MSN Group is conducting a walk-in interview for Executive – Formulation Analytical Research & Development (FAR&D) at its MSN R&D Center, Pashamylaram, Hyderabad. Candidates with M.Pharma or M.Sc qualifications and 1–5 years of relevant experience in Formulation Analytical R&D can attend the walk-in drive on 31 October 2026.
The opportunity is for professionals experienced in analytical method development, method validation, HPLC/UPLC, pharmaceutical formulation analysis, and stability studies.
Job Details
| Particulars | Details |
|---|---|
| Company | MSN Group |
| Position | Executive |
| Department | Formulation Analytical Research & Development (FAR&D) |
| Division | Formulation Division |
| Designation | Executive FAR&D |
| Qualification | M.Pharma / M.Sc |
| Experience | 1–5 Years |
| Job Location | MSN R&D Center, Pashamylaram |
| Number of Openings | 25 |
| Employment Type | Full-Time, Permanent |
| Industry | Pharmaceutical & Life Sciences |
| Interview Date | 31 October 2026 (Saturday) |
| Interview Time | 9:00 AM – 2:00 PM |
Position: Executive – Formulation Analytical R&D
Department: Formulation Analytical Research & Development (FAR&D)
Function: Analytical Development – Formulation
The selected candidates will perform analytical method development, optimization, validation, and testing of pharmaceutical formulations in accordance with applicable regulatory requirements, approved specifications, and Good Laboratory Practices (GLP).
Job Responsibilities
- Develop, optimize, and validate analytical methods using HPLC, UPLC, UV-Visible spectrophotometry, and other relevant analytical instruments.
- Perform analytical testing of formulation development batches, pilot batches, exhibit batches, stability samples, and finished products.
- Execute analytical method transfer activities and support technology transfer from R&D to Quality Control (QC).
- Conduct forced degradation studies and support the development of stability-indicating analytical methods.
- Perform stability sample analysis according to ICH guidelines and approved stability protocols.
- Conduct related substances, assay, dissolution, content uniformity, and other pharmaceutical analytical tests.
- Prepare and review analytical method development reports, validation protocols, validation reports, method transfer documents, and stability reports.
- Maintain laboratory records, raw data, chromatograms, calculations, and documentation in compliance with ALCOA+ data integrity principles.
- Investigate analytical deviations, atypical results, OOS, and OOT results, as applicable.
- Ensure proper calibration, maintenance, and routine performance checks of analytical instruments.
- Coordinate with Formulation Development, QC, QA, and Regulatory Affairs teams.
- Follow laboratory safety procedures, SOPs, GLP, GMP requirements, and applicable regulatory guidelines.
Eligibility and Educational Qualifications
- Educational Qualification: M.Pharma / M.Sc.
- Experience: 1–5 years of relevant experience in Formulation Analytical R&D.
- Candidates should have relevant experience in pharmaceutical analytical development and formulation analysis.
Candidate Preference: Male candidates preferred.
Required Technical Skills
- Hands-on experience with HPLC/UPLC.
- Working knowledge of UV-Visible spectrophotometry.
- Analytical method development, optimization, validation, and verification.
- Understanding of ICH guidelines, particularly Q1, Q2, and Q14.
- Knowledge of pharmaceutical formulation analysis.
- Experience with dissolution testing and stability studies.
- Familiarity with chromatography data systems and laboratory instruments.
- Understanding of electronic data integrity requirements.
- Ability to prepare technical reports, protocols, SOPs, and analytical documentation.
Key Competencies
- Analytical thinking and problem-solving.
- Attention to detail and data integrity.
- Technical documentation and report writing.
- Effective communication and cross-functional coordination.
- Ability to manage multiple analytical activities and meet project timelines.
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