Ipca walk-in Analytical Method Development

M.Pharm Analytical Method Development Roles | Ipca Mumbai

Ipca walk-in for M.Pharm/M.Sc candidates — Analytical Method Development (Research Associate/Scientist). 4–8 yrs exp, Kandivali West, Mumbai.

Ipca Laboratories is inviting experienced analytical scientists to attend a walk‑in interview for its Analytical Development (Formulations) team in Kandivali West, Mumbai. These openings are ideal for M.Pharm or M.Sc (Chemistry) professionals with proven experience in analytical method development, HPLC operation, and technology transfer for regulated and emerging markets. If you have a track record in assay development, dissolution testing, and site troubleshooting — and are willing to travel to manufacturing plants — this role offers high-impact work within a globally compliant R&D environment.

Company Overview

Ipca Laboratories is a leading pharmaceutical company with a strong footprint in global markets. Known for its robust R&D, quality systems, and diverse dosage-form expertise, Ipca supports both regulated (US/EU) and emerging market submissions. The Analytical Development (Formulations) group plays a critical role in ensuring product quality through method development, validation, and transfer — activities that directly support regulatory filings and commercial manufacturing. Working here means contributing to safe, effective medicines and building deep technical competence in analytical chemistry.

Job Role & Responsibilities

Ipca is hiring Research Associates / Research Scientists for Analytical Method Development. The role sits at the intersection of analytical chemistry, method validation, technology transfer, and QC support.

Primary Responsibilities

• Independently develop and optimize analytical methods (HPLC, UV, Dissolution) for assay, related substances, content uniformity, and blend uniformity across dosage forms.
• Execute method validation protocols and produce comprehensive validation reports in line with ICH and regulatory expectations.
• Manage technology transfer activities to QC sites: generate method transfer plans, support site troubleshooting, and ensure data integrity during handover.
• Provide QC support for incoming issues — investigate OOS/OOT results, root cause analysis, and corrective action recommendations.
• Operate chromatography and analytical software (Empower 3.0, Chromeleon 7.2) to generate reliable and auditable data.
• Support stability program sampling and analysis; coordinate with formulation and regulatory groups for analytical requirements.
• Work with multiple dosage forms including oral solids, liquid orals, ophthalmic formulations, and injectables.
• Prepare and review analytical SOPs, method protocols, COAs, and technical documentation for regulatory submissions.

Technical Skills & Tools

• Hands‑on HPLC method development and troubleshooting experience is mandatory.
• Proficiency with Empower and Chromeleon chromatography data systems and experience with dissolution apparatus, UV spectrophotometers, GC, and particle sizing (e.g., Malvern 3000) is desirable.
• Strong understanding of GLP, GMP, data integrity (ALCOA+), and regulatory expectations for analytical methods.
• Experience in analytical method transfer, method validation, system suitability, and stability testing.
• Excellent technical writing skills for preparing validation reports, method transfer documentation, and regulatory‑grade deliverables.

Eligibility / Qualifications

• Educational Qualification: M.Pharm or M.Sc (Chemistry).
• Experience Required: 4–8 years in analytical method development for regulated and emerging markets.
• Relevant Courses (comma-separated): M.Pharm (Pharmaceutics/Pharmaceutical Analysis), M.Sc Chemistry, Analytical Chemistry, Pharmaceutical Chemistry, Method Validation Certification, Chromatography Training.
• Willingness to travel extensively to plant sites for method transfer and troubleshooting — travel is a core part of the role.

Location & Salary

Job Location: Kandivali West, Mumbai (Ipca Laboratories Ltd., Plot No. 48, Kandivali Industrial Estate, Kandivali West, Mumbai – 400067)

Walk‑in Date & Time: 29th November 2025 (Saturday), 10:00 AM – 5:00 PM

Compensation: Competitive and commensurate with experience. Exact salary details will be discussed during the interview and depend on candidate profile and current market bands for analytical chemists and HPLC specialists.

Why This Role Matters

Analytical method development is a high‑impact function in drug development and quality assurance. Methods you develop and validate form the backbone of product release, stability profiling, and regulatory submissions. This role offers exposure to cross‑functional projects (formulation, QC, regulatory) and strengthens expertise in high‑value skills — HPLC method development, method validation, and technology transfer — which are among the most sought‑after competencies in pharmaceutical R&D and analytical chemistry.

Application Process

Confirm your attendance and send your updated CV to jobs.hr@ipca.com with the subject line: Walk‑in ADL – Analytical Development (Your Name). Bring the following documents to the venue:

• Updated resume (hard copy)
• Educational certificates and degree mark sheets
• Experience letters and relieving letters (if any)
• Government ID (Aadhaar/PAN/Passport) and passport-size photograph

Candidates will be screened on a first‑come, first‑serve basis during the walk‑in window. Please ensure you arrive early to complete document verification.

Preparation Tips for Candidates

• Be ready to discuss specific method development and validation projects you handled: objectives, challenges, troubleshooting steps, and final outcomes.
• Prepare examples of technology transfer experiences — explain how you trained QC teams, resolved site-specific issues, and verified method robustness.
• Bring a concise list of instruments and software you have used (e.g., Empower 3.0, Chromeleon 7.2, Malvern 3000, GC models, dissolution apparatus).
• Expect technical questions on chromatographic method parameters, system suitability, impurity profiling, and dissolution interpretation.

FAQs

Q1: What is the minimum experience required?
A1: Candidates should have 4–8 years of experience in analytical method development for regulated and emerging markets.

Q2: Which instruments must I be familiar with?
A2: HPLC and UV spectrophotometer are mandatory; experience with dissolution, GC, and Malvern particle sizing is advantageous.

Q3: Is travel mandatory for this role?
A3: Yes. The role requires extensive travel to plant sites for method transfer and troubleshooting. Only candidates willing to travel should apply.

Q4: Can freshers apply?
A4: No. This position is targeted at experienced professionals with 4–8 years of relevant experience.

Q5: How do I confirm my attendance?
A5: Email your confirmation and updated CV to jobs.hr@ipca.com with the subject line: Walk‑in ADL.

Summary Table

Company	Ipca Laboratories Ltd.
Vacancies	Research Associate / Research Scientist — Analytical Method Development (ADL)
Required Education	M.Pharm, M.Sc (Chemistry), Analytical Chemistry, Pharmaceutical Chemistry
Experience	4–8 years in analytical method development, technology transfer, QC support; willingness to travel