3 method validation opportunities in Vadodara updated today
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Senores Pharmaceuticals LimitedCentral Validation Lab role involving analytical method validation and transfer activities using HPLC. Experience in assay, impurity profiling, dissolution, residual solvent analysis, and preparation of validation protocols and reports is required.
Job Description Job description To Access Study Plan and Standard Operating Procedures and to comply with instructions given in Study Plan and Standard Operating Procedures. To record raw data promptly and accurately and in compliance with the Principles of Good Laboratory Practice, review of raw da
Job Description Job Summary To work as per cGMP and ensure its compliance as per current guideline and SOPs. Responsible to take training before execution of allotted work maintaining the training file. Responsible to follow safety precaution as per laboratory procedure. Responsible to escalate any
Role & responsibilities Qualification : M.Sc. Work Experience : 5 to 7 years Preparation and review of protocols and reports for analytical method validation and method verification. Execution of method as per protocol of method validation and method verification. Coordination with respective de
Role & responsibilities Qualification : M.Sc. Work Experience : 5 to 7 years Preparation and review of protocols and reports for analytical method validation and method verification. Execution of method as per protocol of method validation and method verification. Coordination with respective de
Your future role Take on a new challenge and apply your technical and manufacturing expertise in a new cutting-edge field. Youll work alongside innovative, dedicated, and collaborative teammates. You''ll contribute to defining and validating detailed manufacturing processes for new products. Day-to-
Group Company: # Group Company # Designation: # Designation # Office Location: # Office Location # Position description: # Position description # Primary Responsibilities: # Primary Responsibilities # Additional Responsibilities: # Additional Responsibilities # Reporting Team Reporting Designation:
Pramukh enterpriseA QA (Quality Assurance) Validation Officer is responsible for ensuring that processes, systems, equipment, and products meet required quality standards and regulatory guidelines—especially in industries like pharmaceuticals, biotechnology, healthcare, and manufacturing. Pay: ₹20,000.00 - ₹25,000.00
Kreston OPR Advisors LLPParticipates in financial due diligence activities, pre-IPO assessments on pending M&A transactions and corporate restructurings in South-east Asia Conducts independent valuation for businesses, tangible, intangible assets and financial instruments includes equity and debt securities for financi
Sun Pharmaceutical Industries, Inc.# **Title:** **40005015 - Validation - G12A - Halol - II** Date: Mar 30, 2026 Location: Halol 2 - Validation/Quality Engineering Company: Sun Pharmaceutical Industries Ltd Education : B. Pharm Experience : 1+ years **Key Responsibilities:** Execution, compilation and compliance of qualification and
Ensure thorough understanding of all requirements mentioned in IS16444/IS13779/IS14697 Ensure all testing exposure is gained execute to become independent
Role & responsibilities Govern endtoend cost control for Advance Design Validation Plan (ADVP) activities Establish cost control frameworks for design validation and verification phases Define cost baselines for ADVP scope and monitor planned vs actual expenditure Control costs related to DV, PV
₹5,40,000 – ₹8,60,000/year
Estimation confidence: Low
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