Executive/Sr Executive- QA

Process Validation:Plan and execute process validation activities for sterile injectable products as per cGMP and regulatory expectations.Prepare and review validation protocols and reports, ensuring compliance with internal SOPs and global regulatory guidelines (e.g., USFDA, EU-GMP, WHO).Cleaning Validation:Develop and implement cleaning validation...

Designation: Sr. Executive/Asst. Manager - Accounts & FinanceResponsibilities:Manage GST compliance, return filing, ITC reconciliation, and handling of notices.Oversee TDS/TCS deduction, deposit, return filing, and reconciliations.Handle banking operations including fund management, reconciliations, LCs, and Bank Guarantees.Process vendor payments,...

Roles and ResponsibilitiesReview and approval of Master Documents such as Batch manufacturing record /Batch packaging record, Specification, Standard test procedure, Standard operating procedure, Qualification/ Validation protocols and reports.Preparation and review of Site Master File.Review and approval of Quality System document such as Deviation, Change...

Responsible for New computer Installation, Upgrades, software Installation, Hardware related support, Managing Inventory and providing the end support to users at site.Responsible for but not limited to, User management of software for creation, modification and disabling the users and assigning privilege groups as per the procedure defined in the respective...

Job Responsibility:To file and coordinate for Health Safety and Environment related legal applications to obtain required licenses and permits from State or Central Regulatory Authorities such as Consent to Establish (NOC), Consent to Operate (CCA), CGWA NOC, Bio Medical Waste Authorization, Fire NOC, PESO Storage License as per requirements.To operate,...

Role Overview:The Lab QA/QC Reviewer will be responsible for the comprehensive review and approval of analytical data generated by the QC laboratory.This role ensures data integrity, compliance with regulatory guidelines, and facilitates resolution of quality investigations related to lab incidents.Key Responsibilities:Perform detailed analytical data review...

The purpose of this role is to :-.The Research Scientist in the Formulation and Development (Injectables) department will be responsible for the design, development, optimization, and scale-up of injectable formulations. This role involves working closely with cross-functional teams, including Analytical, Regulatory, Quality, and Manufacturing, to ensure the...

Key Responsibilities:Hardware & Software Maintenance:Install, set up, and maintain computers, printers, servers, and company software.User Support:Help employees (especially production staff) with any computer or software-related problems.HR & Admin Support:Assist the HR and Admin teams with technical support and IT-related tasks.Documentation:Keep records...

Role & responsibilities :Review of all QMS documents related to regulatory submissionsPrepare status of all documents related to submissionCo-ordinate with all stakeholders of plant for collection of documentsProvide all regulatory documents to HO-RA for submission.Evaluation of change control, deviations and out of specifications.Review of specifications,...

Candidate should have good exposure of Analytical Data Review and electronic data review of QC instruments (LCMS/HPLC/ GC/ Dissolution, Malvern 3000 etc) .Should have Strong knowledge of QC investigations (Lab incidents, OOS/OOT etc).