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production_executive

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Tulsi Vihar Colony

Gandhi Nagar

Terraman Infratech Consultants

Madura  

Surya Nagar

1. Production Planning and Scheduling
2. Quality Control
3. Safety Management
4. Labor Management
5.Preferable for chemistry subject students


Vanitha Fireworks Industries

Birubari

NH-37

M/s Delta Force Security & Manpower Services

Rashtrapati Bhavan

Major Mohit Sharma

We need one male candidate for the Profile of 
Production executive. 
Candidate should know 
Packaging 
Dispatch 
Production costing 
Labor handing. 


Mentoring Human Resource

I.I.T.Main Gate

Jui Nagar Station ( Herdilla Company)

We are seeking a skilled Production Technician to support the manufacturing of our medical devices and associated components.  The role demands a strong focus on production excellence, calibration, documentation, and ISO-compliant quality systems. The ideal candidate will have an ITI/Diploma background with prior experience in medical device or healthcare equipment manufacturing.

Key Responsibilities
·      Device Assembly & Testing: Assemble, calibrate, and test machines and caps as per SOPs, BOMs, and drawings.
·      Calibration Activities: Perform and document calibration of production equipment, fixtures, and gauges at defined intervals to maintain compliance.
·      Batch Manufacturing Record (BMR): Accurately fill out and review BMRs, ensuring traceability of materials, processes, and outputs.
·      ISO & Quality Compliance: Follow ISO 13485 and other applicable regulatory requirements in day-to-day production.
·      Quality Control: Conduct in-process inspection, identify defects, and support corrective actions.
·      Documentation: Ensure Good Documentation Practices (GDP) for SOPs, BMRs, calibration logs, and quality records.
·      Production Targets: Meet daily/weekly production output while maintaining high quality standards.
·      Collaboration: Work with quality, engineering, and supply chain teams to resolve issues and optimize processes.

Eligibility & Qualifications
·      Minimum ITI (Fitter/Electrical/Electronics/Instrumentation) or Diploma (Mechanical/Electrical/Electronics).
·      4+ years of experience in production/manufacturing, preferably in medical devices, pharma, or other regulated sectors.
·      Experience with calibration activities and ISO 13485 / ISO 9001 quality systems.
·      Knowledge of Batch Manufacturing Records (BMR), GDP, and traceability requirements.
·      Ability to interpret SOPs, work instructions, and engineering drawings.
·      Strong attention to detail with a quality-first mindset.
·      Basic computer literacy for recording production and calibration data.

Core Competencies
·      Production Process Execution – Accurate assembly, calibration, and testing of devices.
·      SOP & BMR Compliance – Strict adherence to documented processes, BMR, and GDP.
·      Quality & ISO Knowledge – Familiar with ISO 13485 / 9001 standards, CAPA, and audit preparedness.
·      Calibration Expertise – Able to calibrate tools, machines, and maintain calibration logs.
·      Documentation Discipline – Ensures traceability and compliance in every step of manufacturing.
·      Teamwork & Communication – Works effectively across production, quality, and engineering teams.


Stemtech Medical Devices

Executive, Production-ARPL-PLP AR
About Apotex Inc.Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions.For more information visit: <a href="http://www.apotex.com/">www.apotex.com</a>. <h4>Job Summary</h4>A role-holder to handle/supervise the Packagingring activities and to ensure the on-time production and delivery of product with quality compliance and cost improvisation.<h4>Job Responsibilities</h4><ul><li>Works in a safe manner collaborating as a team member to achieve all outcomes.</li><li>Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion.</li><li>Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies.</li><li>All other relevant duties as assigned</li><li>To be well disciplined &amp; maintain the same in the production department.</li><li>To maintain the safety and housekeeping practices at work place.</li><li>To ensure and follow good and online documentation practices.</li><li>To ensure proper labeling procedure wherever applicable as per procedure.</li><li>To ensure that cleaning the area as per related SOP ‘s are conducted and maintained as per proper cleanliness.</li><li>To ensure the Calibration/Preventive maintenance of the equipment as per the schedule.</li><li>To maintain and ensure cleaning and operation activities are performed as per procedure.</li><li>To maintain the batch as per instruction given in batch document / procedure.</li><li>To ensure material movement is conducted as per procedure.</li><li>To ensure training of our self on current version of procedure prior to perform activity.</li><li>To perform the activities assigned to him by the concerned section seniors or by his superiors in area.</li><li>To follow the cGMP practices.</li><li>To showcase the value of collobaration with own/other departments to complete the work assigned.</li><li>To escalate immediately to concerned superior / manager for any deviation / non-compliance /abnormal observation.</li><li>Shall always be ready to accept new challenges &amp; multifunctional activities.</li><li>Shall always stick to the time line provided or assignment given by superiors, to avoid any delays and any non-compliance.</li><li>Works as a member of a team to achieve all outcomes.</li><li>Performs all work in accordance with all established regulatory and compliance and safety requirements.</li><li>To plan the production activities as per the weekly plan on daily basis &amp; deliver the same to down level for its execution.</li><li>To supervise the production process to produce quality formulation at optimum cost and within the time limit.</li><li>To plan for various activities of the process and get it done within the specified time.</li><li>Also maintain the online documentation related to production activities .</li><li>To allocate the Job responsibilities for operators, housekeeping &amp; contract labours in production area.</li><li>To train the concern members on the related SOP’s , newly updated SOP’s , cGMP &amp; documentation practices.</li><li>To supervise the process validation &amp; cleaning validation activities as per protocol in co-ordination with QA/QC.</li><li>Create a culture which values trust and provides the opportunity for Employee development and growth in pursuit of our purpose and demonstrating our core Values – Collaboration, Courage, Perseverance and Passion.</li><li>All other duties as assigned.</li></ul> <h4>Job Requirements</h4><ul><li>Education<ul><li>Pharmacy / M Pharmacy</li></ul></li><li>Knowledge, Skills and Abilities<ul><li>Adequate knowledge and ability in handling /supervising the Packagingring activities</li><li>In depth knowledge of cGMP practices</li><li>Identify and escalate equipment related issues.</li></ul></li><li>Experience<ul><li>3 to 5 Years</li></ul></li></ul> At Apotex, we are committed to fostering a welcoming and accessible work environment, where all everyone feels valued, respected, and supported to succeed. We offer accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation. <h4>Experience Level</h4>Executive Level

Apotex Pharmachem India Pvt Ltd

Executive, Production
About Apotex Inc.Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions.For more information visit: <a href="http://www.apotex.com/">www.apotex.com</a>. <h4>Job Summary</h4>A role-holder to handle/supervise the manufacturing activities and to ensure the on-time production and delivery of product with quality compliance and cost improvisation.<h4>Job Responsibilities</h4><ul><li>Works in a safe manner collaborating as a team member to achieve all outcomes.</li><li>Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion.</li><li>Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies.</li><li>All other relevant duties as assigned</li><li>To be well disciplined &amp; maintain the same in the production department.</li><li>To maintain the safety and housekeeping practices at work place.</li><li>To ensure and follow good and online documentation practices.</li><li>To ensure proper labeling procedure wherever applicable as per procedure.</li><li>To ensure that cleaning the area as per related SOP ‘s are conducted and maintained as per proper cleanliness.</li><li>To ensure the Calibration/Preventive maintenance of the equipment as per the schedule.</li><li>To maintain and ensure cleaning and operation activities are performed as per procedure.</li><li>To maintain the batch as per instruction given in batch document / procedure.</li><li>To ensure material movement is conducted as per procedure.</li><li>To ensure training of our self on current version of procedure prior to perform activity.</li><li>To perform the activities assigned to him by the concerned section seniors or by his superiors in area.</li><li>To follow the cGMP practices.</li><li>To showcase the value of collobaration with own/other departments to complete the work assigned.</li><li>To escalate immediately to concerned superior / manager for any deviation / non-compliance /abnormal observation.</li><li>Shall always be ready to accept new challenges &amp; multifunctional activities.</li><li>Shall always stick to the time line provided or assignment given by superiors, to avoid any delays and any non-compliance.</li><li>Works as a member of a team to achieve all outcomes.</li><li>Performs all work in accordance with all established regulatory and compliance and safety requirements.</li><li>To plan the production activities as per the weekly plan on daily basis &amp; deliver the same to down level for its execution.</li><li>To supervise the production process to produce quality formulation at optimum cost and within the time limit.</li><li>To plan for various activities of the process and get it done within the specified time.</li><li>Also maintain the online documentation related to production activities .</li><li>To allocate the Job responsibilities for operators, housekeeping &amp; contract labours in production area.</li><li>To train the concern members on the related SOP’s , newly updated SOP’s , cGMP &amp; documentation practices.</li><li>To supervise the process validation &amp; cleaning validation activities as per protocol in co-ordination with QA/QC.</li><li>Create a culture which values trust and provides the opportunity for Employee development and growth in pursuit of our purpose and demonstrating our core Values – Collaboration, Courage, Perseverance and Passion.</li><li>All other duties as assigned.</li></ul> <h4>Job Requirements</h4><ul><li>Education<ul><li>Pharmacy / M Pharmacy</li></ul></li><li>Knowledge, Skills and Abilities<ul><li>Adequate knowledge and ability in handling /supervising the manufacturing activities</li><li>In depth knowledge of cGMP practices</li><li>Identify and escalate equipment related issues.</li></ul></li><li>Experience<ul><li>3 to 5 Years</li></ul></li></ul> At Apotex, we are committed to fostering a welcoming and accessible work environment, where all everyone feels valued, respected, and supported to succeed. We offer accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation. <h4>Experience Level</h4>Executive Level

Production Executive PuneProduction Executive Pune<h4>Job Description</h4>As a person, you’re a learner – a natural leader – someone who is always taking initiative to make things better and bring others along with you. You live your life in alignment with the highest values of integrity and quality, always ensuring your responsibilities become a long-term success story. In this role, you’ll help us deliver better care for billions of people around the world. It starts with YOU. About UsHuggies®. Kleenex®. Cottonelle®. Scott®. Kotex®. Poise®. Depend®. Kimberly-Clark Professional®. You already know our legendary brands—and so does the rest of the world. In fact, millions of people use Kimberly-Clark products every day. We know these amazing Kimberly-Clark products wouldn’t exist without talented professionals, like you.At Kimberly-Clark, you’ll be part of the best team committed to driving innovation, growth, and impact. We’re founded on more than 150 years of market leadership, and we’re always looking for new and better ways to perform – so there’s your open door of opportunity. It’s all here for you at Kimberly-Clark.Led by Purpose. Driven by You.About YouYou perform at the highest level possible, and you appreciate a performance culture fueled by authentic caring.  You want to be part of a company actively dedicated to sustainability, inclusion, wellbeing, and career development.You love what you do, especially when the work you do makes a difference. At Kimberly-Clark, we’re constantly exploring new ideas on how, when, and where we can best achieve results.In one of our Manufacturing roles, you’ll focus on winning with consumers and the market, while putting safety, mutual respect, and human dignity at the center. To succeed in this role, you will need the following qualifications:<ul><li>Adopt safety practices that meet safety codes, policies, and guidelines. Achieve business objectives by establishing and following safe workplace practices consistent with KC. Conduct Safety Audits as per set frequency. To Minimize damage or losses. No safety incidents during regular work activities.</li><li>Develop myself to full potential through feedback received during Performance Management discussions, appropriate training and education, goal setting, and career development discussions.</li><li>Expected result will be: 100% completion of Performance Plan.100% completion and implementation of own Individual Development Plan (IDP).</li><li>Ways to Measure Accomplishment: Completion of effective Performance Plan for the year. Completion and implementation of IDP for the year.</li><li>Provide Solution to Processes: Provide leadership to improve production and maintain process stability and capabilities. Plan and manage production as per plan. Keep close communications with other departments. Develop a centerline and make it a daily practice for each activity on the machine. Maintain data for settings and analyze the data to provide solutions. </li><li>The machine will have a stable and consistent run. No unexpected machine breakdown due to process issues to help achieve the mill objectives.</li><li>Ways to Measure Accomplishment: Daily productivity report shows machine consistency in running without major fluctuation in productivity because of process instability.    Trials and Engineering modifications are completed on time and as per budget.</li><li>Quality Assurance: Adopt practices that meet Quality codes, policies, and guidelines. Achieve business objectives by following practices consistent with KC guidelines – QMS, RQGL. Ensure safe, clean &amp; good quality products are delivered to the consumer. Implement short and long-term action plans to deal with recurring quality issues. Ensure defective products are quarantined and sorted out most effectively. Ensure that Quality Indices are achieved as per the target set by the regional QA team and Management.</li><li>Ensure all products being made are up to FPS attributes and variables. Quality Management Systems are followed as per KC guidelines.</li><li>Nullified customer complaint rates.</li><li>Ways of measurement: No. of customer complaints, Quality Indices results of the mill published by QA team. Internal as well as external Quality system audit scores from KC or external authorities.</li><li>Defective product disposal report</li><li>Productivity Improvement: Lead in delay and waste reduction activities. Improve productivity and quality by collecting data on the same and carrying out troubleshooting together with process specialists when they require assistance. Analyses the causes of waste/process / mechanical problems through close communication with the operation support team leader and other engineers, sets up the action plan, and takes action to eliminate the causes. To achieve productivity targets.</li><li>Ways to Measure Accomplishment: Productivity improvement projects completion and improvement in line productivity.</li><li>Owner of Center lining Data: Develop and maintain the best setting on the machine control. Discuss with the process engineer the causes and solutions to move the setting to the next level. Monitor, identify, and seek solutions to the issues that are arising out of specified setting. Ensure center lining data records are accurate and kept up to date.</li><li>Expected result: Issues encountered on specific Center lining sets up is monitored regularly. Solutions to Center lining issues are addressed on time. Center lining setup is continuously improved and moving progressively in accordance with the program.</li></ul>To Be Considered Click the Apply button and complete the online application process. A member of our recruiting team will review your application and follow up if you seem like a great fit for this role.In the meantime, please check out the <a href="https://www.careers.kimberly-clark.com/en/our-careers/career-areas" rel="noopener noreferrer" target="_blank">careers website</a>.And finally, the fine print….For Kimberly-Clark to grow and prosper, we must be an inclusive organization that applies the diverse experiences and passions of its team members to brands that make life better for people all around the world.  We actively seek to build a workforce that reflects the experiences of our consumers.  When you bring your original thinking to Kimberly-Clark, you fuel the continued success of our enterprise. We are a committed equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, sexual orientation, gender identity, age, pregnancy, genetic information, citizenship status, or any other characteristic protected by law.The statements above are intended to describe the general nature and level of work performed by employees assigned to this classification. Statements are not intended to be construed as an exhaustive list of all duties, responsibilities and skills required for this position.#LI-Hybrid<h4>Primary Location</h4>Pune Sanaswadi Mill<h4>Additional Locations</h4><h4>Worker Type</h4>Employee<h4>Worker Sub-Type</h4>Regular<h4>Time Type</h4>Full time

Kimberly Clark Lever Pvt Ltd

Production ExecutiveJob Title: Production Executive – Amli Factory, Silvassa Location: Amli, Silvassa – Manufacturing Unit  Reporting to: Production Manager / Factory ManagerReq ID: R-1164428 Role PurposeTo ensure efficient, safe, and quality-driven production operations at the Amli Factory. The Production Executive will be responsible for managing daily manufacturing activities, driving performance metrics, and supporting continuous improvement initiatives in line with Unilever’s operational excellence standards. Key Responsibilities<ul><li>Oversee end-to-end production processes for assigned lines or units</li><li>Ensure adherence to daily production plans, quality standards, and safety protocols</li><li>Monitor equipment performance and coordinate with maintenance for timely interventions</li><li>Lead shift operations, including manpower deployment and shopfloor discipline</li><li>Maintain accurate records of production output, downtime, and material usage</li><li>Drive root cause analysis for deviations and implement corrective actions</li><li>Support TPM, WCM, and other continuous improvement initiatives</li><li>Collaborate with cross-functional teams (Quality, Engineering, Planning) for seamless operations</li><li>Ensure compliance with Unilever’s SHE (Safety, Health &amp; Environment) and GMP standards</li><li>Train and engage operators to build capability and ownership on the shopfloor</li></ul> Qualifications &amp; Experience<ul><li>Diploma / B.E. / B.Tech in Mechanical, Chemical, Production, or Industrial Engineering</li><li>3-9 years of experience in FMCG / food / beverages / chemical manufacturing</li><li>Exposure to automated production lines and lean manufacturing practices preferred.</li><li>"All official offers from Unilever are issued only via our Applicant Tracking System (ATS). Offers from individuals or unofficial sources may be fraudulent—please verify before proceeding."</li></ul><h4>Experience Level</h4>Executive Level

Hindustan Unilever Limited

Executive - Production ( Drug Product )<ol><li>To carryout filling and packing activities as per BFR, BPR &amp; SOPs. </li><li>To follow &amp; maintain current GMP standards in production area/activities. </li><li>To follow day-to-day production schedule and ensure to complete production activities (filling &amp; packing) as per schedule. </li><li>To take &amp; follow operating instructions for the shift activities from superior/Manger.</li><li>If any abnormality is found in production area / activities, authorized to stop activity immediately &amp; highlight to Production Manager. </li><li>To maintain manufacturing records online &amp; should comply data integrity practices.</li><li>Indenting, issuance &amp; submission of BFR/BPR.</li><li>Verification of Raw material &amp; Packing material during receipt.</li><li>Sample request/submission to QC after filling / packing activity. </li><li>Transfer of finished goods through “Finished Goods Transfer Note” to Stores.</li><li>Carryout cleaning of filters &amp; storage tanks as per schedule. </li><li>Ensure &amp; Maintain cleanliness in production area as per SOP. </li><li>Ensure cleaning of AHU filters as per schedule. </li><li>To Check and ensure minimum stock of consumables, Logbooks &amp; status labels.</li><li>Ensuring preventive maintenance of all equipment as per schedule. </li><li>Maintain temperature &amp; RH within SOP limits in production area. </li><li>Co-ordinate with service departments (QA, QC, stores, E &amp; M and SCM) for various production related activities. </li><li>To follow safety instructions/procedures and ensure use of safety outfit while on works.</li><li>Responsible to carry out the work of his senior in the absence of senior or authorization from senior. </li></ol>

Piramal Pharma

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