350 Who Jobs - Page 3

Sterile Manufacturing based in Waghodia, Vadodara. The ideal candidate brings 1- 7 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). Additio...

The ideal candidate brings 1-6 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) Lead microbiology practices including EM, MLT, sterility assur...

Chief Manager Township Administration (MP 25/13) based in Narmada, Gujarat. 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...

Job Title: Infection Control Nurse Branch Name: Thanal Brain & Spine Medcity Qualification: Bsc/Msc Nursing Experience : 2-3 Years Location: Kanhirode , Kannur Employment Type: Full time Department: Neurorehabilitation Key Responsibilities: Infection Surveillance: Monitor and record hospital-acquired infections and track infection trends. Conduct regular infection control rounds in all patient care areas. Policy Implementation: Develop, update, and enforce infection control policies and standard operating procedures (SOPs). Ensure adherence to aseptic techniques and hygiene protocols across departments. Training & Awareness: Conduct regular training programs for nursing, medical, housekeepin...

Support the technical transfer activity for a multi-phase and multi-year project to transfer programs into a third-party contract manufacturing facility in India. Provide Technical direction and support for third party manufacturing activities including coordination of activities with cross-functional roles from Quality, Regulatory, Development, Project Management, Supply Chain, Procurement and Validation. Be involved in the full project life cycle - successful project completion will include full implementation from initiation to deployment for multiple products, including equipment setup validation, manufacturing process transfer and validation, Test method transfer and validation, and pos...

# Support the manufacturing department to ensure all production operations comply with GMP, QMS & QA standards. # Monitor & maintain the QMS by managing SOPs. # Act as a key pivot between manufacturing operations and QA/QMS functions, Required Candidate profile # Min~5 years of experience in pharmaceutical manufacturing & in QA/QMS documentation, batch review, GMP compliance # Sound understanding of WHO - GMP, regulatory requirements # B. Pharm – essential

Hiring Head – Engineering (Pharma OSD, Wada) to lead maintenance, utilities & projects ensuring cGMP, USFDA, MHRA compliance. Exp: 12–20 yrs in pharma. glocalrise.komal@gmail.com | 9106329670 Food allowance Health insurance Annual bonus Provident fund

1. Preparation and submission of registration and re-registration dossiers as per country requirements of ROW (Preferable Russia, CIS countries and WHO) 2. Arrangement for indent of Samples, Packing Material specimen, Impurities, Reference Standards as per submission requirement. 3. Query evaluation and submission with respective countries requirement within the required time frame. 4. Establish coordination with other departments like QA/QC, R&D, Marketing and Purchase for ensuring the filings and query response within time frame. 5. Post approval activities: Submission of variations to the terms of marketing authorizations for finished products as per respective variation guideline. 6. Pre...

Minimum of 5-7 years of experience in regulatory affairs within the pharmaceutical industry for filing of products in various regulatory agencies Knowledge: Strong understanding of regulatory guidelines and

About The Role : Job titleBond Analytics Analyst Corporate titleAVP LocationBangalore, India Role Description OverviewBusiness Division Deutsche Banks Corporate Bank (CB) a market leader in cash management, trade finance & lending, securities services and Trust & Agency Services. Focusing on the treasurers and finance departments of corporate and commercial clients and financial institutions across the globe, our universal expertise and global network allows us to offer truly integrated and effective solutions. OverviewBusinessTrust and Agency Service (TAS): With offices in New York, California, London, Frankfurt, Milan, Lisbon, Dublin, Hong Kong, Singapore and Tokyo, the Trust and Agency Se...

Role & responsibilities The QA & Regulatory Affairs Manager leads and oversees all regulatory and quality assurance activities within the company, ensuring that all products comply with local and international medical device regulations . The role is responsible for developing and executing regulatory strategies , managing submissions and approvals , and maintaining strong relationships with health authorities, notified bodies, and certification agencies to support product launches and lifecycle management. A core aspect of this position is to build and implement a full Quality Management System (QMS) compliant with ISO 13485:2016 , and to ensure regulatory readiness for global markets inclu...

Job Title: Production Executive/Asst Manager Qualification: B.Pharm / M.Pharm / B.Sc. / M.Sc. Experience: 7-10 years of relevant experience in pharmaceutical production ( Formulation experience is mandatory ). Job Responsibilities: Manage day-to-day formulation production operations , ensuring timely and efficient manufacturing in compliance with GMP. Ensure adherence to regulatory, safety, and environmental requirements , and maintain readiness for internal and external audits. Drive productivity improvement , cost saving initiatives , and rejection reduction across all production processes. Oversee and optimize production schedules, raw material usage, and inventory control to meet busines...

shall be responsible for maintaining and improving all QMS activity, GMP and GLP across the company Handling QMS activities like change control, validations, stability, qualifications, APQR and Risk assessment etc Label artwork review and management Required Candidate profile Assisting HOD in customer complaint analysis and preparation of customer complaint report. Investigation of incidents, deviations, OOS and ensure corrective actions in place.

We are seeking a highly experienced Quality Assurance leader to drive Corporate QA initiatives across multiple formulation manufacturing sites. The incumbent will be responsible for strengthening the company's Audit, Compliance, and Validation/Qualification (VQ) framework, ensuring adherence to global regulatory standards, and maintaining continuous inspection readiness . This is a strategic corporate role requiring close coordination with site QA, manufacturing, and regulatory teams to uphold a consistent culture of quality excellence and compliance across all units. Key Responsibilities: Lead and manage internal and external audits across formulation sites (OSD, Injectables, Topicals). Ens...

1. Production Management & Planning 2. Compliance, Quality & Regulatory Adherence 3. Process Improvement & Operational Excellence 4. Leadership & Team Development 5. Reporting, Budget & Governance Required Candidate profile •Bachelor’s or master’s degree in pharmacy, engineering, or life sciences. •Proven expertise in URS, equipment qualification, SOPs, and manufacturing process •Experience of EU-GMP, WHO and USFDA

Drive on 9th Nov -Assistant Manager – Production (OSD)-Dahej11–13 yrs (Pharma – Tablets/Capsules, OSD)Ensure smooth OSD manufacturing operations (Granulation, Compression, Coating, Packing) in a cGMP-compliant facility. Salary: Flexible

Role & responsibilities Oversee the CDMO sales of marketing functions of medical devices/ Medical related products, Polymer compounding business development, contract manufacturing products Collaborate and strategic alliance/tie-up/mergers with state/central Government team members/WHO/Medical OEMs/Hospitals, pharmaceutical and other healthcare & life science product manufacturers Collaborate with customer R&D & develop the business for new Med-tech/Compounded polymer development Develop marketing plans to showcase the company's products and solutions to potential customers and target markets. Conducting market research to identify trends, customer preferences, and emerging opportunities in ...

Job Title: Formulation ADL - Analyst Division Integrated Product Development Department Global Respiratory Job Purpose Execute the core method development activities and conduct analysis of routine as well as stability samples to finalize specifications and ensure timely delivery of product to unit. Key Accountabilities (1/6) 1.Develop new analytical methods for analysis of routine as well as stability samples by following proper GLPs to provide results or information regarding products to formulators 2. Perform maintenance and calibration of lab instruments / equipment to get accurate and reproducible analytical result for proper interpretation 3.Document and interpret the analytical data i...

1. Project & Engineering Management 2. Maintenance, Reliability & Calibration 3. Energy, Safety & Environmental Compliance 4. People Leadership & Capability Development 5. Digitalization, Operational Excellence & Continuous Improvement Required Candidate profile • Bachelor’s or Master’s degree in Mechanical, Electrical, Instrumentation, or Automation Engineering (B.E./M.E., B.Tech/M.Tech). • 16+ years of experience in pharmaceutical

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 ...

Job Title: Senior Trainer Validation (CQV, Equipment, Injection Mold, HVAC) Location: Remote Job type: Part-time Job Summary: To design, develop, and deliver comprehensive training programs on Commissioning, Qualification & Validation (CQV), Equipment Qualification, Injection Molding Process Validation, and HVAC System Validation. The trainer will ensure technical competency development across engineering and quality teams in compliance with international regulatory standards (USFDA, EU GMP, ISO 13485, etc.). Key Responsibilities: Develop and deliver training modules on: Commissioning, Qualification, and Validation (CQV) lifecycle Equipment Qualification (IQ/OQ/PQ) Process Validation for Inj...

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 (...

1. Quality System Management: Establish, implement, and maintain the Quality Management System (QMS) as per cGMP, WHO, and regulatory norms . Oversee activities related to change control, deviations, CAPA, OOS/OOT investigations, and risk assessments . Ensure all QA processes align with company policies and current regulatory requirements. 2. Documentation & Compliance: Review and approve SOPs, BMRs, BPRs, validation protocols , and analytical reports. Ensure all documentation complies with Good Documentation Practices (GDP) and data integrity requirements. Supervise document control , issuance, archival, and version management systems. 3. Batch Release & In-Process Quality Assurance: Ensure...

Urgent Opening | Global Operations (Humanitarian Logistics) Industry: Freight Forwarding / International Logistics / Humanitarian Supply Chain Location: Mumbai About the Role: We are looking for an experienced logistics professional to manage and coordinate international humanitarian shipments for clients such as UNICEF, WHO, Red Cross, and other NGOs . The role involves close coordination with the Global Operations Team in Copenhagen , ensuring smooth, compliant, and timely delivery of relief cargo worldwide. Key Responsibilities: Manage and execute end-to-end international air/sea shipments for humanitarian and relief projects. Coordinate with global offices, airlines, shipping lines, and ...

We are looking for a skilled ENT professional with 5 years of experience to join our team as an Associate in the field of ENT. The ideal candidate should have a strong background in MS - ENT and be able to work effectively in a fast-paced environment. Roles and Responsibility Conduct thorough examinations and diagnoses of patients with various ear, nose, and throat conditions. Develop and implement effective treatment plans for patients with different levels of severity. Collaborate with other healthcare professionals to ensure comprehensive care. Stay updated with the latest advancements and technologies in the field of ENT. Provide guidance and support to junior staff members. Participate ...