QA Analyst B.Pharma Fresher .

HR Remedy India; Pune District, Chhatrapati Sambhajinagar District, Mumbai; On-site; INR 240,000 - 300,000; Full time

Job summary

HR Remedy India Pvt Ltd is seeking B.Pharm fresh graduates (2026 pass-outs) for entry-level QA and QC trainee positions in a multinational pharmaceutical setting in Pune. The role involves supporting GMP-compliant QA/QC activities, documentation, and laboratory testing under supervision.

The candidate will join either QA or QC streams based on company needs, with exposure to GMP, GLP, SOPs and essential laboratory operations while preparing for a regulated manufacturing environment.

Qualifications

• B.Pharm fresh graduates accepted (2026 pass-out).
• Fresher with interest in QA/QC roles in pharma.
• Willingness to work in shifts may be required.
• Basic understanding of GMP/GLP concepts.
• Strong documentation and analytical skills.

Responsibilities

• QA: assist in GMP documentation review and record maintenance.
• QA: maintain BMR/BPR records and SOPs and related quality docs.
• QA: support in-process quality checks and area inspections.
• QA: learn deviations, CAPA, and change control procedures.
• QC: assist sampling and testing of materials per procedures.
• QC: perform basic lab testing under supervision and maintain records.

Skills

GMP knowledge

GLP understanding

SOP documentation

Quality mindset

Attention to detail

Teamwork

Education

B.Pharm

Tools

HPLC

UV-Vis

Calibration checks

Job description

Job Description: QA / QC Trainee Pharmaceutical MNC

Industry: Pharmaceutical Manufacturing
Position: Quality Assurance (QA) Trainee / Quality Control (QC) Trainee
Employment Type: Full-Time
Experience: Fresher – 2026 Pass-Out
Education: B.Pharm (Bachelor of Pharmacy)
Salary: As per company standards

Job Overview

We are hiring B.Pharm freshers (2026 pass-outs) for entry-level opportunities in Quality Assurance (QA) and Quality Control (QC) with a reputed multinational pharmaceutical company.

1. Job Responsibilities – Quality Assurance (QA)

The QA Trainee will assist the Quality Assurance team in maintaining product quality and ensuring compliance with pharmaceutical quality standards.

• Assist in reviewing and maintaining GMP (Good Manufacturing Practices) documentation.
• Support preparation and maintenance of Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR).
• Assist in maintaining Standard Operating Procedures (SOPs) and other quality documents.
• Support in-process quality checks and manufacturing area inspections.
• Assist in documentation review and verification of compliance with approved procedures.
• Learn about deviations, investigations, CAPA (Corrective and Preventive Actions), and change control procedures.
• Support line clearance activities and production documentation checks, as authorized.
• Assist in maintaining data integrity and proper documentation practices.
• Participate in internal audits, quality reviews, and compliance-related activities under supervision.
• Follow applicable safety, hygiene, and pharmaceutical quality requirements.

2. Job Responsibilities – Quality Control (QC)

The QC Trainee will assist the Quality Control team in laboratory testing and quality evaluation of pharmaceutical materials and products.

• Assist in sampling and testing of raw materials, packaging materials, and finished products as per approved procedures.
• Learn and perform laboratory testing under supervision.
• Understand basic analytical techniques such as titration, pH measurement, and other applicable chemical and physical tests.
• Gain exposure to analytical instruments such as HPLC, UV-Visible Spectrophotometer, and other laboratory equipment, depending on the assigned department.
• Assist in maintaining laboratory records, test reports, worksheets, and analytical documentation.
• Support preparation of reagents, solutions, and laboratory materials as per approved procedures.
• Follow laboratory safety practices, Good Laboratory Practices (GLP), and applicable GMP requirements.
• Assist in calibration checks and routine maintenance documentation of laboratory instruments.
• Understand out-of-specification (OOS) and out-of-trend (OOT) results and their investigation procedures under supervision.
• Maintain cleanliness, organization, and compliance within the laboratory.

Note: Candidates will be assigned to either QA or QC based on the company's requirements, candidate suitability, and available openings.

3. Candidate Eligibility

• B.Pharm graduates who have completed their degree in 2026.
• Freshers with no prior full-time work experience are eligible to apply.
• Basic understanding of pharmaceutical manufacturing, quality assurance, quality control, and GMP concepts.
• Good communication, documentation, and analytical skills.
• Attention to detail and willingness to learn pharmaceutical quality systems.
• Ability to follow standard procedures and work in a regulated manufacturing environment.
• Willingness to work in shifts, if required by the company.
• Candidates must meet the employer's applicable eligibility and documentation requirements.

4. Key Skills Required

• Basic pharmaceutical and analytical knowledge.
• Understanding of GMP, GLP, and SOPs.
• Documentation and record-keeping skills.
• Basic knowledge of laboratory instruments and testing procedures.
• Attention to detail and a quality-oriented mindset.
• Teamwork, discipline, and a learning attitude.

5. Career Opportunities

• Quality Assurance (QA)
• Quality Control (QC)
• Pharmaceutical Manufacturing Quality Systems
• Laboratory Testing and Analytical Quality Control
• GMP Compliance and Documentation
• Pharmaceutical Audits and Quality Management Systems