Ribosome Research Centre Pvt. Ltd. is hiring QA Officers for its Quality Assurance department. This is a valuable opportunity for professionals with 1-8 years experience in OECD GLP and NABL seeking pharma jobs, QA jobs, and pharmaceutical careers in India. Join a company dedicated to quality research and regulatory excellence.
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About the Company
Ribosome Research Centre Pvt. Ltd. is a specialized contract research organization focused on providing high-quality preclinical and analytical services in the pharmaceutical and biotechnology sectors. With a strong emphasis on regulatory compliance, scientific integrity, and innovation, the company operates facilities that meet OECD GLP and NABL (ISO/IEC 17025:2017) standards.
Ribosome Research Centre is committed to delivering reliable data and supporting drug development processes while maintaining the highest levels of quality and ethical practices. The organization continues to grow as a trusted partner for global clients, offering a professional environment for professionals to build successful careers in pharmaceutical research and quality assurance.
Job Details
- Company Name: Ribosome Research Centre Pvt. Ltd.
- Experience: 1-3 years and 4-8 years in OECD GLP & NABL (ISO/IEC 17025:2017)
- Qualification: Relevant qualifications in Pharmacy, Life Sciences or related fields
- Location: Not specified (likely company facility)
- Work Type: On-site
Job Description
Ribosome Research Centre is strengthening its Quality Assurance team with openings for QA Officers. This role is essential for ensuring compliance with international standards through inspections, documentation review, and quality system management. The position supports the company’s commitment to GLP and NABL excellence in a research-driven environment.
QA Officer
- Department: Quality Assurance
- Market: Pharmaceutical Research & CRO
- Role: QA Officer
- Experience: 1-3 years or 4-8 years
- Education/Qualification: Relevant scientific or pharmacy background
Skills/Qualifications
- Hands-on experience in QAU as per OECD GLP and NABL (ISO/IEC 17025:2017)
- Strong knowledge of study-based, process-based, and facility-based inspections
- Experience in review of SOPs, Change Control, Deviation, and CAPA
- Excellent verbal and written communication skills
- Attention to detail and strong documentation abilities
- Familiarity with toxicology or study director roles (advantage for experienced candidates)
- Ability to work effectively in a quality-focused team
- Proactive approach to compliance and quality improvement
Key Responsibilities
- Plan and perform various types of inspections
- Review SOPs, change controls, deviations, and CAPA
- Ensure compliance with OECD GLP and NABL standards
- Maintain accurate quality documentation and records
- Support internal and external audits
- Coordinate with study personnel and departments
- Monitor quality systems and processes
- Contribute to continuous improvement initiatives
Benefits/Perks
- Career growth in a specialized CRO
- Learning opportunities in GLP and NABL compliance
- Competitive salary and benefits package
- Professional and collaborative work culture
- Exposure to international regulatory standards
- Long-term career stability and development
How to Apply
Interested candidates should send their updated CV and portfolio to hrd@ribosomeresearch.com and ceo@ribosomeresearch.com. You can also call +9174349 36627 for more information.
Apply now and join Ribosome Research Centre! For more pharma jobs across India, visit Pharma Recruiter.
Walk-in Interview Details
No specific walk-in interview details available. Applications are accepted via email.
Why You Should Join
Ribosome Research Centre offers a culture of scientific integrity, innovation, and quality excellence where QA professionals play a critical role in ensuring reliable research outcomes. Employees enjoy long-term career stability, continuous learning opportunities in GLP and NABL standards, and a supportive environment focused on regulatory compliance and professional development. Join a company that values expertise and contributes to advancing pharmaceutical research while building a rewarding career in India.
FAQs
Q1: What experience is required for the QA Officer position?
1-3 years or 4-8 years in OECD GLP and NABL (ISO/IEC 17025:2017). Toxicology or study director experience is an advantage.
Q2: What is the qualification needed?
Relevant qualifications in Pharmacy, Life Sciences or related fields.
Q3: How can I apply?
Send your CV to hrd@ribosomeresearch.com and ceo@ribosomeresearch.com.
Q4: What growth opportunities does Ribosome Research Centre offer?
Strong career progression in quality assurance, exposure to international GLP standards, and professional development in a research-focused CRO.
