Qualification & ExpeurienceQualification: Diploma / Bachelor's Degree Experience: 1 - 2 Years (Junior)Note: Male Candidate Preferred

Qualification & ExpeurienceQualification: Diploma/ B.Sc Experience: 4 - 7 Years

Qualification & ExpeurienceQualification: B.Pharm + MBA Experience: 10 - 12 Years

Qualification & ExperienceQualification - B. Pharma/M. Pharma Experience- 0 to 3 years

Qualification & ExperienceQualification - D. Pharma/B. Pharma Delhi Pharmacy Registration is must Experience- 1 to 3 years

ResponsibilitiesResponsible to daily work planning & allocation analytical work of method validation / method verification / method transfer for API and finished products. Preparation and review of SOPs, Protocols, Reports, Summary sheets etc. to review analytical raw data of LNB / Reports for compliance, correctness, and completeness. To coordinate with Analytical development team to ensure timely availability of all pre requisites required for validation and in case of discrepancies observed during validation / verification / transfer. To ensure resources (Chemicals / Reagents / Analytical columns / Standards / Documents / Instruments / Equipment’s etc.) available to smooth line function whenever required. To perform the task assigned by the supervisor/HOD as and when required.

ResponsibilitiesStrong hold on drafting, reviewing, and negotiating global contracts with customers and vendors. Interacting with internal and external stakeholder including law firms for various matter globally Litigation and employment law matters across the globe Any ad hoc matters including compliance, M&A etc. Qualification & ExpeirenceLLB (mandatory), LLM (optional)3-5 years experience Strong hold on drafting, reviewing, and negotiating global contracts with customers and vendors preferably from industries such as manufacturing, pharma and/or IT sector.

ResponsibilitiesInventory Management  Receive and verify incoming raw materials, packing materials, and finished goods.  Ensure proper storage as per material specifications (temperature, humidity, FEFO/FIFO).  Maintain stock levels and monitor inventory to prevent shortages or excess.  Conduct periodic stock verification and reconciliation.  Documentation & Compliance  Maintain accurate records as per GMP and regulatory requirements.  Ensure proper documentation for GRN (Goods Receipt Note), material issuance, and dispatch.  Maintain batch-wise traceability of materials.  Support audits (internal, regulatory, customer audits).  Material Handling & StorageQualification & Experience Bachelor’s degree in pharmacy, Science, Commerce, or related field.2–5 years of experience in pharmaceutical warehouse operations (formulation plant preferred). Knowledge of GMP, GDP, GWP and regulatory guidelines.  Familiarity with SAP/WMS systems and MS Office.

ResponsibilitiesTo ensure cGMP and compliance review in the manufacturing shop floor and packing areas. To supervision of dispensing activity of manufacturing shop floor and packing areas. To Issuance of Bottle label, Ouster and Medication guide for commercial batch. Rsponsible for providing machine and area clearance. To conduct Sampling of reserve sample, stability sample and In-process checks during execution of batch packaging as per Batch Packaging Record (BPR) and stability study protocol. Online Documents and records review like equipment’s logbooks, dispensing logs, housekeeping records, environmental monitoring records, calibration record, batch records etc.. Calibration of IPQA instruments.Qualification & ExpeirenceBachelors Degree (BA/BS) B. Pharm - Required Experience  2 - 4 Years

ResponsibilitiesHaving good knowledge of the regulatory guidelines related to eCTD publishing and submissions, mainly ICH M4, M8 and FDA eCTD guidance.  Prepare, compile, and publish high quality eCTD sequences for ANDAs/NDAs/Amendments/Supplements in alignment with USFDA eCTD technical specifications and ICH guidelines.  Own Module 1 (US regional) requirements and ensure correct placement/metadata for cover letters, forms (356h), labeling (SPL), REMS, correspondence, and ESG submission properties.  Ensure accuracy and consistency across Module 2 summaries and Module 3 (CMC/Quality), with correct granularity, file naming, and document locations per eCTD backbone.  Execute precise PDF publishing standards: pagination, bookmarks, hyperlinks, table of contents, headers/footers, legibility, OCR, and accessibility compliance.  Perform end to end pre-publish checks and validations; resolve all technical errors/warnings; troubleshoot link/file/path, STF, and schema issues prior to finalization.  Manage lifecycle operations (new, replace, append, delete) with proper leaf tracking and sequence continuity, maintaining audit trails and version control.  Define and maintain sequence metadata (submission type, sequence number, submission description, related sequence references) with zero defect accuracy.  Coordinate cross functionally with Regulatory, CMC, Nonclinical/Clinical, and Labeling teams to secure submission ready documents on time.  Prepare and submit through FDA ESG, monitor and interpret ACK1/ACK2/ACK3, and rapidly address transmission errors with IT/ESG support.  Monitor and implement updates to USFDA eCTD Technical Conformance Guide, regional Module 1 specs, validation rules, and eCTD v4.0 transition requirements.  Execute Study Tagging Files (STFs) where applicable; validate structure and relationships for quality/nonclinical/clinical study sections.Qualification & ExperienceB. Pharm M. Pharm Experience 3 - 4 Years