QA Sr. Executive QMS

QA - QMSTo perform Department coordinator, Site coordinator and Learner related training activity Manually as well as through software like LIMSResponsible for scheduling, execution and closing of training as well as hard copy for induction and on the job stage.Responsible for arrange training to employees, Contract workers, vendors, and skilled manpower.To...

Sr. No.Responsibilities1QMS Documents handling1.1To be Prepare New SOP.1.2Prepare, update, amended and review of Store SOP's.1.3To be handling Change control, deviation and CAPA2Materials Received and GRN preparation2.1Ensure that timely unload materials.2.2Prepare Goods received note. (RM, PM & MISC.)2.3Ensure that timely affixed Barcode label3Material...

Department - ALIDAC QA - Job posted on - Oct 03, 2025 - Employment type - C-C8-Confirmed-HO Executive Name : Isha Naik BU : Quality Place : ZLL-SEZ Oncology Injectable, SEZ, Matoda, Ahmedabad. Contact : 9898143494 **Basic Details**: Position : 60047440 Designation : Associate Manager/Deputy Manager Reports to : QA Head Department : Quality...

Validation/Qualification activities➢ Handling and leading QA validation activities (Which include ScheduledRequalification, New qualifications/validations due to Change control ornew projects, New qualifications/validations due to introduction of newproducts etc.) with taking care of 10-15 Nos. of team members.➢ Planning of all qualification related...

Department: Production QMS Designation: Officer to Executive Experience: 3 to 6 Years Location: Bavla, Ahmedabad Key Responsibilities: ✅ Injectable Production Activities Carry out and monitor day-to-day manufacturing of injectable products (aseptic or terminal sterilized). Follow batch manufacturing records (BMRs) and SOPs during production. Coordinate...

Remote: India Open to candidates with experience in global clinical research operations. We are seeking a Senior QA Auditor/ Senior GCP Auditor professional with proven experience in audits, SOP management, and regulatory compliance across global clinical research environments. This role is ideal for someone who has worked within or closely with a global...

Prepare Documents in LIMS Software for all Location. Preparation, Revision and Review of Raw Material, FP and in process specification, MOA and Worksheet. 1.2 Create Assay master, Party master, Test characteristic master, Product unit and Test unit In LIMS software 1.3 Operation and Handling of LIMS Software. Transfer Raw Material/ Finished product...

Sr. No.Responsibilities1.0Work allocation for LIMS Department. 2.0Review Documents in LIMS Software for All location2.1Review of Finished product , Raw Material and In process Specification, MOA  and worksheet In LIMS2.2Preparation, Review and Revision of Packing material Specification, MOA and worksheet.2.3Create Assay master, Market master and test...

Skanttr Lifescience LLP (API Manufacturing)Location - Bavla , AhmedabadKey ResponsibilityDocumentation & CompliancePreparation, review, and control of SOPs, protocols, and quality documents.Review and issuance of BMR (Batch Manufacturing Record) / BPR (Batch Packaging Record).Ensure compliance with cGMP, GLP, and regulatory requirements (USFDA, EU, WHO,...

Job Description About Omega QMS: Omega QMS is India's leading consultancy organization providing end-to-end solutions inconformity assessment,regulatory compliance, andmarket access. Our expertise spansBIS Certification(Domestic, Foreign, and Scheme X for machinery and electrical equipment),BIS Registrationfor electronic and IT products,BEE approvals,TEC...