HAB Pharmaceuticals Recruitment 2026: Multiple Openings in QA, QMS & Documentation at Dehradun Plant

The pharmaceutical industry continues to offer excellent career opportunities for skilled professionals across quality assurance, regulatory compliance, documentation, and manufacturing support functions. If you are looking to build or advance your career in the pharmaceutical sector, a new hiring announcement from HAB Pharmaceuticals & Research Ltd. could be the opportunity you’ve been waiting for.

HAB Pharmaceuticals has announced multiple openings for its Unit-3 manufacturing facility located in Selaqui, Dehradun, Uttarakhand. The company is seeking qualified candidates for various roles in Quality Assurance (QA), In-Process Quality Assurance (IPQA), Quality Management Systems (QMS), Stability Studies, Documentation Control, Artwork Review, Qualification & Calibration, and Documentation Support.

This recruitment drive is ideal for candidates with 1–6 years of pharmaceutical industry experience who want to work in a professional manufacturing environment specializing in Oral Solid Dosage (OSD) and Dry Powder Injection formulations.

About HAB Pharmaceuticals

HAB Pharmaceuticals & Research Ltd. is a recognized pharmaceutical manufacturing company engaged in the development and production of various pharmaceutical formulations. The company focuses on maintaining high-quality standards, regulatory compliance, and continuous innovation within the pharmaceutical manufacturing sector.

The latest recruitment initiative aims to strengthen its quality systems and operational excellence by hiring experienced professionals across multiple departments.

Job Overview

ParticularsDetails
Company NameHAB Pharmaceuticals & Research Ltd.
Plant LocationUnit 3, Selaqui, Dehradun
Job LocationUttarakhand
Qualification12th Pass, B.Sc., M.Sc., B.Pharm
Experience1–6 Years
IndustryPharmaceutical Manufacturing
DepartmentsQA, IPQA, QMS, Documentation, Stability, Calibration
Application ModeEmail

Available Positions

1. IPQA Officer – Dry Powder Injection

Qualification: B.Pharm / M.Sc.

Experience: 3–4 Years

Key Responsibilities:

  • Monitoring manufacturing activities of Dry Powder Injection products.
  • Conducting line clearance activities.
  • Verifying in-process quality parameters.
  • Ensuring compliance with GMP requirements.
  • Performing batch sampling and inspections.

2. IPQA Officer – Oral Solid Dosage (OSD)

Qualification: B.Pharm / M.Sc.

Experience: 3–4 Years

Key Responsibilities:

  • Monitoring granulation, compression, coating, and packaging operations.
  • Reviewing critical process parameters.
  • Conducting shop-floor GMP inspections.
  • Managing in-process quality checks.

3. QMS & Regulatory Compliance Officer/Executive

Qualification: B.Pharm / M.Sc.

Experience: 5–6 Years

Key Responsibilities:

  • Handling deviations, investigations, and root cause analysis.
  • Managing CAPA and change control systems.
  • Supporting internal and external audits.
  • Maintaining regulatory compliance documentation.

4. Document Control Officer

Qualification: B.Pharm / M.Sc.

Experience: 2–3 Years

Key Responsibilities:

  • Managing SOP issuance and archival.
  • Maintaining document control systems.
  • Tracking production records and logbooks.
  • Ensuring compliance with data integrity requirements.

5. Stability Study Officer/Executive

Qualification: B.Pharm / M.Sc.

Experience: 3–4 Years

Key Responsibilities:

  • Managing stability study programs.
  • Handling sample withdrawal and charging activities.
  • Preparing stability protocols and reports.
  • Conducting trend analysis and data reviews.

6. Qualification & Calibration Officer/Executive

Qualification: B.Pharm / M.Sc.

Experience: 3–4 Years

Key Responsibilities:

  • Coordinating equipment qualification activities.
  • Supporting HVAC validation programs.
  • Managing IQ/OQ/PQ documentation.
  • Tracking calibration schedules and records.

7. Artwork Review & Coordination Officer/Executive

Qualification: B.Pharm / M.Sc.

Experience: 3–4 Years

Key Responsibilities:

  • Reviewing packaging artwork and labels.
  • Verifying regulatory compliance requirements.
  • Coordinating with production and regulatory teams.
  • Maintaining artwork approval records.

8. Documentation Support Helper

Qualification: 12th Pass / B.Sc.

Experience: 1–2 Years

Key Responsibilities:

  • Filing and maintaining records.
  • Supporting documentation activities.
  • Managing scanning and photocopying tasks.
  • Assisting departments with administrative support.

Eligibility Criteria

Candidates applying for these positions should possess:

  • Relevant educational qualifications.
  • Pharmaceutical manufacturing experience according to the role applied for.
  • Knowledge of GMP, GDP, and regulatory compliance practices.
  • Good documentation and communication skills.
  • Ability to work in a regulated manufacturing environment.

Job Location

Selected candidates will work at:

HAB Pharmaceuticals & Research Ltd. – Unit 3

122 MI E-State,

Selaqui Industrial Area,

Selaqui, Dehradun,

Uttarakhand – 248197

India

Landmark: Near DBS Global University

Why Consider This Opportunity?

Working with HAB Pharmaceuticals offers several advantages:

✅ Exposure to regulated pharmaceutical manufacturing

✅ Opportunity to work with OSD and Dry Powder Injection facilities

✅ Career growth in Quality Assurance and Compliance functions

✅ Hands-on experience with QMS and regulatory systems

✅ Professional work environment with industry-standard practices

How to Apply

Interested and eligible candidates can apply by sending their updated resume through email.

Application Steps

Step 1: Update your resume with relevant technical skills and experience.

Step 2: Mention the position name clearly in the email subject line.

Example Subject Line:

Application for IPQA Officer – Your Name – 4 Years Experience

Step 3: Attach your updated CV.

Step 4: Send your application to:

Email ID: hra1@habpharma.in

Contact Information

For recruitment-related queries, candidates may contact:

📞 +91 7618261363

📞 +91 9258257210

Important Tips for Applicants

  • Customize your resume according to the role.
  • Highlight experience in QA, QMS, Documentation, Stability, or IPQA.
  • Mention GMP, CAPA, Change Control, Validation, and Compliance experience.
  • Ensure your contact information is updated.
  • Apply as early as possible since vacancies are limited.

Final Thoughts

The HAB Pharmaceuticals Recruitment 2026 drive presents an excellent opportunity for pharmaceutical professionals looking to strengthen their careers in quality systems, compliance, documentation, and manufacturing operations. With openings across multiple specialized departments and a modern manufacturing setup in Dehradun, this recruitment campaign offers promising career prospects for eligible candidates.

Candidates meeting the required qualifications and experience criteria are encouraged to submit their applications promptly and take advantage of this valuable career opportunity.

Disclaimer: Job information is provided for educational and informational purposes only. Applicants are advised to verify details directly with the company before applying.

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