2,819 Sr Manager Agm Ppic Bidar Api Cdmo Manufacturing Facility jobs in India
Sr Manager / AGM - PPIC, Bidar- API - CDMO Manufacturing Facility
Job Viewed
Job Description
Job Description
To operate out of plant and oversee the production planning and materials management with an aim to support in interrupted services to the manufacturing team
and provide the requested information with the objective of converting the opportunities (RFP's/QIFs) into
business (purchase orders).
Key Responsibilities
1. RFP Response
Study the technical package (QIF/RFX) and understand the customer requirements in consultation with BD &
co-ordinate with cross functional team (CFT) i.e., R&D, PE/PPIC, AR&D, SCM, IP, RA, QA, HSE and Projects team,
to gather their inputs. Evaluate the RM costing, technical/commercial feasibility; compare with the market
price; prepare the quote and conduct the review meeting for final pricing; and present the proposal to BD.
2. Preliminary Assessment & Inputs for Key Account Management:
Co-ordinate with the BD team members for a preliminary screening of opportunity, seek clarifications from
customers through BD team in order to evaluate the opportunity and support the BD Team with information
(Market analytics, Financial, Portfolio, etc) to have a common shared understanding and help the BD team
prepare key account plan.
3. Database management
Effective usage of CRM database (Salesforce) and proper archival of all RFP related information and contribute
to the content library by submitting new content or updates related to Sai Life Sciences capabilities,
opportunities and customer related information.
4. Kick off meetings & coordinating for project code creation.
Handing over the evaluation/proposal details to Project execution team on award of project. On receipt of PO
from client coordinate with Finance team & CFT for project code creation.
5. MIS and Reports:
To track result of the RFPs and compile the MIS with relevant information and submit the reports to appraise
the senior management and stake holders.
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Sr Manager / AGM - PPIC, Bidar- API - CDMO Manufacturing Facility
Posted today
Job Viewed
Job Description
Job Description
To operate out of plant and oversee the production planning and materials management with an aim to support in interrupted services to the manufacturing team
and provide the requested information with the objective of converting the opportunities (RFP's/QIFs) into
business (purchase orders).
Key Responsibilities
1. RFP Response
Study the technical package (QIF/RFX) and understand the customer requirements in consultation with BD &
co-ordinate with cross functional team (CFT) i.e., R&D, PE/PPIC, AR&D, SCM, IP, RA, QA, HSE and Projects team,
to gather their inputs. Evaluate the RM costing, technical/commercial feasibility; compare with the market
price; prepare the quote and conduct the review meeting for final pricing; and present the proposal to BD.
2. Preliminary Assessment & Inputs for Key Account Management:
Co-ordinate with the BD team members for a preliminary screening of opportunity, seek clarifications from
customers through BD team in order to evaluate the opportunity and support the BD Team with information
(Market analytics, Financial, Portfolio, etc) to have a common shared understanding and help the BD team
prepare key account plan.
3. Database management
Effective usage of CRM database (Salesforce) and proper archival of all RFP related information and contribute
to the content library by submitting new content or updates related to Sai Life Sciences capabilities,
opportunities and customer related information.
4. Kick off meetings & coordinating for project code creation.
Handing over the evaluation/proposal details to Project execution team on award of project. On receipt of PO
from client coordinate with Finance team & CFT for project code creation.
5. MIS and Reports:
To track result of the RFPs and compile the MIS with relevant information and submit the reports to appraise
the senior management and stake holders.
Operations Manager - Advanced Manufacturing Facility
Posted today
Job Viewed
Job Description
Key responsibilities include:
- Developing and implementing strategic operational plans to meet production targets and quality standards.
- Overseeing all aspects of the manufacturing process, including production scheduling, resource allocation, and workflow optimization.
- Implementing and maintaining lean manufacturing principles and methodologies.
- Managing the production workforce through remote supervision and leadership, focusing on performance management and skill development.
- Ensuring compliance with all health, safety, and environmental regulations.
- Driving cost reduction initiatives and improving overall operational profitability.
- Collaborating with engineering and quality assurance teams to enhance product quality and process reliability.
- Utilizing advanced analytics and IoT technologies for real-time performance monitoring and predictive maintenance.
- Managing supplier relationships and ensuring the timely availability of raw materials and components.
- Reporting on key operational performance indicators (KPIs) to senior management.
The ideal candidate will possess a Bachelor's or Master's degree in Industrial Engineering, Manufacturing Engineering, Operations Management, or a related field. A minimum of 7-10 years of progressive experience in manufacturing operations, with a strong background in production management and process improvement, is required. Proven experience in managing operations remotely, utilizing digital tools and technologies, is essential. Excellent leadership, problem-solving, and strategic thinking skills are paramount. A strong understanding of quality management systems (e.g., ISO 9001) and lean manufacturing principles is crucial. This role offers the flexibility of remote work while impacting a significant manufacturing operation.
General Manager – Facility Setup & Compliances (Biologicals manufacturing)
Posted today
Job Viewed
Job Description
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.
General Manager – Facility Setup & Compliances (Biologicals manufacturing)
Posted today
Job Viewed
Job Description
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.
General Manager – Facility Setup & Compliances (Biologicals manufacturing)
Posted today
Job Viewed
Job Description
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.
General Manager – Facility Setup & Compliances (Biologicals manufacturing)
Posted today
Job Viewed
Job Description
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.
General Manager – Facility Setup & Compliances (Biologicals manufacturing)
Posted today
Job Viewed
Job Description
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.
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General Manager – Facility Setup & Compliances (Biologicals manufacturing)
Posted today
Job Viewed
Job Description
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.
General Manager – Facility Setup & Compliances (Biologicals manufacturing)
Posted today
Job Viewed
Job Description
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.
General Manager – Facility Setup & Compliances (Biologicals manufacturing)
Posted today
Job Viewed
Job Description
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.