Document Controller

Maintain and control project-related documents such as drawings, material lists, schedules, and reports.Ensure proper filing, version control, and traceability of all project documentation.Enter data accurately into project trackers, Excel sheets, and ERP or planning tools.Prepare, update, and circulate document logs, transmittals, and submission...

Responsibilities:Ensuring Compliances: Quality Assurance professionals play an important role in ensuring that all processes & product comply with QMS/IMS and other relevant regulations.Quality Control: Quality Assurance professionals involved in the development, maintenance & implementation of procedures and system in QC and production.Documentation: QA...

To prepare documents Technology Transfer Document, Product scale up report, Product development report, Chemistry manufacturing & control, Polymorphism study etc.To collect necessary information from all concerned Department.To prepare DMF (Drug Master File) for Regulatory Market.To ensure that manufacturing procedure and specification of materials are in...

The ideal candidate brings 5 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environmentsKey responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with...

Perform daily, weekly, and monthly reconciliations of bank statements with internal accounting records. Investigate and resolve discrepancies in a timely and efficient manner. Record and monitor all cash transactions including bank fees, interest, and transfers. Collaborate with Accounts Payable and Accounts Receivable teams to ensure alignment of...

Hands-on experience in monitoring manufacturing and packaging processes, line clearance, and in-process checks.Proficiency in DOC-MS systems, SOP preparation, deviation handling, and change control.Involvement in TT activities including protocol review, execution, and coordination between RCD and manufacturing.Familiarity with validated software systems that...

Responsibilities:Government Liaison:Establish and maintain effective working relationships with central and state drug control authorities (e.g., CDSCO, FDA).Facilitate timely submissions and follow-ups for licenses, approvals, renewals, and NOCs.Handle interactions with bodies such as Ministry of Health, Pollution Control Boards, Customs, Excise, and other...

Job Title:QC Testing Engineer – Radiology & Imaging Systems (X-Ray / C-Arm / DR / CT)Department:Quality Control / Quality Assurance – Radiology DivisionLocation:Vapi, GujaratReports To:QC Supervisor / Manager – Radiology SystemsJob Purpose:To perform quality control testing, inspection, and validation ofradiology and imaging systemsincludingX-Ray,...

Responsibilities:Compilation and review of regulatory dossiers (CTD, ACTD, eCTD) for CIS, LATAM (especially Brazil & Mexico), African, and EU regions.Handle full lifecycle of product registration including new submissions, renewals.Review technical documentation: PDR, DMF, AMV, BMR/BPR, Specifications, Stability Reports, BE Studies, etc.Address Ministry of...

HPLC Operator (01 Position) based in Vapi, Gujarat. The ideal candidate brings 5 to 10 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments.Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control...