GLP GMP Analytical Scientist Jobs for M.Sc, M.Pharm
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities
- Eligibility / Qualifications
- Educational Requirements
- Experience Requirements
- Technical Skills
- Application Process
- Why Join Ribosome Research Centre
- Frequently Asked Questions (FAQs)
- Is CRO experience mandatory?
- What analytical techniques are required?
- Is this role suitable for freshers?
- Does the role involve regulatory documentation?
- Summary Table
Ribosome Research Centre hiring Analytical & Bioanalytical Scientists. CRO jobs for M.Sc, M.Pharm with 1–7 years experience.
Ribosome Research Centre Pvt. Ltd. (RRC) is hiring skilled Analytical Scientist and Bioanalytical Scientist professionals for its Contract Research Organization (CRO) operations. This opportunity is ideal for candidates with strong analytical chemistry and bioanalysis expertise who want to work in a regulated GLP/GMP environment supporting global research and regulatory programs.
Company Overview
Ribosome Research Centre Pvt. Ltd. is a leading global Contract Research Organization delivering high-quality analytical, bioanalytical, and regulatory-compliant research services. RRC supports pharmaceutical, biotechnology, and life sciences companies with method development, validation, impurity profiling, and bioanalysis under stringent GLP and GMP standards.
The organization is recognized for its regulatory alignment, client-focused approach, and technical depth across complex analytical and bioanalytical projects.
Job Role & Responsibilities
RRC is hiring for the role of Analytical Scientist / Bioanalytical Scientist to support regulated CRO projects across pharmaceutical development and regulatory submissions.
Key Responsibilities
- Perform impurity profiling including identification and quantification of nitrosamine and genotoxic impurities as per global regulatory guidelines
- Develop and validate analytical methods using LC-MS/MS, HPLC, GC-HS, and related techniques
- Execute customized method development for diverse matrices and dosage forms
- Conduct raw material and finished product analysis including related substances, residual solvents, and heavy metals
- Perform bioanalysis for PK/TK studies involving whole blood, plasma, urine, tissues, and other biological matrices under GLP conditions
- Carry out dose formulation analysis including stability studies, API quantification, and homogeneity testing
- Perform physico-chemical testing and characterization of pharmaceutical substances as per GLP and GMP standards
- Ensure strict compliance with OECD-GLP, GMP, and applicable regulatory requirements
- Support regulatory documentation and data integrity for submissions
- Deliver client-centric analytical services tailored to sponsor-specific project needs
This role directly contributes to regulatory submissions, product safety, and scientific integrity in global drug development programs.
Eligibility / Qualifications
Educational Requirements
M.Sc Analytical Chemistry, M.Sc Pharmaceutical Sciences, M.Pharmacy (Analytical Chemistry), M.Pharmacy (Pharmaceutical Analysis), or related life science disciplines
Experience Requirements
- 1 to 7 years of relevant experience
- Prior experience in a CRO or regulated laboratory environment preferred
- Strong familiarity with OECD-GLP documentation and regulatory expectations
Technical Skills
- Hands-on experience with LC-MS/MS, HPLC, and GC-HS
- Strong understanding of impurity profiling and bioanalytical workflows
- Knowledge of GLP/GMP compliance and data integrity requirements
- Ability to work on multiple client-driven analytical projects
Application Process
Interested and eligible candidates can apply by sharing their updated CV via email:
Shortlisted candidates will be contacted for further interview rounds.
Why Join Ribosome Research Centre
- Opportunity to work in a global CRO environment
- Exposure to advanced analytical and bioanalytical techniques
- Strong regulatory and compliance-driven work culture
- Direct involvement in client-sponsored research programs
- Professional growth in GLP/GMP-regulated operations
Frequently Asked Questions (FAQs)
Is CRO experience mandatory?
CRO experience is preferred but not mandatory if candidates have strong GLP/GMP laboratory exposure.
What analytical techniques are required?
Hands-on experience with LC-MS/MS, HPLC, and GC-HS is essential.
Is this role suitable for freshers?
No. This role requires prior experience ranging from 1 to 7 years.
Does the role involve regulatory documentation?
Yes. The role involves GLP documentation and regulatory-compliant reporting.
Summary Table
| Category | Details |
|---|---|
| Company | Ribosome Research Centre Pvt. Ltd. |
| Vacancies | Analytical Scientist, Bioanalytical Scientist |
| Required Education | M.Sc Analytical Chemistry, M.Pharm Analytical, Pharmaceutical Sciences |
| Experience | 1–7 years |
To apply for this job email your details to ceo@ribosomeresearch.com
