production

Bridgeworks Co

<div>BridgeWorks Staffing is looking for dedicated MACHINE OPERATORS who are ready to go to work and are ready to put in overtime.
LOTS OF OVERTIME!! 
 Job Title: Machine Operator
Location: Simpsonville
Hours:<ul><li>
Monday to Friday: 5:30 AM - 5:30 PM</li><li>
Saturday: 5:30 AM - 1:30 PM</li></ul>
Rate of Pay: $17/hour with increased overtime pay
Job Description:
We are looking for experienced Machine Operators to work with our machinery from set up to operation. This role involves ensuring that machines are set up properly and are operating effectively to produce high-quality products. Some machines are computer-controlled, while others are mechanically based, so versatility and adaptability are key.
Responsibilities:<ul><li>
Set up machinery for production runs, ensuring all settings are correct for optimal performance</li><li>
Operate machinery during production runs, monitoring performance and making adjustments as needed</li><li>
Ensure that machines are running smoothly and producing quality products</li><li>
Troubleshoot any issues that arise during production, performing maintenance or repairs as necessary</li><li>
Collaborate with team members and supervisors to meet production goals and deadlines</li><li>
Follow safety protocols and guidelines to maintain a safe work environment</li><li>
Maintain accurate production records and reports as required</li></ul>
Requirements:<ul><li>
High school diploma or equivalent</li><li>
Previous experience as a Machine Operator in a manufacturing environment</li><li>
Familiarity with both computer-controlled and mechanically based machines</li><li>
Strong mechanical aptitude and problem-solving skills</li><li>
Attention to detail and commitment to producing high-quality work</li><li>
Ability to work effectively in a fast-paced environment and adapt to changing priorities</li><li>
Basic computer skills for data entry and equipment operation</li></ul>
Requirements:<div><ul><li>
Ample opportunities for additional work hours beyond regular shifts 
</li><li>
Supportive work environment with a focus on teamwork and collaboration</li></ul></div></div>

Production

Coatinks (Private) Limited

Department: Production.Production reporting to : Production/Plant ManagerLocation: DIPPL Factory.Purpose: To support the effective planning, execution, control, and documentation of production operations in order to ensure product conformity, timely order fulfilment, and compliance with ISO 9001:2015 requirements.Job Responsibilities:<ul><li>Plan and implement production schedules to meet customer requirements and delivery timelines.</li><li>Coordinate production activities across multiple product lines to ensure smooth workflow. Monitor and adjust production schedules as necessary to maximize efficiency and productivity.</li><li>Participate in capacity planning and line allocation to achieve production targets.</li><li>Oversee production operations to ensure compliance with quality standards.</li><li>Conduct regular product inspections to identify defects or deviations from specifications. Report and assist in managing nonconforming products, including segregation, rework, and documentation.</li><li>Maintain accurate production records to ensure batch traceability and data integrity.</li><li>Track inventory levels of raw materials and finished goods.</li><li>Liaise with procurement and logistics teams to ensure timely availability of required materials.</li><li>Optimize resource usage to minimize waste and control production costs.</li><li>Facilitate effective communication between Quality, Warehouse, Maintenance, and Planning teams to maintain seamless operations.</li><li>Support continuous improvement initiatives, including Lean, 5S, and Kaizen, to enhance overall efficiency.</li><li>Monitor production downtime and investigate root causes to reduce disruptions.</li><li>Assist in training production staff on SOPs, quality standards, and safety procedures. Support monitoring of team performance and provide constructive feedback to supervisors.</li><li>Ensure adherence to health and safety regulations and company policies.</li><li>Promote a safety-conscious culture and ensure compliance with safety protocols among production staff.</li></ul>Education Requirements:<ul><li>Bachelor&rsquo;s degree in Engineering, Industrial Manufacturing or relevant technical field.</li></ul>(Preferably BE/BS &ndash; Industrial, Mechanical, Chemical, or equivalent)Experience Requirements:<ul><li>2 to 5 years of experience in a production or manufacturing environment.</li><li>Experience in process control, quality inspection, or production planning is preferred. Good understanding of HSE culture and practices.</li><li>Strong communication and interpersonal and time management skills.</li><li>Experience with continuous improvement initiatives and ISO management system will be an advantage.</li></ul>Job Type: Full-timeWork Location: In person

Production Executive

Manufacturing Commercial Vehicles

<div>Company: MCV INDUSTRY ( egypt)- Job Purpose:Responsible for implementing work schedule, issues plans, and follow up with warehouses to deliver chassis of manufactured parts and component parts to production lines according to assigned work centers on timely fashionJob Duties and Responsibilities:<ul><li>Implement and coordinate production plans to deliver chassis, components and manufactured items to production work centers</li><li>Follow up open production orders due dates to ensure meeting deadlines set</li><li>Follow up production lines in different stages</li><li>Review production orders and get feedback in regard to the parts that have no work centers</li><li>Follow up BOM errors to ensure adjusting in line with technology Dept before releasing orders to production line</li><li>Review and arrange shortage of items before entering the batch to production line</li><li>Follow up with production line and trouble shoot and facilitate any appearing problems during production process</li><li>Record any deviations from plans and reasons</li><li>Follow up modifications needed for vehicles with production planning department</li><li>Carry out additional tasks as per job requirements and as directed by line managerMain KPI Key Performance indicators:
</li></ul><ul>
<li>Core Competencies<ul>
<li>Financial Management</li>
<li>Customer Excellence</li>
<li>Process Management</li>
<li>Growth &amp; Development</li></ul> 
</li>
<li>Functional Competencies<ul>
<li>Job Knowledge</li>
<li>Monitoring, Reporting and Trend Thinking</li>
<li>Technology and Cyber Security</li></ul> 
</li>
<li>Leadership Competencies<ul>
<li>Accountability &amp; Focusing on Business Results</li>
<li>Emotional Intelligence</li>
<li>Integrity &amp; Professional Behavior</li></ul></li> 
</ul>
Job Skills and Abilities:<ul><li> Good English language</li><li> Very good communication skills</li><li> Very good computer skills</li><li> Ability to work under pressure</li><li> Enthusiastic, cooperative, and positive behavior</li></ul>Qualifications:<ul><li> Bachelor of commerce accounting section </li><li> 0-3 Years of Experience</li></ul></div>

Production Controller

Mauser Packaging Solutions

<div>Responsibilities:
<ul><li>Provides leadership and training to accomplish production objectives to all employees for Safety, Quality, Production, Packaging, and Maintenance.
</li><li>Coordinates production activities with other departments to ensure production goals/objectives are accomplished in a timely and cost-effective manner.
</li><li>Works with the operations team to ensure vacancies are covered for any planned/unplanned.
</li><li>Establishes and monitors shift performance for safety, quality, and production standards.
</li><li>Enters production data accurately into the system in order to measure and monitor KPIs (Key Performance Indicators) around efficiencies, downtime, inventory and overall production.
</li><li>Updates communication boards to keep production floor team members informed about safety, quality and efficiency metrics. Leads employee start-up meetings
</li><li>Works with other team members to control and improve efficiencies, minimize labor overtime, downtime and repair expenses. Implements cost-effective systems around this as necessary.
</li><li>Promotes shop floor organization, plant housekeeping with employees lean utilizing techniques such as 5S with shift personnel.
</li><li>Acts as the first point of contact for operators regarding mechanical failure or production issues; Directs maintenance employees to troubleshoot mechanical problems and perform preventative maintenance.
</li><li>May conduct tool store inventory reviews to ensure proper tools and/or parts are available for use in the event they are needed.
</li><li>Prepares and reviews employees' worked hours for submission to payroll.
</li></ul>Requirements:
<ul><li>Bachelor's degree in engineering or operations management
</li><li>3 years of supervisory experience in a manufacturing environment or an equivalent combination of education and experience
</li><li>Six Sigma Green or Black Belt Certification a plus
</li><li>Previous Labor Relations experience
</li><li>Previous experience working in a Lean environment; Embraces continuous improvement
</li><li>Self-directed team player
</li><li>Excellent critical thinking and problem-solving skills
</li><li>Flexibility to work multiple shifts
</li></ul>Competencies:
<ul><li>Excellent Communication
</li><li>Strong Business Acumen
</li><li>Results Orientation
</li><li>Building Collaborative Relationships
</li><li>Influencing Others
</li><li>Strategic Thinking
</li><li>Customer Orientation</li></ul></div>

Supervisor, Production

UNIVERSAL ENTERPRISES (UE)

<ul><li>Key Requirements:</li><li>Minimum 10 years of experience in pharmaceutical production or manufacturing.</li><li>Strong knowledge of GMP (Good Manufacturing Practices)</li><li>Proven track record in team management, production planning, and process optimization.</li><li>Excellent problem solving and leadership skills.</li></ul>Responsibilities:<ul><li>Manage and supervise daily production activities in the plant.</li><li>Ensure adherence to quality standards and safety protocols.</li><li>Optimize production processes to improve efficiency and reduce costs.</li><li>Coordinate with quality, maintenance, and supply chain teams to meet production targets.</li></ul>Please send your CV and cover letter to admin@missionpharma.com.pkwith the subject line &ldquo;Production Manager&rdquo; Application.Job Type: Full-timeWork Location: In person

Production Manager

JAMA MARBLE

Key ResponsibilitiesProduction Operations&middot; Supervise daily dairy and juice production activities (milk processing, pasteurization, fermentation, juice extraction, blending, filling, and packaging)&middot; Ensure production schedules are met with optimal use of manpower, materials, and equipment&middot; Monitor processing parameters such as temperature, time, pressure, and hygiene controlsQuality &amp; Food Safety&middot; Ensure compliance with food safety standards (HACCP, GMP, ISO, FSSAI/USDA/FDA as applicable)&middot; Conduct routine quality checks and ensure corrective actions for deviations&middot; Maintain cleanliness and sanitation of equipment and production areas (CIP/SIP systems)Team Supervision&middot; Lead, train, and motivate production operators and technicians&middot; Assign duties, manage shifts, and monitor employee performance&middot; Enforce safety rules and proper use of PPEEquipment &amp; Maintenance&middot; Coordinate with maintenance teams for preventive and breakdown maintenance&middot; Ensure proper operation of pasteurizers, homogenizers, fillers, chillers, and other processing equipment&middot; Minimize downtime and improve equipment efficiencyDocumentation &amp; Reporting&middot; Maintain production records, batch logs, and quality reports&middot; Track wastage, yields, and production efficiency&middot; Report daily production performance to managementContinuous Improvement&middot; Identify opportunities to improve productivity, quality, and cost efficiency&middot; Support implementation of process improvements and new product trials&middot; Product complaint investigation and root cause identification and implementation of CAPA.---Required Skills &amp; Competencies&middot; Strong knowledge of dairy and juice processing technology&middot; Understanding of food safety and quality systems&middot; Leadership and people management skills&middot; Problem-solving and decision-making abilities&middot; Basic computer skills (production reports, ERP systems)&middot; Attention to detail and ability to work under pressure---Qualifications&middot; Diploma or Bachelor&rsquo;s degree in Dairy Technology, Food Technology, or a related field&middot; 3&ndash;5 years of experience in dairy or beverage production, with supervisory experience preferred---Key Performance Indicators (KPIs)&middot; Production output vs. plan&middot; Product quality and rejection rates&middot; Equipment downtime&middot; Compliance with food safety audits&middot; Labor productivity and wastage control---Work Environment&middot; Manufacturing plant / processing facility&middot; Shift-based work, including nights or weekends&middot; Exposure to cold rooms, wet areas, and food-grade chemicals<ul><li>Required: Advantage experience with Baladna and Al Wajba dairy products.</li></ul>Job Type: PermanentPay: QAR5,000.00 - QAR6,500.00 per monthEducation:<ul><li>Bachelor's (Preferred)</li></ul>Work Location: In person

Production Supervisor

Sofie

<div><div>Job Description: Production Manager 
Title: Production Manager 
Department: Radiopharmaceutical Contract Manufacturing 
Training Curriculum: ID TCU.XXX 
Overview:<div>
The Production Manager for Radiopharmaceutical Contract Manufacturing is responsible for 
overseeing the Pharmaceutical Production Chemists and Aseptic Cleaning Technicians, ensuring timely manufacture and 
delivery of all diagnostic and therapeutic radiopharmaceutical finished product to meet customer expectations. The 
Production Manager will be responsible for overseeing the site&rsquo;s production related activities within aseptic and GMP 
areas such as cleaning, manufacturing campaigns for various products, and coordinating/scheduling both resources and 
materials for production. Following SOFIE's master records, SOPs, and QMS requirements, and following cGMP 
guidelines, the Production Manager will ensure that these radiopharmaceuticals are in full compliance with all regulatory 
requirements, including 21 CFR 211/212, EudraLex Volume 4, and all other applicable regulations for drug manufacturing. 
Essential Duties and Responsibilities 
<ul><li>Lead and implement the transfer of established manufacturing processes, records, and procedures for new</li></ul>
radiopharmaceuticals, either directly from customer or from SOFIE development group, or the SOFIE production 
team. 
<ul><li>Schedule and supervise clinical and commercial manufacturing activities, focusing on full compliance with industry</li></ul>
requirements. Lead by example by fully understanding and participating in manufacturing activities as needed. 
<ul><li>Manage implementation, validation, organization, and participation in the production of routine patient dose</li></ul>
manufacturing activities for various radiopharmaceutical drug products. 
<ul><li>Manage and supervise the RCM production and cleaning team (including shift leads and supervisors) beginning</li></ul>
with the transition of radiopharmaceuticals in development to clinical manufacturing and through commercial 
manufacturing. 
<ul><li>Conduct performance review for the direct reports and or indirect reports as assigned. Track performance through</li></ul>
regular 1:1s and staff meetings. 
<ul><li>Develops and maintains working relationships with employees at all levels. Manage current and newly hired</li></ul>
personnel training process and ensures training for direct reports meets expectations as defined in job specific 
training matrices.Ensure aseptic operations by the production team members comply with internal procedures (example: gowning, 
cleaning/sanitation, sterility, environmental monitoring), accepted industry practice and regulatory guidance. 
Assure completeness, accuracy, traceability, and compliance of the site utility and facility monitoring methods and 
records. Provide support to site Microbiologists and QA, as necessary. 
<ul><li>Review and approve clinical dose manufacturing plans, final drug product labels, reagents, manufacturing batch</li></ul>
records, and associated EM data. Properly organize and securely maintain cGMP production documents until 
archived by QA. Keep facility and manufacturing SOPs up to date and ensure no copies of obsoleted documents 
are held by the production team members. 
<ul><li>Work with SOFIE's QA, Regulatory, and EH&amp;S teams to ensure SOFIE's standards are continuously reflected in</li></ul>
all new radiopharmaceutical products and contribute in the generation of regulatory documentation required for 
new radiopharmaceuticals, including Standard Operating Procedures (SOPs), development and validation 
Protocols, and Master Batch Records. 
<ul><li>Oversee the participation of the production team in the installation, qualification, and maintenance of the facility</li></ul>
production equipment. Executes approved protocols to validate manufacturing processes in coordination with 
project managers. Maintain individual qualification requirements and training for entering ISO classified areas. 
<ul><li>Demonstrate proficiency in industry radiation safety procedures. Responsible for tracking radiation exposure of</li></ul>
production personnel and seeing that principles of ALARA are maintained. Maintain a clean and safe working 
environment and perform radiation safety duties in compliance with safety and pharmaceutical regulations. 
<ul><li>Provide oversight to the materials utilized in the manufacturing process and ensure that raw materials,</li></ul>
components, containers, closures, packaging, and labeling are inspected, qualified, and meet acceptance criteria 
before use. 
<ul><li>Lead exception document initiation and investigation for manufacturing processes [Deviation, OOS, Action/Alert</li></ul>
Level Notifications]. Ensure that scientifically sound root causes are identified. Initiate and Implement CAPA plans. Evaluate effectiveness of the CAPA plans through reporting and trending. Ensure SOFIE's Change Control 
procedure is followed as required. 
<ul><li>Monitor site production performance and manage departmental metrics by collecting key performance indicators.</li></ul>
Collaborate cross functionally to discuss operations, issues/concerns, innovative ideas, and continuous quality 
improvements. Keep departmental costs within the budget and determine ways to reduce production costs using 
Lean tools. 
<ul><li>Ability to work various shifts and weekends required. Perform routine production synthesis as needed.</li><li>Write reports, presentations, and other documentation summarizing data. Coordinate the Radiopharmaceutical</li></ul>
Contract Manufacturing team's activities to reach defined objectives. 
<ul><li>Liaise with our contract partners (e.g., biotech and pharma). Effectively communicate with customers, vendors,</li></ul>
and other internal sites. 
<ul><li>Perform other duties as assigned.</li></ul></div>
Qualifications:<ul><li>Bachelor&rsquo;s degree in a scientific field is required with 10+ years of experience in radiopharmaceutical /</li></ul>
pharmaceutical drug product manufacturing and production equipment management (qualification, 
troubleshooting and maintenance) required. Master&rsquo;s degree with 7+ years of experience is preferred. 
<ul><li>Three to five years of people management experience required.</li><li>Familiarity with radiation protection and safe handling of radioactive materials is required. Experience in radiation</li></ul>
safety is highly preferred. 
<ul><li>Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and</li></ul>
procedure manuals required. 
<ul><li>Experience in cGMP manufacturing environment is highly preferred. Knowledge of cGMP requirements, aseptic</li></ul>
process (cleanroom environment), and equipment qualification is required. 
<ul><li>Efficient in the use of MS Office Suite required.</li><li>Excellent organizational skills required. Knowledge of Lean Six Sigma preferred.</li><li>Cross functional communication skills in addition to collaboration and troubleshooting</li></ul></div></div>

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