19 Manufacturing jobs in Nasirabad

About River

River is an electric vehicle company building multi-utility scooters. At River, we’re building scooters of tomorrow for the ambitious youth of today. Because we believe people only need two things to achieve success: the desire to make it to the top, and the means to get there.

With our flagship product River Indie, SUV of Scooters, is designed to help you get things done. Engineered to be a dependable ally on your road to success. We are backed by marquee international investors - these are mobility focused funds backed by Yamaha Motors, Al-Futtaim Automotive Group, Toyota VC and Maniv Mobility.

Key Responsibilities

• Strong communication and interpersonal skills
• Working Knowledge of Data Analysis and Presentation skills
• Problem-solving and analytical abilities
• Organizational and time management skills
• Ability to work well both in a team and independently
• Adaptability and flexibility
• Proficiency in Microsoft & Google Office Suite
• Strong attention to detail
• Basic understanding of business operations and management principles

Ideal Candidate

• Education Qualification :Bachelor Degree in Mech/EE
• Experience Required : 5 to 12 Years
• Automobile Project Management with focus on operations, Sales & Service
• Understanding of Project management methodologies Agile waterfall etc.
• PMP certification is an added advantage
• Should have good knowledge of reports and dashboard development on Excel, Power BI
• Should be proficient with MS office tools
• End to End Project Management and tracking w.r.t cost, quality & Delivery
• Risk Management & Mitigation
• Good knowledge of budgeting and control

About Loopworm:

At Loopworm, we are building the future of recombinant protein production with LoopBac technology , using insects as a reactor-free production platform . This novel process requires meticulous attention to high quality construction, biosafety, and compliance from the ground up.

The Role:

We are hiring a General Manager to embed quality-by-design during facility planning, construction and commissioning. You will be the custodian of regulatory alignment, working closely with engineering, design consultants, and government bodies to ensure the facility is audit-ready and future-proof.

What You’ll Do:

• Ensure facility design, layout, and utilities meet GMP, biosafety, and ISO standards.
• Develop documentation (Facility Master File, SOPs, QA checklists).
• Liaise with consultants and regulators (DBT, CDSCO, local PCB, Factories Act).
• Drive risk assessments to prevent costly compliance errors.

What We’re Looking For:

• Minimum 6 years experience in Biotech/Pharma facilities projects (manufacturing, validation, audits).
• Strong knowledge of GMP, ISO, HACCP, biosafety, and facility approvals.
• Detail-oriented professional who can balance compliance with project agility.

Why Join Us?

You’ll be setting up the commercial facility and compliance foundation for a world-class biotech platform , ensuring India takes a global lead in sustainable recombinant protein production.

About Loopworm:

At Loopworm, we are building the future of recombinant protein production with LoopBac technology , using insects as a reactor-free production platform . This novel process requires meticulous attention to high quality construction, biosafety, and compliance from the ground up.

The Role:

We are hiring a General Manager to embed quality-by-design during facility planning, construction and commissioning. You will be the custodian of regulatory alignment, working closely with engineering, design consultants, and government bodies to ensure the facility is audit-ready and future-proof.

What You’ll Do:

• Ensure facility design, layout, and utilities meet GMP, biosafety, and ISO standards.
• Develop documentation (Facility Master File, SOPs, QA checklists).
• Liaise with consultants and regulators (DBT, CDSCO, local PCB, Factories Act).
• Drive risk assessments to prevent costly compliance errors.

What We’re Looking For:

• Minimum 6 years experience in Biotech/Pharma facilities projects (manufacturing, validation, audits).
• Strong knowledge of GMP, ISO, HACCP, biosafety, and facility approvals.
• Detail-oriented professional who can balance compliance with project agility.

Why Join Us?

You’ll be setting up the commercial facility and compliance foundation for a world-class biotech platform , ensuring India takes a global lead in sustainable recombinant protein production.

Job Title: Good Manufacturing Practice(GMP) Quality Assurance ManagerTiming: Overlap with PST hours - Upto 2 am ISTTravel: International trips once every quarter expectedEmployment Type: Full-timeWorkplace Type: RemoteTHE CELITO TEAMThe Celito Team architects the buildout of simplified, integrated, and compliant technology stacks. With both consulting and products, our expertise can help our customers save time and money as they move from strategic Clinical & Quality management all the way to widespread and profitable commercialization.JOB OVERVIEWWe are seeking a highly skilled and experienced Manager/Sr. Manager of GMP Quality Assurance Operations to join our team. This leadership role is responsible for Quality oversight of CMOs manufacturing drug substance, drug product, and packaged product. This role will work closely with the CMC team to ensure compliance across the entire product lifecycle. The role ensures adherence to GMP and regulatory standards while driving continuous improvement. The ideal candidate will possess significant decision-making authority on quality matters and ensure the efficient operation of the QA department.KEY RESPONSIBLIITIESGMP QA Operations Responsibilities: Perform batch record review and compile documentation packages to support product disposition.Conduct technical reviews and approvals of Master Batch Records and executed batch records.Review and approve Deviations, CAPAs, Change Controls, and Audit reports.Perform technical reviews of Quality Control records, including Certificates of Release, Analytical Protocols, Reports, and Stability reports.Support and contribute to the Annual Product Quality Review.Author, review, and update QA Operations SOPs and other quality documents.Quality Oversight and Compliance Responsibilities:Ensure Quality and Compliance oversight of CMOs per quality agreements, including periodic site visits as needed.Oversee CMO/CSPs through remote collaboration, on-site visits, KPI monitoring, and adherence to quality agreements.Conduct vendor/CMO audits.Prepare, manage, and execute Quality Agreements.Provide Quality oversight and representation on external CDMO project teams; manage CDMO relationships.Coordinate and manage compliance activities in preparation for regulatory and internal inspections, and support interactions.External Audits and Regulatory Inspections:Lead preparations for external audits and regulatory inspections.Serve as the subject matter expert (SME) and host during audits and inspections.Develop and implement strategies to maintain continuous inspection readiness.Additional Responsibilities:Collaborate effectively with functional teams such as CMC, Supply Chain, and Regulatory.Escalate critical quality and compliance issues to management in a timely manner.Manage critical quality issues with Vendors/CMOs and provide prompt resolutions.Identify process gaps proactively and implement mitigation strategies. QUALIFICATIONSBachelor’s degree in a relevant field (e.g., Life Sciences, Pharmacy, Chemistry, Engineering). Advanced degree preferred.13+ years of experience in quality assurance role in the pharmaceutical industry required with at least 5+ years in Quality Operation roles in a current Good Manufacturing Practices (c GMP) environmentStrong working knowledge of FDA regulations (21 CFR, 210/211), ICH guidelines, and global regulations (EU Directives, and ROW) and expertise in the c GMP requirements pertaining to manufacturing and packaging operations (including serialization) in the United States and globally in support of global commercial production activitiesIn-depth knowledge of c GMP and strong understanding of the entire product lifecycle.Proven experience in conducting GMP audits and inspections is preferred.Strong analytical and problem-solving skills.Excellent communication and interpersonal skills.Ability to work independently and as part of a multidisciplinary team.Certification in GMP or related areas is preferred.Experience working with US and European companies is required.

Job Title: Good Manufacturing Practice(GMP) Quality Assurance ManagerTiming: Overlap with PST hours - Upto 2 am ISTTravel: International trips once every quarter expectedEmployment Type: Full-timeWorkplace Type: RemoteTHE CELITO TEAMThe Celito Team architects the buildout of simplified, integrated, and compliant technology stacks. With both consulting and products, our expertise can help our customers save time and money as they move from strategic Clinical & Quality management all the way to widespread and profitable commercialization.JOB OVERVIEWWe are seeking a highly skilled and experienced Manager/Sr. Manager of GMP Quality Assurance Operations to join our team. This leadership role is responsible for Quality oversight of CMOs manufacturing drug substance, drug product, and packaged product. This role will work closely with the CMC team to ensure compliance across the entire product lifecycle. The role ensures adherence to GMP and regulatory standards while driving continuous improvement. The ideal candidate will possess significant decision-making authority on quality matters and ensure the efficient operation of the QA department.KEY RESPONSIBLIITIESGMP QA Operations Responsibilities: Perform batch record review and compile documentation packages to support product disposition.Conduct technical reviews and approvals of Master Batch Records and executed batch records.Review and approve Deviations, CAPAs, Change Controls, and Audit reports.Perform technical reviews of Quality Control records, including Certificates of Release, Analytical Protocols, Reports, and Stability reports.Support and contribute to the Annual Product Quality Review.Author, review, and update QA Operations SOPs and other quality documents.Quality Oversight and Compliance Responsibilities:Ensure Quality and Compliance oversight of CMOs per quality agreements, including periodic site visits as needed.Oversee CMO/CSPs through remote collaboration, on-site visits, KPI monitoring, and adherence to quality agreements.Conduct vendor/CMO audits.Prepare, manage, and execute Quality Agreements.Provide Quality oversight and representation on external CDMO project teams; manage CDMO relationships.Coordinate and manage compliance activities in preparation for regulatory and internal inspections, and support interactions.External Audits and Regulatory Inspections:Lead preparations for external audits and regulatory inspections.Serve as the subject matter expert (SME) and host during audits and inspections.Develop and implement strategies to maintain continuous inspection readiness.Additional Responsibilities:Collaborate effectively with functional teams such as CMC, Supply Chain, and Regulatory.Escalate critical quality and compliance issues to management in a timely manner.Manage critical quality issues with Vendors/CMOs and provide prompt resolutions.Identify process gaps proactively and implement mitigation strategies. QUALIFICATIONSBachelor’s degree in a relevant field (e.g., Life Sciences, Pharmacy, Chemistry, Engineering). Advanced degree preferred.13+ years of experience in quality assurance role in the pharmaceutical industry required with at least 5+ years in Quality Operation roles in a current Good Manufacturing Practices (c GMP) environmentStrong working knowledge of FDA regulations (21 CFR, 210/211), ICH guidelines, and global regulations (EU Directives, and ROW) and expertise in the c GMP requirements pertaining to manufacturing and packaging operations (including serialization) in the United States and globally in support of global commercial production activitiesIn-depth knowledge of c GMP and strong understanding of the entire product lifecycle.Proven experience in conducting GMP audits and inspections is preferred.Strong analytical and problem-solving skills.Excellent communication and interpersonal skills.Ability to work independently and as part of a multidisciplinary team.Certification in GMP or related areas is preferred.Experience working with US and European companies is required.

Job Title : Good Manufacturing Practice(GMP) Quality Assurance Manager

Timing : Overlap with PST hours - Upto 2 am IST

Travel : International trips once every quarter expected

Employment Type : Full-time

Workplace Type : Remote

THE CELITO TEAM

The Celito Team architects the buildout of simplified, integrated, and compliant technology stacks. With both consulting and products, our expertise can help our customers save time and money as they move from strategic Clinical & Quality management all the way to widespread and profitable commercialization.

JOB OVERVIEW

We are seeking a highly skilled and experienced Manager/Sr. Manager of GMP Quality Assurance Operations to join our team. This leadership role is responsible for Quality oversight of CMOs manufacturing drug substance, drug product, and packaged product. This role will work closely with the CMC team to ensure compliance across the entire product lifecycle. The role ensures adherence to GMP and regulatory standards while driving continuous improvement. The ideal candidate will possess significant decision-making authority on quality matters and ensure the efficient operation of the QA department.

KEY RESPONSIBLIITIES

GMP QA Operations Responsibilities:

• Perform batch record review and compile documentation packages to support product disposition.
• Conduct technical reviews and approvals of Master Batch Records and executed batch records.
• Review and approve Deviations, CAPAs, Change Controls, and Audit reports.
• Perform technical reviews of Quality Control records, including Certificates of Release, Analytical Protocols, Reports, and Stability reports.
• Support and contribute to the Annual Product Quality Review.
• Author, review, and update QA Operations SOPs and other quality documents.

Quality Oversight and Compliance Responsibilities:

• Ensure Quality and Compliance oversight of CMOs per quality agreements, including periodic site visits as needed.
• Oversee CMO/CSPs through remote collaboration, on-site visits, KPI monitoring, and adherence to quality agreements.
• Conduct vendor/CMO audits.
• Prepare, manage, and execute Quality Agreements.
• Provide Quality oversight and representation on external CDMO project teams; manage CDMO relationships.
• Coordinate and manage compliance activities in preparation for regulatory and internal inspections, and support interactions.

External Audits and Regulatory Inspections:

• Lead preparations for external audits and regulatory inspections.
• Serve as the subject matter expert (SME) and host during audits and inspections.
• Develop and implement strategies to maintain continuous inspection readiness.

Additional Responsibilities:

• Collaborate effectively with functional teams such as CMC, Supply Chain, and Regulatory.
• Escalate critical quality and compliance issues to management in a timely manner.
• Manage critical quality issues with Vendors/CMOs and provide prompt resolutions.
• Identify process gaps proactively and implement mitigation strategies.

QUALIFICATIONS

• Bachelor’s degree in a relevant field (e.g., Life Sciences, Pharmacy, Chemistry, Engineering). Advanced degree preferred.
• 13+ years of experience in quality assurance role in the pharmaceutical industry required with at least 5+ years in Quality Operation roles in a current Good Manufacturing Practices (cGMP) environment
• Strong working knowledge of FDA regulations (21CFR, 210/211), ICH guidelines, and global regulations (EU Directives, and ROW) and expertise in the cGMP requirements pertaining to manufacturing and packaging operations (including serialization) in the United States and globally in support of global commercial production activities
• In-depth knowledge of cGMP and strong understanding of the entire product lifecycle.
• Proven experience in conducting GMP audits and inspections is preferred.
• Strong analytical and problem-solving skills.
• Excellent communication and interpersonal skills.
• Ability to work independently and as part of a multidisciplinary team.
• Certification in GMP or related areas is preferred.
• Experience working with US and European companies is required.

Job Title : Good Manufacturing Practice(GMP) Quality Assurance Manager

Timing : Overlap with PST hours - Upto 2 am IST

Travel : International trips once every quarter expected

Employment Type : Full-time

Workplace Type : Remote

THE CELITO TEAM

The Celito Team architects the buildout of simplified, integrated, and compliant technology stacks. With both consulting and products, our expertise can help our customers save time and money as they move from strategic Clinical & Quality management all the way to widespread and profitable commercialization.

JOB OVERVIEW

We are seeking a highly skilled and experienced Manager/Sr. Manager of GMP Quality Assurance Operations to join our team. This leadership role is responsible for Quality oversight of CMOs manufacturing drug substance, drug product, and packaged product. This role will work closely with the CMC team to ensure compliance across the entire product lifecycle. The role ensures adherence to GMP and regulatory standards while driving continuous improvement. The ideal candidate will possess significant decision-making authority on quality matters and ensure the efficient operation of the QA department.

KEY RESPONSIBLIITIES

GMP QA Operations Responsibilities:

• Perform batch record review and compile documentation packages to support product disposition.
• Conduct technical reviews and approvals of Master Batch Records and executed batch records.
• Review and approve Deviations, CAPAs, Change Controls, and Audit reports.
• Perform technical reviews of Quality Control records, including Certificates of Release, Analytical Protocols, Reports, and Stability reports.
• Support and contribute to the Annual Product Quality Review.
• Author, review, and update QA Operations SOPs and other quality documents.

Quality Oversight and Compliance Responsibilities:

• Ensure Quality and Compliance oversight of CMOs per quality agreements, including periodic site visits as needed.
• Oversee CMO/CSPs through remote collaboration, on-site visits, KPI monitoring, and adherence to quality agreements.
• Conduct vendor/CMO audits.
• Prepare, manage, and execute Quality Agreements.
• Provide Quality oversight and representation on external CDMO project teams; manage CDMO relationships.
• Coordinate and manage compliance activities in preparation for regulatory and internal inspections, and support interactions.

External Audits and Regulatory Inspections:

• Lead preparations for external audits and regulatory inspections.
• Serve as the subject matter expert (SME) and host during audits and inspections.
• Develop and implement strategies to maintain continuous inspection readiness.

Additional Responsibilities:

• Collaborate effectively with functional teams such as CMC, Supply Chain, and Regulatory.
• Escalate critical quality and compliance issues to management in a timely manner.
• Manage critical quality issues with Vendors/CMOs and provide prompt resolutions.
• Identify process gaps proactively and implement mitigation strategies.

QUALIFICATIONS

• Bachelor’s degree in a relevant field (e.g., Life Sciences, Pharmacy, Chemistry, Engineering). Advanced degree preferred.
• 13+ years of experience in quality assurance role in the pharmaceutical industry required with at least 5+ years in Quality Operation roles in a current Good Manufacturing Practices (cGMP) environment
• Strong working knowledge of FDA regulations (21CFR, 210/211), ICH guidelines, and global regulations (EU Directives, and ROW) and expertise in the cGMP requirements pertaining to manufacturing and packaging operations (including serialization) in the United States and globally in support of global commercial production activities
• In-depth knowledge of cGMP and strong understanding of the entire product lifecycle.
• Proven experience in conducting GMP audits and inspections is preferred.
• Strong analytical and problem-solving skills.
• Excellent communication and interpersonal skills.
• Ability to work independently and as part of a multidisciplinary team.
• Certification in GMP or related areas is preferred.
• Experience working with US and European companies is required.

Job Title: Good Manufacturing Practice(GMP) Quality Assurance Manager

Timing: Overlap with PST hours - Upto 2 am IST

Travel: International trips once every quarter expected

Employment Type: Full-time

Workplace Type: Remote

THE CELITO TEAM

The Celito Team architects the buildout of simplified, integrated, and compliant technology stacks. With both consulting and products, our expertise can help our customers save time and money as they move from strategic Clinical & Quality management all the way to widespread and profitable commercialization.

JOB OVERVIEW

We are seeking a highly skilled and experienced Manager/Sr. Manager of GMP Quality Assurance Operations to join our team. This leadership role is responsible for Quality oversight of CMOs manufacturing drug substance, drug product, and packaged product. This role will work closely with the CMC team to ensure compliance across the entire product lifecycle. The role ensures adherence to GMP and regulatory standards while driving continuous improvement. The ideal candidate will possess significant decision-making authority on quality matters and ensure the efficient operation of the QA department.

KEY RESPONSIBLIITIES

GMP QA Operations Responsibilities:

• Perform batch record review and compile documentation packages to support product disposition.
• Conduct technical reviews and approvals of Master Batch Records and executed batch records.
• Review and approve Deviations, CAPAs, Change Controls, and Audit reports.
• Perform technical reviews of Quality Control records, including Certificates of Release, Analytical Protocols, Reports, and Stability reports.
• Support and contribute to the Annual Product Quality Review.
• Author, review, and update QA Operations SOPs and other quality documents.

Quality Oversight and Compliance Responsibilities:

• Ensure Quality and Compliance oversight of CMOs per quality agreements, including periodic site visits as needed.
• Oversee CMO/CSPs through remote collaboration, on-site visits, KPI monitoring, and adherence to quality agreements.
• Conduct vendor/CMO audits.
• Prepare, manage, and execute Quality Agreements.
• Provide Quality oversight and representation on external CDMO project teams; manage CDMO relationships.
• Coordinate and manage compliance activities in preparation for regulatory and internal inspections, and support interactions.

External Audits and Regulatory Inspections:

• Lead preparations for external audits and regulatory inspections.
• Serve as the subject matter expert (SME) and host during audits and inspections.
• Develop and implement strategies to maintain continuous inspection readiness.

Additional Responsibilities:

• Collaborate effectively with functional teams such as CMC, Supply Chain, and Regulatory.
• Escalate critical quality and compliance issues to management in a timely manner.
• Manage critical quality issues with Vendors/CMOs and provide prompt resolutions.
• Identify process gaps proactively and implement mitigation strategies.

QUALIFICATIONS

• Bachelor’s degree in a relevant field (e.g., Life Sciences, Pharmacy, Chemistry, Engineering). Advanced degree preferred.
• 13+ years of experience in quality assurance role in the pharmaceutical industry required with at least 5+ years in Quality Operation roles in a current Good Manufacturing Practices (cGMP) environment
• Strong working knowledge of FDA regulations (21CFR, 210/211), ICH guidelines, and global regulations (EU Directives, and ROW) and expertise in the cGMP requirements pertaining to manufacturing and packaging operations (including serialization) in the United States and globally in support of global commercial production activities
• In-depth knowledge of cGMP and strong understanding of the entire product lifecycle.
• Proven experience in conducting GMP audits and inspections is preferred.
• Strong analytical and problem-solving skills.
• Excellent communication and interpersonal skills.
• Ability to work independently and as part of a multidisciplinary team.
• Certification in GMP or related areas is preferred.
• Experience working with US and European companies is required.