Document Controller

Analytical testing using GC, HPLC, UV techniquesNew methods for analysis of API samplesQuality AssuranceQuality Control TestingProcess ImprovementDocumentation & ReportingCollaboration & complaint investigationLead Audits

To perform In process, Intermediate, Process validation, Raw material, Packing material, Stability, Working standard and finished product chemical sample analysis with proper documentation.Registration off All stages sample in LIMS etc.Maintain of Inward register, instrument usage log books.Preparation and documentation of volumetric solution/regents.To...

Role & responsibilitiesSecurity operation.Control Room operation.Access Control.Vehicle Management.Billing of security agencies.SOP, Documentation & Auditing.Periodical inspection of vehicles. Checking of transport bills.Supervision of checking at gate.Verification of documents of incoming & outgoing vehicles.Issue of temporary passes.Coordination of all...

Manage QMS (Change Control, Deviation, CAPA, OOS/OOT), vendor qualification, audits, and compliance documentation. Oversee GMP activities including in-process checks, dispatch coordination, labeling, and record review.

Handle quality complaints, aberrations & compliance, Perform RA, RCA, CAPA, Review &approve deviation, batch record, change control, CAPA, SOP, QMS documents, test method, sampling, Vendor Mgt, dispatch, Approve & review validation/qualficn protocols Required Candidate profileM.Sc.(Chem/Pharma) with 4 to 8 yrs exp in API industry. Knowledge of quality...

Key Responsibilities:Oversee daily QA operations in SVP manufacturing and ensure compliance with cGMP and regulatory guidelines.Perform and supervise IPQA activities in production areas including line clearance, in-process checks, aseptic practices, and documentation verification.Review and approve batch manufacturing records, quality control data,...

Roles and ResponsibilitiesShould have Hands on Experience in Handling the Microbiology Tastings/Pathogens Testing's at Quality Control Laboratory.Should have basic knowledge of Media Preparations, Discarding, Environment Monitoring, Swabs Testing's.Should have basic knowledge of CGMP, GLP, GHP. Documentation with Hands on Experience of SAP QA Module.Conduct...

Drafting and adherence to Quality Assurance Procedures including:Standard Operating Procedures & Work InstructionsChange ControlProcess ValidationDocument Control.cGMP CompliancePlanning and Co-ordination for External and Internal AuditsEnsure that CAPA and adhered for NonconformancesInvestigate and Review Customer ComplaintsTraining to stakeholders w.r.t....

1Ensuring resources available BMR, Raw Material, Packing Material Manpower etc.)2Liaison with QC/QA/STORE/Eng. Dept. for solving of trouble shooting problem.3Implementation and monitoring of GMP Standard.4Reporting to higher authority.5Raw material, packing material issuance and receipt from RMS and checking of MRO and verification6Intermediate, Finished...

An Instrumentation Technician installs maintains and repairs instruments and control systems used in various industries These technicians ensure that instruments function accurately and efficiently often working with sensors controllers and measurement devices Key Responsibilities Installation Technicians install new instruments and control...