Manage & approve QMS-related documentation within the RDQA department Oversee the lifecycle of SOPs Review & approve product development reports, validation protocols, documentation generated by the R&D department
Manage corporate communication, newsletter & media relations Create brand content for social media, website & campaigns Support IR with earnings reports, AGM updates & analysis Drive CSR/ESG communication Oversee corporate websites & company magazine
Key Responsibilities 1. Dossier Preparation and Submission CTD/eCTD Compilation: Assemble and submit regulatory dossiers in Common Technical Document (CTD) format, including modules for clinical, non-clinical, and quality data.
2-7 years of experience in Europe CTD dossier preparation Module-1,2,3,4 & 5 Compiling & submitting technical dossiers for export markets Receiving the site registration requirements Query Response Management Preparation of variation data package Perks and benefits Weekly off on all SATURDAYS & SUNDAYS
Change Control & CAPA Management Initiation and documentation of Change Controls and CAPAs related to: SOP revisions Equipment qualification and modifications Deviations, self-inspections, and facility changes
Handle end-to-end recruitment & staffing Coordinate & review BGV process Manage onboarding & exit formalities. Maintain employee records & documentation Track HR data via internal systems & trackers Oversee Monthly Probation, Confirmation processes
Job Description: We are looking for an experienced Officer to join our team at our pellet manufacturing facility in Nagpur. The ideal candidate will have 4–6 years of experience in manufacturing operations.
Job Description: We are seeking experienced Operators for our manufacturing facility in Nagpur. The ideal candidates should have 2–4 years of hands-on experience in pellet manufacturing or related industrial operation's:
Handling QMS with audit compliance, Preparation of SOP, Protocol, Reports & Formats Preparation of PMS & check list of Equipment & utilities. Facility Qualification, Protocol & Report of filter cleaning records of AHU,LAF/RLAF, Dust collector
Seeking for experienced & strategic Regulatory Affair leader. will oversee all regulatory submission activities, maintain compliance with evolving global health authority requirements & provide expert regulatory guidance for pharmaceutical products
Authorizing Purchase, expenses & journal approvals. Ageing report analysis & ledger reconciliation. Vendor coordination & entry issue resolution. Period-end closure & audits. TDS, tax compliance & GST-TDS reconciliation. Income tax compliance & forms
Job Title: Executive Assistant / Personal Assistant (Stenography & Shorthand Expertise) Location: Nagpur Job Type: Full-Time Experience Required: 3+ years Reports To: Technical Director
Basic understanding of pharmaceutical manufacturing process Good documentation and observation skills Team player with adaptability and learning mindset
Review & approval of laboratory analytical data, test reports, and chromatographic data HPLC/GC/UV. Ensure GLP & cGMP standards, Participate in investigations of Out of Specification & Out of Trend, deviations, & lab incidents. SOP Review, CAPA.
We are looking for a motivated and detail-oriented fresher to join our pharmaceutical warehouse operations as a trainee.
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