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| Senior Manufacturing Engineer Blue Signal Search Hammonton Upgrade your resume prior to applying with resumeandcareerservices.com. Our client manufactures and delivers top-notch packaging products and components nationwide. They are hiring a Senior Manufacturing Engineer to support manufacturing processes for a large plastic manufacturing plant. The Senior Manufacturing Engineer will lead process improvement, automation development, and product design. They will be responsible for project management and aiding the engineering operations team in delivering best-in-class production to support capital infrastructure projects. This Role Offers Competitive pay, plus comprehensive benefits including health/dental/vision, 401K matching, etc. Stable company with decades of experience developing and producing top of the line packing products. Lean, efficient manufacturing environment. High degree of freedom to refine operational and manufacturing processes. Company prioritizes sustainability efforts and environmental impact. Focus: Lead project management of capital projects, supporting engineering and design initiatives. Be involved in all stages of the product lifecycle from requirements to design, to development, to testing, and implementation. Design and implement highly scalable and reliable plastics molding processes and products. Automate manual processes and improve efficiency related to plant safety, equipment, production, and more. Write and participate in reviewing of specifications and validation plans. Assist with troubleshooting, risk management, and maintenance for injection molding processes. Maintain design standards and technical documentation across all manufacturing projects. Work with engineering and manufacturing teams to develop fixes for workflow problems and recurring issues. Leverage extensive technical knowledge of molding machines to create fluidity and excellence within the engineering function. Skill Set: 4 years of process engineering/manufacturing. Experience in healthcare, medical devices, plastics, and/or packaging industry, preferred. 4 years of experience in project management. BS in Engineering or related engineering field. PMP or Lean Six Sigma certifications, preferred. Background in injection molding environment, a plus. Proven success in troubleshooting issues and creating reactive process that get to the root cause of the issue and fix it. Knowledge of basic manufacturing standards, best practices, and equipment. Understanding of materials, tooling, and injection mold design procedures. Proficiency with ERP, IQMS, and Excel. Detail oriented with the ability to translate project requirements into actionable tasks. Strong interpersonal and communication skills and the ability to work effectively in a team environment with people of varying skills and backgrounds. 2023-02-05T02:15:09Z | |
| Full-Time Door Manufacturer 84 Lumber Company Egg Harbor Overview: The Door Shop Manufacturer is responsible for, but not limited to: Working on a Door Pre-hanging assembly line and keeping up on routine maintenance of equipment. Responsibilities: Using Power Saws, Air Nail Guns, Staplers and other tools needed to prep wood material used to assemble doors.Safely operate a forklift to assist in moving material to appropriate area of the shop.Pick and pull production material as needed.Load, unload, store and package material as needed.Maintain a clean and safe work environment and observe all safety rules posted. Qualifications: Ability to read and comprehend simple instructions, short correspondence and memos; write simple correspondence; effectively present information to others one-on-one.Ability to apply common sense understanding and carry out simple one or two-step instructions; deal with standardized situations with only occasional or no variables. 2023-02-06T19:34:48Z | |
| Director, Biologics Regulatory Chemistry, Manufacturing and Control Organon & Co Atlantic City Organon is a Women's Health Company that believes in a better and healthier every day for every woman We are a passionate, global community of thousands dedicated to redefining the future of women's health. Our mission is to deliver impactful medicines and solutions for a healthier every day. But what really makes it work at Organon is our people. We're looking for real, passionate team players, curious innovators, forward thinkers, empowered by the idea of shaping their career, and ready to bring their fire to embrace change and the opportunities it brings for progress. At Organon, you'll get to enjoy the best of both worlds: the open, agile, collaborative culture of a start-up, and operating at the scale of a Fortune 500 company with an international footprint that serves people in more than 140 markets. It's going to be an exciting future-come be a part of it Reporting to the Executive Director in Regulatory Chemistry, Manufacturing and Control (CMC), the candidate is responsible for developing and implementing Regulatory CMC strategies for assigned biological products in accordance with global regulations, guidance, and our Company's procedures. The candidate will lead the preparation and submission of CMC dossiers for original registrations, life-cycle maintenance submissions, and post-approval changes. The candidate may manage a small group of individual contributors and/or outsourcing partners in support of project execution. The candidate may also support project team goals and organizational initiatives on an as needed basis. OPEN to the Boston, MA to Washington DC area. Primary Responsibilities: Serve as the CMC Product Lead for assigned products and be accountable for the delivery of all regulatory milestones for assigned products through initial product registration and launch, and across the product's lifecycle. Lead the development and execution of global product and project regulatory strategy(ies) by ensuring robust assessment of CMC changes, identification of global regulatory requirements and critical evaluation of supporting documentation to confirm acceptability and identification of potential risks. Execute regulatory strategies by leading the development, authoring, and review of CMC submission components and documentation to support investigational new drug (IND)/clinical trial application (CTA) submissions, post-approval supplements, annual reports, registration renewals, and responses to health authority questions per established business processes and systems. Interact with relevant Health Authorities to support submissions, response to questions, and agency meetings. Identify, communicate, and escalate potential regulatory issues to our Company's Regulatory CMC management, and propose mitigation strategies, as needed. Collaborate with our Company's Manufacturing & Supply colleagues and external partners to support compliant execution of change management and conduct all activities with an unwavering focus on regulatory conformance. Demonstrate an understanding of regulatory affairs and apply this understanding to the benefit of the company to ensure approval and product supply continuity. Provide regulatory leadership as needed to product in-license/due diligence review, product divestment, and product withdrawal. May manage a small number of individual contributors or outsourced staff who are responsible for their products/projects. Education Minimum Requirement: Bachelor's Degree in a science, engineering, or a related scientific field. Fields of study include Chemistry, Biochemistry, Chemical Engineering, Biology, Pharmacy, Microbiology, Virology, or Molecular Biology with at least 10 years of relevant experience including biological research, manufacturing, quality or related field. OR Advanced degree (MS, MBA, Ph.D., PharmD) with at least 5 years of relevant experience including biological research, manufacturing, quality or a related scientific field. Required Experience and Skills: At least five (5) years of relevant regulatory CMC experience, including biological research, manufacturing, analytical testing, quality, or related fields. Technical writing experience for regulatory CMC submissions compliant with current CTD requirements including, new biologics license application BLA/marketing authorization application (MAA), IND/CTA, post-approval variations, Agency meeting briefing packages, and health authority queries. Proficient in relevant ICH guidelines and registration requirements. The candidate must be proficient in English; additional language skills are a plus. Develop CMC regulatory strategy to advance product development with track record of biologics product registration in major markets. Evaluation of subject matter expert (SME) technical documentation for completeness and sufficient details in order to make accurate regulatory assessments through utilization of current global regulatory guidelines. Proven experience in critically reviewing detailed scientific information to assess technical merits and suitability of scientific rationale to ensure information is presented clearly and conclusions are adequately supported by data. Demonstrated superior oral and written communication skills in multicultural settings and ability to communicate complex issues in a succinct and logical manner. Strong listening skills. Demonstrated sound understanding of related fields (e.g., manufacturing, analytical, quality assurance) and the ability to be creative and imaginative in the approach to new and diverse problem solving. Ability to lead communications with regulatory agencies to facilitate review and approval of submissions. Demonstrated ability to generate innovative solutions to complex regulatory problems and effectively work with and communicate to key stakeholders. Demonstrated flexibility in responding to changing priorities or dealing with unexpected events. Demonstrated effective leadership, communication, interpersonal, and negotiating skills. Ability to lead a team of direct or matrixed colleagues to deliver on business commitments and project timelines. Managing multiple projects to ensure on-time deliverables and timely submissions to ensure product supply continuity. Preferred Experience and Skills: Strong experience in developing global regulatory strategies for biological products. Strong technical leadership skills, as well as demonstrated understanding of related biological operations (e.g., biologics manufacturing and quality). Device and/or combination product regulatory. CMC Who We Are: Organon delivers ingenious health solutions that enable people to live their best lives. We are a $6.5 billion global healthcare company focused on making a world of difference for women, their families and the communities they care for. We have an important portfolio and are growing it by investing in the unmet needs of Women's Health, expanding access to leading biosimilars and touching lives with a diverse and trusted portfolio of health solutions. Our Vision is clear: A better and healthier every day for every woman. Subject to applicable law, all prospective US Organon hires will be required to demonstrate that they have been fully vaccinated against COVID-19 with a vaccine authorized or approved by the Food and Drug Administration (FDA), or qualify for a medical or religious accommodation to this vaccination requirement, as a precondition of employment. Residents of Colorado: to request this role's pay range: email: coloradopayactorganon.com Jersey City, New York City, Washington State & California Positions: to request this role's pay range and benefits, email: jcnycpayorganon.com US and PR Residents Only If you require reasonable accommodation(s) in completing an application, interviewing, or otherwise participating in the employee selection process, please email us at staffingaadarorganon.com. For more information about personal rights under Equal Employment Opportunity, visit: EEOC Poster EEOC GINA Supplement OFCCP EEO Supplement OFCCP Pay Transparency Rule Organon is an equal opportunity employer, Minority/Female/Disability/Veteran - proudly embracing diversity in all of its manifestations. Search Firm Representatives Please Read Carefully Organon LLC., does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Regular Relocation: Domestic VISA Sponsorship: Yes Travel Requirements: 10% Flexible Work Arrangements: Telecommuting Shift: 1st - Day Valid Driving License: No Hazardous Material(s): Number of Openings: 1 2022-12-21T14:09:06Z | |
| Director, Biologics Regulatory Chemistry, Manufacturing and Control Organon & Co. Atlantic City Job Description Organon is a Women's Health Company that believes in a better and healthier every day for every woman We are a passionate, global community of thousands dedicated to redefining the future of women's health. Our mission is to deliver impactful medicines and solutions for a healthier every day. But what really makes it work at Organon is our people. We're looking for real, passionate team players, curious innovators, forward thinkers, empowered by the idea of shaping their career, and ready to bring their fire to embrace change and the opportunities it brings for progress. At Organon, you'll get to enjoy the best of both worlds: the open, agile, collaborative culture of a start-up, and operating at the scale of a Fortune 500 company with an international footprint that serves people in more than 140 markets. It's going to be an exciting future-come be a part of it Reporting to the Executive Director in Regulatory Chemistry, Manufacturing and Control (CMC), the candidate is responsible for developing and implementing Regulatory CMC strategies for assigned biological products in accordance with global regulations, guidance, and our Company's procedures. The candidate will lead the preparation and submission of CMC dossiers for original registrations, life-cycle maintenance submissions, and post-approval changes. The candidate may manage a small group of individual contributors and/or outsourcing partners in support of project execution. The candidate may also support project team goals and organizational initiatives on an as needed basis. OPEN to the Boston, MA to Washington DC area. Primary Responsibilities: - Serve as the CMC Product Lead for assigned products and be accountable for the delivery of all regulatory milestones for assigned products through initial product registration and launch, and across the product's lifecycle.? - Lead the development and execution of global product and project regulatory strategy(ies) by ensuring robust assessment of CMC changes, identification of global regulatory requirements and critical evaluation of supporting documentation to confirm acceptability and identification of potential risks. - Execute regulatory strategies by leading the development, authoring, and review of CMC submission components and documentation to support investigational new drug (IND)/clinical trial application (CTA) submissions, post-approval supplements, annual reports, registration renewals, and responses to health authority questions per established business processes and systems. - Interact with relevant Health Authorities to support submissions, response to questions, and agency meetings. - Identify, communicate, andescalate potential regulatory issues to our Company's Regulatory CMC management, and propose mitigation strategies, as needed. - Collaborate with our Company's Manufacturing & Supply colleagues and external partners to support compliant execution of change management and conduct all activities with an unwavering focus on regulatory conformance. - Demonstrate an understanding of regulatory affairs and apply this understanding to the benefit of the company to ensure approval and product supply continuity. - Provide regulatory leadership as needed to product in-license/due diligence review, product divestment, and product withdrawal. - May manage a small number of individual contributors or outsourced staff who are responsible for their products/projects. Education Minimum Requirement: - Bachelor's Degree in a science, engineering,?or a related scientific field.?? Fields of study include?Chemistry, Biochemistry, Chemical Engineering,?Biology, Pharmacy, Microbiology, Virology, or Molecular Biology with at least 10 years of relevant experience including biological research, manufacturing, quality or related field. - OR Advanced degree (MS, MBA, Ph.D., PharmD) with at least 5 years of relevant experience including biological research, manufacturing, quality or a related scientific field. Required Experience and Skills: - At least five (5) years of relevant regulatory CMC experience, including biological research, manufacturing, analytical testing, quality, or related fields. - Technical writing experience for regulatory CMC submissions compliant with current CTD requirements including, new biologics license application BLA/marketing authorization application (MAA), IND/CTA, post-approval variations, Agency meeting briefing packages, and health authority queries. - Proficient in relevant ICH guidelines and registration requirements. - The candidate must be proficient in English; additional language skills are a plus. - Develop CMC regulatory strategy to advance product development with track record of biologics product registration in major markets. - Evaluation of subject matter expert (SME) technical documentation for completeness and sufficient details in order to make accurate regulatory assessments through utilization of current global regulatory guidelines. - Proven experience in critically reviewing detailed scientific information to assess technical merits and suitability of scientific rationale to ensure information is presented clearly and conclusions are adequately supported by data. - Demonstrated superior oral and written communication skills in multicultural settings and ability to communicate complex issues in a succinct and logical manner.? Strong listening skills. - Demonstrated sound understanding of related fields (e.g., manufacturing, analytical, quality assurance) and the ability to be creative and imaginative in the approach to new and diverse problem solving. - Ability to lead communications with regulatory agencies to facilitate review and approval of submissions. - Demonstrated ability to generate?innovative solutions to complex regulatory problems and effectively work with and communicate to key stakeholders. - Demonstrated flexibility in responding to changing priorities or dealing with unexpected events. - Demonstrated effective leadership, communication, interpersonal, and negotiating skills.? - Ability to lead a team of direct or matrixed colleagues to deliver on business commitments and project timelines. - Managing multiple projects to ensure on-time deliverables and timely submissions to ensure product supply continuity. Preferred Experience and Skills: - Strong experience in developing global regulatory strategies for biological products. - Strong technical leadership skills, as well as demonstrated understanding of related biological operations (e.g., biologics manufacturing and quality). - Device and/or combination product regulatory. CMC Who We Are: Organon delivers ingenious health solutions that enable people to live their best lives. We are a $6.5 billion global healthcare company focused on making a world of difference for women, their families and the communities they care for. We have an important portfolio and are growing it by investing in the unmet needs of Women's Health, expanding access to leading biosimilars and touching lives with a diverse and trusted portfolio of health solutions. Our Vision is clear: A better and healthier every day for every woman. Subject to applicable law, all prospective US Organon hires will be required to demonstrate that they have been fully vaccinated against COVID-19 with a vaccine authorized or approved by the Food and Drug Administration (FDA), or qualify for a medical or religious accommodation to this vaccination requirement, as a precondition of employment. Residents of Colorado: to request this role's pay range: email: coloradopayactorganon.com Jersey City, New York City, Washington State & California Positions: to request this role's pay range and benefits, email: jcnycpayorganon.com US and PR Residents Only If you require reasonable accommodation(s) in completing an application, interviewing, or otherwise participating in the employee selection process, please email us at staffingaadarorganon.com . For more information about personal rights under Equal Employment Opportunity, visit: EEOC Poster EEOC GINA Supplement OFCCP EEO Supplement OFCCP Pay Transparency Rule Organon is an equal opportunity employer, Minority/Female/Disability/Veteran - proudly embracing diversity in all of its manifestations. Search Firm Representatives Please Read Carefully Organon LLC., does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Regular Relocation: Domestic VISA Sponsorship: Yes Travel Requirements: 10% Flexible Work Arrangements: Telecommuting Shift: 1st - Day Valid Driving License: No Hazardous Material(s): Number of Openings: 1 Requisition ID: R514260 2022-11-03T17:33:30Z | |
| PRICING ANALYST Confidential Vineland Description: The Pricing Analyst is responsible for managing product pricing. This will include ensuring timely updating of the monthly price lists and all associated master data. This individual will generate pricing reports/analytics/tools in an effort to monitor, control and/or improve pricing policies and profitability (includes but is not limited to pricing KPIs, price erosion, quote conversion & quote compliance). In conjunction with the Sales team, the individual will assist in the analysis and evaluation of product pricing. Principle Duties & Responsibilities: Manage annual updates to standardized price lists and other pricing tools. Track and coordinate annual price increases by customer The role of this position is to work up the price quote using various pricing tools unique to each area of the business. Maintain pricing master data in ERP system Monthly analysis of outbound freight. Coordinate and manage monthly customer/item profitability review Knowledge, Skills, and Abilities A Bachelor's degree in Business Administration, Marketing or Economics or related field is required. An MBA is preferred. A minimum 2-3 years analytical experience, preferably in a food manufacturing environment or in a pricing department is required. Experience in either sales or marketing discipline in addition to pricing a plus for the added perspective. Experience working with cross-functional groups is preferred. Proficiency in Microsoft Excel is required. A self-starter with the ability to work independently as needed. PI202393198 2023-01-31T06:07:31Z | |
| Sanitation Manager The Judge Group Vineland Location: Vineland, NJ Salary: $80,000.00 USD Annually - $100,000.00 USD Annually Description: Our food manufacturing client is currently seeking a Sanitation Manager for their plant in Vineland, NJ. This position directs and manages the overall housekeeping and sanitation of food contact areas and manufacturing equipment to ensure compliance to required standards for cleanliness at the plant. Assures quality and safety while achieving established goals and objectives. Responsibilities: Promotes integrity, respect, accountability, continuous improvement and positive interactions with all Team Members, customers & vendors. Directs and supervises sanitation employees. Coordinates the master sanitation schedule/program for all processing and packaging equipment and storage vessels in accordance with company and FDA standards. Responsible for meeting established sanitation objectives and controls and minimizes the overtime labor costs, maintenance / repair costs and equipment downtime. Works with HR for hiring, training and scheduling of production work force. Responsible for and coordinates shift activities through planning and communication with employees to ensure all sanitation objectives are accomplished in a timely, cost-effective and safe manner. Ensures scheduling of the sanitation department. Compiles required sanitation reporting accurately and timely. Maintains close working relationship with all departments and responds to deviations from standards immediately. Monitors CIP equipment to ensure proper operation by shift personnel. Monitors the usage & storage of all cleaning/sanitizing chemicals and agents to ensure compliance to safety requirements & no unauthorized access or usage occurs. Coordinates with department managers and shift supervisors to ensure a trouble-free shift start-up. Responsible for & maintains positive employee, corporate and community relations along with appropriate interface with customer service, vendors & contractors. Regular Attendance is required in accordance with Company attendance policy and procedures. Performs tasks or responsibilities as assigned by Management. Complete initial/annual training to ensure the individual is properly qualified (QI) to perform all required job tasks as outlined in training programs/records. Qualifications: 3-5 years of management or high level supervisory experience in a food manufacturing plant preferably a union manufacturing environment, Associates degree in business or equivalent experience/training in CIP systems and chemical usage. Working knowledge of sanitation equipment, methods and chemicals. 2-3 years production/group leader experience in a manufacturing environment, preferably in a food-related industry. Working knowledge of scheduling and production processes. Contact: apattjudge.com This job and many more are available through The Judge Group. Find us on the web at www.judge.com 2023-01-28T16:20:20Z | |
| Manager - Sanitation Rich Products Corporation Vineland Rich's, also known as Rich Products Corporation, is a family-owned food company dedicated to inspiring possibilities. From cakes and icings to pizza, appetizers and specialty toppings, our products are used in homes, restaurants and bakeries around the world. Beyond great food, our customers also gain insights to help them stay competitive, no matter their size. Our portfolio includes creative solutions geared at helping food industry professionals compete in foodservice, retail, in-store bakery, deli, and prepared foods, among others. Working in 100 locations globally, with annual sales exceeding $4 billion, Rich's is a global leader with a focus on everything that family makes possible. Rich's-Infinite Possibilities. One Family. PURPOSE STATEMENT The Sanitation Manager manages all plant units responsible for monitoring and ensuring proper sanitation throughout the facility and meets all regulatory requirements. Also recommends improvements in manufacturing methods and sanitation practices to management. In addition to developing and implementing short-term and mid-term business plans for department, and assists in the development of the strategic plan for the plant and meets all regulatory requirements. KEY ACCOUNTABILITIES/OUTCOMES Plans, manages and directs plant sanitation procedures, programs and regulatory requirements, ensuring all plant equipment is clean and safe for production. Ensures compliance with all standard operating procedures. Develops, implements and communicates short-term and mid-term (1 - 2 years) business plans for the operations, ensuring associates understand the link to the plant's, division's and the corporation's business plans and understand their role in accomplishing these plans. Assists in establishing the longer-term strategic plans for the plant. Develops operating policies and procedures as necessary. Oversees the tailoring and documenting of plant procedures related to approved cleaning chemicals and cleaning schedules. Mentors and motivates associates, providing training and development to optimize their performance and personal growth. Communicates performance standards to associates, recognizing and rewarding individual and team accomplishments and counseling performance problems. Ensures all associates have the resources and capabilities to effectively accomplish their responsibilities. May serve as a member of the plant's Steering Team. Monitors rodent and insect control program, including periodically checking weekly rodent reports and traps. Monitors microbiological reports from the plant to determine whether cleaning procedures are being followed.Implements corrective action as necessary. Participates in regular meetings with plant management to discuss quality and sanitationimprovements.Facilitates problem resolution related to sanitation and quality issues. Develops, maintains and reports required operational information to management. Ensures that all GMP and Safety standards are in compliance. Participates in weekly GMP, sanitation and safety inspections throughout the production departments and corrects, or issues work orders to correct, any identified deficiencies. Follows up on work orders, with the appropriate Associates to ensure expeditious performance of the requested work. Keeps abreast of latest manufacturing technologies, systems, and sanitation practices. Performs other related responsibilities, as needed, to support Rich Products Corporation's business objectives. KNOWLEDGE/SKILLS/EXPERIENCE BA/BS degree in Business, Supply Chain Operations, Food Science, Engineering or related field 5 years supervisory experience in a food-processing, pharmaceutical or chemical manufacturing organization, preferably using computerized manufacturing equipment Working knowledge of FDA regulations, Good Manufacturing Practices (GMPs), sanitation processes/procedures and HACCP Demonstrated understanding of production scheduling and other production variables such as run-rates, processing times, change-over times, etc. Demonstrated knowledge of efficient and safe manufacturing operations to include product and associate safety, OSHA standards, product quality (success rates), throughput delivery and cost control (minimizing downtime and waste, optimizing yield) Demonstrated ability to direct, coach, and train associates as well as plan, monitor and schedule work Demonstrated ability to analyze and resolve problems Demonstrated mechanical and spatial aptitude, including the ability to disassemble and reassemble equipment Demonstrated ability to formulate and understand complex mathematical equations Proficient using Excel or other spreadsheet software Rich Products Corporation, its subsidiaries and affiliates ("Rich's"), are committed to a policy of Equal Employment Opportunity and will not discriminate against an applicant or employee on the basis of race, color, religion, creed, national origin or ancestry, sex, age, physical or mental disability, veteran or military status, genetic information, gender identity, sexual orientation, marital status or any other legally recognized protected basis under federal, state, or local law. The information collected by this application is solely to determine suitability for employment, verify identity, and maintain employment statistics on applicants. Applicants with disabilities may be entitled to reasonable accommodation under the Americans with Disabilities Act and certain state or local laws. A reasonable accommodation is a change in the way things are normally done which will ensure an equal employment opportunity without imposing undue hardship on Rich's. Please contact Rich's Human Resources department at ascrich.comif you need assistance completing this application or to otherwise participate in the application process. PDN-9841e83d-79bc-43cd-86a1-c87a0a3f56e8 2023-02-07T02:20:46Z | |
| Cybersecurity Operation Technology Engineer Job Juncture Vineland We have an opening in Cybersecurity for an Operation Technology Engineer in southern New Jersey (about an hour south of Philadelphia, PA) with a global manufacturing company This is a permanent position with full benefits starting minute one day one including unlimited PTO and relocation, if needed. You will have multi-plant responsibility for a food plant in New Jersey, Pennsylvania and Florida. Operations Technology Engineer (OTE) will be the single point of contact (SPOC) for deploying OT strategy in a manufacturing plant and work as a liaison between plant operations and the central automation team. OTE will maximize the availability of industrial automation systems (Hardware, Network, Scada Software, Database, Integration of new components and solutions) and use cybersecurity tools (Claroty, Factory Talk Security, Factory Talk Asset Center) for threat mitigation and unauthorized access to industrial control systems. Job Specifications: Troubleshoot and resolve complex, ambiguous issues and escalate when necessary Project Management related to industrial networking, applications upgrade / deployments Industrial Automation Asset Management using Claotry / SolarWinds Management of vendor access in PLC and Scada application Continuous improvement of Cybersecurity KPI (Vulnerability mitigation, threat detection, access management) Maintain and update industrial automation architecture Industrial automation hardware and software life cycle management Organize windows patch install in industrial automation servers and workstations with the Americas server infrastructure team Master plan development for industrial networking and industrial applications roadmap Share knowledge and learnings through company North America networking Enforce company North America automation standards / specifications Identify opportunities to evolve applications by proposing improvement actions to the Manager to satisfy business needs according to OT and IT standards Identify and communicate breakdowns and gaps in performance with respective personnel / systems Facilitate meetings regarding continuous improvement of system performance Experience Requirement: 5-7 years of job experience in operations technology Educational Requirement: Bachelor’s degree in Computer Science/ Information Technology/Management Information system or any related field Minimum of 5 years of experience in food manufacturing related to information systems and automation technologies OR minimum of 10 years of experience in food manufacturing related to information systems and automation technologies in lieu of degree Knowledge, Skills and Abilities Experience and working knowledge in plant wide automation network design Experience and working knowledge in logic controller communications Experience and working knowledge of Allen Bradley/ Rockwell PLC programming Experience and working knowledge in Industrial networking Experience and working knowledge in Auto Cad and Microsoft Visio Experience and working knowledge of the following distributed Scada systems such as Inductive Automation’s Ignition Platform, Wonderware System platform, Factory Talk View SE Experience and working knowledge in Microsoft Office suite and windows operating system Must be highly self-directed and able to work independently as well as part of a team. Must be organized and self-disciplined to accommodate the management of concurrent multiple projects. Excellent conflict resolution and interpersonal skills. Experience in IT and OT network segregation using Purdue model Fast learner, open to learn new things (attending training & certification related to the role as needed) and adapts to change Certificates, Licenses, Registrations ISA/IES 62443 Cybersecurity Certification is a plus 2023-01-28T16:22:10Z | |
| Process Technician II - Sign On Bonus Comar Buena PROCESS TECHNICIAN II Actively Hiring – Immediate Openings Hours: full-time position. Competitive pay & benefits: paid overtime, health, dental, vision, paid time off, 401k with match…and more “Come Build your Career in our Growing, Fast-Paced, Customer-Focused Company that fosters Training & Professional Development” WHAT YOU WILL DO: “Quality & Safety are Top Comar Priorities” Set up molds and establish process parameters in various molding machines using established documentation, tools, quality, and production concepts in accordance with established safety procedures. Startup machines to produce quality product within validated molding processes. Operate Injection Molding machines and auxiliary equipment to manufacture product which conforms to quality specifications, at the rated output. Perform and maintain safe and efficient tool and machine set-up, operation, and process capabilities to meet customer on-time delivery and quality expectations. Perform startups including completion of all required quality management system documentation. Troubleshoot quality/part issues by confirming plastic conditions and performing root cause analysis to determine true root cause solutions. Verify process parameters prior to start up and assure process is running to validated parameters. Identify machine problems and communicate to maintenance as required. Resolve basic mold issues and/or secondary packing equipment issues. Work with other molding team members to keep equipment running during breaks and callouts. Perform thorough product inspections and make appropriate decisions relative to product quality requirements. Work flexible shifts and overtime as needed and maintain reliable attendance. Maintain a clean and safe work environment. Adhere to and communicate to others all plant Health, Safety and Quality guidelines and GMP. Safety and Cleanliness “We have put in place Covid-19 practices for our employees’ safety” Adhere to safety policies. Maintain a clean and safe work area and report any unsafe conditions to supervisor. Wear company issued personal protective equipment (PPE) such as uniforms, gloves, masks, hairnets. WHO WE ARE LOOKING FOR: “A Comar employee who will represent the customer and be the consumer’s advocate” Are You…? A High School, Vo-Tech, or equivalent graduate with a minimum of 2 years related experience as a Manufacturing Production Operator III or Set Up Mechanic. Proficient in basic computer use with the ability learn and use new systems quickly and efficiently. Knowledge of raw materials and product quality specifications. Proficient producing product with molds, mold, and packaging equipment. Proficient with controlled documents (Work Instructions, Forms, Standard Operating Procedures, Safety & Quality specifications, etc.), preventative maintenance task lists and equipment manuals which pertain to operation of equipment. An understanding of continuous improvement, six sigma or lean manufacturing concepts. Preferred: Vocational or trade school in related trade. Pursuing RJG certification. Two (2) years of experience working in a manufacturing environment using Injection or Extrusion Blow Molding mold machines. Do You…? Good time management, organizational and communication skills to work independently and also in a team environment. Self-motivated, conscientious, with a results-oriented mindset. Ability to read and follow verbal and written instructions; write simple correspondence. Ability to operate in the Enterprise Resource Planning system, IQMS and accurately enter production data and complete production forms (batch record). Strong basic math skills with the ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, percentages, and decimals. Ability to use measuring devices such as Comparator, Dial indicator, Go/No Go gauges. Use Quality Control instruments such as calipers, gram scales and magna mike. Ability to work in a fast-paced manufacturing environment with demonstrated ability to handle and prioritize multiple tasks and demands. Strong technical aptitude, as well as analytical and problem-solving skills. Sound judgment - ability to work efficiently with many competing demands. Effectively present information in one-on-one and small group situations to customers, clients, and other employees of the organization. Do you Enjoy Physical Work where you will…? Stand for most of the work shift. Use hands and fingers to handle or feel; reach with hands and arms; stoop, crouch, bend, twist, and only occasionally sit. Lift and/or move up to 10 pounds. Heavier amounts can be moved with assistance of equipment. If YES , don't delay, Apply Today CB 2023-01-28T16:25:01Z | |
| Cybersecurity Operations Technology Engineer Job Juncture Vineland Job description: We have an opening in Cybersecurity for an Operation Technology Engineer in southern New Jersey (about an hour south of Philadelphia, PA) with a global manufacturing company This is a permanent position with full benefits starting minute one day one including unlimited PTO and relocation, if needed. You will have multi-plant responsibility for a food plant in New Jersey, Pennsylvania and Florida. Operations Technology Engineer (OTE) will be the single point of contact (SPOC) for deploying OT strategy in a manufacturing plant and work as a liaison between plant operations and the central automation team. OTE will maximize the availability of industrial automation systems (Hardware, Network, Scada Software, Database, Integration of new components and solutions) and use cybersecurity tools (Claroty, Factory Talk Security, Factory Talk Asset Center) for threat mitigation and unauthorized access to industrial control systems. Job Specifications: Troubleshoot and resolve complex, ambiguous issues and escalate when necessary Project Management related to industrial networking, applications upgrade / deployments Industrial Automation Asset Management using Claotry / SolarWinds Management of vendor access in PLC and Scada application Continuous improvement of Cybersecurity KPI (Vulnerability mitigation, threat detection, access management) Maintain and update industrial automation architecture Industrial automation hardware and software life cycle management Organize windows patch install in industrial automation servers and workstations with the Americas server infrastructure team Master plan development for industrial networking and industrial applications roadmap Share knowledge and learnings through company North America networking Enforce company North America automation standards / specifications Identify opportunities to evolve applications by proposing improvement actions to the Manager to satisfy business needs according to OT and IT standards Identify and communicate breakdowns and gaps in performance with respective personnel / systems Facilitate meetings regarding continuous improvement of system performance Qualifications: Experience Requirement: 5-7 years of job experience in operations technology Educational Requirement: Bachelors degree in Computer Science/ Information Technology/Management Information system or any related field Minimum of 5 years of experience in food manufacturing related to information systems and automation technologies OR minimum of 10 years of experience in food manufacturing related to information systems and automation technologies in lieu of degree Knowledge, Skills and Abilities Experience and working knowledge in plant wide automation network design Experience and working knowledge in logic controller communications Experience and working knowledge of Allen Bradley/ Rockwell PLC programming Experience and working knowledge in Industrial networking Experience and working knowledge in Auto Cad and Microsoft Visio Experience and working knowledge of the following distributed Scada systems such as Inductive Automations Ignition Platform, Wonderware System platform, Factory Talk View SE Experience and working knowledge in Microsoft Office suite and windows operating system Must be highly self-directed and able to work independently as well as part of a team. Must be organized and self-disciplined to accommodate the management of concurrent multiple projects. Excellent conflict resolution and interpersonal skills. Experience in IT and OT network segregation using Purdue model Fast learner, open to learn new things (attending training & certification related to the role as needed) and adapts to change Certificates, Licenses, Registrations ISA/IES 62443 Cybersecurity Certification is a plus Why is This a Great Opportunity: Relocation Paid for by company & unlimited Paid Time Off Policy with health & 401K etc. benefits starting minute day one. Salary Type : Annual Salary Salary Min : 110000 Salary Max : 125000 Currency Type : US Dollars 2023-01-17T16:02:05Z |
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