Manage daily production to meet quality, output & efficiency targets. Plan schedules, supervise staff, ensure GMP/ISO compliance, handle liquid filling lines, reduce wastage, maintain records, provide SOP training; Candidate required 2P/3P exp.
Manages daily purchase tasks, creates POs, coordinates with suppliers, controls inventory, and maintains records. Ensures timely material supply, follows safety norms, assists audits, updates reports, and supports monthly review data preparation.
Create and optimize CNC lathe programs using G/M-code, set up machines, interpret blueprints, select tools, inspect parts, and ensure precision. Collaborate with teams, maintain documentation, and perform machine maintenance for quality output.
Manufacturing operations, ensuring GMP compliance and safety. Monitor Manufacturing/production, maintain batch records and SOPs, assist with audits, and drive process improvements to enhance efficiency, reduce costs, and improve product quality.
Follow PTW system, attend breakdowns, repair equipment, maintain history records, coordinate with departments, ensure equipment functionality, support preventive maintenance, ensure safety.
Manage vendor sourcing, procurement, material receipt, and inventory. Ensure accurate stock entry, issue items per requisition, handle hazardous/non-hazardous materials safely, and maintain vendor relations, contracts, and timely deliveries.
QMS, Handling Customer and Marketing Complaints, Deviations, Change Control, CAPA, Documentation, IPQA, Data control, Regulatory, Stability, SIP, BOS, GLP, Various Audit Compliance - Clients & Regulatory i.e. USFDA, GMP, ISO 22716, 9001, 45001, etc. Required Candidate profile Must have 10+ yrs of experience in Quality for 3rd Party contact Manufacturing Company. Can handle Multinational & Multi Clients for Pharma or Personal Care Products, Resolve the issues of clients.
Mechnical, Machinist, Fitter, Welder and Electrical Trade, Specifically Polytechnic pass out candidates required Only. Apply or send on hrsai@wonderproduction.co.in
1-Lead QA/QC team,2-Implementation of QMS,3-implementation of good housekeeping, Safety in QC.4-Review & approval STP,SOP, Calibration record, CAPA, Audit compliance, Handling Training,Co-ordination with Production Warehouse,Quality Coordination.
1-Formulation Development 2-Pre-formulation Studies 3-Process Development & Optimization 4-Documentation 5-Technology Transfer 6-Analytical Support 7-Regulatory Compliance 8-Cross-Functional Collaboration
1-Lead QA team,2-Implementation of QMS,3-implementation of good housekeeping, Safety .4-Review & approval STP,SOP, Calibration record, CAPA, Audit compliance, Handling Training,Co-ordination with Production Warehouse,Quality Coordination.
Looking for a proactive and detail-oriented HR Time Office Officer/Executive to manage employee attendance, leave records, and time office activities. male Candidates with experience in HRMS (preferably Savior HRMS or any HRMS) will be given priority
Sai Corporation is looking for experienced and responsible Production Incharges to oversee cosmetics and personal care manufacturing operations in a 3P environment. Candidates with a pharmaceutical background will be preferred.
Sai Corporation seeks a Recruitment Officer/Executive (2–3 yrs exp) for its HR team in Kala Amb. strong communication skills, prior recruitment experience, and ability to manage end-to-end hiring and onboarding processes.male candidates will preffer
Production Shift Incharge will supervise and manage shift operations to ensure smooth workflow, quality compliance, and target achievement. Requires strong leadership, problem-solving skills, and hands-on manufacturing experience.
Executive Assistant to Director will handle scheduling, travel, communication, and documentation, ensuring smooth office operations. Requires strong organization, confidentiality, and proactive communication in a dynamic work environment.
Mechanical Engineer will design, analyze, maintain, and improve mechanical systems to ensure efficiency and reliability. Requires strong technical expertise, analytical ability, and hands-on experience in manufacturing or plant operations.
1 Line clearance, 2 In process activity, 3 IPQA, 4 BMR, BPR.
Documentation- BMR review, Day to day documentation, Qualification, Validation, Deviation ,Change control, OSS, Incident, Market complainant, CAPA.
The QA Executive ensures implementation and maintenance of Quality Assurance systems as per GMP and GDP standards, maintaining documentation accuracy, adherence to procedures, and continuous improvement in product quality and reliability.
FIND ON MAP