Cleaning Validation - 24+ job offers

Responsible for line clearance activity before commencing the different operations like dispensing, manufacturing, filling, inspection, sealing, labelling, and packing. Responsible for Process validation, cleaning validation/verification, hold time study, media fill & routine batch sampling as per p

To review of URS, DQ, QRM, FAT, SAT, and vendor/ supplier’s documents related to qualification. To conduct sampling activities as per the protocols (Hold time, Process validation and cleaning validation etc.). To execute Qualification / Re-Qualification and Validation activities of Equipment / Syste

Apotex Research

Job Description About Apotex Inc. Apotex Inc. is a Canadian-based global health company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 6000 people worldwide in manufacturing, R&D, and commercial operations. Apotex medicines are accessible to

Amneal

1. Responsible to perform Quality Function responsibilities pertaining to Validation. 2. Responsible for preparation and review of URS, DQ and vendor/ supplier’s documents related to qualification. 3. Responsible to co-ordinate with manufacturing, Engineering and QC personnel for respective Qualific

Amneal

Responsible for Process validation, cleaning validation/verification, hold time study, media fill & routine batch sampling as per protocol/SOP. Responsible for review of URS, DQ and vendor/ supplier’s documents related to qualification. Responsible for preparation and review of Validation/ Qualifica

Amneal

Description: .The Senior Manager, Quality Control is responsible for overseeing activities within the quality control laboratory to ensure Quality Control Lab tasks are managed according to company procedures, and cGMP, assess business needs and make decisions based on changing conditions and manufa

📍 India (Remote + Mumbai Lab Setup) | Full-Time | Supporting U.S. Operations | IST - EST Overlap Required Reporting to: Director of Technical & Analytical Sciences - Hubot CDMO, South Bend, Indiana, USA Build the science. Own the methods. Shape a lab from the ground up. Hubot, Inc. is a U.S.-based

Job Description Job Description Review of documents such as executed Batch Production Records, Analytical records, Change Controls, Deviations, OOS, process Validation, Cleaning Validation, Equipment Qualification, stability data and CAPA for IRF Market and US formulation CM sites. Routine/ new site

Job Description Job Description Responsible for overall QA function compliance with various regulatory guidelines and standard operating procedures in practice at the site. Review and monitor quality systems and provide guidance to team for implementation. Responsible for Review and approval of Batc

Job Description This is where your work makes a difference. At Baxter, we believe every person-regardless of who they are or where they are from-deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delive

Validation Specialist - Cleaning (India Role to Support US Operations) Hubot, Inc. 📍 India (Remote/Hybrid) | Full-Time | US Shift Overlap Required | Technical Support Role Reporting To: Sr. Validation Engineer (USA) Hubot, Inc. is seeking a Validation Specialist - Cleaning to serve as the Technical

Novartis

Job Description Summary The Purpose of the Validation expert role is to support Site Manufacturing Science & Technology (MS&T) by providing expertise in process and cleaning validation for aseptic Drug product manufacturing. The role ensures that validation strategies and lifecycle activities are sc

Validation Specialist - Cleaning (India Role to Support US Operations) Hubot, Inc. India (Remote/Hybrid) | Full-Time | US Shift Overlap Required | Technical Support Role Reporting To: Sr. Validation Engineer (USA) Hubot, Inc. is seeking a Validation Specialist - Cleaning to serve as the Technical Co

Validation Specialist - Cleaning (India Role to Support US Operations) Hubot, Inc. India (Remote/Hybrid) Full-Time US Shift Overlap Required Technical Support Role Reporting To: Sr. Validation Engineer (USA) Hubot, Inc. is seeking a Validation Specialist - Cleaning to serve as the Technical Control

Validation Specialist - Cleaning (India Role to Support US Operations) Hubot, Inc. India (Remote/Hybrid) Full-Time US Shift Overlap Required Technical Support Role Reporting To: Sr. Validation Engineer (USA) Hubot, Inc. is seeking a Validation Specialist - Cleaning to serve as the Technical Control

MSD

Job Description The External Manufacturing, Associate Director will support a technical team interfacing between our Company and External Partners (EP) in the Biologics Drug substance manufacturing area. This individual will support the platform lead(s) in the execution of technical transfers to and

MSD

Job Description The External Manufacturing, Associate Director will support a technical team interfacing between our Company and External Partners (EP) in the Biologics Drug substance manufacturing area. This individual will support the platform lead(s) in the execution of technical transfers to and

IOTA Diagnostic

₹5,00,000 - ₹6,00,000 /year

About The Opportunity IOTA Diagnostic is an innovation-driven MedTech company developing affordable and accessible diagnostic solutions. With products such as BioSampler (Blood Microsampling Device) and M-Strip (Menstrual Blood Self-Sampling Device), we are redefining home-based sample collection an

Preparation and Review of Standard Operating Procedures. Review of BMR, BPR, ECR, PFD etc. Responsible for Change Control Management. Preparation and Review of Annual Product Quality Review. Responsible for label management. Responsible for Process Performance Qualification and Cleaning Validation.

To perform IPQA Activity To Handle change control To perform process validation and cleaning validation To prepare APQR To handle Training To handle CAPA To review Master BMR and ECR