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📑 For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma pa ...

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📑 Job DescriptionCSV consultant to evaluate laboratory equipment's CSV protocols for a pharma-biotech industry.RequirementsBachelor’s degree in science & 5 years of experience in laboratory CSV.<li ...

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📑 For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma ...

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📑 Job DescriptionCSV Specialist for  validation of laboratory instruments with LIMS connection (HPLC, Gas Chromatographer, Instron pull testers) <span id=s ...

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📑 Job DescriptionPSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements.Our goal is to skyrocket our clients’ success, and you can be a part of our team’s achievements. Employing ...

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📑 Job DescriptionPSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in co ...

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📑 Department Details Role Summary Manufacuring IT System support, including implementation, installation, CSV and support activities Key Responsibilities Manufacuring IT System support, including implementation, installation, CSV and support activities Educational Qualifications Required Education Qualification: Required Expe ...

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📑 Department Details Role Summary Manufacuring IT System support, including implementation, installation, CSV and support activities Key Responsibilities Manufacuring IT System support, including implementation, installation, CSV and support activities < ...

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📑 Department Details Role Summary •Having hands on experience in ABB 800xA DCS. •Planning & Execution of different types of maintenance & trouble shooting of instruments / control systems (PLC /DCS / MES) and its accessories •Review / execution of CSV of control systems /instrument qu ...

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📑 A CSV consultant will use his/her knowledge of FDA cGMP and related regulations and guidelines, and specific knowledge of computer validation methodologies and principles to perform CSV on a variety of systems and programs. Experience of QA in a FDA regulated environment is preferred. At least 2 years of Computer System Validation or any validation ...

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📑 About CAI CAI is a 100% employee-owned company established in 1996, that has grown year over year to nearly 850 people worldwide. We provide commissioning, qualification, validation, start-up, project management and consulting services related to operational readiness to FDA regulated and other mission critical industries. Meeting a High ...

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📑 A CSV consultant will use his/her knowledge of FDA cGMP and related regulations and guidelines, and specific knowledge of computer validation methodologies and principles to perform CSV on a variety of systems and programs. Experience of QA in a FDA regulated environment is preferred. <str ...

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📑 Job DescriptionPSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements.Our goal is to skyrocket our clients’ success, and you can be a part of our team’s achievements. Employing ...

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📑 Job DescriptionQA/CSV Consultant with experience in Electronic Record Software and quality regulations review.Software Validations knowledgeStrong knowledge of Electronic Record Review Quality Systems </div ...

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📑 Job Description<span class=size style ...

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📑 About CAI CAI is a 100% employee-owned company established in 1996, that has grown year over year to nearly 850 people worldwide. We provide commissioning, qualification, validation, start-up, project management and consulting services related to operational readiness to FDA regulated and other mission critical industries. Meeting a High ...

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📑 • Experience on more than one project or more than two years performing CSV for ERP • Ability to create and execute computer systems validation scripts • Experience performing computer systems validation with a risk-based approach • Ability to create and execute computer systems validation plans • Strong written communication skills ...

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📑 • Experience on more than one project or more than two years performing CSV for ERP • Ability to create and execute computer systems validation scripts • Experience performing computer systems validation with a risk-based approach • Ability to create and execute computer systems validation plans • Strong written communication skills ...

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📑 A Computer System Validation (CSV) Engineer is responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals, medical devices, and biotechnology, meet the necessary quality, safety, and compliance requirements. The qualifications for a CSV Engineer typically include: ResponsibilitiesTo maintain consistent and ...

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📑 A Computer System Validation (CSV) Engineer is responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals, medical devices, and biotechnology, meet the necessary quality, safety, and compliance requirements. The qualifications for a CSV Engineer typically include: ResponsibilitiesTo maintain consistent and ...

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📑 Job DescriptionLooking to onboard a seasoned Senior Information Security Project Manager (m/f/d) for a thrilling opportunity with a renowned manufacturing powerhouse nestled in the picturesque surroundings of Bubendorf, BL.ResponsibilitiesManagement of multiple simultaneous projects including their dependencies, creation and delivery of presentatio ...

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📑 A Computer System Validation (CSV) Engineer is responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals, medical devices, and biotechnology, meet the necessary quality, safety, and compliance requirements. The qualifications for a CSV Engineer typically include:ResponsibilitiesTo maintain cons ...

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📑 A Computer System Validation (CSV) Engineer is responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals, medical devices, and biotechnology, meet the necessary quality, safety, and compliance requirements. The qualifications for a CSV Engineer typically include:ResponsibilitiesTo maintain cons ...

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📑 A Computer System Validation (CSV) Engineer is responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals, medical devices, and biotechnology, meet the necessary quality, safety, and compliance requirements. The qualifications for a CSV Engineer typically include:ResponsibilitiesTo maintain cons ...

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📑 Job DescriptionEURHASI is recruiting for its client a CSV Engineer French-English<span class=font style=fo ...

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📑 **Job Responsibilities:** + Perform review of Computerized System Validation of IT systems of Manufacturing Sites + Support various phases of Computer System including Planning, Implementation, Maintenance and retirement activities by ensuring compliance with internal / external regulatory requirements + Perform ...

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📑 GST FilingExport DocumentationPreparing debit & credit note**Salary**: ₹18,000.00 - ₹25,000.00 per monthSchedule:- Day shift- Monday to Friday**Education**:- Bachelor's (preferred)**Experience**:- Taxation: 1 year (preferred)- total work: 2 years (preferred)**La ...

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📑 Experience - 2 to 4 Years (Herbal Extracts & essential oils)Company profile:We CSV Pharmaceuticals a Contract manufacturer & supplier of Herbal Extracts & Essential oils.**Responsibilities**:- Conducting product research and sourcing new suppliers and vendors.- Sourcing materials, herbal products, and services and ne ...

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📑 Business: PPL Central Partner Functions Department: IT Location: Kurla, Mumbai Travel: Moderate Job Overview To perform and document Computer System Validation as per defined processes at Corporate IT and across Piramal Pharma sites. Key Stakeholders: Internal Business – Site / Corporate functions IT Team ( SAP/ Infra / Quality IT / Al ...

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📑 For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma par ...

🔗 View Salary and More Information 🎯 Get Ai Resume Score for this Job

📑 For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma par ...

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📑 Verista's 600 experts team up with the world's most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world's most pressing healthcare challenges. Verist ...

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📑 Verista's 600 experts team up with the world's most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world's most pressing healthcare challenges. Verist ...

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📑 A CSV consultant will use his/her knowledge of FDA CGMP and related regulations and guidelines, and specific knowledge of computer validation methodologies and principles to perform CSV on a variety of systems and programs. Experience of QA in a FDA regulated environment is preferred.At least 2 years of Computer System Validation or any validation ...

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📑 Working with UsChallenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transfor ...

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📑 Working with UsChallenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transfor ...

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📑 • Experience on more than one project or more than two years performing CSV for ERP• Ability to create and execute computer systems validation scripts• Experience performing computer systems validation with a risk-based approach• Ability to create and execute computer systems validation plans• Strong written communication skills ...

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📑 • Experience on more than one project or more than two years performing CSV for ERP • Ability to create and execute computer systems validation scripts • Experience performing computer systems validation with a risk-based approach • Ability to create and execute computer systems validation plans • Strong written communication sk ...

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📑 • Experience on more than one project or more than two years performing CSV for ERP• Ability to create and execute computer systems validation scripts• Experience performing computer systems validation with a risk-based approach• Ability to create and execute computer systems validation plans• Strong written communication skills ...

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📑 • Experience on more than one project or more than two years performing CSV for ERP • Ability to create and execute computer systems validation scripts • Experience performing computer systems validation with a risk-based approach • Ability to create and execute computer systems validation plans • Strong written communication sk ...

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📑 A CSV consultant will use his/her knowledge of FDA CGMP and related regulations and guidelines, and specific knowledge of computer validation methodologies and principles to perform CSV on a variety of systems and programs. Experience of QA in a FDA regulated environment is preferred. At least 2 years of Computer System Validation or any validation ...

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📑 A CSV consultant will use his/her knowledge of FDA cGMP and related regulations and guidelines, and specific knowledge of computer validation methodologies and principles to perform CSV on a variety of systems and programs. Experience of QA in a FDA regulated environment is preferred. At least 2 years of Computer System Validation or any validation ...

🔗 View Salary and More Information 🎯 Get Ai Resume Score for this Job

📑 A Computer System Validation (CSV) Engineer is responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals, medical devices, and biotechnology, meet the necessary quality, safety, and compliance requirements. The qualifications for a CSV Engineer typically include:ResponsibilitiesTo maintain consistent and d ...

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📑 A Computer System Validation (CSV) Engineer is responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals, medical devices, and biotechnology, meet the necessary quality, safety, and compliance requirements. The qualifications for a CSV Engineer typically include: ResponsibilitiesTo maintain consistent and ...

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📑 Dear Aspirants, Greetings from !!We have an amazing opportunity for Sr. Software Engineer who can join our team immediately!Primary Skill set : CSV, GAMP, MES, QMS, VMP, 21 CFRExperience: 8+ yearsLocation: HyderabadNotice period: Immediate to 15 DaysJob DescriptionDeveloping validation documentation for pharmaceut ...

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📑 Python Technical Lead 7 to 9 years of experience Essential: •Experience working with Python (Pandas, NumPy, Openpyxl, logger, Asynchronous methods, CSV, CSV to DF) •Good understanding on Data Structures •Basic knowledge on Insurance domain. •Create and maintain technical documentation, design documents, and code documentation •Conduct cod ...

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📑 A Computer System Validation (CSV) Engineer is responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals, medical devices, and biotechnology, meet the necessary quality, safety, and compliance requirements. The qualifications for a CSV Engineer typically include:ResponsibilitiesTo maintain consiste ...

🔗 View Salary and More Information 🎯 Get Ai Resume Score for this Job

📑 A Computer System Validation (CSV) Engineer is responsible for ensuring that computer systems used in regulated industries, such as pharmaceuticals, medical devices, and biotechnology, meet the necessary quality, safety, and compliance requirements. The qualifications for a CSV Engineer typically include:ResponsibilitiesTo maintain consistent a ...

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📑 Working with UsChallenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that tran ...

🔗 View Salary and More Information 🎯 Get Ai Resume Score for this Job

📑 Working with UsChallenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that tran ...

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