GMH Organics, a leading Indian pharmaceutical company specializing in small volume parenteral manufacturing, is hiring for multiple roles at its EU-GMP certified sterile plant in Baddi, Himachal Pradesh. Established in 2005, GMH Organics is renowned for its expertise in injectable manufacturing and contract services for top pharmaceutical companies in India. With a commitment to quality and innovation, GMH Organics offers exciting career opportunities for skilled professionals in the pharmaceutical industry. Explore our urgent job openings for Sterile Manufacturing Chemist, QA, QC, DRA, Warehouse, and QMS roles, and take the next step in your pharma career today!
Job Openings at GMH Organics
1. Sterile Manufacturing Chemist (Production)
- Experience: 3-5 years in sterile manufacturing
- Vacancies: 2 (Male candidates only)
- Responsibilities:
- Oversee sterile production processes for dry powder injections.
- Ensure compliance with EU-GMP standards.
- Monitor equipment operation and troubleshoot issues.
- Maintain documentation for regulatory audits.
- Qualifications:
- B.Pharm or M.Pharm with sterile manufacturing experience.
- Knowledge of GMP and sterile production protocols.
- Strong attention to detail and problem-solving skills.
2. QA Validation Senior Officer
- Experience: 3-5 years in sterile QA validation
- Vacancies: 2
- Responsibilities:
- Conduct validation of sterile manufacturing processes.
- Prepare and review validation protocols and reports.
- Ensure compliance with regulatory standards.
- Support internal and external audits.
- Qualifications:
- B.Pharm/M.Pharm with experience in sterile QA validation.
- Familiarity with EU-GMP and ICH guidelines.
- Analytical and organizational skills.
3. QA Assistant Manager
- Experience: 12-15 years in sterile QA
- Vacancies: 1 (Male candidates only)
- Responsibilities:
- Lead QA team in sterile manufacturing operations.
- Implement quality management systems (QMS).
- Oversee compliance with regulatory requirements.
- Conduct risk assessments and CAPA implementation.
- Qualifications:
- B.Pharm/M.Pharm with extensive sterile QA experience.
- Leadership skills and in-depth GMP knowledge.
- Proven track record in managing audits.
4. QC Officer (HPLC)
- Experience: 2-4 years in HPLC analysis
- Vacancies: 4 (Male candidates only)
- Responsibilities:
- Perform HPLC testing for quality control of injectables.
- Maintain and calibrate analytical equipment.
- Document test results and ensure compliance with SOPs.
- Support stability studies and method validation.
- Qualifications:
- B.Sc./M.Sc. in Chemistry or B.Pharm with HPLC expertise.
- Knowledge of GMP and analytical techniques.
- Precision and accuracy in testing procedures.
5. DRA Officer
- Experience: 3-4 years in regulatory affairs
- Vacancies: 1 (Male/Female)
- Responsibilities:
- Prepare and submit regulatory dossiers for injectables.
- Coordinate with regulatory authorities for approvals.
- Ensure compliance with CDSCO and international guidelines.
- Maintain documentation for regulatory submissions.
- Qualifications:
- B.Pharm/M.Pharm with DRA experience.
- Understanding of regulatory requirements for injectables.
- Strong communication and organizational skills.
6. Warehouse Officer (PM)
- Experience: 1-2 years in pharma warehouse management
- Vacancies: 2
- Responsibilities:
- Manage inventory of raw materials and finished products.
- Ensure proper storage conditions for sterile products.
- Coordinate material dispatch and receipt.
- Maintain warehouse documentation and compliance.
- Qualifications:
- B.Pharm or equivalent with pharma warehouse experience.
- Knowledge of GMP and inventory management systems.
- Organizational and multitasking abilities.
7. Production QMS Officer
- Experience: 2-3 years in sterile QMS
- Vacancies: 1
- Responsibilities:
- Implement and monitor QMS in sterile production.
- Conduct internal audits and ensure compliance.
- Prepare SOPs and quality documentation.
- Support CAPA and deviation management.
- Qualifications:
- B.Pharm/M.Pharm with sterile QMS experience.
- Familiarity with EU-GMP and QMS protocols.
- Strong analytical and documentation skills.
Benefits of Working at GMH Organics
- Competitive salary (INR 3,00,000–8,00,000 annually, based on role and experience).
- Opportunities for career growth in a leading pharmaceutical company.
- Exposure to EU-GMP certified sterile manufacturing processes.
- Supportive work environment with a focus on innovation and quality.
- Access to training and development programs.
How to Apply
Interested candidates should send their CV to humanresource@gmh.co.in or contact 7876456719 via WhatsApp/call. Ensure your application highlights relevant experience in sterile manufacturing or pharmaceutical operations. Only shortlisted candidates will be contacted for interviews. Apply by September 19, 2025, to be considered for these urgent openings at GMH Organics’ dry powder injection manufacturing plant in Baddi, Himachal Pradesh.
FAQs
Q: What qualifications are required for the Sterile Manufacturing Chemist role?
A: Candidates need a B.Pharm/M.Pharm with 3-5 years of experience in sterile manufacturing, particularly in dry powder injections, and knowledge of EU-GMP standards.
Q: Can female candidates apply for the DRA Officer position?
A: Yes, the DRA Officer role is open to both male and female candidates with 3-4 years of experience in regulatory affairs.
