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Analytical Development Executive

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Onsite

Analytical Development Executive

Archerchem Healthcare

Analytical Development Executive

Skills

Testing & QARCompliance

1 month ago

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Important information


Contract type:

Permanent

Salary:

₹300,000 – ₹600,000 / year

Location:

Mumbai, Maharashtra, India

Work mode:

Onsite

Published on:

21 September 2026

What they need


Job Description: Analytical Development Executive

Department: Analytical Development / R&D

Industry: Pharmaceutical CMO / Formulation

Location: Mumbai - Malad

Experience: 3 - 8 Years

About the Role

We are looking for an Analytical Development Executive with hands-on experience in pharmaceutical formulation development and analytical method development/validation. The candidate will support analytical activities for CMO/formulation projects, ensuring robust analytical methods, accurate testing, documentation, and timely project execution.

Key Responsibilities

  • Develop, optimize, and validate analytical methods for pharmaceutical formulations.
  • Perform analytical method development for solid, liquid, and injectable formulations.
  • Conduct method validation, verification, and transfer as per applicable guidelines and SOPs.
  • Perform testing using HPLC, GC, UV, Dissolution, FTIR and other relevant analytical instruments.
  • Develop and optimize analytical methods for assay, related substances, dissolution, content uniformity and other quality attributes.
  • Execute forced degradation studies and establish stability-indicating analytical methods.
  • Prepare and review analytical protocols, reports, specifications, STPs and related documentation.
  • Support analytical method transfer between R&D, QC and manufacturing/CMO sites.
  • Investigate OOS, OOT, deviations and analytical discrepancies and support root-cause analysis.
  • Review analytical data and ensure compliance with data integrity requirements.
  • Coordinate with Formulation R&D, QC, QA, Regulatory and Manufacturing teams.
  • Support stability studies and evaluation of stability data.
  • Maintain proper documentation in accordance with GMP, GLP and regulatory requirements.
  • Support preparation of analytical sections of regulatory and customer/CMO documentation.
  • Ensure timely completion of analytical activities as per project timelines.
  • Stay updated with current CH, pharmacopoeial and regulatory requirements.
  • Travelling to CMO all over India.

Required Qualifications

  • M.Sc. / B.Pharm / M.Pharm / equivalent qualification in Pharmaceutical Analysis, Analytical Chemistry or related field.
  • 26 years of relevant experience in Analytical R&D / Analytical Development within the pharmaceutical industry.
  • Experience in formulation development and/or CMO/CDMO projects will be preferred.
  • Strong hands-on experience with HPLC and other analytical instruments.
  • Good understanding of analytical method development, validation, transfer and stability studies.
  • Knowledge of ICH guidelines, pharmacopoeial requirements and GMP/GLP.
  • Strong documentation, analytical problem-solving and communication skills.

Preferred Experience

Candidates with experience in analytical development for generic formulations, contract manufacturing projects, technology transfer, and regulatory submissions will be preferred.

Key Competencies

  • Analytical Method Development
  • Method Validation & Transfer
  • HPLC / GC / UV / Dissolution
  • Stability & Forced Degradation Studies
  • OOS / OOT Investigation
  • GMP / GLP / Data Integrity
  • Pharmaceutical Formulation
  • Technical Documentation
  • Cross-functional Coordination
  • Problem Solving

Interested candidate can share their cv on [email protected] or can contact us on 90288 71352.

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