Gracure hiring R&D Research Associate
- MPharm MSc R&D Research Associate Openings – Gracure Bhiwadi
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities
- Eligibility / Qualifications
- Required Education
- Experience
- Desired Skills
- Location & Salary
- Application Process
- FAQs
- Is experience in ADL mandatory?
- Are freshers eligible?
- What formulation background is preferred?
- Do I need experience in impurity profiling?
- Is documentation experience necessary?
- Summary Table
MPharm MSc R&D Research Associate Openings – Gracure Bhiwadi
Gracure Pharmaceuticals hiring M.Pharm/M.Sc candidates (1–4 yrs) for R&D ADL roles in Bhiwadi. Apply via email.
Gracure Pharmaceuticals is hiring Research Associates and Senior Research Associates for its R&D division in Bhiwadi, Rajasthan. These openings are suited for candidates with hands-on analytical experience in ADL/QC, particularly in method development and method validation for OSD formulations. Professionals with strong documentation skills and exposure to regulatory expectations will find this an impactful role within a growing research environment.
Company Overview
Gracure Pharmaceuticals Ltd. is a formulation-driven organization with a strong focus on high-quality research, technology transfer, and regulatory compliance. The company’s R&D centre supports global filings and develops robust analytical methods that ensure product quality and safety. Working at Gracure provides structured exposure to analytical research, impurity profiling, regulatory documentation and GLP-driven laboratory operations.
Job Role & Responsibilities
The Research Associate/Sr. Research Associate will support analytical method development, validation and documentation activities required for OSD formulations.
Key Responsibilities
- Develop and finalize analytical methods with specifications and STPs.
- Prepare dissolution method development reports.
- Create comparative dissolution profile protocols and reports.
- Conduct risk assessments for elemental impurities, nitrosamine impurities and residual solvents.
- Prepare analytical method development reports.
- Draft analytical incident reports and CAPA documentation.
- Deliver GLP and SOP training to departmental scientists.
- Perform analytical document gap assessments and ensure compliance with agency expectations.
- Prepare method equivalency or superiority reports.
- Support creation and maintenance of other analytical documents required for regulatory submissions.
These responsibilities require solid analytical reasoning, strong documentation discipline and familiarity with regulatory expectations for global markets.
Eligibility / Qualifications
Required Education
- M.Pharm (Pharmaceutics/Pharmaceutical Analysis/Quality Assurance)
- M.Sc (Chemistry/Analytical Chemistry)
Relevant Courses (comma-separated): Pharmaceutical Analysis, Analytical Chemistry, Quality Assurance, Instrumental Methods of Analysis, Chromatography, Dissolution Science, Impurity Profiling.
Experience
- 1 to 4 years in ADL/QC with proven experience in analytical method development and validation for OSD formulations.
- Experience handling dissolution profiling, impurity assessment, documentation and incident/CAPA management.
Desired Skills
- Strong understanding of GLP, data integrity and documentation practices.
- Ability to conduct scientific assessments and prepare structured analytical reports.
- Good communication, analytical interpretation and problem-solving capability.
Location & Salary
Location: Gracure Pharmaceuticals Ltd., Bhiwadi, Rajasthan.
Salary will be based on experience and analytical expertise, aligned with industry standards for R&D roles in formulation development.
Application Process
Eligible candidates may share their updated resume at:
shivani.singh@gracure.com
Use a clear subject line such as: “Application – R&D Research Associate | Your Name.”
FAQs
Is experience in ADL mandatory?
Yes, ADL/QC experience with method development and validation is required.
Are freshers eligible?
No. Minimum 1 year relevant experience is required.
What formulation background is preferred?
OSD analytical experience is essential.
Do I need experience in impurity profiling?
Yes. Experience with elemental, nitrosamine and residual solvent risk assessment is valued.
Is documentation experience necessary?
Absolutely. Strong documentation and report-writing skills are crucial.
Summary Table
| Category | Details |
|---|---|
| Company | Gracure Pharmaceuticals Ltd. |
| Vacancies | Research Associate / Sr. Research Associate (R&D – ADL) |
| Required Education | M.Pharm, M.Sc |
| Experience | 1–4 years in ADL/QC with method development & validation |
To apply for this job email your details to shivani.singh@gracure.com
