523 Sop Preparation Jobs

1. To prepare annual equipment qualification planner with respect to validationmaster plan. 2. To prepare HVAC / compressed air / effectiveness of cleaning validation planner. 3. Preparation of protocols for qualifications of newly procured equipments and ofequipments transferred from other location. 4. Preparation of protocols for re-qualifications of HVAC system. 5. Preparation and execution of re-qualification protocols and reports as per schedule ofvalidation master plan and as on when required. 6. Toperform cleaning validation cleaning verification. 7. Preparationreview of cleaning assessment report. 8. Preparation review of process validation protocols and reports. 9. Preparation revie...

experience in Vaccine or Biosimilar manufacturing Strong exposure to In-Process Quality Assurance & Quality Management Systems and review system Knowledge of GMP guidelines and documentation practices fast-paced, regulated environment Perks and benefits 5- days working, Pf , health insurance

protocol & reports of equipment / utility qualification Responsible for execution of equipment / utility qualification. process validation cleaning validation Annual Product review Validation Master Plan. Computer System Validation/ PLC validation Perks and benefits Food & Transportation, Bonus & Gratuity Separately

Role & responsibilities Responsible for preparing SOPs and conducting planned/random process audits across Big Basket warehouses to ensure operational compliance. Set and monitor SCM process standards, KPIs, and performance dashboards for continuous improvement. Coordinate with inter-department teams and DC Managers for reviews, manpower budgeting, and performance reporting. Investigate major process deviations and develop efficiency improvement techniques. Handle vendor liaison and support all SCM-related meetings and tasks assigned by management.

Job Summary: The Transition Specialist will play a critical role in supporting the seamless transition of clinic operations from the US to India. This individual will attend all relevant training programs, capture process knowledge, and develop comprehensive Standard Operating Procedure (SOP) documents. The role demands strong documentation skills, attention to detail, and the ability to collaborate across teams to ensure operational readiness and compliance. Key Responsibilities: Attend and actively participate in all training sessions related to clinic operations, systems, and workflows. Document processes in detail to create accurate and user-friendly SOPs for various operational function...

About the Role We are looking for a Procedural Writer who specializes in developing clear, structured, and actionable documentation such as Standard Operating Procedures (SOPs) and process guides . The ideal candidate will have a strong understanding of operational workflows, cross-functional processes, and compliance frameworks , ensuring that procedures are accurate, compliant, and easy to follow. This role goes beyond task documentation it involves analyzing how processes work across systems (e.g., Gateway), identifying gaps, and ensuring alignment with organizational standards and audit requirements. Key Responsibilities Analyze and document complex workflows involving multiple teams and...

1. Training Strategy & Execution Design and implement training programs alligned with business goals and operational needs. Drive compliance on training mandays, role deployment certifications, and onboarding effectiveness. Lead initiatives like Learning Fridays and SOP standardization across stores. 2. Talent Development Build internal talent pipelines by enabling career progression from frontline to managerial roles. Oversee panel-based hiring and structured onboarding for new hires. Monitor and improve first-attempt training clearance rates and readiness for promotions. 3. Digital Learning & LMS Optimization Enhance LMS usage and content quality; eliminate manual tracking dependencies. Ro...

Role & responsibilities 1 Preparation of standard operating procedure. 2 Preparation of quality documents. 3 Initiate / review of change control system. 4 Initiate / review of deviation. 5 Initiate / review of CAPA. 6 To control, issue, retrieve, retention and disposal of GMP documents as per standard procedure. 7 Review of MFR/BMR/BPR/ECR. 8 Review of validation protocols and report. 9 To participate in investigation of OOS for RM/intermediate/FP. 10 To participate in market complaint handling. 11 Review of vendor qualification documents. 12 Review of executed manufacturing and analytical records. 13 Preparation of annual product quality review. 14 To take plant round and ensure compliance ...

Competent in design and planning Familiar with construction and project management processes Ability to produce detailed drawings and specifications Assist in the development of architectural projects Collaborate with senior architects and project teams Prepare and modify architectural documents and drawings Show more Show less

Competent in design and planning Familiar with construction and project management processes Ability to produce detailed drawings and specifications Assist in the development of architectural projects Collaborate with senior architects and project teams Prepare and modify architectural documents and drawings Show more Show less

Manager - Quality Control (Formulations) 10 to 15 years of experience in Pharmaceutical Industry especially in Formulations Unit. Should have experience in successfully handling Quality Audits. Thorough knowledge in all types of Analytical instruments, analytical methods, HPLC, Method validation and method development etc., Should possess profound knowledge and skills in OSD/Formulations products. Total Quality Management (TQM), preparation and successful implementation of SOP's. Should lead a team in QC department and responsible for TQM. Sound working knowledge in MS Office and computer skills. Responsible for day-to-day and periodical MIS reports. Coordination with Production, QA and othe...

As a candidate for this position, you should have 3-5 years of hands-on experience in Granulation, Compression, and Coating processes. Your role will involve utilizing your good machine handling skills, specifically with RMG, FBD, Compression, and Coating equipment. Key Responsibilities: - Monitor and supervise production processes - Maintain online documentation - Ensure compliance with SOP and GMP standards - Prepare and review SOP, BMR, and BPR - Demonstrate skill in handling manpower - Plan and execute production activities - Utilize Pharma Cloud software for work tasks Qualifications Required: - 3-5 years of experience in Granulation, Compression, and Coating - Proficiency in machine ha...

Location: Hyderabad-WFO Experience: 2+ years Work timings: US work hours Must have Seasoned Level 1 (2 - 4 years) or early Level 2 support resources Excellent Communications Experience with ticketing tools (Zendesk or any) Should be flexible to work in US hours Resolving support tickets, configuring printers, Wi-Fi, and laptops, as well as managing Windows operating systems and other technical setups. Technical Skills: Understands system configurations, networks, printers, imaging, VPN, Office 365, Windows OS. Documentation Skills: Able to create or update SOPs and KBs. Interaction: Comfortable on video calls with customers, clinic staff (dentists, assistants, admin). Soft Skills: Clear comm...

Hi, Position Title : Odoo Specialist Department: Operations / IT Location : Gurugram, India Employment Type : Full-time Experience : 2-5 years Role Overview: The Odoo Specialist is responsible for overseeing the configuration, customization, and management of the Odoo ERP system across all Seitz operations. The role ensures that business processes are effectively mapped within Odoo, supporting operational efficiency and seamless inter-departmental coordination. Key Responsibilities: Implement, configure, and maintain Odoo ERP modules across functions including Sales, CRM, Purchase, Inventory, Accounting, HR, and Project. Customize workflows and reports based on departmental requirements. Coo...

We Are Hiring!! Role : QA Executive (Only Males) | Nacharam, Hyderabad Location: Nacharam, Hyderabad Qualification: M.Sc Organic Chemistry Experience: 2 to 4 Years Industry Preference: Pharma / Chemical / Cosmetics Industry (API QA experience preferred) Working Days: 6 Days a Week Roles and Responsibilities: Ensure compliance with GMP, ISO, and regulatory standards in all QA activities. Preparation, review, and control of QA documentation, SOPs, change controls, deviations, and CAPA records. Conduct internal audits and assist in external regulatory or customer audits. Monitor process validations, equipment qualifications, and calibration activities . Handle in-process checks and ensure produ...

He is responsible for implementing and maintaining quality systems to ensure manufacturing processes and products meet regulatory standards like cGMP and ICH guidelines, reviewing & approving documentation such as batch records and SOPs. Required Candidate profile cGMP and ICH guidelines, reviewing & approving documentation such as batch records and SOPs, supporting internal and external audits, participating in process equipment validation. manage deviations Perks and benefits SALARY WITH PF, ESIC, BONUS ,GRATUTITY BENEFITS

Preparation review of Comparative threshold analysis reports for Drug-device combination products Design history files for Drug-device combination products Preparation of Packaging Development SOPs Co-ordination with CFT to complete the review and approval of documents Preparation and review of packaging material specifications Preparation and review of packaging material STPs Review and approval of shade cards Preparation and review of BOM (Bill of Materials) Preparation of Master Packaging Record Initiation and handling of Change Controls Archival of all packaging development documents with respective to the product

Job Summary : Responsible for supervising and executing equipment operation, visual inspection, and packing activities in compliance with GMP and quality protocols. The role involves documentation, coordination with cross-functional teams, equipment qualification, and QMS adherence. Key Responsibilities : To perform equipment operation and cleaning To supervise visual inspection and batch packing execution as per plan To perform documentation as per batch record and SOP To perform equipment qualification as per protocols and SOP Responsible for maintaining documents as per cGMP norms Coordinate with cross-functional teams for day-to-day activities Responsible for SOP, MPR, and BPR preparatio...

Roles and Responsibilities Conduct Process Validation, Equipment Qualification, and Cleaning Validation activities according to SOPs. Prepare documents for Capa, MACO, OSD, and SOP preparation. Ensure compliance with regulatory requirements through quality control measures. Collaborate with cross-functional teams to resolve quality issues. Maintain accurate records of all quality-related activities. Desired Candidate Profile 5-10 years of experience in Quality Assurance (QA) or related field. Bachelor's degree in Pharmacy (B.Pharma) or Master's degree in Pharmacy (M.Pharma). Strong understanding of pharmaceutical industry regulations and standards. Proficiency in equipment qualification, cle...

As a Microbiologist at our company, your role will involve the following responsibilities: - Reporting and reviewing microbiology results of Raw Materials, Packing Materials, In-process Materials, and Finished Products as required. - Reviewing and approving Microbiological analysis reports including Water, Microbial monitoring of clean rooms, MLT, and BET. - Preparation of SOPs related to QC Microbiology. - Maintaining media stock and related GPT records. - Implementing Good Microbiological Laboratory Practices at work. - Reviewing microbial test results of water samples as required. - Maintaining reference standard cultures / subcultures; preparation and maintenance of working cultures as a...

Role Summary The Optimization Specialist focuses on observing, documenting, and refining processes across departments and clients. This role requires precision, structure, and a deep understanding of how to design workflows that are clear, consistent, and ready for automation. Core Responsibilities - Observe existing workflows, document them in comprehensive detail, and develop clear SOPs and process maps. - Identify inefficiencies and provide actionable recommendations to streamline operations. - Collaborate with automation teams to prepare workflows for implementation. - Maintain uniformity and clarity in all documentation, meeting Abraham Advisors standard of luxury-grade documentation wi...

Role & responsibilities Work closely with clients to gather, analyze, and document business requirements for various banking and finance processes. Analyze data to identify insights, and areas for improvement. Suggest process improvements and explore automation opportunities. Collaborate with cross-functional teams to ensure business and technical goals align. Understand technology and software applications and ideate new processes with objective of process efficiencies. Develop clear and practical Standard Operating Procedures (SOPs), checklists and preparing policies. Lead meetings to discuss and review new suggested process improvement. Prepare process, workflows, SOPs and Checklists. Giv...

Position Title : Odoo Specialist Location : Gurugram, India Experience : 2-5 years Key Responsibilities: Implement, configure, and maintain Odoo ERP modules across functions including Sales, CRM, Purchase, Inventory, Accounting, HR, and Project

Dear Candidates, V-Ensure Pharma (USFDA & EU GMP approved Formulation plant ) located at additional Patalganga MIDC near Panvel is hiring for Sr. Officer / Executive HR & Admin role. Role & responsibilities 1. Talent Acquisition & Management 2. Employee life cycle management 3. Supervision of Time office Management 4. Supports to PMS activity 5. Handling QMS activities such as SOP Preparation, SOP Compliance & Pharma Audits 6. Sound Knowledge of Statutory compliances. Preferred candidate profile Candidate having experience in Pharmaceutical Company is preferable

Greeting from INTELIZIGN! Job Description PMO (Design) – Automotive Domain Manage and support design-related projects ensuring alignment with project timelines, technical requirements, and organizational objectives. Coordinate with cross-functional teams such as design, engineering, manufacturing, and program management to deliver design outcomes efficiently. Plan, track, and report design project activities, milestones, and deliverables. Define project scope, schedules, and resource requirements in collaboration with stakeholders. Manage design documentation, version control, and change management processes. Facilitate design review meetings, track action items, and ensure timely closure. P...