8 Unskilled Workers jobs in Tamil Nadu

Job description: Assistant Manager - Production

Primary Responsibilities:

· Responsible for overseeing and managing the production processes, ensuring efficient operations, quality output, and timely delivery of fabricated products.

· Completely responsible for the day to day output.

· Involve in coordinating with various teams, implementing production plans, monitoring resources, and maintaining a safe working environment. Your ultimate goal will be to optimize productivity, minimize costs, and achieve production targets while adhering to quality standards.

· Develop production schedules and plans in collaboration with other departments to meet customer demands and deadlines.

· Ensure availability of raw materials, equipment, and labor resources for smooth production operations.

· Monitor production progress and adjust schedules as needed to meet targets.

· Supervise and allocate resources effectively, including manpower, machinery, tools, and equipment, to maximize productivity.

· Monitor inventory levels of raw materials and consumables, and liaise with procurement to ensure timely replenishment.

· Maintenance of machinery in tact condition to avoid disruption in production activities

· Optimize resource utilization to minimize waste, reduce downtime, and control costs.

· Implement quality control procedures and standards to ensure fabrication processes and products meet or exceed customer expectations. 

· Conduct regular inspections and audits to identify and resolve quality issues or non-conformity.

· Collaborate with the quality assurance and design team to implement corrective and preventive actions.

· Monitor adherence to safety regulations and promote a culture of safety among production staff.

· Lead and motivate production teams, providing guidance, coaching, and performance feedback.

· Identify training needs and facilitate skill development programs to enhance the capabilities of production personnel.

· Foster a positive work environment that encourages teamwork, collaboration, and continuous improvement.

· Resolve conflicts and address any performance or disciplinary issues that may arise.

· Identify opportunities for process improvement, cost reduction, and efficiency enhancement within the fabrication department.

· Implement lean manufacturing principles and other best practices to optimize production processes.

· Analyze production data, generate reports, and present findings to management for decision-making.

· Stay updated with industry trends, technological advancements, and regulatory requirements related to fabrication processes.

Skills for Success:

· Proven experience (typically 5+ years) in production management, preferably in a fabrication or sheet metal fabrication

· Strong knowledge of fabrication processes, equipment, and materials.

· Familiarity with quality control standards and practices.

Qualification:

lB.E (EEE/ECE/Mech)

Perks and Benefits:

lPerformance based incentives

lAnnual Vacation

lMonthly Employee Engagement

lEmployee friendly work environment

KEY RESPONSIBILITIES

Production Management :

• Oversee and manage day-to-day production operations to meet quality, cost, and delivery

targets.

• Develop and implement production schedules to ensure the timely delivery of products.
• Ensure adherence to Good Manufacturing Practices (GMP) and compliance with USFDA

regulations.

Regulatory Compliance :

• Maintain and ensure compliance with USFDA, WHO, and other regulatory standards in all production processes.
• Coordinate with the Quality Assurance (QA) team to prepare for and manage regulatory audits and inspections.
• Ensure proper documentation of all manufacturing processes as per USFDA requirements.

Team Leadership :

• Lead, mentor, and train the production team to ensure optimal performance and awareness of regulatory requirements.
• Foster a culture of continuous improvement, accountability, and teamwork.

Process Improvement :

• Identify and implement process optimizations to improve productivity, efficiency, and quality.
• Collaborate with cross-functional teams such as R&D, Quality Control (QC), and Supply Chain to resolve production-related issues.

Equipment and Facility Management :

• Ensure proper maintenance and calibration of production equipment and facilities.
• Implement safety protocols to maintain a hazard-free work environment.

Resource Planning :

• Manage inventory of raw materials and ensure uninterrupted production.
• Prepare and manage the production budget to optimize costs without compromising quality

Educational Qualifications

• Bachelor’s or Master’s degree in Pharmacy, Pharmaceutical Sciences, Microbiology, Chemistry, Biotechnology, or a related field.
• Minimum of 5-14 experience in pharmaceutical manufacturing in a managerial role .
• Proven experience working in a USFDA-regulated environment, with knowledge of cGMP, CAPA, and regulatory submissions.

Technical / Functional Skills

• Strong understanding of pharmaceutical production processes, including tablet, capsule, injectable, or API manufacturing.
• Familiarity with validation protocols, including IQ, OQ, and PQ processes.
• Exceptional leadership, communication, and interpersonal skills.
• Strong analytical, problem-solving, and decision-making abilities.
• Ability to work under pressure and meet tight deadlines.

KEY RESPONSIBILITIES

Production Management:

• Oversee and manage day-to-day production operations to meet quality, cost, and delivery

targets.

• Develop and implement production schedules to ensure the timely delivery of products.
• Ensure adherence to Good Manufacturing Practices (GMP) and compliance with USFDA

regulations.

Regulatory Compliance:

• Maintain and ensure compliance with USFDA, WHO, and other regulatory standards in all production processes.
• Coordinate with the Quality Assurance (QA) team to prepare for and manage regulatory audits and inspections.
• Ensure proper documentation of all manufacturing processes as per USFDA requirements.

Team Leadership:

• Lead, mentor, and train the production team to ensure optimal performance and awareness of regulatory requirements.
• Foster a culture of continuous improvement, accountability, and teamwork.

Process Improvement:

• Identify and implement process optimizations to improve productivity, efficiency, and quality.
• Collaborate with cross-functional teams such as R&D, Quality Control (QC), and Supply Chain to resolve production-related issues.

Equipment and Facility Management:

• Ensure proper maintenance and calibration of production equipment and facilities.
• Implement safety protocols to maintain a hazard-free work environment.

Resource Planning:

• Manage inventory of raw materials and ensure uninterrupted production.
• Prepare and manage the production budget to optimize costs without compromising quality

Educational Qualifications

• Bachelor’s or Master’s degree in Pharmacy, Pharmaceutical Sciences, Microbiology, Chemistry, Biotechnology, or a related field.
• Minimum of 5-14 experience in pharmaceutical manufacturing in a managerial role.
• Proven experience working in a USFDA-regulated environment, with knowledge of cGMP, CAPA, and regulatory submissions.

Technical / Functional Skills

• Strong understanding of pharmaceutical production processes, including tablet, capsule, injectable, or API manufacturing.
• Familiarity with validation protocols, including IQ, OQ, and PQ processes.
• Exceptional leadership, communication, and interpersonal skills.
• Strong analytical, problem-solving, and decision-making abilities.
• Ability to work under pressure and meet tight deadlines.

KEY RESPONSIBILITIES

Production Management :

• Oversee and manage day-to-day production operations to meet quality, cost, and delivery

targets.

• Develop and implement production schedules to ensure the timely delivery of products.
• Ensure adherence to Good Manufacturing Practices (GMP) and compliance with USFDA

regulations.

Regulatory Compliance :

• Maintain and ensure compliance with USFDA, WHO, and other regulatory standards in all production processes.
• Coordinate with the Quality Assurance (QA) team to prepare for and manage regulatory audits and inspections.
• Ensure proper documentation of all manufacturing processes as per USFDA requirements.

Team Leadership :

• Lead, mentor, and train the production team to ensure optimal performance and awareness of regulatory requirements.
• Foster a culture of continuous improvement, accountability, and teamwork.

Process Improvement :

• Identify and implement process optimizations to improve productivity, efficiency, and quality.
• Collaborate with cross-functional teams such as R&D, Quality Control (QC), and Supply Chain to resolve production-related issues.

Equipment and Facility Management :

• Ensure proper maintenance and calibration of production equipment and facilities.
• Implement safety protocols to maintain a hazard-free work environment.

Resource Planning :

• Manage inventory of raw materials and ensure uninterrupted production.
• Prepare and manage the production budget to optimize costs without compromising quality

Educational Qualifications

• Bachelor’s or Master’s degree in Pharmacy, Pharmaceutical Sciences, Microbiology, Chemistry, Biotechnology, or a related field.
• Minimum of 5-14 experience in pharmaceutical manufacturing in a managerial role .
• Proven experience working in a USFDA-regulated environment, with knowledge of cGMP, CAPA, and regulatory submissions.

Technical / Functional Skills

• Strong understanding of pharmaceutical production processes, including tablet, capsule, injectable, or API manufacturing.
• Familiarity with validation protocols, including IQ, OQ, and PQ processes.
• Exceptional leadership, communication, and interpersonal skills.
• Strong analytical, problem-solving, and decision-making abilities.
• Ability to work under pressure and meet tight deadlines.

KEY RESPONSIBILITIES

Production Management :

• Oversee and manage day-to-day production operations to meet quality, cost, and delivery

targets.

• Develop and implement production schedules to ensure the timely delivery of products.
• Ensure adherence to Good Manufacturing Practices (GMP) and compliance with USFDA

regulations.

Regulatory Compliance :

• Maintain and ensure compliance with USFDA, WHO, and other regulatory standards in all production processes.
• Coordinate with the Quality Assurance (QA) team to prepare for and manage regulatory audits and inspections.
• Ensure proper documentation of all manufacturing processes as per USFDA requirements.

Team Leadership :

• Lead, mentor, and train the production team to ensure optimal performance and awareness of regulatory requirements.
• Foster a culture of continuous improvement, accountability, and teamwork.

Process Improvement :

• Identify and implement process optimizations to improve productivity, efficiency, and quality.
• Collaborate with cross-functional teams such as R&D, Quality Control (QC), and Supply Chain to resolve production-related issues.

Equipment and Facility Management :

• Ensure proper maintenance and calibration of production equipment and facilities.
• Implement safety protocols to maintain a hazard-free work environment.

Resource Planning :

• Manage inventory of raw materials and ensure uninterrupted production.
• Prepare and manage the production budget to optimize costs without compromising quality

Educational Qualifications

• Bachelor’s or Master’s degree in Pharmacy, Pharmaceutical Sciences, Microbiology, Chemistry, Biotechnology, or a related field.
• Minimum of 5-14 experience in pharmaceutical manufacturing in a managerial role .
• Proven experience working in a USFDA-regulated environment, with knowledge of cGMP, CAPA, and regulatory submissions.

Technical / Functional Skills

• Strong understanding of pharmaceutical production processes, including tablet, capsule, injectable, or API manufacturing.
• Familiarity with validation protocols, including IQ, OQ, and PQ processes.
• Exceptional leadership, communication, and interpersonal skills.
• Strong analytical, problem-solving, and decision-making abilities.
• Ability to work under pressure and meet tight deadlines.

Our Client is a subsidiary of a Japanese corporation that has businesses in various fields such as industrial gas, energy, agriculture, and health. They use green technology to harvest water from the humidity in the air and purify it with ozone. They also provides solutions for water scarcity and environmental issues

Exp:10Years

Location: Chennai

Job Description:

Responsible for running the plant in shifts and maintaining & monitoring the plant parameters on continues basis.

Achieving the agreed production targets and involves in process related trouble shooting.

Prepare the daily MIS and production confirmation on the basis of production.

Take charge as a site controller as shift in-charge (after office hours).

Achieve maximum output by monitoring of machine efficiencies and plant performance through various available tools to take corrective action in consultation with / Manager Production / Plant Manager / or respective maintenance in charge.

Start up and shutdown of plant.

Carrying out day to day maintenance and co-ordinating with maintenance team to ensure working of the machines.

Understanding of plant P&ID, involved in turbine thawing , cryo pumps thawing and plant thawing