Verified Job
Back Office / Data Entry
Assistant Manager Third Party Risk Management
Back Office / Data Entry
#560576
Remote / WFH
Job Description
Cummins Inc.
Team Leader – Customer Order Management O2C
Cummins Inc. • Pune, Maharashtra • via SimplyHired
2 days ago
Full–time
Apply on SimplyHired
Apply on Glassdoor
Apply on Expertini
Apply on Recruit.net
Apply on Latest Jobs
Apply on CallCenterJob.co.in
Job description
DESCRIPTION
Key Responsibilities:
• Perform order management tasks for specific customers/accounts, handling the entire order life cycle (order entry, modification, invoicing, credits/debits, logistics documentation).
• Provide consultative support to customers regarding lead time, availability, minor technical support, and policy.
• Act as a single point of contact for customer inquiries and esc...
Report this listing
D
deloitte
Assistant Manager Third Party Risk Management Pune CSV
deloitte • Pune, Maharashtra • via Deloitte South Asia Careers
16 hours ago
Full–time
Apply on Deloitte South Asia Careers
Apply on LinkedIn
Apply on Jooble
Apply on Tech Funding News Jobs
Apply on Glassdoor
Apply on BeBee
Apply on Mail Jobs
Apply on SimplyHired
Job description
The Team
Deloitte helps organizations anticipate and adapt to changes in the compliance requirements, and build better programs and controls to address the wide variety of risks. We work with clients and regulators on effective remediation in response to compliance events.
Work you’ll do
As a part of our Technology & Transformation team, You’ll:
• Support on IT quality systems framework design and implementation
• Managing the reviews and assessments for IT quality
• Assist in Computer System Validation (CSV) compliance of GxP processes for pharmaceutical companies or experience on quality compliance services for global consumer health care, medical devices, and pharmaceutical companies
• GxP Business process review
• Development of integrated GxP and IT compliance
• Standard operating procedures and guidelines
• GxP and IT compliance assessment
• Define the Validation strategy of IT Software and Systems
• Actively participate in the Validation Life Cycle of regulated IT projects or platforms by planning validation deliverables, working on validation documentation, participating in authoring deliverables, functional requirements definition, traceability matrix, validation protocol development,
• Validation testing and deviation management; and working closely with cross-functional project teams.
• Ensure 21 CFR Part 11 compliance for Computerized system
• Provide User training on CSV and increase awareness about compliance
• Responsible for reducing Gaps identified in various GAP/Risk Assessments existing and new computerized systems and providing a remedial action plan for compliance.
• Carrying out an Audit of IT systems to ensure regulatory compliance
• Manage the specified business/systems requirements, working closely with the designated Project Manager to facilitate the progress of the project Coach/mentor staff and provide technical leadership, as needed
The key skills required are as follows:
• IT Quality, Regulatory, Compliance (IT-QRC)
• Quality guidelines mentioned by FDA, MHRA, and other regulatory bodies
• GxP practices and GAMP5 guidelines.
• Computer System Validation of various COTS products like COGNOS, IMPACT, BAELN and other related applications used in pharmaceutical industries
• Experience in activities like Business Analysis, Risk Identification, FRS creation and other validation testing deliverables.
• Good understanding & practical experience of 21CFR Part 11 and other FDA GxP regulations.
Additional Skills
• Excellent verbal and written communication skills
• Experience in consulting domain to handle/manage different clients
Qualifications
• B.E./B.Tech./MCA/MBA/M.Sc/B.Pharm/M.Pharm or similar
• Experience range– 3years to 5years
Team Leader – Customer Order Management O2C
Cummins Inc. • Pune, Maharashtra • via SimplyHired
2 days ago
Full–time
Apply on SimplyHired
Apply on Glassdoor
Apply on Expertini
Apply on Recruit.net
Apply on Latest Jobs
Apply on CallCenterJob.co.in
Job description
DESCRIPTION
Key Responsibilities:
• Perform order management tasks for specific customers/accounts, handling the entire order life cycle (order entry, modification, invoicing, credits/debits, logistics documentation).
• Provide consultative support to customers regarding lead time, availability, minor technical support, and policy.
• Act as a single point of contact for customer inquiries and esc...
Report this listing
D
deloitte
Assistant Manager Third Party Risk Management Pune CSV
deloitte • Pune, Maharashtra • via Deloitte South Asia Careers
16 hours ago
Full–time
Apply on Deloitte South Asia Careers
Apply on LinkedIn
Apply on Jooble
Apply on Tech Funding News Jobs
Apply on Glassdoor
Apply on BeBee
Apply on Mail Jobs
Apply on SimplyHired
Job description
The Team
Deloitte helps organizations anticipate and adapt to changes in the compliance requirements, and build better programs and controls to address the wide variety of risks. We work with clients and regulators on effective remediation in response to compliance events.
Work you’ll do
As a part of our Technology & Transformation team, You’ll:
• Support on IT quality systems framework design and implementation
• Managing the reviews and assessments for IT quality
• Assist in Computer System Validation (CSV) compliance of GxP processes for pharmaceutical companies or experience on quality compliance services for global consumer health care, medical devices, and pharmaceutical companies
• GxP Business process review
• Development of integrated GxP and IT compliance
• Standard operating procedures and guidelines
• GxP and IT compliance assessment
• Define the Validation strategy of IT Software and Systems
• Actively participate in the Validation Life Cycle of regulated IT projects or platforms by planning validation deliverables, working on validation documentation, participating in authoring deliverables, functional requirements definition, traceability matrix, validation protocol development,
• Validation testing and deviation management; and working closely with cross-functional project teams.
• Ensure 21 CFR Part 11 compliance for Computerized system
• Provide User training on CSV and increase awareness about compliance
• Responsible for reducing Gaps identified in various GAP/Risk Assessments existing and new computerized systems and providing a remedial action plan for compliance.
• Carrying out an Audit of IT systems to ensure regulatory compliance
• Manage the specified business/systems requirements, working closely with the designated Project Manager to facilitate the progress of the project Coach/mentor staff and provide technical leadership, as needed
The key skills required are as follows:
• IT Quality, Regulatory, Compliance (IT-QRC)
• Quality guidelines mentioned by FDA, MHRA, and other regulatory bodies
• GxP practices and GAMP5 guidelines.
• Computer System Validation of various COTS products like COGNOS, IMPACT, BAELN and other related applications used in pharmaceutical industries
• Experience in activities like Business Analysis, Risk Identification, FRS creation and other validation testing deliverables.
• Good understanding & practical experience of 21CFR Part 11 and other FDA GxP regulations.
Additional Skills
• Excellent verbal and written communication skills
• Experience in consulting domain to handle/manage different clients
Qualifications
• B.E./B.Tech./MCA/MBA/M.Sc/B.Pharm/M.Pharm or similar
• Experience range– 3years to 5years
