QA Documentation

Drlogy

Solan

On-site

INR 350,000 - 550,000

Full time

14 days+

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Job summary

Unix Biotech is seeking a QA Documentation Executive for its Jharmajri, Solan facility. The role involves preparing, reviewing, and maintaining GMP/GDP-compliant quality documents, batch records, and related quality systems within a GMP environment.

The position supports audits, regulatory inspections, and continuous QMS improvements. Requires 1–3 years experience and B.Pharm/M.Pharm/B.Sc Life Sciences; full-time on-site work.

Qualifications

  • QA documentation preparation, review and control.
  • Maintain SOPs, specifications, batch records and logs.
  • Ensure GMP/GDP compliance, data integrity and regulatory guidelines.

Responsibilities

  • Prepare, review, issue, revise, and archive quality documents and records.
  • Maintain SOPs, specifications, protocols, batch records, formats, and logbooks.
  • Ensure compliance with GMP, GDP, data integrity, and regulatory guidelines.
  • Control document versioning, numbering, and distribution.
  • Review BMR and BPR.

Skills

Quality assurance documentation
BMR/BPR Review
SOP compliance
Record Maintenance

Education

B.Pharm
M.Pharm
B.Sc (Life Sciences)

Job description

Free to Apply Verified Employer Secure & Private No Hidden Charges

Job Requirements

Experience 1 - 3 Years Experience

Education

  • B.Pharm
  • M.Pharm
  • B.Sc (Life Sciences)

All Gender

Vacancy 2

Last Date to Apply 03, February 2027

Job Role

Work Location Jharmajri, Solan

Work Mode Work From Office

Department Quality Assurance

Employment type

  • Full time
Key Skills

Quality assurance documentation

BMR/BPR Review

SOP compliance

Record Maintenance

Preference Languages

Any Language

Job Story
Job Description

A QA Documentation Executive is responsible for preparing, reviewing, controlling, and maintaining quality assurance documents to ensure compliance with Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), Standard Operating Procedures (SOPs), and regulatory requirements. The supports document control, batch record management, quality systems, audits, and regulatory inspections while ensuring documentation accuracy and data integrity.

Role & Responsibilities
  • Prepare, review, issue, revise, and archive quality documents and records.
  • Maintain SOPs, specifications, protocols, batch records, formats, and logbooks.
  • Ensure compliance with GMP, GDP, data integrity, and regulatory guidelines.
  • Control document versioning, numbering, and distribution.
  • Review Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR).
  • Coordinate with QA, QC, Production, Engineering, Warehouse, and Regulatory Affairs departments.
  • Support deviation, CAPA, change control, and risk assessment documentation.
  • Maintain document control registers and archival records.
  • Assist in qualification, validation, and regulatory documentation activities.
  • Support internal audits, customer audits, and regulatory inspections.
  • Ensure timely retrieval and secure storage of controlled documents.
  • Prepare quality reports and documentation metrics.
  • Train employees on documentation practices and SOP compliance.
  • Maintain confidentiality of quality and manufacturing records.
  • Contribute to continuous improvement of the Quality Management System (QMS).

Unix Biotech is a rapidly growing pharmaceutical manufacturing and marketing company headquartered in Baddi, Solan, Himachal Pradesh, India. Established in 2005, the company was founded by a team of experienced professionals with a strong commitment to improving healthcare through the development and supply of high-quality pharmaceutical products. Over the years, Unix Biotech has built a strong presence in the Indian pharmaceutical industry by focusing on innovation, quality, affordability, and customer satisfaction.

The company manufactures and markets a broad portfolio of pharmaceutical formulations, including tablets, capsules, syrups, dry syrups, protein powders, and nutraceuticals. With modern manufacturing facilities that comply with WHO-GMP quality standards, Unix Biotech serves both domestic and international markets while maintaining stringent quality control throughout the manufacturing process. The company's commitment to research, quality assurance, and ethical business practices has helped establish it as a trusted partner for healthcare professionals, distributors, and patients.

Vision

To become a leading and trusted pharmaceutical company in both the domestic and international markets by delivering innovative, high-quality, and affordable healthcare solutions.

Mission
  • To provide high-quality pharmaceutical products that improve patient health.
  • To make quality medicines accessible and affordable.
  • To uphold the highest standards of quality, safety, and regulatory compliance.
  • To continuously innovate and expand the product portfolio.
  • To serve humanity with integrity, commitment, and excellence.
Core Values
  • Quality
  • Integrity
  • Commitment
  • Customer Satisfaction
  • Trust
  • Service to Humanity

Unix Biotech manufactures and markets a wide range of pharmaceutical products, including:

  • Tablets
  • Capsules
  • Syrups
  • Dry Syrups
  • Specialty Pharmaceutical Formulations
  • Generic Medicines
  • Export-oriented Pharmaceutical Products
Manufacturing & Infrastructure

Unix Biotech is equipped with:

  • WHO-GMP compliant manufacturing facilities
  • Modern pharmaceutical production units
  • Advanced quality control and quality assurance laboratories
  • Research and development support
  • Efficient warehousing and distribution network
  • Export-focused manufacturing capabilities
  • Regulatory-compliant production processes
Quality Commitment

Unix Biotech is committed to:

  • Manufacturing safe, effective, and reliable medicines.
  • Following stringent quality control procedures.
  • Maintaining international manufacturing standards.
  • Ensuring timely delivery through an efficient supply chain.
  • Building long-term relationships based on trust, transparency, and customer satisfaction.
Why Choose Unix Biotech?
  • Established in 2005 with nearly two decades of pharmaceutical expertise.
  • WHO-GMP compliant manufacturing practices.
  • Wide portfolio of pharmaceutical and nutraceutical products.
  • Presence in domestic and international markets.
  • Strong focus on quality, innovation, and affordability.
  • Experienced professional management team.
  • Commitment to ethical business practices and healthcare excellence.
Corporate Office

Unix Biotech Plot No. 27, Export Promotion Industrial Park – Phase I, Jharmajri, Baddi, Solan – 173205, Himachal Pradesh, India.

Our Commitment

Unix Biotech is dedicated to enhancing global healthcare by delivering innovative, high-quality, and affordable pharmaceutical products. Through continuous investment in quality manufacturing, ethical business practices, and patient-focused solutions, the company strives to improve patient outcomes while contributing to the advancement of the pharmaceutical industry.

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