Ortiv-Q3 Hiring Analytical R&D
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities:
- Core Expertise Required:
- Eligibility / Qualifications
- Required Education:
- Experience:
- Key Skills:
- Location & Salary
- Job Location:
- Salary:
- Application Process
- Apply via Email:
- Contact:
- Why This Role Matters in Pharma Industry
- Frequently Asked Questions (FAQs)
- 1. Who can apply for these roles?
- 2. Are freshers eligible?
- 3. What instruments should I know?
- 4. What is the selection process?
- 5. What is the career growth?
- Summary
Ortiv-Q3, a SOTAX Joint Venture, is hiring for 10 vacancies across multiple roles including Research Scientist, Research Associate, and Trainee Research Scientist/Associate in the Analytical Research & Development domain. This is an excellent opportunity for both freshers and experienced candidates (0–5 years) to build a strong career in pharmaceutical analytical development. The positions are ideal for candidates with expertise in HPLC, LC-MS, dissolution testing, and method validation. Candidates will be working in a high-end analytical laboratory environment with exposure to regulated pharmaceutical standards.
Company Overview
Ortiv-Q3 is a joint venture with SOTAX, a globally recognized leader in pharmaceutical testing equipment and analytical solutions. The organization focuses on delivering advanced analytical services, method development, and validation support to pharmaceutical companies.
With a strong presence in analytical research, Ortiv-Q3 plays a critical role in ensuring drug quality, stability, and compliance with international regulatory standards. The company operates with modern laboratories equipped with high-end analytical instruments and follows stringent quality systems aligned with global guidelines.
Working at Ortiv-Q3 offers exposure to advanced analytical techniques, regulatory compliance, and high-value pharmaceutical research projects, making it a strong platform for career growth in analytical R&D.
Job Role & Responsibilities
As part of the Analytical Research & Development team, candidates will be involved in method development, validation, and analytical testing using advanced instrumentation.
Key Responsibilities:
- Perform analytical method development and validation for pharmaceutical products
- Conduct technology transfer (TT) activities and support analytical studies
- Operate and calibrate analytical instruments such as HPLC, LC-MS, and dissolution systems
- Execute routine and non-routine analytical testing
- Ensure compliance with GLP, GMP, and regulatory guidelines
- Maintain proper documentation and analytical records
- Support stability studies and analytical troubleshooting
Core Expertise Required:
- Hands-on experience with HPLC, LC-MS, dissolution apparatus, and PSD
- Understanding of analytical method validation protocols
- Knowledge of calibration, maintenance, and troubleshooting of instruments
- Familiarity with regulatory guidelines and documentation practices
Eligibility / Qualifications
Required Education:
M.Pharm, M.Sc (Analytical Chemistry, Organic Chemistry, Pharmaceutical Sciences, Chemistry, Biotechnology)
Experience:
- 0 to 5 years in analytical laboratory or pharmaceutical R&D
- Freshers with strong academic background in analytical techniques can apply
Key Skills:
- Analytical method development and validation knowledge
- Hands-on experience with HPLC, LC-MS, Dissolution testing
- Understanding of pharmaceutical quality systems and compliance
- Strong documentation and data analysis skills
Location & Salary
Job Location:
India (Location to be communicated during hiring process)
Salary:
Competitive salary package based on experience, analytical expertise, and technical skills. Freshers and experienced candidates will be offered compensation aligned with industry standards.
Application Process
Interested candidates can apply by sharing their updated CV through email.
Apply via Email:
hr@ortiv.in
Talent.acquisition@ortiv.in
Contact:
+91 7676707801
Ensure your resume highlights your experience in analytical techniques, instrument handling, and method validation to improve your chances of selection.
Why This Role Matters in Pharma Industry
Analytical Research & Development is a core function in the pharmaceutical industry, ensuring the quality, safety, and efficacy of drug products. Professionals in this domain are responsible for developing validated analytical methods that support regulatory approvals and product lifecycle management.
By joining Ortiv-Q3, candidates contribute to the development of high-quality medicines that meet global standards. This role provides long-term career growth in analytical sciences, regulatory compliance, and pharmaceutical innovation.
Frequently Asked Questions (FAQs)
1. Who can apply for these roles?
Candidates with M.Pharm or M.Sc degrees and 0–5 years of experience in analytical R&D can apply.
2. Are freshers eligible?
Yes, freshers with knowledge of analytical techniques are eligible.
3. What instruments should I know?
HPLC, LC-MS, Dissolution apparatus, and related analytical instruments.
4. What is the selection process?
Resume screening followed by technical and HR interviews.
5. What is the career growth?
Candidates can grow into senior analytical scientists, regulatory experts, or R&D leads.
Summary
| Company | Ortiv-Q3 (A SOTAX Joint Venture) |
|---|---|
| Vacancies | Research Scientist, Research Associate, Trainee (10 Positions) |
| Required Education | M.Pharm, M.Sc (Analytical Chemistry, Pharma, Chemistry, Biotechnology) |
| Experience | 0–5 Years (Freshers Eligible) |
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