2863 Sop Jobs - Page 16

Candidate should be B.Pharm Candidate should have regulatory exposure/ in previous organisation Candidate should have well command on IPQA activities Candidate should have Command on packaging operations Candidate should be able to work in shift well aware with regulatory requirement

Perform daily production as per SOPs & batch instructions. Operate reactors, filters, centrifuges. Maintain BMRs, ensure GMP/EHS compliance, proper labeling & raw material handling. Coordinate with shift in-charge for smooth operations.

Job Title: Manager - Regulatory Affairs / Quality Assurance Company: GreenSignal Bio Pharma Pvt Ltd Location: Gummidipoondi, Chennai, Tamil Nadu Experience: 10-15 years in Quality Assurance and Regulatory Affairs, specifically within the Vaccine, Injectable, and Sterile Industry Educational Qualification: Bachelors or Masters in Pharmacy M.Sc in Biotechnology, Microbiology, or a related field Additional qualifications in life sciences or pharmaceutical sciences are a plus Job Overview: As the Manager QA / Regulatory Affairs , you will play a pivotal role in ensuring that our vaccine , injectable , and sterile pharmaceutical products meet global regulatory requirements and quality assurance (...

Key Responsibilities: Gather and analyze business requirements to prepare BRDs and FRS Map out As-Is and To-Be processes for criminal justice and e-Governance systems Assess existing technology landscapes and recommend appropriate infrastructure sizing Design solution architecture for interoperability, scalability, and data quality Ensure compliance with Government IT/security standards Develop SOPs, user guides, training materials, and maintain project documentation Execute UAT scenarios and validate dashboards and analytics Advise on best practices for integrated dashboards and e-Governance systems

Job Vacancy Location : Padi, Mahindra World City & Madurai. Qualification : B.E (Mech) /Automobile. B.E (EEE), B.E (ECE) B.Tech (Mech) / Automobile B.Tech (EEE), B.Tech (ECE) Job Description Quality Control Engineer Looking for experienced Quality Control candidates with strong knowledge of PPAP and IATF 16949 documentation. Must be capable of handling customer complaints, root cause analysis, and corrective actions. Responsible for monitoring in-process and final product quality as per standards. Should have hands-on experience in quality tools and report generation. Ability to face and support internal/external audits independently. Join our team to ensure consistent quality and drive cont...

Responsibilities well trust you with: Project Management Oversight: Efficiently allocate and manage project resources, including personnel, equipment, and materials. Gather, organize, and disseminate essential project information to all relevant stakeholders. Project Planning: Break down projects into actionable tasks and establish realistic timeframes for their completion. Collaborate with teams to assign tasks and responsibilities, considering individual strengths and expertise. Progress Monitoring and Issue Resolution: Proactively manage and resolve project-related issues, collaborating with relevant teams and stakeholders to find solutions. Risk Management and Analysis: Identify potentia...

Skillsets: Must have exp in the Property &Casualty Insurance domain. Exp in training new joiners and conducting refresher training. Experienced in quality audits. Experience in SOP creation or modification & escalation management.

Sodexo Food Solutions India Pvt. Ltd.ces is looking for STEWARDING EXECUTIVE to join our dynamic team and embark on a rewarding career journey Supervise and manage the stewarding team, including hiring, training, scheduling, and performance management. Develop and implement standard operating procedures (SOPs) for stewarding operations to ensure efficient workflow and compliance with health and safety regulations. Maintain cleanliness and hygiene standards in the kitchen, dining areas, and other food and beverage service areas. Monitor and ensure proper handling, cleaning, and storage of all food and beverage equipment, utensils, and supplies. Coordinate with the purchasing department to ens...

Location: Bangalore and Hyderabad Experience in SAP PP" Must have S4 HANA knowledge and Fiori apps. Experience in implementation, roll out, support Experience in supporting processes in PP- MTS, MTO, ETO, ATO, MRP, Production Execution, LTP, SOP Experience of Production Planning & Execution, Direct & Indirect Procurement process, Subcontracting process, Consignment process Functional integration aspects with other SAP modules Customizing experience in BOM, Routing, Work center, Production Orders, Batch Management, Serialization and Handling Units management "Knowledge of Debugging Very good experience in client communication & working with the client from offshore

Be responsible to lead downstream manufacturing compliance. Ensure quality management systems in line with cGMP and regulatory requirements and handling training requirements Handling Change control management system including CCF impact assessment, preapproval, cross functional CCF evaluation, monitoring of closure of change controls and change control action item. Coordinate with investigator in identifying appropriate CAPA and tracking for closure of the CAPA. Responsible for the review and approval of Master manufacturing records for the commercial batches. Responsible for review and approval of scale up, exhibit, intended and Process validation master manufacturing records. To review an...

Q.A Preparation & review QMS (SOPs, wise and formats) technical files for all products, manufacturing licenses, ensuring accuracy & completeness assist Required Candidate profile conducting internal audit assist in competition of country specific sanitation and registration requirements

Looking for immediate joiners Designation: Content Rating Expert (SME) Business Vertical: IOA Reporting Manager: Team Manager (TM) Location: Bangalore (Work from Home) Typical Background: 5–8 years in HR domain with experience authoring SOPs, managing escalations, and enforcing policy. Role Purpose: Apply policy judgment to complex HR cases; define acceptance criteria, mentor Generalists, and refine training data and rubrics to improve model quality . Core Responsibilities: • Interpret complex outputs involving eligibility, documentation, SLAs • Define golden examples and edge case boundaries for high-risk flows. • Conduct RCA on recurring defects and suggest rubric/prompt changes. • Mentor ...

Role: Internal Audit & Risk Advisory - Consultant / Senior Consultant / Deputy Manager (Non-FS) Travelling: Candidate must be comfortable travelling within India & to overseas for projects. Interested candidates can also share their updated resumes at kirti.goyal@protivitiglobal.in Key Responsibilities: Spearhead internal client facing teams and guide them on solution delivery. Independently lead smaller modules of the engagement. Identify, assess and monitor risks by developing a risk management plan and strategy and identify opportunities to improve business processes. Assist clients in addressing compliance, financial, operational and strategic risk. Assist team members in developing tech...

Key Responsibilities: Overall looking for documentation work of Engineering Department and presenting as Engineering Q.A. Active Participation with Q.A in Audit Works. Active participation in QMS work i.e QAP and relevant documents for EU Audits. Scheduling, Planning, Executing Departmental working & documentation work for Engineering Drafting of QAP, SOP, Logbooks, Documents, etc and timely revision according to schedule. Drafting of Engineering SOPs for all machines/utilities accordance with manufacturer recommendations along with performing Qualification activities and accordingly designing logbooks and records. Drafting of In-house Qualification documents with respect to manufacturers do...

A) Execution and Recording: Perform the manufacturing activities as per the BMR and SOP’s. Batch related documents in manufacturing area. Preparation of shift schedule and batch schedule. Readiness related to batch manufacturing. Execution and monitoring of activities in compliance to cGMP. Execution of activities during product change over Checking and timely submission of Batch Manufacturing records to QA. Decontamination and disposable of bio waste. Preparation of MCB/WCB. Automated or manual CIP and SIP of equipment in the manufacturing area. Follow safety norms in the manufacturing area. Self-Inspection of manufacturing area and compliance as per regulatory norms. Operation of SAP S/4 H...

Job Responsibilities: A) Execution and Recording: Perform the manufacturing activities as per the BMR and SOP’s. Batch related documents in manufacturing area. Preparation of shift schedule and batch schedule. Readiness related to batch manufacturing. Execution and monitoring of activities in compliance to cGMP. Execution of activities during product change over Checking and timely submission of Batch Manufacturing records to QA. Decontamination and disposable of bio waste. Preparation of MCB/WCB. Automated or manual CIP and SIP of equipment in the manufacturing area. Follow safety norms in the manufacturing area. Self-Inspection of manufacturing area and compliance as per regulatory norms. ...

Process planning Complete process design in consultation with Product Design and Launch team Preparation, verification & maintenance of production BOM (Bill of Materials) Conduct Process FMEA for input to facility & process set up for new projects Preparation of Fixtures Tools & Gauges (FTG), estimation, justifications, procurement process initiation, Design approval process, installation & commission and buy-off according to project time lines Design of Material handling Trolleys, Pallets, Lifting Tackles & other facilities related to manufacturing Ensures manufacturing process documentation (Process sheets, Control Plan, Tool Drawings etc.) Facility planning Preparation of FTG requirements...

Knowledge in IAFT 16949 2016, ISO 14001 & ISO 45001, PPAP, SPC, G8D, APQP, SOP, Internal auditor, Drawing study, Process & product auditor

About the Role We are seeking enthusiastic and driven BBA graduates to join our HR Shared Services team as Apprentices. This opportunity offers hands-on experience in global HR operations, with exposure to onboarding, employee lifecycle management, and compliance processes. Key Responsibilities Support pre-onboarding, onboarding, and post-onboarding activities Assist in employee lifecycle processes including offboarding and background verification Participate in AskHR ticket resolution and other transactional HR tasks Follow standard operating procedures (SOPs) and maintain compliance Rotate across HR functions to gain broad exposure and identify areas of strength Eligibility Criteria Must b...

JOB DESCRIPTION Purpose: Define, establish, and monitor quality management systems at EM&S APAC as per cGMP and Sanofi Global Quality policies to ensure the quality of products DP and DS. To ensure regulatory compliance for domestic and export Drug products and API manufactured by External Manufacturing sites of Sanofi. Collaborate with Quality Operations Cluster Head Quality Operations for rolling-out best practices and governance for CMO Quality Management within the EM&S APAC Quality network, ensuring quality oversight. Lead and coordinate quality and compliance of transversal projects for the EM&S APAC. Ensuring the renewal, registration, and maintenance of product dossiers & regulatory ...

Utility Operator HVAC / Water / Electrical (01 Position) based in Vapi, Gujarat. The ideal candidate brings 5 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvemen...

The ideal candidate brings 15-20 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen). Plan resources, ensure statutory compliance, drive traini...

The ideal candidate brings 3- 8 Years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen). Own production execution and shift supervision; ensure lin...

The ideal candidate brings 5 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen) Own production execution and shift supervision; ensure line clea...

The ideal candidate brings 8 to 10 year and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen) Additional info: Key Skills: QMS (Change Control, Deviation...