available

QA Officer

Senior Officer – Quality Assurance

Department

Quality Assurance (QA)

OSD Manufacturing Unit

Educational Qualification

Applicants should possess any of the following qualifications:

M.Sc

Bachelor of Pharmacy (B.Pharm)

Experience Required

Minimum: 2 Years

Maximum: 6 Years

Experience in OSD Formulation Manufacturing is mandatory.

Job Responsibilities

Selected candidates will be responsible for:

Performing IPQA (In-Process Quality Assurance) activities.

Conducting Line Clearance before production.

Performing In-process Checks and Finished Product Inspection.

Ensuring compliance with cGMP, SOPs, and Quality Standards.

Reviewing Batch Manufacturing Records (BMR) and maintaining Data Integrity.

Coordinating with Production, QC, and QA teams.

Investigating Deviations and supporting CAPA implementation.

Handling APQR (Annual Product Quality Review) activities.

Executing Validation and Qualification activities, including:

Process Validation

Cleaning Validation

Equipment Qualification

Utility Qualification

Computer System Validation (CSV)

Required Skills

Candidates should have knowledge of:

cGMP Guidelines

Good Documentation Practices (GDP)

IPQA Activities

Line Clearance

Batch Record Review

Deviation Investigation

CAPA

APQR

Validation & Qualification

Data Integrity

SOP Compliance

Why Join Aristo Pharmaceutical?

Dynamic and growth-oriented work environment.

Opportunity to work in a modern OSD manufacturing facility.

Exposure to advanced pharmaceutical quality systems.

Excellent learning and career development opportunities.

Opportunity to work with experienced pharmaceutical professionals.

Job Location

Sikkim, India

How to Apply

Interested and eligible candidates can send their updated resume to the official email addresses below:

Email IDs

vishal.chanday@aristopharma.co.in

sailesh.rai@aristopharma.co.in

Subject Line Example:

Application for QA Officer / Senior Officer – OSD Manufacturing

Selection Process

The recruitment process may include:

Resume Screening

HR Interview

Technical Interview

Final Selection

Offer Letter

Documents Required

Updated Resume

Educational Certificates

Experience Certificates

Latest Salary Slip (if applicable)

Government Photo ID

Passport-size Photograph

5 Technical FAQs

1. What is IPQA in pharmaceutical manufacturing?

IPQA (In-Process Quality Assurance) involves monitoring manufacturing activities during production to ensure products comply with GMP requirements and predefined quality standards.

2. What is the purpose of Line Clearance?

Line Clearance ensures that equipment and production areas are free from materials, labels, and documents from previous batches before starting a new batch, preventing cross-contamination and mix-ups.

3. What is CAPA in Quality Assurance?

CAPA (Corrective and Preventive Action) is a quality management system used to identify the root cause of deviations or non-conformities and implement corrective and preventive measures to avoid recurrence.

4. What is APQR (Annual Product Quality Review)?

APQR is a periodic review of manufacturing and quality data for a product to verify process consistency, identify trends, and ensure continuous compliance with regulatory requirements.

5. What are Validation and Qualification activities?

Validation and Qualification confirm that processes, equipment, utilities, cleaning procedures, and computerized systems consistently perform as intended and produce products meeting quality specifications.