Cadila Pharmaceuticals Walk-in Quality Control (HPLC) – Executive/Supervisor

SEO Optimized Job Post: B.Sc/M.Sc Chemistry Vacancies in QC (HPLC) – Cadila Pharmaceuticals, Dholka

Quality Control Executive/Supervisor Jobs for B.Sc/M.Sc Chemistry Graduates – Cadila Pharmaceuticals

Walk-in for B.Sc/M.Sc Chemistry graduates with 2–5 years’ experience in HPLC at Cadila Pharmaceuticals, Dholka Plant. Interview in Vadodara on 10 August 2025.

URL Slug: cadila-bsc-msc-hplc-jobs-dholka-vadodara

Career Opportunity in Quality Control (HPLC) – Cadila Pharmaceuticals, Dholka Plant

Cadila Pharmaceuticals Limited, a leading name in the pharmaceutical industry and certified as a “Great Place to Work,” is conducting a walk-in interview for experienced professionals in the Quality Control Department. The opportunity is for their state-of-the-art manufacturing facility located in Dholka, Gujarat.

This hiring is for professionals specialized in High-Performance Liquid Chromatography (HPLC), an essential analytical technique in pharmaceutical testing. Candidates with relevant industry experience are encouraged to apply.

Why Join Cadila Pharmaceuticals?

As a trusted global pharmaceutical company, Cadila Pharmaceuticals continues to provide outstanding healthcare solutions and career growth opportunities. Employees benefit from a dynamic work culture, learning environment, and long-term career advancement.

Walk-In Interview Details

Interview Location:

Baroda Productivity Council, 2nd Floor, Productivity House,
BPC Road, Vishwas Colony, Alkapuri,
Vadodara, Gujarat 390007

Interview Date & Time:

Date: Sunday, 10th August 2025
Time: 9:30 AM – 4:00 PM

Contact:

• Mr. Sanjay Makwana – HR: 8347434234
• Mr. Jimit Sharma – HR: 7069824377
  Email CV: Jimit.sharma@cadilapharma.com

Note: Please carry your updated resume along with Aadhar card and salary proof.

Job Overview

Department: Quality Control (QC)

Role: Technical Supervisor / Executive

Section: HPLC (High-Performance Liquid Chromatography)

Responsibilities:

• Conduct routine HPLC analysis of raw materials, in-process samples, and finished products.
• Ensure adherence to cGMP, GLP, and data integrity standards.
• Prepare and review SOPs, validation reports, and test protocols.
• Maintain HPLC instruments and troubleshoot technical issues.
• Assist in regulatory audits and documentation compliance.

Required Qualifications:

• Education: B.Sc or M.Sc in Chemistry (Analytical, Organic, General Chemistry)
• Experience: 2–5 years of hands-on HPLC experience in the pharmaceutical industry

Eligibility Criteria:

• Must have experience specifically in HPLC operations.
• Background in pharmaceutical QC environments is mandatory.
• Excellent knowledge of GMP compliance and audit readiness.

Application Process

Walk in with your resume, identity proof, and salary documents at the given venue. Ensure your CV highlights relevant HPLC experience.

Courses Relevant for This Job:

B.Sc Chemistry, M.Sc Chemistry, Analytical Chemistry, Organic Chemistry, Industrial Chemistry, Pharmaceutical Chemistry

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