Executive - Analytical Validation with CDMO Partner For Derma

1 - 4 years

2 - 4 Lacs

Posted:-1 days ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

Greetings! & very warm welcome to BEST-FIT Recruitment Riders,

highly specialized Recruitment & Executive Search Partner for Pharmaceutical, Biotech, CRO, Chemicals, Medical Devices & Turnkey Pharma Projects Engineering-Construction Design Sectors.

professional career opportunity

Please see the following position summary:

  • Client Name: Globally Preferred CDMO Partner for Derma

  • Position: Officer / Executive

  • Department: ADL

  • Location: Mumbai

Job Profile:

  • To ensure accurate and compliant analytical testing of raw materials, finished products, and stability samples through routine instrument calibration, method development, validation, and documentation. The role supports product quality and regulatory standards by maintaining lab equipment, preparing analytical solutions, and adhering to Good Laboratory and Documentation Practices.
  • Perform Analytical Method Validation of Assay of Preservative, Antioxidant, Related Substance by HPLC, Residual Solvent by GC.
  • Analytical Method transfer of validated method to QC department of respective manufacturing location.
  • Providing analytical method development support & perform routine analysis on HPLC, GC, UV, FTIR, Density meter, Polarimeter, KF auto titrator etc.
  • Documentation of analytical reports.
  • To ensure accurate and compliant analytical testing of raw materials, finished products, and stability samples through routine instrument calibration, method development, validation, and documentation.
  • Routine calibration and/or verification of laboratory instruments and equipment.
  • Analysis of raw material finished product and stability samples of sterile ophthalmic and non-sterile dermatological products.
  • The role supports product quality and regulatory standards by maintaining lab equipment, preparing analytical solutions, and adhering to Good Laboratory and Documentation Practices.
  • Good Documentation Practices and Good Laboratory Practices.
  • Chemicals, Reagents, Buffer solution, Mobile phase, solutions preparation required for analysis.
  • Purified Water analysis.
  • Handling and maintenance of laboratory consumables, glassware, chemicals, reference standards, working standards and chromatographic columns etc.
  • Participate in continuous improvement initiatives for method performance.

Desired Profile:

  • M.Sc. (Analytical / Organic / Pharmaceutical Chemistry) or B.Pharm / M.Pharm with 2 to 4 years experience in in Analytical Research & Development with well reputed Pharma Formulations companies.
  • Must have strong experience in Analytical Method Validation.
  • Strong knowledge of analytical chemistry, chromatography techniques, and method validation principles.
  • Candidate with semi solid experience would preferred first.
  • Hands-on experience with HPLC/GC/UV/KF/FTIR instruments.
  • Understanding of ICH guidelines and regulatory expectations.
  • Skills in Analytical Competency, Technical Proficiency, Time Management, Team Collaboration.
  • Excellent documentation skills and attention to detail.
  • Ability to work independently and manage multiple validation projects.
  • All round of interviews will be F2F.

Recruiter's Contact Details:

BEST-FIT Recruitment Riders

G-7, Amrit Complex, R.V. Desai Road,

Near Goyagate Circle, Vadodara-390001, Gujarat

Mobile: 07226009222, 09722042906

E-Mail: hrd@bfrr.in

Website: www.bestfitrecruitment.co.in

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