4089 Gmp Jobs - Page 31

About The Role Skill required: KYC Screening - Know Your Customer (KYC) Designation: Regulatory Compliance New Associate Qualifications: Any Graduation Years of Experience: 0 to 1 years What would you do? Help clients transform their compliance function from reactive to proactive through an intelligent compliance operating model powered by data, intelligent technologies and talentLooking for someone with KYC experience along with ECDD/OCDD knowledgeBusiness and regulatory requirements, governance, operating model, process and system controls to verify the identity, suitability, and risks involved with onboarding and/or maintaining a business / customer relationship. This includes driving cus...

About The Role Skill required: KYC Screening - Know Your Customer (KYC) Designation: Regulatory Compliance Associate Qualifications: Any Graduation Years of Experience: 1 to 3 years What would you do? Experience working in Client On-boarding, Account Maintenance, Customer Identification Program (CIP) and Know Your Customer (KYC) processes.Conducting PEPs (Politically Exposed Persons) screening and adverse media checksProven analytical skills, problem solving ability, and a control mentality paired with meticulous attention to detail.Aptitude for building relationships and ability to communicate complex issues to a wide array of internal clients with differing levels of product experience.Sel...

About The Role Skill required: KYC Screening - Know Your Customer (KYC) Designation: Regulatory Compliance New Associate Qualifications: Any Graduation Years of Experience: 0 to 1 years What would you do? Help clients transform their compliance function from reactive to proactive through an intelligent compliance operating model powered by data, intelligent technologies and talentLooking for someone with KYC experience along with ECDD/OCDD knowledgeBusiness and regulatory requirements, governance, operating model, process and system controls to verify the identity, suitability, and risks involved with onboarding and/or maintaining a business / customer relationship. This includes driving cus...

We are looking for a highly skilled and experienced professional to join our team as a Kitchen Bakery, Asian, and Butchery Section in Trident. The ideal candidate will have 1-3 years of experience in the hospitality industry. Roles and Responsibility Manage and maintain high standards of food quality and presentation in the bakery section. Prepare and cook a variety of dishes, including bread, pastries, and desserts. Maintain cleanliness and organization in the kitchen area. Collaborate with other chefs to ensure seamless service delivery. Develop new recipes and menus to enhance culinary offerings. Ensure compliance with health and safety regulations. Job Requirements Proven experience in a...

JOB DESCRIPTION 1, PURPOSE OF THE JOB: Job Context: To support the running of the factory by resolving breakdowns and by delivering maintenance. Also required to drive improvement across the site in terms of new machinery, hygiene, quality, and performance. Responsible for supervising and improving production at plants and factories. Support engineering teams, draw up safety protocols, report issues to the manager, and develop strategies to improve efficiency and profit. 2, DETAILS OF THE JOB: Job Role/ Title: Production Level: M01-M02 Business Unit: Gorakhpur Function: Production Country: India Work Location: Gorakhpur Reporting Manager: Manager’s Manager: Matrix Manager: - Team Size: - No....

Role & responsibilities Perform daily monitoring of laboratory activities as per defined SOPs. Experience in handling GMP documentation and regulatory audits preferred. Carry out calibration of instruments such as the pH meter and weighing balance. Conduct Environmental Monitoring (EM) through microbial methods. Perform water sampling and microbiological analysis of purified and process water. Conduct sterility and bacterial endotoxin tests (BET) as per standard methods. Perform Liquid Particle Count (LPC) testing and maintain trend data. Maintain all laboratory documentation and records in compliance with GMP and regulatory requirements.

Responsibilities: * Conduct regular audits & inspections * Ensure compliance with quality standards * Monitor KPIs & report findings * Lead capa investigations & implement corrective actions * Manage change controls process

Responsibilities: * Conduct audits and inspections. * Collaborate with cross-functional teams on product development. * Ensure compliance with quality standards. * Develop and implement quality plans.

Gaining an understanding of the client's needs and requirements and communicating them and the quality standards to the production teams. Devising ways to improve the manufacturing process to ensure higher-quality goods. Required Candidate profile Strong attention to detail, observation, organizational, and leadership skills. Knowledge of quality control procedures and legal standards. Good technical and IT skills. Perks and benefits Bonuses Flexible Work Arrangements Paid Time Off

Roles & Responsibilities: Good Communication skills (Hindi, Gujarati and English) candidate who has experience or are from pharma/biotechnology/medical devices industry. Experience with SAP S4 HANA is must. Good understanding of dispatch activities, understanding of inventory management, domestic and export dispatches etc. Familiarity with GMP, GDP, and 5S practices. Ensure proper documentation and control of records related to incidents, deviations, change controls, and other QMS-related activities. Maintain and update records as per established SOPs and regulatory requirements. Oversee day-to-day warehouse activities, including material receipt, storage, issuance, and handling. Manage mate...

Job Title: Deputy Manager- Formulation Location: Govandi, Mumbai Department: Corporate Quality Assurance Qualification, Experience and Technical Competency: 1. Master’s Degree in Pharmacy or Science or equivalent scientific field. 2. Minimum 10 years experience in Pharmaceutical Industry (Strong background of Formulation industry with 2 to 3 years experience in Quality Control.) 3. Work experience in Regulatory Sites (USFDA, MHRA, EU GMP) 4. Knowledge of current Good Manyfacturing Practices (cGMP), Quality Management Systems (QMS) and regulatory guidelines. Key Requirements: Responsible for Quality Functions across Own Sites and Contract Sites with adherance to cGMP, Regulatory standards and...

Senior Manager 1

Role & responsibilities 1. To ensure that all documents are updated according to audits & regulatory. 2. To calibrate the instruments as per the calibration schedule and maintain the records. 3. To develop SOPs and updating documents based on audits. 4. To ensure the QMS activities of instrument department. 5. To impart training to the shop- floor staff on handling & operation of the instruments. 6. Overall responsibility for calibration 7. Responsible for maintain concerned area as per Audit requirement. 8. Identify and perform calibration activities of all instruments as per schedule. 9. To highlight the non-safe working practices and conditions to the department in-charge so that these is...

Job Responsibility To implement and follow the cGMP, GLP, GDP and aseptic practices at microbiology laboratory. To follow the entry and exit procedure at microbiology and production area as per the applicable SOP. To maintain microbiology laboratory in clean condition. To operate and to maintain all equipment in microbiological laboratory, like Calibration, Validation, AMC and Break down. Store, prepare, sterilize and use the dehydrated media as per the SOP and document the same. To check the disinfectant solution preparation, sanitization and fumigate the microbiology laboratory. To monitor and record the temperature of microbiology laboratory and refrigerator as per the scheduled frequency...

Introduction: Jubilant Bhartia Group is a global conglomerate founded by Mr Shyam S Bhartia and Mr Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Life Science Ingredients, Contract Research & Development Services, Therapeutics, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services Group has global presence employing around 42,000 people across the globe with over 2,400 in North America, Jubilant Pharmova Limited Jubilant Pharmova Limited (formerly Jubilant Life Sciences Limited) is a company with global presence that is involved in Radio pharma, Allergy Immunotherapy, CDMO Sterile Injectable, Contract Research Develo...

Develop and execute regulatory strategies for Class I, II, and III medical devices in compliance with US FDA (21 CFR Part 820) and EU MDR (2017/745). Prepare, review, and submit regulatory submissions including 510(k), PMA, Technical Documentation, and Design Dossiers. Collaborate with cross-functional teams including R&D, Quality, Clinical, and Manufacturing to ensure regulatory compliance throughout product lifecycle. Assess the regulatory impact of product and process changes and ensure proper documentation and notification. Support internal and external audits, including FDA inspections and Notified Body audits, ensuring readiness and timely response to findings. Review and approve produ...

Description. At West, were a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, Wests indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future. Theres no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supp...

Description. At West, were a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, Wests indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future. Theres no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supp...

Key Responsibilities: Shift Supervision: Supervise PET bottling operations during the assigned shift. Plan, allocate, and monitor manpower and machine usage. Ensure smooth shift handover and maintain accurate shift reports/logbooks. Production & Efficiency: Monitor production processes and optimize machine uptime and output. Ensure production targets are met within time, quality, and cost parameters. Minimize line downtime, rework, and wastage. Machine & Process Handling: Operate and monitor PET bottling machines such as: Preform feeding Filling and capping machines Labelling and packing machines Coordinate with maintenance team for breakdowns and preventive maintenance. Quality & Hygiene Co...

You will be responsible for conducting WET, GC, and HPLC analysis as an Expert in the field. Your role will involve ensuring compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), Good Documentation Practices (GDP), and ALCOA+ guidelines. Key Responsibilities: - Conduct WET, GC, and HPLC analysis - Ensure compliance with GMP, GLP, GDP, and ALCOA+ guidelines Qualification Required: - M.Sc. in Chemistry - 3 to 5 years of experience - Good knowledge of GMP, GLP, GDP, ALCOA+ - Expertise in WET, GC, HPLC Analysis,

As a Process Equipment Engineer, you will be responsible for designing and specifying process equipment systems for pharmaceutical manufacturing plants, ensuring alignment with project goals and regulatory standards. This includes selecting appropriate equipment based on factors such as material compatibility, process requirements, automation, and cost-effectiveness. Additionally, you will develop equipment specifications, datasheets, and technical documentation for procurement and installation. - Design and specify process equipment systems for pharmaceutical manufacturing plants. - Select appropriate equipment based on material compatibility, process requirements, automation, and cost-effe...

Role Overview: As a Quality Control Inspector at our company, your role involves performing inspections, tests, and evaluations to identify defects or deviations from specifications. You will be responsible for collecting and analyzing data to identify trends and areas for improvement. Additionally, you will ensure that all required documentation complies with industry standards such as GMP, ISO, and GDP. Your contribution in helping implement and maintain quality control processes and procedures will be crucial. Collaborating with production and manufacturing teams to identify and resolve quality issues will also be part of your responsibilities. Furthermore, you will play a key role in ass...

Role Overview: As a QC Microbiologist, you play a crucial role in ensuring the quality and safety of products through microbiological testing. Your responsibilities include: Key Responsibilities: - Sampling and Analysis: Collect and analyze samples from raw materials, in-process, and finished products using microbiological techniques such as plate counting and molecular assays. - Quality Control Testing: Ensure that microbial levels meet regulatory specifications and product safety standards. - Environmental Monitoring: Monitor microbial levels in production areas to detect any contamination risks, including air, surfaces, and water systems. - Aseptic Techniques: Follow aseptic practices dur...

Role & responsibilities Job Title: Quality Control / Quality Assurance Executive (Fresher) Industry: Pharmaceuticals Manufacturing Department: Quality Control (QC) / Quality Assurance (QA) Company: Vivek Pharmaceuticals Pvt Ltd Location: Jammu Employment Type: Full Time Experience: 0 2 Years Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc (Chemistry, Microbiology, Biotechnology or related field) Job Summary: We are looking for passionate and detail-oriented candidates to join our Quality team. The selected candidates will be part of controlling product quality, compliance with regulatory requirements, and in all quality operations. Key Responsibilities: Quality Control (QC): Conduct routine t...

As a SAP ECC Functional Consultant, you will be responsible for leading functional activities for ECC company code rollout in a greenfield environment for a leading pharmaceutical client. Your role will also involve preparing for a future S/4HANA conversion, requiring awareness of the S/4HANA landscape and delta changes. Collaboration with business stakeholders, gathering requirements, performing detailed analysis, and ensuring compliance with pharma industry standards will be key aspects of your role. - Lead functional activities for ECC company code rollout in a greenfield environment. - Work closely with business stakeholders to gather requirements and perform detailed analysis. - Prepare...