39 Manufacturing jobs in Karachi
Head of Manufacturing
Karachi, Sindh
Abbott
Posted 4 days ago
Job Viewed
Job Description
**The Opportunity**
This role provides direction to the Manufacturing and Finishing Operations team at the Korangi Plant in Karachi. Reporting to the Operations Director, this position is responsible for ensuring compliance with local Regulatory requirements, cGMP, EHS & and Abbott Quality standards during manufacturing and finishing operations.
**Core Job Responsibilities**
+ Prepare and Monitor Operational Plan for Optimum utilization of Resources i.e. Material, Labour & Overheads
+ Ensure that products are manufactured under conditions that meet Abbott Policies, EHS Standards, and Regulatory and cGMP requirements.
+ Ensure compliance with labor laws, security standing orders & code of Business conduct.
+ Ensure provision of the necessary resources (area, equipment, workforce, etc.) to produce products of the required quality.
+ Ensure that required initial and continuing training of production personnel including GMP training is carried out and adapted according to need.
+ Provide strategic direction in Mfg. technology and equipment. Ensure that maintenance of premises and equipment, calibrations, and Process Validation are performed and recorded.
+ Coordinate with Quality regarding QA Audits, CAPA, Complaints, ERs, Market Returns, and Trend Analysis Reports, etc.
+ Coordinate with QA, Regulatory, Technical Centre, Engineering, and Supply Chain in the resolution of quality problems, disposition of nonconforming issues, and ensure uninterrupted product deliveries to Commercial.
+ Prepare Plant annual budget in consultation with Finance and get it approved by Management.
+ Take into account all demands, including forecasts, contracts, customer orders, samples, special prototypes, spares, interplant, etc in creating a Master Schedule that directs and drives all manufacturing, purchasing, and manufacturing-related engineering activities.
+ Monitor KPIs and perform Root Cause Analysis where applicable.
+ Review and approve technical documents including SOPs, Manufacturing and Finishing Directions including in-process controls, Shop Orders, Validation documents, Change requests, CAPA and ERs, etc.
+ Ensure that the production records are re-evaluated and signed by a designated person before they are made available to the Quality Assurance department.
+ Review new product dossiers and Manufacturing input for preparation of product registration / re-registration and their submission to the Regulatory Department.
+ Review batch variance/yield reports with production managers and take appropriate steps for improvement.
+ Expose, prioritize, and stimulate the reduction or elimination of non-value-added activities.
+ Ensure employee development, Goal Setting, Performance Assessment, and succession planning within the department.
+ Any other task assigned by Director Operations.
**Qualifications**
+ B.Pharm/Pharm.D
+ 10 years of working experience in Manufacturing and Finishing operations
+ Knowledge of Drug Rules, cGMP requirements, and Quality Standards
+ Understanding of Supply Chain Management of Multi-National Companies
+ Awareness of Operational Finance and Capital Budgeting
+ Understanding of Business Excellence (CI) and New Product Development activities
**_Competencies required:_**
+ Good communication and Interpersonal skills
+ Proven Leadership qualities
+ Ability to thrive in a fast-paced environment
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
This role provides direction to the Manufacturing and Finishing Operations team at the Korangi Plant in Karachi. Reporting to the Operations Director, this position is responsible for ensuring compliance with local Regulatory requirements, cGMP, EHS & and Abbott Quality standards during manufacturing and finishing operations.
**Core Job Responsibilities**
+ Prepare and Monitor Operational Plan for Optimum utilization of Resources i.e. Material, Labour & Overheads
+ Ensure that products are manufactured under conditions that meet Abbott Policies, EHS Standards, and Regulatory and cGMP requirements.
+ Ensure compliance with labor laws, security standing orders & code of Business conduct.
+ Ensure provision of the necessary resources (area, equipment, workforce, etc.) to produce products of the required quality.
+ Ensure that required initial and continuing training of production personnel including GMP training is carried out and adapted according to need.
+ Provide strategic direction in Mfg. technology and equipment. Ensure that maintenance of premises and equipment, calibrations, and Process Validation are performed and recorded.
+ Coordinate with Quality regarding QA Audits, CAPA, Complaints, ERs, Market Returns, and Trend Analysis Reports, etc.
+ Coordinate with QA, Regulatory, Technical Centre, Engineering, and Supply Chain in the resolution of quality problems, disposition of nonconforming issues, and ensure uninterrupted product deliveries to Commercial.
+ Prepare Plant annual budget in consultation with Finance and get it approved by Management.
+ Take into account all demands, including forecasts, contracts, customer orders, samples, special prototypes, spares, interplant, etc in creating a Master Schedule that directs and drives all manufacturing, purchasing, and manufacturing-related engineering activities.
+ Monitor KPIs and perform Root Cause Analysis where applicable.
+ Review and approve technical documents including SOPs, Manufacturing and Finishing Directions including in-process controls, Shop Orders, Validation documents, Change requests, CAPA and ERs, etc.
+ Ensure that the production records are re-evaluated and signed by a designated person before they are made available to the Quality Assurance department.
+ Review new product dossiers and Manufacturing input for preparation of product registration / re-registration and their submission to the Regulatory Department.
+ Review batch variance/yield reports with production managers and take appropriate steps for improvement.
+ Expose, prioritize, and stimulate the reduction or elimination of non-value-added activities.
+ Ensure employee development, Goal Setting, Performance Assessment, and succession planning within the department.
+ Any other task assigned by Director Operations.
**Qualifications**
+ B.Pharm/Pharm.D
+ 10 years of working experience in Manufacturing and Finishing operations
+ Knowledge of Drug Rules, cGMP requirements, and Quality Standards
+ Understanding of Supply Chain Management of Multi-National Companies
+ Awareness of Operational Finance and Capital Budgeting
+ Understanding of Business Excellence (CI) and New Product Development activities
**_Competencies required:_**
+ Good communication and Interpersonal skills
+ Proven Leadership qualities
+ Ability to thrive in a fast-paced environment
An Equal Opportunity Employer
Abbot welcomes and encourages diversity in our workforce.
We provide reasonable accommodation to qualified individuals with disabilities.
To request accommodation, please call or email
This advertiser has chosen not to accept applicants from your region.
0
Head of Manufacturing
Karachi, Sindh
Abbott
Posted 12 days ago
Job Viewed
Job Description
Overview The Opportunity: This role provides direction to the Manufacturing and Finishing Operations team at the Korangi Plant in Karachi. Reporting to the Operations Director, this position is responsible for ensuring compliance with local regulatory requirements, cGMP, EHS and Abbott Quality standards during manufacturing and finishing operations.
Responsibilities
Prepare and monitor operational plans for optimum utilization of resources, including materials, labor, and overheads.
Ensure that products are manufactured under conditions that meet Abbott Policies, EHS Standards, Regulatory and cGMP requirements.
Ensure compliance with labor laws, security standing orders, and the Code of Business Conduct.
Provide the necessary resources (area, equipment, workforce, etc.) to produce products of the required quality.
Ensure that initial and ongoing training of production personnel, including GMP training, is carried out and updated as needed.
Provide strategic direction in manufacturing technology and equipment. Ensure maintenance of premises and equipment, calibrations, and process validation are performed and recorded.
Coordinate with Quality regarding QA audits, CAPA, complaints, ERs, market returns, and trend analysis reports.
Coordinate with QA, Regulatory, Technical Centre, Engineering, and Supply Chain in the resolution of quality problems, disposition of nonconforming issues, and ensuring uninterrupted product deliveries to Commercial.
Prepare Plant annual budget in consultation with Finance and secure management approval.
Consider all demands, including forecasts, contracts, customer orders, samples, special prototypes, spares, interplant needs, etc., in creating a Master Schedule that directs and drives all manufacturing, purchasing, and manufacturing-related engineering activities.
Monitor KPIs and perform root cause analysis where applicable.
Review and approve technical documents including SOPs, Manufacturing and Finishing Directions, in-process controls, shop orders, validation documents, change requests, CAPA and ERs.
Ensure that production records are re-evaluated and signed by a designated person before they are made available to the Quality Assurance department.
Review new product dossiers and manufacturing input for preparation of product registration/re-registration and submission to the Regulatory Department.
Review batch variance/yield reports with production managers and take appropriate steps for improvement.
Expose, prioritize, and stimulate the reduction or elimination of non-value-added activities.
Ensure employee development, goal setting, performance assessment, and succession planning within the department.
Any other task assigned by the Director of Operations.
Qualifications
B.Pharm/Pharm.D
10 years of working experience in manufacturing and finishing operations
Knowledge of drug rules, cGMP requirements, and quality standards
Understanding of supply chain management of multinational companies
Awareness of operational finance and capital budgeting
Understanding of business excellence (CI) and new product development activities
Competencies Required
Good communication and interpersonal skills
Proven leadership qualities
Ability to thrive in a fast-paced environment
Seniority level
Director
Employment type
Full-time
Job function
Production and Manufacturing
Industries
Hospitals and Health Care
#J-18808-Ljbffr
Responsibilities
Prepare and monitor operational plans for optimum utilization of resources, including materials, labor, and overheads.
Ensure that products are manufactured under conditions that meet Abbott Policies, EHS Standards, Regulatory and cGMP requirements.
Ensure compliance with labor laws, security standing orders, and the Code of Business Conduct.
Provide the necessary resources (area, equipment, workforce, etc.) to produce products of the required quality.
Ensure that initial and ongoing training of production personnel, including GMP training, is carried out and updated as needed.
Provide strategic direction in manufacturing technology and equipment. Ensure maintenance of premises and equipment, calibrations, and process validation are performed and recorded.
Coordinate with Quality regarding QA audits, CAPA, complaints, ERs, market returns, and trend analysis reports.
Coordinate with QA, Regulatory, Technical Centre, Engineering, and Supply Chain in the resolution of quality problems, disposition of nonconforming issues, and ensuring uninterrupted product deliveries to Commercial.
Prepare Plant annual budget in consultation with Finance and secure management approval.
Consider all demands, including forecasts, contracts, customer orders, samples, special prototypes, spares, interplant needs, etc., in creating a Master Schedule that directs and drives all manufacturing, purchasing, and manufacturing-related engineering activities.
Monitor KPIs and perform root cause analysis where applicable.
Review and approve technical documents including SOPs, Manufacturing and Finishing Directions, in-process controls, shop orders, validation documents, change requests, CAPA and ERs.
Ensure that production records are re-evaluated and signed by a designated person before they are made available to the Quality Assurance department.
Review new product dossiers and manufacturing input for preparation of product registration/re-registration and submission to the Regulatory Department.
Review batch variance/yield reports with production managers and take appropriate steps for improvement.
Expose, prioritize, and stimulate the reduction or elimination of non-value-added activities.
Ensure employee development, goal setting, performance assessment, and succession planning within the department.
Any other task assigned by the Director of Operations.
Qualifications
B.Pharm/Pharm.D
10 years of working experience in manufacturing and finishing operations
Knowledge of drug rules, cGMP requirements, and quality standards
Understanding of supply chain management of multinational companies
Awareness of operational finance and capital budgeting
Understanding of business excellence (CI) and new product development activities
Competencies Required
Good communication and interpersonal skills
Proven leadership qualities
Ability to thrive in a fast-paced environment
Seniority level
Director
Employment type
Full-time
Job function
Production and Manufacturing
Industries
Hospitals and Health Care
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This advertiser has chosen not to accept applicants from your region.
1
Head of Manufacturing
Karachi, Sindh
Abbott
Posted 18 days ago
Job Viewed
Job Description
JOB DESCRIPTION:
The Opportunity
This role provides direction to the Manufacturing and Finishing Operations team at the Korangi Plant in Karachi. Reporting to the Operations Director, this position is responsible for ensuring compliance with local Regulatory requirements, cGMP, EHS & and Abbott Quality standards during manufacturing and finishing operations.
Core Job Responsibilities
Prepare and Monitor Operational Plan for Optimum utilization of Resources i.e. Material, Labour & Overheads Ensure that products are manufactured under conditions that meet Abbott Policies, EHS Standards, and Regulatory and cGMP requirements. Ensure compliance with labor laws, security standing orders & code of Business conduct. Ensure provision of the necessary resources (area, equipment, workforce, etc.) to produce products of the required quality. Ensure that required initial and continuing training of production personnel including GMP training is carried out and adapted according to need. Provide strategic direction in Mfg. technology and equipment. Ensure that maintenance of premises and equipment, calibrations, and Process Validation are performed and recorded. Coordinate with Quality regarding QA Audits, CAPA, Complaints, ERs, Market Returns, and Trend Analysis Reports, etc. Coordinate with QA, Regulatory, Technical Centre, Engineering, and Supply Chain in the resolution of quality problems, disposition of nonconforming issues, and ensure uninterrupted product deliveries to Commercial. Prepare Plant annual budget in consultation with Finance and get it approved by Management. Take into account all demands, including forecasts, contracts, customer orders, samples, special prototypes, spares, interplant, etc in creating a Master Schedule that directs and drives all manufacturing, purchasing, and manufacturing-related engineering activities. Monitor KPIs and perform Root Cause Analysis where applicable. Review and approve technical documents including SOPs, Manufacturing and Finishing Directions including in-process controls, Shop Orders, Validation documents, Change requests, CAPA and ERs, etc. Ensure that the production records are re-evaluated and signed by a designated person before they are made available to the Quality Assurance department. Review new product dossiers and Manufacturing input for preparation of product registration / re-registration and their submission to the Regulatory Department. Review batch variance/yield reports with production managers and take appropriate steps for improvement. Expose, prioritize, and stimulate the reduction or elimination of non-value-added activities. Ensure employee development, Goal Setting, Performance Assessment, and succession planning within the department. Any other task assigned by Director Operations. Qualifications
B.Pharm/Pharm.D 10 years of working experience in Manufacturing and Finishing operations Knowledge of Drug Rules, cGMP requirements, and Quality Standards Understanding of Supply Chain Management of Multi-National Companies Awareness of Operational Finance and Capital Budgeting Understanding of Business Excellence (CI) and New Product Development activities Competencies required:
Good communication and Interpersonal skills Proven Leadership qualities Ability to thrive in a fast-paced environment The base pay for this position is
N/A
In specific locations, the pay range may vary from the range posted.
JOB FAMILY: Manufacturing DIVISION: EPD Established Pharma LOCATION: Pakistan > Karachi : Opp: Radio Pakistan Transmission, Hyderabad Road, Landhi ADDITIONAL LOCATIONS:
WORK SHIFT: Standard TRAVEL: No MEDICAL SURVEILLANCE: No SIGNIFICANT WORK ACTIVITIES: Not Applicable #J-18808-Ljbffr
The Opportunity
This role provides direction to the Manufacturing and Finishing Operations team at the Korangi Plant in Karachi. Reporting to the Operations Director, this position is responsible for ensuring compliance with local Regulatory requirements, cGMP, EHS & and Abbott Quality standards during manufacturing and finishing operations.
Core Job Responsibilities
Prepare and Monitor Operational Plan for Optimum utilization of Resources i.e. Material, Labour & Overheads Ensure that products are manufactured under conditions that meet Abbott Policies, EHS Standards, and Regulatory and cGMP requirements. Ensure compliance with labor laws, security standing orders & code of Business conduct. Ensure provision of the necessary resources (area, equipment, workforce, etc.) to produce products of the required quality. Ensure that required initial and continuing training of production personnel including GMP training is carried out and adapted according to need. Provide strategic direction in Mfg. technology and equipment. Ensure that maintenance of premises and equipment, calibrations, and Process Validation are performed and recorded. Coordinate with Quality regarding QA Audits, CAPA, Complaints, ERs, Market Returns, and Trend Analysis Reports, etc. Coordinate with QA, Regulatory, Technical Centre, Engineering, and Supply Chain in the resolution of quality problems, disposition of nonconforming issues, and ensure uninterrupted product deliveries to Commercial. Prepare Plant annual budget in consultation with Finance and get it approved by Management. Take into account all demands, including forecasts, contracts, customer orders, samples, special prototypes, spares, interplant, etc in creating a Master Schedule that directs and drives all manufacturing, purchasing, and manufacturing-related engineering activities. Monitor KPIs and perform Root Cause Analysis where applicable. Review and approve technical documents including SOPs, Manufacturing and Finishing Directions including in-process controls, Shop Orders, Validation documents, Change requests, CAPA and ERs, etc. Ensure that the production records are re-evaluated and signed by a designated person before they are made available to the Quality Assurance department. Review new product dossiers and Manufacturing input for preparation of product registration / re-registration and their submission to the Regulatory Department. Review batch variance/yield reports with production managers and take appropriate steps for improvement. Expose, prioritize, and stimulate the reduction or elimination of non-value-added activities. Ensure employee development, Goal Setting, Performance Assessment, and succession planning within the department. Any other task assigned by Director Operations. Qualifications
B.Pharm/Pharm.D 10 years of working experience in Manufacturing and Finishing operations Knowledge of Drug Rules, cGMP requirements, and Quality Standards Understanding of Supply Chain Management of Multi-National Companies Awareness of Operational Finance and Capital Budgeting Understanding of Business Excellence (CI) and New Product Development activities Competencies required:
Good communication and Interpersonal skills Proven Leadership qualities Ability to thrive in a fast-paced environment The base pay for this position is
N/A
In specific locations, the pay range may vary from the range posted.
JOB FAMILY: Manufacturing DIVISION: EPD Established Pharma LOCATION: Pakistan > Karachi : Opp: Radio Pakistan Transmission, Hyderabad Road, Landhi ADDITIONAL LOCATIONS:
WORK SHIFT: Standard TRAVEL: No MEDICAL SURVEILLANCE: No SIGNIFICANT WORK ACTIVITIES: Not Applicable #J-18808-Ljbffr
This advertiser has chosen not to accept applicants from your region.
2
Financial Projects Lead — Manufacturing
Karachi, Sindh
AGILE HR
Posted today
Job Viewed
Job Description
Position Title: Financial Projects Lead
Location: DHA Phase 7, Karachi
Experience: 5–7 years (Manufacturing)
Benefits: Car, Fuel & benefits
Key Responsibilities
- Full-cycle finance & compliance (GL, AP/AR, audits, tax).
- Financial modeling, feasibilities & cash-flow forecasts.
- Costing (BOM/BOQ, variances) & inventory management.
- Budgets, FP&A, MIS & board reporting.
- ERP utilization & process improvement.
Requirements
- Strong independence & ownership.
- Manufacturing finance/costing background.
- Advanced Excel & ERP skills.
- Preferred: ACCA/CMA/ICMA/MBA Finance.
Job Type: Full-time
Pay: Rs250, Rs300,000.00 per month
Work Location: On the road
This advertiser has chosen not to accept applicants from your region.
3
Project / Planning Engineer – Switchgear Manufacturing
Karachi, Sindh
Accrescent Engineers Pvt Limited
Posted today
Job Viewed
Job Description
Responsibilities:
- Review project technical drawings, Single Line Diagrams (SLDs), and costing sheets provided by the Estimation and Sales teams.
- Conduct detailed handover meetings with Estimation and Sales teams to ensure clear understanding of project scope and cost structure.
- Collaborate with the Design team to ensure project design aligns with approved budget and scope.
- Develop and submit detailed project schedules in line with contractual timelines.
- Review and validate design documents; coordinate with clients for approvals, submissions, and variations.
- Ensure all client comments and feedback are properly incorporated into project design.
- Verify that all components issued for procurement align with approved designs and client expectations.
- Coordinate with the Supply Chain team to manage alternatives and design changes, ensuring all modifications are client-approved.
- Liaise with the Planning team to ensure accurate scheduling and effective project control.
- Work closely with Production teams and external vendors to resolve production-related issues affecting project delivery.
- Coordinate with clients for scheduling and conducting Factory Acceptance Tests (FAT).
- Manage project delivery logistics, ensuring timely delivery within client expectations.
- Support clients during installation and commissioning, addressing any related issues or after-sales service requirements.
- Follow up with clients for payments and ensure timely collection of receivables.
- Lead the project team to meet defined milestones and ensure successful execution.
- Create and maintain comprehensive project documentation and records.
- Monitor project progress, identify potential risks or delays, and implement corrective actions.
- Develop resource allocation plans and track utilization to optimize efficiency.
Qualifications & Experience:
- Bachelor's degree in Electrical Engineering from a recognized university.
- 2–4 years of relevant experience in project planning and execution, preferably in the switchgear or electrical equipment industry.
- Proficiency in project management tools such as Primavera P6, MS Project, or equivalent is highly desirable.
- Strong analytical, organizational, and problem-solving skills.
- Excellent client-facing and internal communication skills.
- Ability to manage multiple tasks, prioritize effectively, and maintain professionalism under pressure.
- Team player with strong coordination skills across departments.
What We Offer:
- Opportunity to work with a growing and innovative company in the switchgear industry.
- Exposure to high-value projects and professional development opportunities.
- Competitive salary and benefits package.
Job Type: Full-time
Work Location: In person
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4
Sr. Manager Finance – Manufacturing Sector
Karachi, Sindh
AGILE HR
Posted today
Job Viewed
Job Description
Job Title: Sr. Manager Finance – Manufacturing Sector
Location: DHA Phase 7, Karachi, Pakistan
Work Schedule: Monday to Saturday
Key Responsibilities:
- Lead and manage all financial reporting processes, ensuring accuracy and compliance with relevant standards.
- Oversee budgeting, forecasting, and variance analysis to support strategic business decisions.
- Manage costing and cost-control measures to optimize profitability.
- Supervise taxation processes, ensuring compliance with all statutory requirements.
- Direct accounting operations, including accounts receivable/payable, general ledger, and reconciliations.
- Handle treasury operations, including cash flow management, banking relationships, and funding strategies.
- Provide financial insights and recommendations to senior management for business improvement.
- Ensure internal controls and processes are in place for risk mitigation.
- Lead, train, and mentor the finance team to achieve departmental objectives effectively.
Required Qualifications & Skills:
- Education: CMA Qualified / ACCA Finalist or Qualified
- Experience: Minimum 8-10 years of progressive finance experience, preferably in the manufacturing sector.
- Strong expertise in:
- Financial Reporting
- Costing
- Taxation
- Budgeting & Forecasting
- Accounting Operations
- Treasury Operations
- Excellent analytical, problem-solving, and decision-making skills.
- Proficiency in financial ERP systems and MS Office (especially Excel).
- Strong leadership, communication, and team management abilities.
Benefits:
- Company Car & Fuel Allowance
- Performance Bonus
- Professional Development Opportunities
- Collaborative Work Environment
Job Type: Full-time
Pay: Up to Rs400,000.00 per month
Work Location: On the road
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5
QC Manager - Medical Device Manufacturing
Karachi, Sindh
Kamion Pharma
Posted 9 days ago
Job Viewed
Job Description
QC Manager - Medical Device Manufacturing
Location:
SITE, Super Highway, Phase-II, Karachi Position Overview: The Quality Control (QC) Manager will be responsible for overseeing quality control activities in a medical device manufacturing facility, ensuring products meet high standards, regulatory requirements, customer expectations, and QMS compliance. This role includes managing a team, coordinating testing, improving quality processes, and supporting other departments like Quality Assurance and technical problem resolution. The QC Manager is also responsible for using and maintaining inspection methods and equipment to ensure timely and compliant results. Key Responsibilities: Supervise and support QC inspectors and technicians to ensure adherence to company standards and prevent delays or product unavailability. Develop and implement quality control procedures to ensure compliance with ISO 13485 and DRAP regulations, demonstrating technical proficiency in analytical methodology and adherence to GMP and ICH standards. Ensure the timely disposition of raw materials, packaging materials, and finished products based on priorities set with Manufacturing, Marketing, and Materials Management, while overseeing inspection and testing to meet quality and efficiency standards. Review the daily QC Lab planning schedule. Monitor adherence to quality standards, regulations, and best practices. Perform regular audits of QC processes. Ensure the implementation of the product stability testing & evaluation as per SOP to verify shelf-life compliance and identify quality issues related to product stability. Gather and analyze quality data, generate reports, and suggest actions for quality improvement. Investigate quality issues or non-conformities and collaborate with other departments to resolve them. Oversee Quality Risk Management and Change Controls within the QC and Micro Lab domains, identifying areas for improvement and implementing changes to enhance product quality and manufacturing processes. Ensure all vendors are qualified and comply with vendor standards, collaborating with suppliers to maintain material quality and conducting evaluations and audits as necessary. Assist in preparing for and participating in external audits and inspections, providing required documentation and evidence of compliance. Maintain accurate records of quality control activities, including inspection and testing reports. Required Skills and Qualifications: Must have a pharmacy, biomedical engineering, or biotechnology degree recognized by HEC. A minimum of 5-6 years of experience in quality control and testing, preferably within a medical device manufacturing environment, with at least 4 years in a supervisory position. Certification in quality control or quality management systems (e.g., CQE, CQA) is preferred. In-depth knowledge of ISO 13485, DRAP regulations, and other relevant standards for medical device manufacturing. Exceptional leadership and team management skills, strong analytical and problem-solving abilities, meticulous attention to detail, and effective communication skills required. This position offers a unique opportunity to work in a dynamic and challenging environment where you can apply your skills and experience to drive improvements and ensure the success of the Quality Control Department. Application Process: Please submit your CV/Resume detailing your experience and qualifications with the subject line ‘QC Manager’.
#J-18808-Ljbffr
Location:
SITE, Super Highway, Phase-II, Karachi Position Overview: The Quality Control (QC) Manager will be responsible for overseeing quality control activities in a medical device manufacturing facility, ensuring products meet high standards, regulatory requirements, customer expectations, and QMS compliance. This role includes managing a team, coordinating testing, improving quality processes, and supporting other departments like Quality Assurance and technical problem resolution. The QC Manager is also responsible for using and maintaining inspection methods and equipment to ensure timely and compliant results. Key Responsibilities: Supervise and support QC inspectors and technicians to ensure adherence to company standards and prevent delays or product unavailability. Develop and implement quality control procedures to ensure compliance with ISO 13485 and DRAP regulations, demonstrating technical proficiency in analytical methodology and adherence to GMP and ICH standards. Ensure the timely disposition of raw materials, packaging materials, and finished products based on priorities set with Manufacturing, Marketing, and Materials Management, while overseeing inspection and testing to meet quality and efficiency standards. Review the daily QC Lab planning schedule. Monitor adherence to quality standards, regulations, and best practices. Perform regular audits of QC processes. Ensure the implementation of the product stability testing & evaluation as per SOP to verify shelf-life compliance and identify quality issues related to product stability. Gather and analyze quality data, generate reports, and suggest actions for quality improvement. Investigate quality issues or non-conformities and collaborate with other departments to resolve them. Oversee Quality Risk Management and Change Controls within the QC and Micro Lab domains, identifying areas for improvement and implementing changes to enhance product quality and manufacturing processes. Ensure all vendors are qualified and comply with vendor standards, collaborating with suppliers to maintain material quality and conducting evaluations and audits as necessary. Assist in preparing for and participating in external audits and inspections, providing required documentation and evidence of compliance. Maintain accurate records of quality control activities, including inspection and testing reports. Required Skills and Qualifications: Must have a pharmacy, biomedical engineering, or biotechnology degree recognized by HEC. A minimum of 5-6 years of experience in quality control and testing, preferably within a medical device manufacturing environment, with at least 4 years in a supervisory position. Certification in quality control or quality management systems (e.g., CQE, CQA) is preferred. In-depth knowledge of ISO 13485, DRAP regulations, and other relevant standards for medical device manufacturing. Exceptional leadership and team management skills, strong analytical and problem-solving abilities, meticulous attention to detail, and effective communication skills required. This position offers a unique opportunity to work in a dynamic and challenging environment where you can apply your skills and experience to drive improvements and ensure the success of the Quality Control Department. Application Process: Please submit your CV/Resume detailing your experience and qualifications with the subject line ‘QC Manager’.
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6
General Manager (Meter Manufacturing Plant)
Karachi, Sindh
Sui Southern Gas Company Limited
Posted 26 days ago
Job Viewed
Job Description
General Manager (Meter Manufacturing Plant) December 25, 2023 JOB DETAILS: Qualification & Experience: Engineering Graduate preferably in Mechanical or Industrial with at least 14 years of relevant experience. Responsibilities: Job Summary To lead the Meter Manufacturing Plant with complete management of production, quality & supply chain. To acquire and sustain business and thus effectively manage the portfolio as a profit generation unit for the organization. Job Responsibilities Overall plant management Manage Supply chain aspects as the location in-charge of meter plant stores, being responsible for inventory control Planning & management of production targets Labor management Business development (SSGC and SNGPL meters) Planning & forecasting Preparing budgets & gaining approval from the management Adherence to the quality management system Logistics arrangement To stay abreast with international quality standards & seek to achieve the same. Process & product improvement Technology transfers with the help of OEMs General factory administration To ensure succession planning by identifying, developing and maintaining pool of successors for key positions within the division / department. Foster and encourage continuous learning and development culture and encourage continuous education at all levels within the division / department.
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7
Senior Engineer - Plastic Parts Manufacturing
Karachi, Sindh
Sui Southern Gas Company Limited
Posted 26 days ago
Job Viewed
Job Description
Senior Engineer - Plastic Parts Manufacturing February 26, 2024 JOB DETAILS: Qualification & Experience: Bachelors in Polymer / Mechanical / Chemical / Plastic Engineering with at least 4 years of relevant experience. Master’s Degree shall be preferred. Candidates having experience in Plastic Injection Molding shall be an added advantage. Responsibilities: Awareness of plastics injection-mold fabrication processes. Create and improve injection-mold machinery. Research and develop new manufacturing processes. Analyze manufacturing data and suggest improvements. Analyze production and machinery line. Ensure quality output of molded components. Develop and design engineered plastic parts, inject molded parts and assemblies. Interact with customers, suppliers, and internal resources. Establish the parameters for an optimal molding environment. Ensure environment to make plastics is appropriate. Analyze quality control and correct flaws. Work with other team members and vendors. Create new reports and verifications. Analyze mold flow, part advisor analysis, finite element analysis, and stress/fatigue analysis on plastics. Create water diagrams and hot runner wiring schematics. Enforce all health and safety rules and regulations according to state/federal laws and company protocol. Prepare production planning for different plastic parts of gas meters.
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8
IR / ER Officer - (Textile / Manufacturing / Food Industry)
Karachi, Sindh
Fulcrum Pvt Ltd
Posted today
Job Viewed
Job Description
Job Title: IR / ER Officer - (Textile / Manufacturing / Food Industry )
Location: Korangi Industry Area, Karachi
Employment Type: Full-time
Job Description:
We are looking for an IR / ER Officer who can manage both HR operations and labour workforce handling. The candidate will be responsible for payroll, compliance, and statutory requirements while also dealing with workers' daily matters, discipline, transportation, canteen, and government agencies.
Key Responsibilities:
- Manage workers' attendance, payroll, and salary distribution.
- Handle EOBI, SESSI, labour laws, and compliance requirements.
- Deal with worker hiring, documentation, police verification, and replacements.
- Resolve labour issues and maintain discipline as per company SOPs.
- Coordinate with government agencies (Labour Dept., SESSI, EOBI, etc.).
- Supervise canteen, bus contractors, and employee welfare facilities.
- Support HR audits, safety, and training initiatives.
Requirements:
- Bachelor's degree in HR / Business Administration (preferred).
- 3+ years of experience in HR and labour handling.
- Strong knowledge of payroll & labour law compliance.
- Excellent communication and problem-solving skills.
- Ability to work closely with workers and management simultaneously.
Job Type: Full-time
Pay: Rs45, Rs50,000.00 per month
Work Location: On the road
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9