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<h3>Job Description</h3>
Job DescriptionDescription:
Job Title: Mechanical Engineer Reports To: Director of Engineering
Classification: Exempt Pay Range: Min $73,615- Max $126,500
 
Job Summary:
The Mechanical Engineer position is quite varied with regard to the scope of work performed. Workers who are designated as a Mechanical Engineer may also be tasked with other general work tasks not specifically covered under the Mechanical Engineer job description. Tasks may include the following but are not limited to; as job duties may change throughout day depending on the workload. 
 
Essential Functions of Position:
<ul>
<li>Provide technical support in the form of design calculations and adherence to project specifications, codes, and standards.</li>
<li>Create and revise CAD drawings, and models for project approval and in-house fabrication.</li>
<li>Developing, initiating, monitoring, and influencing all aspects of an order/project. </li>
<li>Maintain, document, and communicate project schedules.</li>
<li>Communicate daily with customers. </li>
<li>Collaborate with multi-disciplinary engineering teams, and work with vendors and contractors.</li>
<li>Perform detailed documentation to track project development and design process.</li>
<li>Perform other duties as assigned.</li>
</ul>
Physical Requirements: 
· Required to sit, stand, and walk; for up to 8 hours per day.
· Continuous use of the hand, arm, and fingers to operate a computer keyboard, telephone, and other office equipment.
· Ability to lift up to 20 pounds occasionally.
· Ability to communicate professionally, in written and oral communications. 
Requirements:
Minimum Qualifications:
<ul>
<li>CAD experience </li>
<li>Associates degree in relevant field with related work experience. Bachelor’s degree preferred.</li>
<li>Knowledge of how mechanical systems and processes work.</li>
<li>Comfortable working in a fast-paced environment.</li>
<li>Exceptional organizational and time management skills</li>
<li>Excellence in verbal and written communication and ability to work as part of a team.</li>
</ul>
 
Preferred Qualifications:
· Bachelor’s in mechanical engineering
· 3-5 years in a manufacturing environment completing Engineering design work

Mechanical Engineer

<h3>Job Description</h3>
Job DescriptionJob Summary: The Packaging Designer is responsible for creating innovative, functional, and aesthetically appealing packaging solutions for a variety of products within the accessories division (legwear, bodywear, bags, hats) that ensure alignment with brand identity, consumer expectations, regulatory standards, and production requirements. This role involves working in a fast-paced environment on both the creative and technical sides of packaging to achieve company goals and enhance customer experience. Essential Functions (Including but not limited to): 
<ul>
<li>Create and design packaging for a variety of brands and product categories; bellybands, hangtags, boxes, and more.</li>
<li>Ensure packaging for each program reflect the design direction, brand’s identity, and customer/distribution requirements.</li>
<li>Create conceptual design boards and appealing presentations for internal teams (design, sales) and external partners (brands, customers).</li>
<li>Digital and physical packaging submissions to the license and/or customer for approvals.</li>
<li>Packaging development with multiple factories; detailed layout review, cost and lead time comparison, and sample execution to establish approved color and quality standards.</li>
<li>Prepare artwork, dielines, mockups, technical files, and production-ready assets for manufacturing.</li>
<li>Work with suppliers and vendors to ensure that packaging is produced to specification and within the required timelines.</li>
<li>Ensure packaging meets both aesthetic and functional standards before mass production.</li>
</ul>
Perform any other duties as assigned in support of the company needs and operations. Qualifications/Requirements:
<ul>
<li>Bachelor’s degree in design or related area and some work experience in the design industry.</li>
<li>Highly proficient in MAC OS, Adobe Illustrator and Photoshop </li>
<li>Experience in Graphic and Packaging Design and Development</li>
<li>High creativity and artistic abilities with keen attention to detail and ability to visualize in three dimensions.</li>
<li>Proficient computer skills to include Adobe Suite programs and Microsoft Office (Excel and Word).</li>
<li>Strong organizational skills that reflect ability to perform and prioritize multiple tasks and workload efficiently and seamlessly and follow-up. </li>
<li>Excellent written and verbal skills as required for effective interpersonal communication. </li>
<li>Ability to work independently and collaboratively with a team under critical time frames. </li>
</ul>
Self-driven and experience working in a fast-paced environment and ability to apply good work habits to effectively complete assigned tasks and contribute to the smooth operation of the company/department. Physical Demands and Working Conditions: The physical demands and working conditions of this position are representative of what must be met to successfully perform the essential functions of the position. Reasonable accommodations may be made to enable an individual with disabilities to perform the essential functions. The functions of this position are typically performed in an office setting and the noise level in the work environment is usually quiet to moderate.While performing the duties of this position, the employee is regularly required to sit; use hands to finger, handle, or feel; reach with hands and arms and talk or hear. The employee is frequently required to walk. The employee is occasionally required to stand and stoop, kneel, crouch, or crawl. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this position include close vision and distance vision. General Acknowledgement &amp; Employment At-Will: Employment in this position requires adherence to all policies and procedures set forth by United Legwear &amp; Apparel Company. This position description is not an exhaustive list of all duties and responsibilities of the position, is not a contract and is subject to change at any time, with or without notice, by the employer. Furthermore, all employees are employed at-will with United Legwear &amp; Apparel Company and are employed for no definite period of time and employment may be terminated without cause or notice.
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Packaging Designer

<h3>Job Description</h3>
Job Description
Company Overview:
GTI specializes in the design, engineering, fabrication, and deployment of custom modular structures, shipping container-based structures, and ballistic metal fabrication. We serve multiple industries, including DOD contractors, military, disaster relief, and commercial markets. Our containerized and modular solutions are all built in-house at our factory in Buffalo, NY. Manufacturing capabilities range from military training, live fire enclosures, bathroom/shower units, expeditionary camps, medical facilities, water treatment, electrical/energy storage enclosures, and much more. 
The GTI team consists of professionals spanning from fabrication and engineering to government and military specialists. Our combination of expertise allows us to provide top quality solutions and customer service for various industries and missions.
The QC Technician is responsible for the inspection and testing of materials and finished products at various stages of the manufacturing process to ensure they comply with all applicable laws, industry codes &amp; standards, as well as Company and Customer specifications/standards.
This is a 2nd shift position with a standard schedule of Monday-Friday, 3:30pm-12:00am
Job Responsibilities:
<ul>
<li>Develop and maintain inspection reports.</li>
<li>Ensure compliance with federal and state laws, as well as company standards and specifications.</li>
<li>Maintain calibration of quality control equipment.</li>
<li>Perform inspections across all stages of production.</li>
<li>Prepare and maintain test data for review.</li>
<li>Evaluate data and draft reports, noting any relevant deviations from existing standards.</li>
<li>Identify areas for quality control improvement and implement new methods accordingly.</li>
<li>Communicate quality or compliance concerns with urgency.</li>
<li>Other duties as assigned by the QA Manager.</li>
</ul>
Required Qualifications:
<ul>
<li>High school diploma or general education degree (GED) required.</li>
<li>Solid understanding of measuring, inspection and test equipment.</li>
<li>Minimum of 2-5 years of inspection and/or production experience in the metals fabrication industry.</li>
<li>Visual weld and welding inspection experience.</li>
<li>Proficiency with Microsoft Office programs, specifically Excel.</li>
<li>Strong working knowledge of various mathematical concepts including fractions, ratios, and proportions.</li>
<li>Ability to lift and/or move up to 50 pounds occasionally.</li>
<li>Specific vision abilities required include close vision, color vision, and the ability to adjust focus. (minimum required visual acuity - 20/20 corrected or uncorrected)</li>
<li>Demonstrated ability to work independently with minimal supervision.</li>
<li>Excellent organizational skills.</li>
<li>Demonstrated ability to analyze and interpret information.</li>
<li>Ability to read and interpret mechanical, electrical, and fabrication drawings.</li>
</ul>
Preferred Qualifications:
<ul>
<li>Associate or bachelor’s Degree in a related field.</li>
<li>AWS Certified Welding Inspector - CWI.</li>
</ul>
 
GrowTech Industries, LLC is committed to equal opportunity for all, without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, or any other protected characteristic.

Quality Control Technician - 2nd Shift

<h3>Job Description</h3>
Job Description
Albany Fire Extinguisher, an established and growing sales &amp; service company with a 70 plus year history in the Capital Region, is seeking reliable and motivated individuals to assist in servicing our ever-growing customer base. Both shop and field technician positions available. No experience necessary. Our in-depth training program will teach you all you need to know to excel in our field! Do you have what it takes to join our team? We offer consistent Monday through Friday schedules, no nights or weekends, a 401K retirement plan with a generous company match, paid vacations and paid holidays! Salary ranges from $16.00 - $25.00 per hour commensurate with experience.

Fire Extinguisher & Suppression Systems Technician

<h3>Job Description</h3>
Job Description
Ultralife Corporation is a leading provider of advanced, highest quality products and services ranging from power solutions to communications and electronics systems to customers across the globe in the government &amp; defense, medical, safety &amp; security, energy, industrial and robotics sectors.
We are a global business with strategic locations in the Americas, Europe, and Asia, ideally positioned to service global customers.
The Quality Director will serve a key role in the Battery &amp; Energy Products (B&amp;EP) organization by leading teams and successfully developing, implementing, maintaining and continuously improving, effective quality systems. The position requires a proven, natural leader, with solid manufacturing/engineering experience, who can demonstrate the ability to collaborate in a pro-active, hands-on manner across the organization. This position is the QMS representative for the B&amp;EP organization and is responsible for regulatory responsibilities for the United Nations, DOT, UL, IEC, Reach, RoHs, EUMDR, etc. 
ULBI is a government contractor therefore this position requires the individual to be a US citizen. 
<ul>
<li>Provide day-to-day direction, coaching, development and performance appraisal for quality team.</li>
<li>Establish, publish and communicate goals, objectives, policies and procedures pertaining to quality assurance.</li>
<li>Develop department budget and control all quality and electrical test lab related expenses to meet approved budget.</li>
<li>As QMS representative, monitor and report on the performance of the quality management system; facilitate senior management reviews of QMS.</li>
<li>Lead teams and drive success by developing, implementing, maintaining and continually improving, effective quality systems.</li>
<li>Support the design, qualification and ensure ongoing manufacturing of products that meet or exceed internal, customer, regulatory and other applicable requirements.</li>
<li>Coordinate external QMS registration and surveillance audits to ensure continuing registration to applicable ISO standards.</li>
<li>Represent Quality Department during customer, regulatory and 3rd-party audits of manufacturing operations and the QMS.</li>
<li>Process owner for Control of Records in accordance with QAP19, QAP51; Customer Property in accordance with QAP13, QAP31; Reporting to Regulatory Authorities in accordance with QAP35, QAP44, QAP49; Internal Audit in accordance with QAP20; Monitoring and Measurement of Processes in accordance with QAP48; Control of Non-Conforming Product in accordance with QAP15, QAP17, QAP44; Analysis of Data in accordance with QAP48; Document Control in accordance with QAP04 and Corrective Action in accordance with QAP16.</li>
<li>Establish, publish and communicate goals, objectives, policies and procedures pertaining to quality assurance and electrical test lab operations.</li>
<li>Develop department budget and control all quality and electrical test lab related expenses to meet approved budget.</li>
<li>As QMS representative, monitor and report on the performance of the quality management system; facilitate senior management reviews of QMS.</li>
<li>Lead teams and drive success by developing, implementing, maintaining and continually improving, effective quality systems.</li>
<li>Support the design, qualification and ensure ongoing manufacturing of products that meet or exceed internal, customer, regulatory and other applicable requirements.</li>
<li>Coordinate external QMS registration and surveillance audits to ensure continuing registration to applicable ISO standards.</li>
<li>Represent Quality Department during customer, regulatory and 3rd-party audits of manufacturing operations and the QMS.</li>
<li>Fulfill the Quality Department responsibilities for customer complaint investigation and response through the Return Material Authorization (RMA) process. Collaborate with manufacturing, product and quality engineers on failure analyses. Coordinate with Sales and senior management on customer communications.</li>
<li>Manage corrective and preventive action processes and maintain CAR and PAR status report, records and supporting documents.</li>
<li>Assumes overall responsibility and compliance for; performance score cards, quality management, and surveys. Including joint responsibility for REACH, ROHS, and WEEE compliance.</li>
</ul>
Education / Training / Skills / Experience: 
<ul>
<li>Proven record of effective quality management leadership in a manufacturing environment; electronics and medical device manufacturing preferred.</li>
<li>Demonstrated results achieving excellence in customer satisfaction, process and product quality.</li>
<li>Strong, proven, communication and personnel management skills that inspire and motivate teams.</li>
<li>Must have experience in working with and managing multiple projects and teams simultaneously.</li>
<li>BS in Quality, Engineering or similar degree required; advanced degree preferred.</li>
<li>Minimum 5 years’ experience in quality management leadership role within a manufacturing environment; electronics and medical device manufacturing preferred.</li>
<li>Must have strong working knowledge of ISO 9001 and ISO 13485 requirements and at least 5 years of experience working in an ISO certified environment.; familiarity with FDA QSR preferred.</li>
<li>Knowledge and working application of process validation principles, production control systems (e.g. SPC, MES), risk management methodologies (e.g. DFMEA, PFMEA).</li>
<li>Proficient with various testing and measurement equipment to include digital multi-meters, thermocouples, oscilloscopes, environmental chambers, current meters, dial gauges, and data collection.</li>
<li>Knowledge of Lean manufacturing, Six Sigma Certification preferred.</li>
</ul>
<ul>
<li>High level of drive and initiative, flexibility and strong work ethic.</li>
<li>Extensive experience with industry regulations (e.g., ISO, CE, UL, RoHS, WEEE, FCC) and product certification processes. </li>
</ul>
Physical Requirements:
While performing the duties of this job, the employee is occasionally required to stand; walk; sit; use hands to finger, handle, or feel objects, tools or controls; reach with hands and arms; climb stairs; balance; stoop, kneel, crouch or crawl; talk and hear. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by the job include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus.
The wage range for this role considers the wide range of factors that are considered in making compensation decisions including but not limited to skill sets; experience and training; licensure and certifications; and other business and organizational needs.
This job description is intended to convey information essential to understanding the scope of the position described above and it is not intended to be an exhaustive list of skills, efforts, duties, responsibilities or working conditions associated with the position.
Ultralife Corporation is an Equal Opportunity Employer, and as such affirms the right of every person to participate in all aspects of employment without regard to race, color, religion, sexual orientation, gender identity, national origin, citizenship, sex, age, veteran status, disability, genetic information, or any other protected characteristic. If you are interested in applying for employment and need special assistance or an accommodation to apply for a posted position, contact our Human Resources department via phone at 315- 332-7100

UL - Quality Director

<h3>Job Description</h3>
Job Description
$17.00/hour
DUTIES AND RESPONSIBILITIES:
1.&nbsp;&nbsp; &nbsp;Receive and follow laundry schedule and instructions from his/her supervisor and/or as outlined in the St. Luke established laundry service policies and procedures.
2.&nbsp;&nbsp; &nbsp;Gather personals that need labeling or repair as instructed.
3.&nbsp;&nbsp; &nbsp;Make labels that need to be sewn on.
4.&nbsp;&nbsp; &nbsp;After labeling, mending, altering, etc., ensure personals are delivered to the resident's room and labeling form is left in the resident's room
5.&nbsp;&nbsp; &nbsp;Keep an updated folder of resident personal clothing that has been or will be labeled.
6.&nbsp;&nbsp; &nbsp;When not sewing, labeling and mending, the Seamstress/Laundry worker will collect, sort and weigh soiled laundry, linen, garments, etc., and place in appropriate containers and/or assigned areas.
7.&nbsp;&nbsp; &nbsp;Sort soiled laundry, linen, garments, etc., and separate those items that require special stain removal/treatment.
8.&nbsp;&nbsp; &nbsp;Sort, count, and wash soiled laundry, linen, garments, etc., as established by our operating policies and procedures and as instructed by your supervisor.
9.&nbsp;&nbsp; &nbsp;Press/iron garments as instructed
10.&nbsp;&nbsp; &nbsp;Fold, count, stack, hang and distribute clean laundry, linen, garments, etc., as necessary.
11.&nbsp;&nbsp; &nbsp;During emergency conditions, ensure that clean laundry, linen, garments, etc., are distributed to designated areas.
12.&nbsp;&nbsp; &nbsp;Load and unload washers and dryers.
13.&nbsp;&nbsp; &nbsp;Other related duties that may become necessary or as directed by the supervisor, Department Head and/or Administrator.
QUALIFICATIONS:&nbsp;
<ul>
<li>Related experience or training with sewing procedures preferred.&nbsp;</li>
<li>Must be able to read, write and speak the English language.&nbsp;</li>
<li>Must possess the ability to make independent decisions when circumstances warrant such action.&nbsp;</li>
<li>Must possess the ability to deal tactfully with personnel, residents, visitors and the general public.&nbsp;</li>
<li>Must learn to operate commercial laundry equipment in a safe efficient manner. Must know how to sew, mend, alter, sew labels, etc.&nbsp;</li>
<li>Must know how to maintain and update files.&nbsp;</li>
<li>Existing employees must have a satisfactory work record in their prior positions.&nbsp;</li>
<li>Related experience or training with sewing procedures preferred.&nbsp;</li>
<li>Must be able to read, write and speak the English language.&nbsp;</li>
<li>Must possess the ability to make independent decisions when circumstances warrant such action.&nbsp;</li>
<li>Must possess the ability to deal tactfully with personnel, residents, visitors and the general public.&nbsp;</li>
<li>Must learn to operate commercial laundry equipment in a safe efficient manner. Must know how to sew, mend, alter, sew labels, etc.&nbsp;</li>
<li>Must know how to maintain and update files.&nbsp;</li>
<li>Existing employees must have a satisfactory work record in their prior positions.&nbsp;</li>
</ul>

Seamstress / Laundry Worker

<h3>Job Description</h3>
Job Description
Ultralife Corporation is a leading provider of advanced, highest quality products and services ranging from power solutions to communications and electronics systems to customers across the globe in the government &amp; defense, medical, safety &amp; security, energy, industrial and robotics sectors.
We are a global business with strategic locations in the Americas, Europe, and Asia, ideally positioned to service global customers.

The Quality Systems Engineer will serve a key role in the Battery &amp; Energy Products (B&amp;EP) organization by leading teams and successfully developing, implementing, maintaining and continuously improving, effective quality systems. The position requires a proven, natural leader, with solid manufacturing/engineering experience, who can demonstrate the ability to collaborate in a pro-active, hands-on manner across the organization.
Essential Functions:
<ul>
<li>Support the design, qualification and ensure ongoing manufacturing of products that meet or exceed internal, customer, regulatory and other applicable requirements.</li>
<li>Coordinate external QMS registration and surveillance audits to ensure continuing registration to applicable ISO standards.</li>
<li>Represent Quality Department during customer, regulatory and 3rd-party audits of manufacturing operations and the QMS.</li>
<li>Fulfill the Quality Department responsibilities for customer complaint investigation and response through the Return Material Authorization (RMA) process. Collaborate with manufacturing and product engineers on failure analysis. Coordinate with Sales and senior management on customer communications.</li>
<li>Manage corrective and preventive action processes and maintain CAR and PAR status report, records and supporting documents.</li>
<li>Partner with the Quality Director and other key personnel to maintain and update Ultralife’s quality management system to ISO, FDA QSR, FAA and other applicable requirements.</li>
<li>Coordinate 3rd-party internal audits of QMS to ensure continuing conformance to applicable ISO standards; including response and closure of audit findings.</li>
<li>Collaborate with manufacturing team and use quality improvement tools/methods to drive focused defect reduction efforts.</li>
<li>Manage and maintain quality inspection and product release processes for finished goods.</li>
<li>Monitor, support and promote process validation activities for new product introductions and current manufacturing operations.</li>
<li>Support new product development teams in the creation of requirements documents, specifications and qualification test plans.</li>
<li>Facilitate risk analysis and control throughout product realization (i.e. from concept to finished good); particularly in support of ISO 13485 requirements. Includes active participation and leadership of DFMEA and PFMEA activities, control plan development and authoring of manufacturing test/inspection procedures.</li>
<li>Actively participate in new product development teams and serve as a key technical contributor to successful transition to production.</li>
</ul>

Education and Experience:
<ul>
<li>Proven record of experience in the medical device industry in development and implementation of quality systems, process controls and continuous improvement methodologies; electronics and medical device manufacturing preferred</li>
<li>Knowledge and working application of process validation principles, guidelines and industry practice</li>
<li>Knowledge and working application of production control systems (e.g. SPC, MES)</li>
<li>Knowledge and working application of risk management methodologies (e.g. DFMEA, PFMEA)</li>
<li>Knowledge and working application of quality management system requirements, in particular ISO 9001 and ISO 13485; familiarity with FDA QSR preferred</li>
<li>Solid technical understanding of manufacturing engineering principles and statistical analysis</li>
<li>Internal Quality System auditing experience, especially ISO 13485 and FDA QSR</li>
<li>Ability to multi-task and methodically manage multiple projects</li>
<li>Ability to work effectively both independently and in teams across organizational levels</li>
<li>BS in Quality, Engineering or similar degree preferred</li>
<li>Certified Quality Engineer (CQE) or Certified Quality Auditor (CQA)</li>
<li>Minimum 7 years’ experience in product development or manufacturing environment</li>
<li>Strong written and verbal communication skills</li>
<li>Knowledge of Lean manufacturing, Six Sigma Certification preferred</li>
<li>High level of drive and initiative, flexibility and strong work ethic</li>
</ul>


This job description is intended to convey information essential to understanding the scope of the position described above and it is not intended to be an exhaustive list of skills, efforts, duties, responsibilities or working conditions associated with the position.
Ultralife Corporation is an Equal Opportunity Employer, and as such affirms the right of every person to participate in all aspects of employment without regard to race, color, religion, sexual orientation, gender identity, national origin, citizenship, sex, age, veteran status, disability, genetic information, or any other protected characteristic. If you are interested in applying for employment and need special assistance or an accommodation to apply for a posted position, contact our Human Resources department via phone at 315- 332-7100

UL - Quality Systems Engineer

<h3>Job Description</h3>
Job Description
Bright Eye is an oasis of discovery, creativity and life supporting nutrition and enjoyment. Our production kitchen for Happier Grocery is a place of community, a place of positivity, a step toward a happier world based in Brooklyn. We connect consumers with products defined by quality, sustainability, and ethical sourcing. Our space serves as a portal to discovery, encouraging exploration, learning, and a deeper connection with every aspect of daily life. 
Website: happiergrocery.com
Our mission is to create a buying experience where shoppers need not scrutinize every food label, and to provide a place of community, positivity, and life-affirming nutrition and enjoyment. 
Role Description
A Juice Production Associate plays a key role in overseeing the day-to-day operation of a beverage bar, ensuring exceptional customer service, maintaining quality standards, and maximizing profitability. With strong leadership, communication, and organizational skills, they contribute to the success and reputation of the establishment.
The ideal candidate will quickly be able to adapt to the brand, values, and culture of the company, evoking passion and excitement for the process in all involved while providing an upbeat and positive client and team experience. Because we are a small team, we all wear many hats and are happy to roll up our sleeves and lend a hand whenever needed. Can-do attitudes and respectful, inclusive outlooks are greatly valued and expected of all team members. 
Location: Brooklyn, New York
Responsibilities:
<ul>
<li>Oversee and manage all aspects of the beverage bar operation.</li>
<li>Ensure adherence to company policies and procedures, as well as health and safety regulations.</li>
<li>Maintain high standards of beverage quality, presentation, and customer service.</li>
<li>Foster a welcoming and friendly atmosphere for guests, providing exceptional customer service.</li>
<li>Address customer inquiries, complaints, and feedback in a professional and timely manner.</li>
<li>Proactively engage with customers to promote special offers, new products, or promotions.</li>
<li>Conduct regular performance evaluations and provide constructive feedback to employees.</li>
<li>Ensure cleanliness and organization of the bar area, including equipment, utensils, and workstations.</li>
<li>Collaborate with other departments, such as kitchen staff and management, to coordinate food and beverage service.</li>
<li>Communicate effectively with colleagues to ensure smooth operation and guest satisfaction.</li>
<li>Participate in the development and updating of beverage menus</li>
<li>Handle situations such as customer complaints, staffing issues, or equipment malfunctions promptly and effectively.</li>
<li>Implement contingency plans as needed to maintain smooth operation during busy periods or unforeseen circumstances.</li>
</ul>
 
Requirements:
<ul>
<li>Previous experience in a supervisory role in the hospitality industry, preferably in a bar or beverage service environment.</li>
<li>Strong leadership and communication skills, with the ability to motivate and inspire a team.</li>
<li>Excellent customer service skills and a passion for creating memorable experiences for guests.</li>
<li>Knowledge of health and safety regulations, particularly as they apply to food and beverage service.</li>
<li>Ability to work flexible hours, including evenings, weekends, and holidays.</li>
</ul>
 
At Happier Management, we provide a fair and equal employment opportunity for all candidates regardless of race, color, religion, national origin, gender, pregnancy, sexual orientation, gender identity/expression, age, marital status, disability, or any other legally protected characteristic. Happier Management hires and promotes individuals solely based on qualifications for the position to be filled and business needs. 
Benefits:
<ul>
<li>Training &amp; Development</li>
</ul>
<ul>
<li>Team Member Referral Program - $250 for any referrals if your referral stays for 3 months, we are always looking for great candidates at fine dining places that have like-minded individuals. Please feel free to forward resumes.</li>
</ul>
The base pay range for this position is a salary range of $18.00 USD per hour. The determination of what a specific employee in this job classification is paid within the range depends on a number of factors, including, but not limited to, prior employment history/job-related knowledge, qualifications and skills, etc.

Juice Production Associate

<h3>Job Description</h3>
Job Description
The Press Operator is responsible for the safe and efficient operation of a press while adhering to customer specification, quality requirements, company standards, and guideline and safety standards. This position is responsible for the overall completion of the job assigned to the Press Operator 2nd shift 4:20pm - 2:40am Monday - Thursday. Mandatory over-time on Fridays.
<ul>
<li>Inspections of printed material to ensure the correctness in all areas of color, registration, stock, and all other customer specifications.</li>
<li>Adjusting and maintaining registration, color, perforations, and other customer specific printing specifications.</li>
<li>Observes the press operations to detect any machine or equipment malfunctions and moves to correct the issues.</li>
<li>Makes adjustments to all press machine parts and equipment: feeders, grippers, guides, feed wheels, cameras, and other machines parts, using proper equipment.</li>
<li>Conducts a visual inspection prior to printing of all material stock and ink for defects or noncompliance to job specifications.</li>
<li>Carries out the final inspection to ensure the material, ink, plates or screens, cylinder/rollers, tension, and all other necessary customer specifications are correct prior to the start of the running the job.</li>
<li>Review and interpret job specifications and work order instructions, delegates or carries out directions as needed.</li>
<li>Ensures all job-related data (time and material) are entered into the ERP system (DISO).</li>
<li>Ensures all unused material goes back to the designated area after each job is finished running.</li>
<li>Ensure complete and proper line clearance has been conducted. Maintain the daily activity production log and all other required documentation for the press and work orders. Performs the general maintenance of the press or minor repairs.</li>
</ul>
Experience:
<ul>
<li>Knowledge of cGMP, ISO and Lean Manufacturing is a plus. Reading, analyzing, and interpreting technical procedures, manuals and manufacturing documents including the system of Graphic specification/Graphic identical/Articles.</li>
<li>Experience with inks and material.</li>
<li>High School Diploma or General Equivalent Degree (GED)</li>
<li>Experience with handling and proper caring of die cutting tools.</li>
<li>Experience with machine set-up</li>
<li>Experience with UV and water-based inks preferred.</li>
<li>Experience working with vision systems preferred.</li>
<li>Working knowledge of quality procedures in the pharmaceutical industry preferred.</li>
<li>Intermediate level of computer knowledge in the Microsoft Office Suites.</li>
</ul>
Physical Requirements
<ul>
<li>Ability to lift 50 pounds.</li>
<li>Standing for long periods of time.</li>
<li>Work activity requires repetitive bending, reaching, walking, stooping, and crouching, lifting, and climbing.</li>
</ul>
 Monday - Thursday 04:20pm - 02:40am

Press Operator

<h3>Job Description</h3>
Job Description
About NECI 
NECI is the leading Automation solutions provider transforming manufacturing, lab operations, process development and process control across a range of process industries in Northeast. NECI relentlessly seeks to drive the outcomes that ‘change the game’ for our clients and is seeking team members to join in our mission.
Here’s What You’ll Get 
<ul>
<li>Highly competitive Medical, Dental, and Vision Insurance</li>
<li>Flexible Spending or Health Savings Accounts</li>
<li>Unlimited Vacation Time</li>
<li>10 Paid Holidays</li>
<li>12 Paid Weeks Maternity Leave</li>
<li>Pet Insurance</li>
<li>Retirement Savings: 401(k) and Employee Stock Ownership Plan</li>
<li>Employee Referral Bonus</li>
<li>Professional Development Reimbursement</li>
<li>Company Paid STD, LTD, and Life Insurance</li>
</ul>
Position Summary
NECI’s Asset Reliability Business is engaged in the delivery of Instrumentation and Calibration services to industrial sites throughout New England &amp; New York. We work closely with our customers in solving problems and providing technical solutions.
As a member of the NECI Asset Reliability team, you are expected to deliver industry leading services to our customers as it pertains to instrumentation support &amp; calibration. Technicians working as a member of a team, or independently are required to execute site services efficiently and accurately. In addition to technical expertise, NECI seeks individuals with superior attention to detail and reporting skills.
Principal Duties and Responsibilities
<ul>
<li>
<ul>
<li>Execute field service work as a member of a team or individually as required</li>
<li>Perform advanced maintenance, troubleshooting, and repair of field instruments</li>
<li>Collect, compile, measure, summarize, and record data gathered during calibration</li>
<li>Identify out-of-tolerance conditions and perform corrective action via adjustments, component replacement, correction factors, etc. </li>
<li>Write detailed site reports, calibration reports, and certificates</li>
<li>Interact with other technicians, schedulers, account managers, and customers.</li>
<li>Lead service technicians during customer engagements.</li>
<li>Train subordinates in calibration concepts and procedures</li>
<li>Manage and maintain equipment in a manner to ensure accuracy</li>
<li>Responsible for providing uncompromising quality to all work processes in designated area of responsibility. Has the authority to stop those work processes at any time it is believed that quality is being compromised</li>
<li>Performs other duties as assigned; responsibilities and activities may change or be assigned at any time with or without notice.</li>
<li>Physical demands: Lifting up to 50 lbs. without assistance. </li>
<li>Travel: 90% travel within the New England area</li>
</ul>
</li>
</ul>
Minimum qualifications: 
<ul>
<li>Minimum High School diploma or equivalent.</li>
<li>Minimum 5 years of calibration experience.</li>
<li>Experience in entering information into a calibration management system.</li>
<li>Knowledge of or experience with ISO 17025.</li>
<li>Must be able to perform advanced math and algebra functions.</li>
<li>Must process excellent written and oral, communication skills.</li>
<li>Self-starter, honest, responsible, timely, detail oriented and self-sufficient.</li>
<li>Basic computer skills.</li>
<li>Proficient in use of MS Word and Excel.</li>
<li>Must have very good interpersonal and customer service skills.</li>
<li>Excellent interpersonal skills</li>
<li>Strong attention to details.</li>
<li>Appropriate and professional demeanor and appearance.</li>
<li>Valid Drivers License </li>
</ul>
Preferred qualifications:
<ul>
<li>
<ul>
<li>ISA Certification (Level 1&amp;2).</li>
<li>Military experience or certification in electronics.</li>
</ul>
</li>
</ul>
Competencies
<ul>
<li>Hands on experience testing, troubleshooting, and repairing pressure, temperature, analytical, liquid flow, mass flow, level, multivariable, humidity, weight, and speed instruments.</li>
<li>Experience using pressure calibrators (e.g. BEAMEX multi-calibrator / Fluke 721), multimeters, resistance simulators, conductivity solutions, pH buffers, tachometers, and temperature standards (e.g. Fluke 1523). </li>
<li>Prefer previous experience working in Pharma, Power, or Utilities.</li>
<li>Proficient in viewing, programming, and adjusting a variety of instruments via HART / FF communication.</li>
<li>Experience with 4-20 mA current loops </li>
<li>Experience in various BUS communication protocols </li>
<li>Ability to perform tasks by referencing standard operating procedures (SOP’s)</li>
<li>Ability to troubleshoot, program, and adjust instruments by referencing instrument manuals</li>
<li>Experience and understanding of P&amp;ID’s, and electrical drawings</li>
</ul>
Must be currently authorized to work in the United States.
Policy on Third-Party Unsolicited Resume Submissions: Please note that any third-party unsolicited resume submissions will immediately become the property of NECI. NECI will not pay any fee to a submitting employment agency, person, or entity unless a signed agreement is established.
Please Note NECI is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status or any other characteristic protected by law.

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