Manufacturing Manager

08512 Cranbury, New Jersey Medix

Posted 9 days ago

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Job Description

You are applying for a position through Medix, a staffing agency. The actual posting represents a position at one of our clients.Company InformationOur client is a leading global open-access biologics technology platform offering end-to-end solutions to empower organizations to discover, develop, and manufacture biologics from concept to commercial manufacturing.Job SummaryReporting to the Manufacturing Director, the Manufacturing Manager will play a pivotal role in establishing the Manufacturing Department by supporting operational readiness and leading the manufacturing team to consistently deliver on specific Key Performance Indicators (KPIs). The Manufacturing Manager will work closely with the MSAT (Manufacturing Science & Technology) teams to ensure the effective and efficient tech transfer of products and processes to the facility.Key Responsibilities Member of the Manufacturing leadership team. Support the execution of the overall Manufacturing strategy aligned with the facility's strategic business plans and global Manufacturing strategy. Lead a team of Supervisors and Manufacturing Bioprocessing Associates to execute routine manufacturing activities of therapeutic proteins in a mammalian cell culture facility. Manage daily downstream manufacturing activities and ensure production timelines are met. Collaborate with MSAT and engineering teams on technical transfer, process validation, etc. Collaborate with QC & QA groups to ensure GMP compliance, manage deviation investigation and CAPA implementation, and support client auditing and agency inspections. Provides working knowledge and technical leadership in Downstream operations. Schedules and/or delivers training to manufacturing personnel to ensure staff can perform manufacturing operations safely and compliantly. Motivate, retain, develop existing group members and recruit new staff to build a strong Downstream manufacturing team. Contribute to continual improvement of all manufacturing documentation (SOP's, MBR's, OJT's) to ensure they are current, accurate, and clear. Communicate operational status regularly to senior management, as required, at the appropriate level of detail. Assist the Manufacturing Director to coordinate the work between the Downstream groups and other functional groups to meet the production objectives and timelines. Perform all duties in accordance with GMP requirements, SOPs, and controlled documents. Will be flexible to take on additional tasks and responsibilities at the discretion of the Manufacturing Director. Will act as a role model for the Manufacturing function and also the wider organisation in adherence to corporate core values and company culture.Qualifications Comprehensive knowledge and experience of relevant cGMP, safety and environmental regulations within the biopharmaceutical industry. Ideally, experienced in establishing a Manufacturing department and building a team of similar size and scale. 10+ years in biopharmaceutical manufacturing with extensive experience in Downstream processing. Experience in the large-scale chromatography, ultrafiltration/diafiltration, viral inactivation, filtration, etc. Experience in dealing with FDA, and/or EMA, and have a solid understanding of quality system in terms of deviation, investigation, CAPA and change control. Experience in working with cross-functional teams. Experience in troubleshooting and investigation of the critical deviation, and making the risk analysis on the development, technical transfer and process validation. Must be quality-focused with knowledge and understanding of cGMP quality systems and how they apply to manufacturing operations.Experience 10+ years in biopharmaceutical manufacturing.Skills Technical skills relevant to downstream processing operations. Strong leadership abilities and the ability to adapt to a dynamic manufacturing environment. Excellent verbal and written communication and presentation skills. Strong interpersonal skills to work effectively with all levels of staff. Ability to work independently and proactively. Results-oriented, with the ability to manage multiple priorities in a short period of time. Excellent organizational and planning skills, strong attention to detail.Education Certificate, Diploma, Degree in Science, Engineering or related field, or equivalent experience in the biopharmaceutical industry is essential. BSc, MSc, or PhD in Chemical Engineering, Bioscience, or Biotechnology is advantageous.Additional Requirements Must be willing to travel as required internationally to fulfill the responsibilities of the position.Medix Overview:With over 20 years of experience connecting organizations with highly qualified professionals, Medix is a leading provider of workforce solutions for clients and candidates across the healthcare, scientific, technology, and government industries. Through our core purpose of positively impacting lives, we're dedicated to creating opportunities for job seekers at some of the nation's top companies. As an award-winning career partner, Medix is committed to helping talent find fulfilling and meaningful work because our mission is to help you achieve yours.

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Quality Control Inspector

08628 West Trenton, New Jersey Macom Technology Solutions Holdings, Inc.

Posted 2 days ago

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Job Description

Company Overview:

MACOM designs andmanufactures semiconductor products for Data Center, Telecommunication, andIndustrial and Defense applications. Headquartered in Lowell, Massachusetts,MACOM has design centers and sales offices throughout North America, Europe,and Asia. MACOM is certified to the ISO9001 international quality standard andISO14001 environmental management standard.

MACOM has more than 65years of application expertise with multiple design centers, Si, GaAs and InPfabrication, manufacturing, assembly and test, and operational facilitiesthroughout North America, Europe, and Asia. In addition, MACOM offers foundry servicesthat represents a key core competency within our business.
MACOM sells anddistributes products globally via a sales channel comprised of a direct fieldsales force, authorized sales representatives, and leading industrydistributors. Our sales team is trained across all of our products to give ourcustomers insights into our entire portfolio.

Title: Quality ControlInspector

Asa Quality Inspector, you will be responsible for verifying all requireddocuments that are involved/required with the parts/products you areinspecting. Document any non-conformances in detail on the Company's Q-notesystem. This includes all areas of quality control, incoming inspection, in-processinspection and final inspection. When not working with the microscope, you willbe verifying measurements with handheld measuring tools.

Key Responsibilities:
  • Perform incoming inspection, in-process inspection, first article inspection and final inspection of electronic and mechanical components with little to no assistance.
  • Schedule source inspections as required.
  • Generate internal and external reports.
  • Generate and maintain data for the control of documentation, effectively report information, and accurately respond to questions from team members, internal suppliers, and customers.
  • Communicate non-conformances and work with Quality and Manufacturing to drive corrective actions. Ensure all incoming, in-process and final materials meet specifications.
  • Perform routine SAP transactions to move, disposition, and route material.
Key Competencies & Skills Required:
  • Safe handling of ESD sensitive materials.
  • Working knowledge of SAP, Agile, Excel, MSWord and Outlook.
  • Ability to prepare oral and written reports clearly and concisely.
  • Excellent internal and external communication skills.
  • Advanced understanding of quality control standards and testing techniques.
  • Knowledge of statistical sampling techniques.
  • Able to lift up to 20 pounds.
  • Able to sit for periods of time working with a microscope.
Required Qualifications and Experience:
  • High School diploma (or equivalent) or AS degree (preferred).
  • Minimum 2 years Quality Control inspection experience (preferred).
  • Self-motivated with the ability to evaluate complex issues in a high-pressure environment.
  • Knowledge of all aspects of inspection and testing.
  • Experience with Mil-PRF-38534, class H & K; Hybrids, Mil-STD-883; methods 2008, 2009, 2010, 2017 Semiconductors and Passive devices.
  • Knowledge of IPC-600 and 610, J-STD-001.
  • Knowledge and experience in performing mechanical and electronic inspections.
  • Ability to work from technical drawings, sketches and specifications.
  • Due to ITAR regulations, U.S. citizenship or permanent residency required.

The Salary Range for this position is $25.00-$28.00.Actual salary offered to candidate will depend on several factors, includingbut not limited to, work location, relevant candidates' experience, education,and specific knowledge, skills, and abilities.

Benefits: This position offers a comprehensive benefits packageincluding:
Health, dental, and vision insurance.
Employer-sponsored 401(k) plan.
Potential for performance-based bonus.
Paid time off.
Professional development opportunities.

EEO:

MACOM is an EqualOpportunity Employer committed to a diverse workforce. MACOM will not discriminateagainst any worker or job applicant on the basis of race, color, religion, sex,gender identity, sexual orientation, national origin, age, disability, geneticinformation, veteran status, military service, marital status, or any othercategory protected under applicable law.

Reasonable Accommodation:

Reasonable Accommodation. MACOM is committed to working with and providingreasonable accommodations to qualified individuals with physical and mentaldisabilities. If you have a disability and are in need of a reasonableaccommodation with respect to any part of the application process, please call or email Provide your name, phone number andthe position title and location in which you are interested, and nature ofaccommodation needed, and we will get back to you. We also work with currentemployees who request or need reasonable accommodation in order to perform theessential functions of their jobs.
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Clinical Manufacturing Associate

07059 Warren, New Jersey Omni Inclusive

Posted 3 days ago

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Job Description

Detailed Position Responsibilities
•Production of blood component lots through cell culture, harvest, and cryopreservation.
•Aseptic technique
•Become fully trained and qualified in all aspects of assigned processes
•Develop a high level of technical knowledge of project(s)
•Weigh and measure in-process materials to ensure proper quantities are added/removed.
•Adhere to the production schedule ensuring on-time, internal production logistics.
•Record production data and information in a clear, concise, format according to proper GDPs.
•Work in a team based, cross-functional environment to complete production tasks required by shift schedule.
•Assist tech transfers in and out of the clinical facility.
•Motivated, team consciousness individuals are needed to fulfill job requirements.
•No direct reports will be assigned to this job role.
•Perform other tasks as assigned.
Desired Experience Required:
- Basic understanding of cell culture, cryopreservation, purification, and aseptic processing or lab technique
- Experience within cGMP/FDA regulated industry
- Basic mathematical skills
- Technical writing capability
- Proficient in MS Office applications
- Background to include an understanding and application within industry of biology, chemistry, medical or clinical practices

Ideal Candidates Would Also Have:
- Advanced understanding of cell culture

Other Qualifications:

- Bachelor's degree in an applicable science or engineering field and a minimum of 2 years relevant experience

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HR Manager- Manufacturing

08302 Hopewell, New Jersey Solomon Page

Posted 5 days ago

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Job Description

Direct message the job poster from Solomon Page

Solomon Page is searching for a Human Resources Manager for a unionized manufacturing plant located in Upper Deerfield Township in Cumberland County, NJ, which offers a vibrant lifestyle, with lifestyle with tons of amenities and career opportunities! The HR Manager and responsible for the overall administration, coordination, and implementation of the operational human resources function at a union facility with over 200 employees. The role oversees all elements of day-to-day HR operations including employee relations, performance management, safety, benefits administration, recruitment and retention, new employee orientation and onboarding, EEO and new hire reporting, and coordination of company events at the facility.

  • Salary range 102k to 128K plus bonus

Responsibilities:

  • Ensure hands-on execution of all site HR functions.
  • Partner with leaders to help drive business performance using sound HR knowledge in the areas of workforce planning, change management, employee productivity, recruitment and selection, and employee relations.
  • Counsel managers and employees consistent with policies/practices, legal considerations, etc., and facilitate resolution of employee relations issues.
  • Implement and execute employee relations programs/practices that create a positive organizational culture and enable management effectiveness.
  • Roll out and drive corporate programs (policies, development, employee engagement, etc.)
  • Assist management in the creation of career development plans that foster growth, based on performance reviews, Talent Review, etc.
  • Develop, coordinate, and manage training initiatives; annual Talent Review, leadership development, employee skills training, and development.
  • Coordinate and manage the performance management process, and drive management in the execution of performance-related action plans.
  • Schedule meetings and ensure an HR presence with off-shift employees (2nd and 3rd shift).
  • Represent function on the business units leadership team, providing appropriate input in key annual strategic processes.
  • Manage and execute the recruitment process; advertising, job descriptions, applicant screening, interview scheduling, and reference checks. placement).
  • Manage the new employee onboarding process.
  • Maintain the HRIS, payroll systems, time and attendance systems, and ensure data integrity.
  • Support the corporations benefits team with the coordination and management of benefits plans; annual open enrollment, and issue resolution.
  • In conjunction with the sites safety committee, implement best-demonstrated safety practices to mitigate risk, reduce exposure, and effectively manage claims.
  • Serve as the groups Safety & Risk Management Officer.
  • Partner with leadership to manage all required and agreed-upon safety programs and training.
  • Supervise and develop staff within the Human Resources Department.
  • Ensure compliance with applicable federal, state and local laws and regulations.
  • Work closely with the members of the United Food and Commercial Workers International Union in the following areas:
  • Represent the company in the day-to-day communications with the Union.
  • Provide resolution of employee concerns and/or grievances.
  • Implement Company policies and practices as related to the members of the Union.
  • Assure that the company is in compliance with the Collective Bargaining Act.
  • Responsible for any other items as it is related to our relationship Perform other related duties as required and assigned.

Required Qualifications:

  • Bachelor's degree in Business, Human Resources, or a related field
  • Five plus (5+) years of progressive HR generalist experience in manufacturing or related experience
  • Two plus (2+) years at the management level, preferred
  • Experience with union
  • Experience in report writing
  • Must have excellent verbal and written communication skills
  • Must be detail-oriented and have the ability to multi-task
  • Must have excellent time management skills
  • Professional in Human Resources (PHR) certification preferred, or the ability to obtain certification.
  • Ability to work independently
  • Stays current on laws and regulations affecting HR practices
  • Credibility and Integrity
  • Builds and maintains relationships

If you meet the required qualifications and are interested in this role, please apply today.

The Solomon Page Distinction

Our teams, comprised of subject matter experts, develop an interest in your preferences and goals and we act as an advisor for your career advancement. Solomon Page has an extensive network of established clients which allows us to present opportunities that are well-suited to your respective goals and needs this specialized approach sets us apart in the industries we serve.

About Solomon Page

Founded in 1990, Solomon Page is a specialty niche provider of staffing and executive search solutions across a wide array of functions and industries. The success of Solomon Page reflects an organic growth strategy supported by a highly entrepreneurial culture. Acting as a strategic partner to our clients and candidates, we focus on providing customized solutions and building long-term relationships based on trust, respect, and the consistent delivery of excellent results. For more information and additional opportunities, visit: solomonpage.com and connect with us on Facebook, and LinkedIn.

Opportunity Awaits.

Seniority level
  • Seniority level Not Applicable
Employment type
  • Employment type Full-time
Job function
  • Job function Human Resources
  • Industries Food and Beverage Services

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Project Manager - Manufacturing

08829 High Bridge, New Jersey DaVita

Posted 20 days ago

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Job Description

Project Manager - Manufacturing

High Bridge, NJ

Department: Production Control

Company: Trident Maritime Systems - Custom Alloy Division

Are you an experienced project manager who thrives in a fast-paced manufacturing environment? Trident Maritime Systems - CAC, LLC is looking for a driven and organized Project Manager to lead cross-functional teams, ensure compliance, and drive key projects to completion in our High Bridge, NJ facility. This is a full-time, on-site role in a dynamic division that serves both government and commercial clients with custom-fabricated pipe, tube, and fitting solutions.

What You'll Do:
  • Lead projects from initiation to close, ensuring alignment with scope, schedule, and budget.

  • Develop detailed project plans, set timelines, and coordinate internal and external resources.

  • Serve as the main point of contact for customers, vendors, and regulatory agencies.

  • Monitor project progress, address roadblocks, and manage scope changes.

  • Mitigate risks with proactive planning and contingency strategies.

  • Optimize resource use and deliver measurable results.

  • Create reports, presentations, and documentation to support project transparency.


What You Bring:
  • U.S. Citizenship required (due to government contracting work).

  • Strong leadership, communication, and problem-solving skills.

  • Experience managing multiple projects in a manufacturing setting.

  • High proficiency in Microsoft Office, especially Excel.

  • Ability to work under pressure and maintain composure in a production environment.

  • Bilingual (English/Spanish) is a plus.


Qualifications:
  • High school diploma or GED required.

  • Associate or Bachelor's degree in Business, Engineering, or a related field preferred.

  • 3+ years of project management experience in manufacturing.

  • Prior supervisory experience is required.

  • Knowledge of manufacturing processes, supply chain logistics, and regulatory compliance.


Physical & Work Environment:
  • Ability to sit, walk, kneel, and occasionally lift up to 25 lbs.

  • Traditional industrial environment - hot/cold/dirty at times, but safety is our priority.

  • Close/distance vision and depth perception needed for visual tasks.


About Us:

At Trident Maritime Systems - Custom Alloy Division , we manufacture mission-critical custom pipe and fittings for defense and commercial applications. We don't do mass production - we engineer solutions tailored to unique specifications, using heavy-duty equipment and a skilled workforce. Our work is demanding, but meaningful.

What We Offer:
  • Cigna Medical, Dental, VSP Vision

  • FSA & HSA with company contributions

  • 401(k) Retirement Plan

  • Paid Time Off + 10 Paid Holidays

  • $200 Safety Shoe Reimbursement

  • Prescription Safety Glasses Program

  • Company-Paid & Voluntary Life Insurance

  • Supplemental Insurance Options

  • Employee Referral Bonus Program

  • Paid Training & Career Development


Ready to make an impact? Apply today and help build the future of maritime manufacturing.

Offers of employment are contingent upon a successful background check and drug screening.

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Forklift Operator - Chemical Manufacturing

08543 Princeton, New Jersey A-Line Staffing Solutions

Posted today

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Job Description

A-Line Staffing is now hiring Forklift Operator in Princeton, NJ 08540. The Forklift Operator would be working for a Major Chemical Manufacturer and has career growth potential.

Forklift Operator Highlights:
? Location: Princeton, NJ 08540
? Schedule: Second shift ? 3:00 PM to 11:00 PM
? Pay Rate: $22.90/hour

Forklift Operator Responsibilities:
? Deliver and retrieve palletized materials to/from production environment
? Ensure safe operation of powered industrial trucks (stand-up/sit-down fork truck and walk-behind)
? Safely handle motorized and non-motorized drum handling equipment
? Use of scanning equipment
? Maintain a safe and clean work area in accordance with GMP

Forklift Operator Qualifications:
? High school diploma required
? Prior forklift experience
? 1?3 years of inventory and chemical manufacturing experience
? Knowledge of inventory systems and manufacturing processes
? Knowledge of Good Manufacturing Practices (GMPs)

Physical Requirements:
? Must be able to operate a forklift for 95% of the workday
? Frequently move, lift, pull, and push up to 50 lbs
? Required to wear personal protective equipment (PPE)
? Willingness and ability to work in a facility with minimal temperature control

If you are interested in this Forklift Operator position, please apply to this posting with Luke H. at A-Line!

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Industry Advisor Pharma Manufacturing

08818 Edison, New Jersey TEPHRA

Posted 3 days ago

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Job Description

Description:

Responsibilities:

• Lead discussions with the prospective customers in positioning advisory services with focus on the Pharma Mfg operations transformation & Digital Plant Solution.

• Work closely Industry Solutions unit to formulate business strategies for new growth avenues in the target account

• Provide subject matter expertise, solution strategies, domain competence development and dissemination of knowledge on new technology trends in the domain to delivery teams.

• Build ROI models and the KPI's for monitoring success of the investments proposed.

• Support Geo sales teams in sales process cycle and help new logo acquisition team in Go-to-Market Strategy.

Qualifications:

The candidate must have :

• Excellent Understanding of Pharma Manufacturing ( Chem API , Bio API, Formulations , CRO's, CRAMS)

• Understanding of Pharma Mfg challenges from operations, Quality and Regulatory perspective and ability to prescribe strategic solutions to address the challenges.

• Experience of developing ROI based Mfg operations transformation prepositions to the Leading global Pharma Mfg consultants.

• Exposure to the latest technology trends in the Digital Manufacturing and IOT based solutions.

• Excellent Knowledge on Information technology and Architecture applied to business process/rules in a pharma mfg environment.

• Conversant with the usage of Enterprise as well as Plant IT applications across ISA S95 ERP, PLM, Plant Engineering, MES, Lab informatics, DCS, SCADA, HMI, etc. in the pharma manufacturing industry.

• Familiarity with S95 & S88 standard- Language, definition and guidelines for integration of enterprise business systems and manufacturing control systems, viz level 0 - level 4.

• Familiarity with leverage of Mfg IT system like ERP-SAP, Asset Management solutions - Maximo, Plant Engineering - Intergraph (Smart Plant), MES - Werum, Pharma Suite, Lab Informatics - Labware, BioVia, Sample Manager etc. and DCS - Emerson for connected digital enterprise.

• Good familiarity with the regulatory environment viz the cGxP requirements of the US FDA . Familiarity to the GAMP, CFR Part 11, IQ, OQ, PQ and their relationship to the GMP

• Plant Engineering would be an added advantage. Being abreast with latest trends in pharma industry like, Digital Tech Transfer, Global Recipe Management, Real-time Batch Release, Predictive Quality & Maintenance for Yield improvement, Quality by Design , Lean Pharma, PAT would be an added advantage.

1) Years of experience required for position - 15+ years of industry Experience
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About the latest Manufacturing Jobs in Hillsborough !

Financial Analyst - Cost/Manufacturing

08543 Princeton, New Jersey Collins Consulting

Posted 4 days ago

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This is an onsite position.

Job Description
The client is a global leader in providing critical medical diagnostic and informatics products for rapid blood analysis that are intuitive, reliable, and cost-effective. Our i-STAT System is an advanced, portable diagnostic tool that provides real-time, lab-quality results within minutes to accelerate patient-care decision-making as well as optimize resource utilization for our customers and the patients that they serve. The i-STAT System has the industrys most comprehensive menu of tests in a single, with-patient platform, including tests for respiratory, metabolic, coagulation, hematology, glucose, and cardiac function. By delivering lab-quality results in minutes, on just a few drops of blood, our i-STAT System fosters a collaborative, patient-centered environment while driving improved operational performance.

The client has a new opening for a Sr. Financial Analyst. This role will support the Division FP&A HQ team with providing financial planning & analysis for the business by building and managing financial reports, preparing analysis for business reviews and other adhoc request.

Responsibilities include:
  • Prepare financial analysis and reports (such as Plans, Latest Best Estimate (LBE's) and Long Range Projections (LRP)) for P&L and balance sheet metrics that meet the timing and quality of presentation requirements, facilitate management review and decision making while ensuring integrity of data and compliance with GAAP as well as client's operating policies
  • Maintain an effective and efficient planning process for the division and functional areas being supported, including the coordination of a planning calendar with key dates and deliverables
  • Develop flexible, comprehensive tools and templates to support the consolidation and timely completion of corporate schedules as well as develop system solutions and process improvements that meet the needs of the financial planning and/or reporting requirements
  • Support the Sales & Operations Planning (S&OP) process by managing the reporting of monthly financial performance metrics such as: sales and expense variances, cash conversion cycle (CCC), Integrated Business Planning (IBP), etc
  • Provide financial support to Global Marketing organization. Partner with marketing team to create annual budget and forecast
  • Complete month-end close activities: tie out monthly revenue, prepare journal entries, expense summaries, and project spend analysis
  • Prepare and analyze daily and weekly sales reporting / projections
  • Maintain finance scorecard on deliverables from other APOC finance organizations
  • Perform adhoc requests and drive cross-business analytic projects for senior management, with financial modeling, data mining and presentation support
Education Requirements:
  • Bachelors degree, preferably in accounting or finance, or an equivalent combination of education and work experience.
Minimum Qualifications:
  • Position requires 7+ years of finance experience to include roles of increasing responsibility in accounting and/or finance
  • Strong Excel skills, demonstrate initiative, analytical thinking, critical-thinking and problem-solving skills
  • Demonstrated ability to provide data and analysis to support decision making, methodical approach to problem solving and rational ideas supporting them, ability to keep learning and to teach others, traditional accounting knowledge and facilitator of management needs, streamlining functions within the department and an efficient work ethic.


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Manufacturing Manager - Switchboard Assembly

07083 Union, New Jersey Lincoln Electric Products Co.

Posted 9 days ago

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Manufacturing Manager - Switchboard Assembly

1 week ago Be among the first 25 applicants

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Description

Manufacturing Manager - Switchboard Assembly

Work Arrangement: Onsite Hours: Monday-Friday

Compensation

Salary will be determined based on the candidates experience, skills, and demonstrated expertise during the hiring process, ensuring competitive compensation aligned with industry standards and internal equity.

About The Company

At Lincoln Electric Products Co. Inc., we specialize in designing, manufacturing, and distributing custom equipment tailored to meet our customers' specific applications and requirements. Our product range includes:

  • Panelboards: Up to 2000A
  • Service and Distribution Switchboards: Up to 8000A
  • Generator Connection Boxes
  • Generator Output Switchboards
  • Single and Double-Ended Substations
  • We pride ourselves on delivering high-quality, custom-designed solutions that address the unique needs of our clients across various industries.

Position Summary

Lincoln Electric Products Co. Inc. seeks a highly motivated and experienced Manufacturing Manager - Switchboard, Panelboard, Wiring, and EV Assemblyto join our team in Union, NJ. This individual will play a critical role in overseeing the assembly department's daily operations, driving efficiency, and ensuring the seamless execution of organizational goals. The Production Operations Manager - Switchboard, Panelboard, Wiring, and EV Assembly will work collaboratively across departments to enhance productivity, implement process improvements, and contribute to the overall success of the business.

While this role primarily operates Monday through Friday, occasional Saturday work may be required based on business demands.

This full-time, exempt position reports directly to the Chief Operating Officer and involves a hands-on approach.

Working Conditions: Office/ Assembly Shop Floor Environment

What We Offer

  • Competitive Salary: Paid every week.
  • Comprehensive Benefits Package, Including Health, Dental, and Vision Plans.
  • Retirement Plan: 401(k)
  • Paid Time Off (PTO): For vacation and personal days.
  • Sick Leave

Job Responsibilities

  • Oversee and manage daily switchboard, panelboard, wiring, and EV assembly operations to ensure adherence to production schedules and customer delivery timelines.
  • Supervise the production and assembly of low-voltage switchgear systems, ensuring compliance with UL standards and other relevant industry regulations.
  • Lead and manage assembly personnel, including team leads, mechanical assemblers, and wiremen, ensuring efficient workflows and high-quality output.
  • Develop, manage, and maintain production assembly schedules, adjusting them as needed to account for delays, material shortages, or equipment issueswhile minimizing downtime and maintaining delivery commitments.
  • Create and implement effective assembly scheduling processes, ensuring coordination across multiple production lines to optimize resource utilization.
  • Implement and enforce standardized production processes, quality control measures, and safety protocols.
  • Monitor key performance indicators (KPIs) and other operational metrics to evaluate performance and identify opportunities for improvement.
  • Collaborate with engineering, project management, quality assurance, procurement, and supply chain teams to resolve production challenges and streamline workflows.
  • Coordinate with procurement and logistics to ensure timely availability of materials and components required for all assembly operations.
  • Develop and manage production budgets, resource planning, and cost-control strategies.
  • Ensure consistent compliance with company policies, safety regulations, and industry standards.
  • Promote and lead continuous improvement initiatives, including Lean Manufacturing and Six Sigma methodologies.
  • Identify and address training needs for team members to support growth and performance enhancement.
  • Partner with the maintenance team to address equipment reliability and minimize disruptions.
  • Foster a culture of safety, accountability, and operational excellence within the production environment.
  • Ensure seamless coordination across switchboard, panelboard, and EV assembly lines, driving cross-functional efficiency and alignment.
  • Regularly review and refine production plans and schedules to identify bottlenecks and implement proactive solutions.

Skills, Requirements, And Specifications

  • Bachelor's degree in Engineering (Master's degree preferred).
  • Minimum of 5-7 years of experience in engineering, production, or operations management, preferably in switchboard, panelboard, EV assembly, and wiring departments.
  • Experience as a General Electrical Foreman in a manufacturing or industrial setting will also be considered.
  • Proficiency in ERP systems.
  • Proven experience in managing large production teams and driving operational excellence.
  • Strong knowledge of Lean Manufacturing, Six Sigma, and other process improvement methodologies.

If youre ready to move to an organization where you will have an integral role in shaping future growth, where you will interact across company functions from the top down, and be valued and appreciated by ownership and senior leadership, this is where you need to be! Seniority level
  • Seniority level Mid-Senior level
Employment type
  • Employment type Full-time
Job function
  • Job function Management and Manufacturing
  • Industries Electrical Equipment Manufacturing

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Manufacturing - Business Operations Specialist

07902 Summit, New Jersey TechDigital Group

Posted 10 days ago

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Job Description

100% onsite

Job Responsibilities:
  1. Supports Cell Therapy External Manufacturing with facilitation of service contracts, agreements, purchase orders, approvals and payments as needed, vendor monitoring, and oversight executed from Client ERP systems.
  2. Create contract review and approval request in Icertis, contract management system.
  3. Create Oracle & Ariba purchase requests and help to drive them through the system.
  4. Accounting, Basware invoice tracking and report generation in OBIEE.
  5. Assist in tracking KPIs and preparation of monthly dashboards and reports.
  6. Assist Sr GBO Specialist in facilitating monthly Working Group Meeting for work alignment.
  7. Coordinate ERP system reports to assist with Monthly Budget review.
  8. Liaise with Client Buy team to assist in supplier inquiries, late payments, update banking details, supplier account payment term updates, etc.
  9. Liaise with Client AP team to assist with invoice issue resolution, purchase order reconciliation, etc.
  10. Adhoc Project assistance as requested by GBO Lead.
  11. Update and maintain departmental electronic records using Sharepoint.

Requirements:
  1. Bachelor's degree or equivalent experience.
  2. 5+ years experience in business operations, contract management or related systems supporting these activities.
  3. Knowledge & experience in Icertis, Oracle, SAP and Ariba systems.
  4. Demonstrated organizational skills and time management with focus on processes, projects, and systems to efficiently meet business needs.
  5. Requires moderate direction to complete more complex tasks, complete routine tasks with little or no supervision.
  6. Excellent interpersonal and communication skills. Must be a team player and be willing to work in an environment where individual initiative, accountability to the team and professional maturity are required.

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