Bilingual Chocolate Production Associate (Overnight Shift)
Production worker job in Piscataway, NJ
Schedule:
Overnight Shift: Monday,Wednesday,Friday | 8:30 PM - 9:00 AM
Training required on 1st shift (6:00 AM - 2:30 PM) for the first three weeks
Pay Rate: $18.00 / hour
Type: Temp-to-Hire
Position Summary:
We are seeking reliable and motivated Production Associates to join our overnight team in a fast-paced food manufacturing environment. In this role, you will assist with daily production activities, including machine setup, material handling, and process monitoring, while ensuring compliance with GMP, HACCP, and SQF standards. This position requires attention to detail, teamwork, and the ability to follow procedures to maintain safety, quality, and efficiency.
Key Responsibilities:
Follow all safety, GMP, and food quality guidelines as outlined in company programs.
Assemble and disassemble production equipment such as extruders and enrobbers.
Fill raw materials (e.g., chocolate chips, yogurt) into processing tanks and maintain proper flow levels.
Operate or assist with flow pack machines, including changing packaging materials, adjusting settings, and monitoring product quality.
Perform product changeovers and monitor equipment performance throughout the shift.
Conduct basic quality checks such as weight reports and metal detector inspections.
Maintain clean and organized workstations and production areas.
Accurately complete required production and QA documentation for traceability.
Communicate deviations, waste, or quality issues to supervisors promptly.
Support continuous improvement and adhere to company food safety and sanitation standards.
Required Qualifications:
High School Diploma or GED preferred.
Minimum 1 year of experience in a production or packaging environment (food manufacturing experience preferred).
Ability to lift up to 50 lbs frequently and stand/walk for extended periods.
Comfortable working in refrigerated and manufacturing environments.
Strong teamwork and communication skills.
Willingness to learn and adapt to new tasks and schedules.
Flexibility to train on 1st shift prior to transitioning to overnight schedule.
Physical Demands
Regular lifting and carrying up to 50 lbs.
Frequent standing, walking, bending, and pushing/pulling of materials.
Occasional exposure to noise, temperature changes, and moving mechanical parts.
Work Environment
Fast-paced, hands-on food manufacturing setting.
Frequent exposure to moderate temperature changes, machinery, and production noise.
Team-oriented culture focused on safety and product quality.
How to Apply / Next Steps:
If you're looking to grow within a dynamic production team and contribute to a leading food manufacturing operation, apply today to join us!
About Us
PrideNow is Pride Global's light industrial staffing organization, specializing in workforce solutions for manufacturing and production environments. As part of the Pride Global network, we are committed to empowering diversity, ensuring compliance, and driving success for both our clients and employees.
Production Operator
Production worker job in Cranbury, NJ
Production Operator
Department: Operations
Reports To: Production Manager
Classification: Full time-On site
FLSA Status: Non-Exempt
SUMMARY/OBJECTIVE:
Under minimal supervision, this position is responsible for operation of pharmaceutical manufacturing equipment in a GMP environment for the purpose of making clinical supplies and performing development experiments. Incumbent is also responsible for leading manufacturing activities in assigned production rooms.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
Train on, comply with, and understand all policy and procedures at Experic including Regulatory, Safety, SOPs, Work Instructions, etc.
Assist in the development of new processes in procedures under the management direction including: Becoming subject matter expert for pharmaceutical manufacturing equipment.
Adapting understanding of equipment into (write) new SOPs and work instructions and assisting in the training of additional staff on equipment specialty.
Front line troubleshooting of processes and equipment.
Perform Pharmaceutical Manufacturing activities including: Batch Documentation/Record Generation, Materials sampling, staging, dispensing, and return. Pharmaceutical Equipment and Room set-up, operation, and cleaning. Use of appropriate personal safety equipment and engineering controls. In-process inspection and sampling. Use Experic IT Platform.
Perform developmental manufacturing experiments under the direction of management.
Support investigational and quality systems activities.
Assist maintenance in the performance of preventative maintenance activities, troubleshooting and repair of equipment.
Participate in continuous improvement activities at Experic.
Carries out duties in compliance with all federal and state regulations and guidelines.
Complies with all company and site policies and procedures.
Mechanical Aptitude, curiosity to explore complex machinery, and a desire to learn new processes.
An ability to learn and remain self-directed on tasks that are both well-defined and more exploratory.
Learn, become and remains current in profession and industry trends.
Makes a positive contribution as demonstrated by: making suggestions for improvement and learning new skills, procedures, and processes.
Is available for other duties as required.
QUALIFICATIONS AND EXPERIENCE:
Requires a bachelor's degree in an Engineering or Scientific Field with one (1) year of experience in Pharmaceutical or Life Science area or a High School Diploma and four (4) years of experience in pharmaceutical manufacturing with an emphasis on working on the implementation of new equipment and processes.
COMPETENCIES/SKILLS:
LANGUAGE SKILLS
Read and interpret documents such as standard operating procedures, manuals, batch records, work instructions and specifications.
Legible Handwriting
Communicate clearly in writing and orally including in the creation of standard operating procedures and work instructions.
MATHEMATICAL SKILLS
Apply concepts of basic arithmetic such as addition, subtraction, fractions, percentages, ratios, and proportions to practical solutions.
Graph data using spreadsheets and perform simple statistical analyses (means, standard deviations, linear regression).
REASONING ABILITY
Identify simple and moderate problems related to job function.
Scientific Reasoning the ability to gather data based on observations and measurement, formulate hypotheses, propose experimental tests, and draw conclusions, systematically.
Deductive Reasoning: Demonstrated experience applying general and complex rules to specific problems to produce answers that make sense.
Inductive Reasoning: Demonstrated experience applying a logical process in which multiple premises, all believed true or found true most of the time, are combined to obtain a specific conclusion (includes finding a relationship among seemingly unrelated events).
Knowledge of cGMP. o Familiar with Pharmaceutical Manufacturing.
Successfully completes regulatory and job training requirements.
Computer skills:
Enter data into computer using software applications for data entry and word processing. Work and be proficient with e-mail systems.
Ability to perform repetitive tasks while maintaining speed of work and attention to detail without loss to production.
Ability to work individually in a self-directed manner with less than daily oversight.
Ability to work with others in a team environment.
SUPERVISORY RESPONSIBILITIES: None
WORK ENVIRONMENT:
This job operates in a manufacturing/packing/warehouse setting.
PHYSICAL DEMANDS:
While performing the duties of this job, the employee is frequently required to stand, walk, use hands to touch, handle or feel, and talk or hear.
The employee is occasionally required to sit and reach with hands and arms.
The ability to lift and/or move up to 50 pounds frequently is preferred.
The employee is occasionally required to sit; climb or balance; and stoop, kneel, crouch or crawl.
Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus.
TRAVEL:
Travel will be required less than 10% of the time, domestic and international.
SALARY RANGE:
From $25 to $28 per hour
If you're interested in this position, please email *************************** with your resume and any relevant documentation, including proof of certifications if specified in the .
Be sure to include the position title in the subject line of your email.
We look forward to connecting with you!
The job demands described here are representative of those that must be met by an employee to successfully perform the functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. This job description is not intended and should not be construed to be exhaustive list of all responsibilities, skills, efforts, or working conditions associated with the job. It is intended to be a reflection of those principal job elements essential for recruitment and selection, for making fair job evaluations and for establishing performance standards. The percentage of time spent performing the various job duties is not absolute. The incumbent shall perform all other functions and/or be cross trained as shall be determined by the sole discretion of management, who has the right to amend, modify, or terminate this job in part or in whole. This document is not a contract for employment.
EXPERIC is an Equal Opportunity Employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.
Production Operator (Pharmaceuticals - Solid Dosage)
Production worker job in Cranbury, NJ
Job Specification - Production Operator (Pharmaceuticals - Solid Dosage)
Shift: Second Shift (3:00 PM - 11:30 PM), Monday-Friday
Employment Type: Full-time
Industry: Pharmaceuticals - Oral Solid Dosage Manufacturing
Role Purpose:
The Production Operator is responsible for executing all aspects of solid-dosage pharmaceutical manufacturing, including dispensing, granulation, sifting, milling, drying, encapsulation, coating, compression, and equipment cleaning.
This role requires strict adherence to cGMP, SOPs, batch record accuracy, safety, and good housekeeping practices.
Key Responsibilities:
Perform commercial and non-commercial manufacturing activities according to schedule.
Set up, operate, clean, and troubleshoot solid-dosage pharmaceutical production equipment.
Follow all cGMP standards, SOPs, Safety Data Sheets, and Batch Records.
Maintain a clean, compliant manufacturing environment at all times.
Participate in quality investigations as needed.
Collaborate with production management and site support teams.
Complete all documentation clearly, accurately, and in English.
Required Experience & Skills
Must-Haves
Minimum 3 years of recent experience as a Production Operator in solid dosage (tablets) pharmaceutical manufacturing.
Hands-on experience in:
Dispensing
Granulation
Sifting
Milling
Drying
Encapsulation
Coating
Compression
Cleaning activities
Proficiency with cGMP solid-dosage manufacturing equipment.
Ability to set up, operate, clean, and troubleshoot equipment independently.
Strong understanding of SOPs, cGMP, batch records, and safety protocols.
Ability to read and write in English.
Job stability (no frequent job changes).
Able to work with minimal supervision.
Able to stand throughout an 8-hour shift.
Able to lift up to 30 lbs (14 kg) unassisted.
Able to wear full PPE, including partial and full facepieces per OSHA guidelines.
Education Requirements
High School Diploma or GED (mandatory)
Bachelor's degree in Physical Sciences or Pharmaceutical Life Sciences (preferred)
Work Authorization
US Citizens or Green Card Holders only
(No visa sponsorship available.)
Additional Details
Department Needs:
3 Operators - Compression
3 Operators - Coating
4 Operators - Granulation/Blending
Shift:
Second Shift only (3:00 PM - 11:30 PM)
Application Process:
Please submit your resume and a cover letter detailing your experience and qualifications.
Equal Opportunity Employer: We are committed to creating a diverse environment and are proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.
Contact Person: Elvis Eckardt
General Production Worker
Production worker job in Sayreville, NJ
Job Title: General Production Worker
Reports to: Production Manager
Shift: Monday - Friday (6:00am - 3:00pm) Salary: $18.00/hour
Who Are We: At Wonder Meats, we are committed to becoming the leading provider of high-quality meat products, focusing on excellence, innovation, and customer satisfaction. Upholding a legacy of quality, consistency, and dedication for over 50 years, we aim to continue delivering exceptional products while embracing new ideas to shape the future of the food industry. Join our team and help us feed the world!
Position Summary
The Production Worker's responsibilities include keeping the production area clean, preparing machinery and equipment for use, working the production line as instructed, and strictly following health and safety guidelines.
To be successful as a production worker you should be able to work on the production line with consistent speed and accuracy. An outstanding production worker should be able to maintain production standards and work towards improving productivity without compromising quality. The hours for this position are Mon- Fri 6am-3:00pm.
Key Duties and Responsibilities:
· Work at different stations as production requires
· Inspect, weigh, and package products
· Monitor flow of product into processing machinery
· Verify compliance with quality, safety, production standards, work rules, and efficient operation of equipment
· Report potential production downtime, scrap production, and quality of each machine and summarize data from shift
· Maintain a clean and safe work environment
· Follow company packing procedures and standards
· Handle inventory with care and attention to detail
· Adhere to safety programs and OSHA compliance for a safe work environment
· Ensure product orders are packed and moved carefully
· Perform other job duties or administrative tasks as needed by Supervisor
Skills and Abilities:
· Great communication skills
· Basic computer skills
· Strong work ethic and organizational skills, attention to detail
· Ability to lift up to 50 pounds and work on foot for extended periods of time
· Able to work in 40° F refrigerated facility
Education/Experience:
· High school diploma or GED certificate (preferred)
· Previous experience a plus but not required
Comprehensive Benefits: Comprehensive insurance benefits, including medical, dental, vision, ensuring financial security and well-being for employees and their families
Time-off: Competitive time off including sick leave and site closures for selected holidays
Corporate Discounts: Get discounts on travel, subscriptions and more!
Auto-ApplyProduction Worker
Production worker job in South River, NJ
Paragon Staffing, LLC is a company that specializes in connecting job seekers with employers who are seeking temporary, contract, or permanent positions.
Responsibilities:
Line Leader
Caping
Palletizing
Apply Labels
Forklift Experience
Pallet Loading/ Combining
Scanner
Pay Rate :
$18/HR
Schedule
7:30 AM - 4:00 PM
Monday to Friday
Location:
South River, NJ
Auto-ApplyGeneral Production Worker
Production worker job in East Hanover, NJ
Job Description
Join Weiss-Aug - A Leader in Precision Manufacturing and Innovation
Weiss-Aug, is a leading provider of advanced manufacturing and engineering solutions with advanced facilities across the U.S. and Mexico for over 50 years.
Why Join Us?At Weiss-Aug we are driven by a commitment to excellence, innovation, and continuous improvement. As a recognized leader in the industrial and commercial sectors, specializing in high-volume metal stamping, thermoplastic molding, and value-added assembly solutions for the medical, aerospace & defense, automotive, interconnect, telecommunications and consumer goods industries, we take pride in cultivating a collaborative and forward-thinking work environment.
*General Production Worker - Stamping & Molding 1st & 2nd Shift *Responsibilities:- Change and set up production reel.
Rewind production reels.
Edit reels for Quantity, Quality, etc.
Rewind interliner.
Change production totes.
Maintain clean work area.
Maintain Lot Control ticket system.
During production run, maintain sample submission to Q.C. according to Routing.
Coordinate packaging material requirements between Press Room and Warehouse.
Perform required visual checks to verify quality of product.
During production run perform gauging verification (Go - No Go gauges).
Interface with Die Setter and Q. C. providing support functions.
Operate Power Press according to Weiss-Aug Co. Inc. standards.
Requirements
High School Diploma or equivalent.
Fluent in English.
Ability to read precision measuring instruments and conduct basic arithmetic calculations.
This position is at our
East Hanover, NJ
location.
1st Shift:Pay Range:
**2nd shift: **2:00pm - 10:30pm
Pay Range: $18.50 per hour plus 15% shift differential
Other Benefits Include
Medical, Dental and Vision
401 (k) with company match
Holiday, Vacation and Sick Time
Tuition Reimbursement
Health Savings Accounts (HAS)
Flexible Spending Accounts (FSA)
Cigna Wellness Incentive Program
Employee Assistance Program (EAP)
Short Term Disability
Group Life and Accidental Insurance
Sun Life - Accident, Critical Illness, and Hospital Indemnity Insurance
Smoking Cessation Program
Pet Insurance
US Pay Transparency
The base salary for this role will be determined on a case-by-case basis and may vary based on the following considerations: job-related knowledge and skills, experience, and internal consistency.
Weiss-Aug is an Equal Opportunity/Affirmative Action Employer. Applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, protected veteran status, disability, or any other characteristics protected by applicable federal, state, or local law.
You should be proficient in:
Machine Setups for Production Runs
Manual Machining Skills
High School / GED
Experience in a Manufacturing Environment
Injection Molding Experience
Machines & technologies you'll use:
Injection Molding Machine (Arburg)
Punch Press
Press Brake
Stamping Press (Minster)
Production Operator II - Soft Gel Encapsulation - 1st shift
Production worker job in East Brunswick, NJ
The role of Production Operator II is a mid-level position within our manufacturing department, tasked with proficiently carrying out manufacturing procedures and operating diverse manufacturing equipment. This position requires strict adherence to company Standard Operating Procedures (SOPs), compliance with cGMP guidelines, and a commitment to upholding environmental, health, and safety standards. The Production Operator II ensures that operations meet high compliance and quality standards.
Reporting Relationships
Individual Contributor
This position works under moderate supervision.
Essential Functions and Detailed Duties
Must be able to fully perform all Production Operator I tasks, including operating manufacturing equipment independently, including setup, cleanup, sanitization, material movement, and safely operating the manufacturing equipment to perform manufacturing functions in two processes/machines such as coating, compression, encapsulation, granulation/blending and soft gel function per Manufacturing batch record.
In addition, must be able to:
Perform intermediate mechanical functions, including troubleshooting, correcting machine malfunctions, and identifying problems such as bottlenecks.
Clearly document activities in batch records, forms and other GMP documents.
Offer suggestions to superiors and follow up on process improvements related to safety, compliance, cost, and productivity.
Identify and report both machine or manual deviations to supervisor or designee.
Operator will have intermediate knowledge of multiple manufacturing machines.
After 1 year of experience and consistently satisfactory performance, able to train Level I Operators and help guide new Level II Operators.
Follow all Good Manufacturing Practices (GMP) and guidelines.
Adhere to cGMP's and Standard Operating Procedures as required. Must report unsafe conditions, near misses, and/or injuries in a timely manner.
Maintain a clean and sanitary workplace.
Follow applicable safety guidelines while operating the production equipment.
Be able to perform other duties as assigned.
Specialized Skills and Knowledge:
Basic mathematical skills.
Good mechanical abilities.
Basic computer skills
Excellent verbal and written communication skills in English
Must complete departmental SOP, GMP, and any required Qualifications.
Ability to work in a team.
Experience and Education
High school diploma or equivalent.
Minimum of 3 years of previous manufacturing experience in the pharmaceutical industry with soft gel encapsulation experience preferred.
Physical Demands/Factors:
While performing the duties of this job, the employee is regularly required to stand. The employee is frequently required to walk; sit; use hands; talk; and hear. The employee is occasionally required to reach with hands and arms; climb or balance; stoop; kneel; crouch. The employee must occasionally lift and or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, and color vision.
The physical demands described here represent those that an employee must meet to perform the essential functions of this job successfully. Reasonable accommodation may be made to enable individuals with disabilities to perform essential functions.
Based on the highly regulated workplace at Avet, employees will be required to meet minimum English proficiency requirements.
All applicants must be legally authorized to work in the U.S. for any employer. We are unable to sponsor any applicants for a work visa or take over sponsorship of a work visa for any applicants, at this time.
Avet is proud to be an Equal Opportunity Employer.
This job description is not all-inclusive. It acts as a guideline and is subject to change over time. Additional duties may be assigned based on business needs.
Compensation and Benefits
Compensation:
This is a non-exempt position with a starting pay of $28.42 per hour.
This pay represents the base hourly rate. In addition, this position is eligible for an annual bonus which aligns to both individual and company performance.
Benefits:
401 (k) matching - vested immediately
Medical, Dental and Vision
Employee Assistance Program
Employee discount through Life Mart
Flexible Spending Account and Dependent Care Account
Paid Holidays
Paid Time Off
Auto-ApplyAutomated Production Operator 2nd Shift
Production worker job in Plainsboro, NJ
Changing lives. Building Careers.
Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what's possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care.
The Automated Production Operator 2nd Shift, performs chemical processing and batch mixing in a new state of the art automated manufacturing environment. Responsibilities include batch execution, in-process quality verifications, equipment cleaning, entering production activities in Oracle MRP system, product inspections, HMI input for robots, and providing support for other activities within the team. All processing operations are performed in ISO Class 7 area and require proper Clean Room gowning. All processing is performed in compliance with Good Manufacturing Practices (GMP), Quality Systems Regulations), Standard Operating Procedures (SOP's) and Health and Safety requirements.
This is a second shift role. (3:00 p.m. - 11:30 p.m.)
SUPERVISION RECEIVED: Under the direct supervision of the Operations Manager
SUPERVISION EXERCISED: NA
ESSENTIAL DUTIES AND RESPONSIBILITIES
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
Responsible for accurately maintaining accurate records, required logs and other procedures to comply with regulatory requirements, Good Manufacturing Practices (GMP), Quality Systems Regulations, Standard Operating Procedures (SOP's), and Health and Safety requirements.
Performs and supports daily manufacturing operations inclusive of batch execution, product inspections, setup, operation, disassembly, and cleaning of manufacturing equipment.
Enter and record production activities in Oracle MRP systems to issue material and labor hours to specific work orders.
Supports equipment maintenance and troubleshooting activities to minimize process downtime or re-occurrence. Support investigational activities around events/non-conformances or customer complaints.
Supports equipment evaluations and validation activities associated with the developed manufacturing processes
Communicate with team members and support teams to ensure continuous production of the correct product at high quality levels with minimal wasted time and materials
Responsible for performing precise measurements and using measurement equipment to accurately add chemicals to batches.
Interfacing with HMIs.
Support department and plant Safety goals by continuously demonstrating safe behavior.
Maintain, analyze problems, troubleshoot, and make adjustments to process equipment as needed and detect when equipment is not operating correctly.
DESIRED MINIMUM QUALIFICATIONS
The requirements listed below are representative of the knowledge, skill, and/or ability required for this position.
High School Diploma or equivalent with 2+ years of experience in the Medical Device industry or Pharmaceutical industry within a clean room environment preferred.
Must work and collaborate as part of a team.
Ability to operate, maintain and troubleshoot process equipment, and make adjustments as needed.
Strong mechanical abilities as applied to an automated production line.
Must read, write, and speak in English, and communicate clearly and concisely.
TOOLS AND EQUIPMENT USED
Lyophilizers, homogenizers, HMI, pH meters, balances (scales), Steris Washer, Printers, Crosslink chambers.
Oracle MRP System
PHYSICAL REQUIREMENTS
The physical requirements listed in this section include, but are not limited, to the motor/physical abilities and skills require of this position in order to successfully undertake the essential duties and responsibilities of this position. In accordance with the Americans with Disabilities Act (ADA), reasonable accommodations may be made to empower individuals with disabilities to undertake the essential duties and responsibilities of the position.
While undertaking the essential duties and responsibilities of the position, the employee must repeatedly
sit, listen, and speak. The employee is required to go to all areas of the company. The employee may be required to periodically lift and/or move up to 25 pounds.
ADVERSE WORKING CONDITIONS
The adverse working conditions listed in this section include, but are not limited to, those environmental conditions to which the employee may be exposed while undertaking the essential duties and responsibilities of this position, which is that of a general plant environment.
Daily interaction with hazardous materials used in a controlled environment.
SELECTION GUIDELINES
Formal application, rating of education and experience; oral interview and reference check; job related tests may be required.
DISCLAIMER
The duties listed above are intended only as illustrations of the various types of work that may be performed. The omission of specific statements of duties does not exclude them from the position if the work is similar, related, or a logical assignment to the position.
The job description does not constitute an employment agreement between the employer and employee and is subject to change by the employer as the needs of the employer and requirements of the job change.
Salary Pay Range:
$19.19 - $25.43 USD Hourly
Our salary ranges are determined by role, level, and location. Individual pay is determined by several factors including job-related skills, experience, and relevant education or training. In addition to base pay, employees may be eligible for bonus, commission, equity or other variable compensation. Your recruiter can share more about the specific salary range for your preferred location during the hiring process.
Additional Description for Pay Transparency:
Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance, and savings plan (401(k)).
Subject to the terms of their respective policies and date of hire, Employees are eligible for the following *******************************************
Integra LifeSciences is an equal opportunity employer, and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status.
This site is governed solely by applicable U.S. laws and governmental regulations. If you'd like more information on your rights under the law, please see the following notices:
EEO Is the Law | EOE including Disability/Protected Veterans
Integra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the ADA. If you have difficulty using our online system due to a disability and need an accommodation, please email us at ***********************.
Unsolicited Agency Submission
Integra LifeSciences 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. A formal written agreement is required before engaging any agency, and it must be executed and authorized by the Vice President, Talent Acquisition. Where agency agreements are in place, introductions (the initial sharing of a candidate's name, resume, or background) are position-specific and may only occur within the scope of that approved agreement. Please, no phone calls or emails.
Integra - Employer Branding from Integra LifeSciences on Vimeo
Auto-Apply2nd Shift Production Technician
Production worker job in Hackettstown, NJ
The Role
As a Production Tech, you'll be an essential part of the process of turning raw cannabis flower into our beautiful line of medicated products. Under the guidance of the management team, you will produce, package, and handle products, perform inventory duties, adhere to compliance requirements, and keep safety as your top priority while working daily in our facility. Here at GTI, we are looking for true team players who are the perfect hybrid between precision and energy.
Responsibilities
Deliver on production goals, while focused on safety and quality
Produce product per recipes and SOP's, maintaining high quality standards
Package product into proper containers with proper labeling to ensure compliance with state regulations
Ensure all standards for processing procedures and laboratory protocols are followed
Compliance with local and state regulations
Adherence to quality control methods throughout entire process
Documentation of manufacturing methods are created and maintained
Electronically convert packaged products in the state traceability system
Manage time efficiently to meet goals while consistently producing quality product
Practice good housekeeping habits throughout the facility with focus and personal contributions towards a clean and organized assigned work area at the end of the assigned shift
Exhibit competency in basic organizational skills, communication skills and Windows based operating software
Use independent judgment regarding product processing, keeping quality and goals in mind
Help create a positive environment by having a positive attitude and by being self-motivated
Other duties as assigned
Qualifications
High School Education or GED graduate; some college or college graduate preferred
1-2 years' experience in manufacturing, food processing, warehousing, and/or inventory preferred
Equivalent combinations of education and experience may be considered
Must be able to work well in a group and independently; demonstrate self-motivation and initiative
Must be able to adapt quickly to changes in policy, procedure, and technique
Employee must exhibit personal hygiene and follow the health guidelines set forth by GTI
Ability to listen well and communicate effectively with various audiences
Ability to perform monotonous tasks with great efficiency without losing qualities
Must be able to follow basic instructions and accept constructive criticism
Prior cannabis experience not required
Additional Requirements
Must have a valid driver's license or State ID card
Must be a minimum of 21 years of age
Must pass all required background checks
Must be and remain compliant with all legal and company regulations for working in the industry
Must be approved by the Cannabis Compliance Board to receive an Agent Card
Working Conditions
While performing the duties of this job, the employee is regularly required to perform reaching, grasping, bending, stooping, talking, hearing, seeing and repetitive motions.
Must be able to sit and/or stand for extended periods of time while maintaining focus.
PHYSICAL DEMANDS: Must be able to lift, carry, and balance up to 50 pounds AND must be able to do so with extreme care and caution when working with product.
Work involves daily exposure to allergens (such as cannabis, tree nuts, and coconut oil).
The pay range is competitive and based on experience, qualifications, and/or location of the role. Positions may be eligible for a discretionary annual incentive program driven by organization and individual performance.
Green Thumb Pay Range$19-$19 USD
Auto-ApplyProduction Operator - Mon - Fri Night Shift (11pm - 7:30am)
Production worker job in Flemington, NJ
Luxfer MEL Technologies is a global leader in the development, manufacture and supply of Magnesium and Zirconium based products and services to technology industries worldwide. We provide innovative products and solutions to customers worldwide for use in a broad range of markets including Aerospace, Automotive, Oil & Gas, Ceramics and Healthcare. We have a wide range of products, including Hazardous, Non-Hazardous and Export shipments. We are an innovative technology driven business where we have a relentless drive and a passion to achieve high standards. At Luxfer Customer First, Integrity, Accountability, Innovation, Personal Development and Teamwork are our core values.
The main purpose of the role is to work as part of a team with responsibilities on the production line reporting to the Team Leader. You will also be required to work flexibly and may be required to work on other related activities when the business need requires.
Benefits
Medical, Dental, Vision Insurance, eligible on the 1st of the month following hire
Disability and Life Insurance
401k Plan with Company Match
Tuition Reimbursement
Career Advancement Opportunities
Hourly rate $20-$25
Main responsibilities:
Understanding the basic chemistry involved in the process in order to effectively monitor and troubleshoot. Operators are expected to continually upgrade their skills until they fully understand the entire plant process flow in addition to the basic chemistry of all the plant processes.
Maintaining the work area in a safe and tidy condition. Adhering to Health & Safety policy and procedures.
Monitors processes, performs required measurements and tests, monitors the operation of equipment and sets equipment controls in maintain right-first time quality products.
Maintains production line operation by following SOP's, solving production process problems and reporting to others to achieve the short-term manufacturing plans.
Understanding the basic mechanical operations of the process in order to effectively monitor and troubleshoot. Through continuous improvement, Operators upgrade their skills until they understand the basic mechanical aspects of the entire plant.
Monitors equipment operation on a day-to-day basis. Performs basic troubleshooting, notifying Team Leader and Maintenance when a situation is beyond limits. Assists in the repairs to equipment and other simple maintenance tasks. Participates in equipment PM and project installation as necessary.
Documents production and production processes by completing production log sheets, recording the receipt and usage of raw materials, and calculating material usage.
Understands customer and product requirements, monitors and adjusts processes to ensure compliance.
Understands environmental regulations and complies fully.
Requirements and Qualifications:
High school diploma or GED
2-5 years working in a manufacturing environment
Experience working in a team
Ability to work in a logical organized manner
Able to work safely using tools and equipment
Ability to work effectively, efficiently and safely to schedules and deadlines
Chemical manufacturing experience Desired
Lean manufacturing (including 5S) Desired
Familiarity with SAP S4 Hana or equivalent ERP system would be beneficial
Skills & Knowledge:
Must have the ability to prioritize tasks and work well under pressure
Computer literate - Experience using MS Office; Excel, Word & Outlook
Basic mathematics
Accurate data entry
Forklift truck license desired
Boiler license desired
Luxfer MEL Technologies is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status. Women, minorities and veterans are encouraged to apply.
This role may involve access to Controlled Unclassified Information (CUI) and export-controlled data subject to the International Traffic in Arms Regulations (ITAR). Employees are expected to follow company policies and security protocols for handling, storing, accessing, and transmitting sensitive information. Compliance training will be required after hire.
Due to federal export control requirements, access to certain information is limited to U.S. Citizens, U.S. Lawful Permanent Residents, and individuals lawfully admitted as asylees or refugees, unless a valid export authorization is obtained. Employment is contingent upon meeting these eligibility requirements and adhering to applicable CUI and ITAR policies.
We are committed to a safe, drug-free work environment and pre-employment drug screening and background checks are required.
Auto-ApplyProduction Operator - Mon - Fri Day Shift (7am - 3:30pm)
Production worker job in Flemington, NJ
Luxfer MEL Technologies is a global leader in the development, manufacture and supply of Magnesium and Zirconium based products and services to technology industries worldwide. We provide innovative products and solutions to customers worldwide for use in a broad range of markets including Aerospace, Automotive, Oil & Gas, Ceramics and Healthcare. We have a wide range of products, including Hazardous, Non-Hazardous and Export shipments. We are an innovative technology driven business where we have a relentless drive and a passion to achieve high standards. At Luxfer Customer First, Integrity, Accountability, Innovation, Personal Development and Teamwork are our core values.
The main purpose of the role is to work as part of a team with responsibilities on the production line reporting to the Team Leader. You will also be required to work flexibly and may be required to work on other related activities when the business need requires.
Benefits
* Medical, Dental, Vision Insurance, eligible on the 1st of the month following hire
* Disability and Life Insurance
* 401k Plan with Company Match
* Tuition Reimbursement
* Career Advancement Opportunities
* Hourly rate $20-$25
Main responsibilities:
* Understanding the basic chemistry involved in the process in order to effectively monitor and troubleshoot. Operators are expected to continually upgrade their skills until they fully understand the entire plant process flow in addition to the basic chemistry of all the plant processes.
* Maintaining the work area in a safe and tidy condition. Adhering to Health & Safety policy and procedures.
* Monitors processes, performs required measurements and tests, monitors the operation of equipment and sets equipment controls in maintain right-first time quality products.
* Maintains production line operation by following SOP's, solving production process problems and reporting to others to achieve the short-term manufacturing plans.
* Understands the basic mechanical operations of the process in order to effectively monitor and troubleshoot. Through continuous improvement, Operators upgrade their skills until they understand the basic mechanical aspects of the entire plant.
* Monitors equipment operation on a day-to-day basis. Performs basic troubleshooting, notifying Team Leader and Maintenance when a situation is beyond limits. Assists in the repairs to equipment and other simple maintenance tasks. Participates in equipment PM and project installation as necessary.
* Documents production and production processes by completing production log sheets, recording the receipt and usage of raw materials, and calculating material usage.
* Understands customer and product requirements, monitors and adjusts processes to ensure compliance.
* Understands environmental regulations and complies fully.
Requirements and Qualifications:
* High school diploma or GED
* 2-5 years working in a manufacturing environment
* Experience working in a team
* Ability to work in a logical organized manner
* Able to work safely using tools and equipment
* Ability to work effectively, efficiently and safely to schedules and deadlines
* Chemical manufacturing experience Desired
* Lean manufacturing (including 5S) Desired
* Familiarity with SAP S4 Hana or equivalent ERP system is beneficial
Skills & Knowledge:
* Must have the ability to prioritize tasks and work well under pressure
* Computer literate - Experience using MS Office; Excel, Word & Outlook
* Basic mathematics
* Accurate data entry
* Forklift truck license desired
* Boiler license desired
Luxfer MEL Technologies is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status. Women, minorities and veterans are encouraged to apply.
This position requires access to our export-controlled commodities, technical data, technology, and services. These items are restricted under the International Traffic in Arms Regulations (ITAR) to U.S. Citizens, Lawful Permanent Residents of the U.S., and properly licensed foreign persons. To conform to U.S. Government export regulations, applicant must be a i) a U.S. citizen or national, ii) U.S. lawful permanent resident (aka green card holder), iii) refugee under 8 U.S.C. §1157, or iv) asylee under 8 U.S.C. § 1158, or be a properly licensed foreign person. Therefore, employment is contingent on compliance with ITAR regulations and successfully obtaining and maintaining the necessary export authorization license from the U.S. Department of Commerce Bureau of Industry and Security (BIS) or U.S. Department of State Directorate of Defense Trade Controls (DDTC). Candidates must be authorized to work in the US.
We are committed to a safe, drug-free work environment and pre-employment drug screening and background checks are required.
Production Operator (Pharmaceuticals - Solid Dosage)
Production worker job in Cranbury, NJ
Job Specification - Production Operator (Pharmaceuticals - Solid Dosage)
Shift: Second Shift (3:00 PM - 11:30 PM), Monday-Friday Employment Type: Full-time Industry: Pharmaceuticals - Oral Solid Dosage Manufacturing
Role Purpose
The Production Operator is responsible for executing all aspects of solid-dosage pharmaceutical manufacturing, including dispensing, granulation, sifting, milling, drying, encapsulation, coating, compression, and equipment cleaning.
This role requires strict adherence to cGMP, SOPs, batch record accuracy, safety, and good housekeeping practices.
Key Responsibilities
Perform commercial and non-commercial manufacturing activities according to schedule.
Set up, operate, clean, and troubleshoot solid-dosage pharmaceutical production equipment.
Follow all cGMP standards, SOPs, Safety Data Sheets, and Batch Records.
Maintain a clean, compliant manufacturing environment at all times.
Participate in quality investigations as needed.
Collaborate with production management and site support teams.
Complete all documentation clearly, accurately, and in English.
Required Experience & Skills
Must-Haves
Minimum 3 years of recent experience as a Production Operator in solid dosage (tablets) pharmaceutical manufacturing.
Hands-on experience in:
Dispensing
Granulation
Sifting
Milling
Drying
Encapsulation
Coating
Compression
Cleaning activities
Proficiency with cGMP solid-dosage manufacturing equipment.
Ability to set up, operate, clean, and troubleshoot equipment independently.
Strong understanding of SOPs, cGMP, batch records, and safety protocols.
Ability to read and write in English.
Job stability (no frequent job changes).
Able to work with minimal supervision.
Able to stand throughout an 8-hour shift.
Able to lift up to 30 lbs (14 kg) unassisted.
Able to wear full PPE, including partial and full facepieces per OSHA guidelines.
Education Requirements
High School Diploma or GED (mandatory)
Bachelor's degree in Physical Sciences or Pharmaceutical Life Sciences (preferred)
Work Authorization
US Citizens or Green Card Holders only
(No visa sponsorship available.)
Additional Details
Department Needs:
3 Operators - Compression
3 Operators - Coating
4 Operators - Granulation/Blending
Shift:
Second Shift only (3:00 PM - 11:30 PM)
Application Process:
Please submit your resume and a cover letter detailing your experience and qualifications.
Equal Opportunity Employer: We are committed to creating a diverse environment and are proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.
Contact Person: Elvis Eckardt
Production Operator - Pharmaceutical Solid Dosage
Production worker job in Cranbury, NJ
Job Description
Shift: Second Shift Employment Type: Full-Time
Mandatory Requirement:
- Minimum 3 years of current relevant experience as a production operator
-Familiarity with working in a regulated pharmaceutical solid dosage facility (SOLID - TABLETS)
-performing tasks like dispensing, granulation, sifting, milling, drying, encapsulation, coating, compression, and cleaning activities
-Proficiency in setup, operation, and cleaning of all cGMP production equipment, combined with strict adherence to Standard Operating
Procedures (SOPs), Batch Records, safety procedures, and good housekeeping practices, ensuring efficient, compliant, and safe manufacturing operations
-Ability to read and write documents written in English.
- Familiarity with various cGMP solid dosage Pharmaceutical manufacturing equipment.
- Able to work with minimal supervision.
- Able to stand on feet throughout an eight-hour work day.
- Maintain personal hygiene habits consistent with working in a cGMP environment
- Be capable of wearing all required PPE; including partial and full facepieces based on OSHA guidelines.
Education :High School Diploma or GED Equivalent.
Bachelors degree in Physical Sciences or Pharmaceutical life science-related field of study.
Job Purpose:Responsible for the execution of all aspects of solid-dosage manufacturing which includes, but is not limited to, the dispensing, granulation, sifting, milling, drying, encapsulation, coating, compression, and cleaning related activities. Must be able to interact daily with all site support personnel as required. Must be able to complete all required batch record documentation in a thorough, accurate, and legible manner in English. Must be capable of reading and understanding all documented Standard Operating Procedures in English plus demonstrate competency through action and written evaluation.
Essential Duties and Responsibilities include the following. Other duties may be assigned:
Assist Production Management with all scheduled and requested activities in an efficient and smooth operation.
Ensure all scheduled commercial and non-commercial manufacturing activities are completed on time.
Become proficient in the setup, operation, and cleaning of all cGMP equipment used during production operations.
Participate in all Quality Investigations as required.
Adhere to all approved Standard Operating Procedures, Batch Records, and Safety Procedures as written when performing all daily activities.
Ensure the cGMP area is cleaned and maintained following all SOPs and good housekeeping practices.
Must use required PPE during cGMP activities as specified in the Batch Records and Safety Data Sheets.
To perform this job successfully, an individual should have:
Familiarity with working in a regulated pharmaceutical solid dosage facility.
Ability to read and write documents written in English.
Excellent written communication skills.
Familiarity with various cGMP solid dosage Pharmaceutical manufacturing equipment. Able to set up, operat,e clean, and troubleshoot the solid dosage Pharmaceutical manufacturing equipment being used.
Able to work with minimal supervision.
Able to stand on feet throughout an eight-hour workday.
Able to lift up to 30 Ibs (14 Kgs) without assistance.
Maintain personal hygiene habits consistent with working in a cGMP environment
Be capable of wearing all required PPE; including partial and full facepieces, based on OSHA guidelines.
Education :
High School Diploma or GED Equivalent.
Bachelors degree in Physical Sciences or Pharmaceutical life science related field of study.
Production Operator
Production worker job in Maplewood, NJ
SUMMARY/OBJECTIVE
A Production Operator is responsible for operating and maintaining equipment in the manufacturing plant as well as preparing items for distribution. The position involves sanitation of equipment, assembling and checking product, and ensuring that all machinery runs smoothly .
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed must be representative of the knowledge, skills, minimum education, training, licensure, experience and/or ability required.
JOB RESPONSIBILITIES
Responsible for maintaining production equipment.
Responsible for shift change overs.
Maintain a clean production area.
Load and unload items from machines, carts, and dollies.
Feed or place supplies onto equipment for processing.
Responsible for quality control of items produced.
Provide packaging duties, as required.
Work in a fast-paced environment.
Provide high standards of production are met.
Inspect final products to assess compliance with quality standards and establish tolerances.
Set up and adjust machines for day-to-day operations.
Monitor machinery in operation to identify concerns and make corrections or report complex problems.
Demonstrate effective communication skills through positive interactions with site managers, outside contractors, and junior on-site staff.
All other duties, as required or needed.
PHYSICAL DEMANDS
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of the job.
While performing the duties of this job, the employee is regularly required to talk or hear and see. The employee frequently is required to stand; walk; use hands to handle or feel and reach with hands and arms.
The employee must regularly lift and/or move objects up to 50 pounds.
JOB REQUIREMENTS
HSD or equivalent
Ability to pay attention to details.
Ability to stand for entire shift.
Ability to work long hours.
Ability to multi-task
Please note this Job Description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.
Auto-ApplyMachine Operator
Production worker job in Trenton, NJ
Maintains parts flow to machine using auto load or hand load and uses caution when hand loading
Reads blueprint or job order for product specifications, such as dimensions and tolerances, and tooling instructions, such as fixtures, feed rates, cutting speeds, depth of cut, and determines sequence of operations.
Works in teams.
Maintains the ability and knowledge to make size adjustments if needed.
Observes operation of machine and verifies conformance of machined work piece to specifications, using measuring instruments, such as fixed gauges, calipers, and micrometers.
Maintains ability to effectively present information in one on one and small group situations to technicians, operators, supervisor, and management
Maintains knowledge on how to change the wheel and installing guarding.
Maintains understanding of machine controls and process control plans and Associate Gauging.
Changes worn diamonds and rotates diamonds as needed
Maintains adjustments on taper.
Maintains ability to be able to move heavy baskets using pallet jacks.
Examines and feels surface of work piece for defects.
Must be able to understand how to power up, power down, start and stop machines.
Troubleshoots and adjusts auto loading mechanisms
Turns valve handle to direct flow of coolant or cutting oil against tool and work piece.
Perform daily inspections on equipment
Perform preventive maintenance per instructions for machine or equipment
Record required information, either in written or electronic form, pertinent to production, quality, and time records.
Maintain a clean work area. Follow all safety and housekeeping rules, policies and procedures.
Works from written and verbal instructions.
Loading and unloading forklift for non-production purposes only. Employee must regularly lift up to 10 pounds and occasionally lift and/or move up to 40 pounds.
Grind Set-up
Summary: Sets up and operates grinding machines to grind diameter surfaces on metal objects to specifications by performing the following duties.
Must be Grind Operator qualified
Troubleshoots and repairs equipment as needed.
Moves controls to position tool and work pieces in relation to each other, and to set specified feeds, speeds, and depth of cut.
Selects positions of machine to insure product being made meets specifications.
EDUCATION:
High school diploma or general education degree (GED) and one to three months related experience and/or training; or equivalent combination of education and experience.
SKILLS/CERTIFICATIONS:
Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals; Ability to write routine reports and correspondence.
Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals; Ability to compute rate, ratio, and percent and to draw and interpret bar graphs.
Ability to apply common sense understanding to carry out instructions furnished in written, oral, or diagram form; Ability to deal with problems involving several concrete variables in standardized situations. #CB
General Production Worker
Production worker job in Sayreville, NJ
Job Description
Job Title: General Production Worker
Reports to: Production Manager
Shift: Monday - Friday (6:00am - 3:00pm) Salary: $18.00/hour
Who Are We:
At Wonder Meats, we are committed to becoming the leading provider of high-quality meat products, focusing on excellence, innovation, and customer satisfaction. Upholding a legacy of quality, consistency, and dedication for over 50 years, we aim to continue delivering exceptional products while embracing new ideas to shape the future of the food industry. Join our team and help us feed the world!
Position Summary
The Production Worker's responsibilities include keeping the production area clean, preparing machinery and equipment for use, working the production line as instructed, and strictly following health and safety guidelines.
To be successful as a production worker you should be able to work on the production line with consistent speed and accuracy. An outstanding production worker should be able to maintain production standards and work towards improving productivity without compromising quality. The hours for this position are Mon- Fri 6am-3:00pm.
Key Duties and Responsibilities:
· Work at different stations as production requires
· Inspect, weigh, and package products
· Monitor flow of product into processing machinery
· Verify compliance with quality, safety, production standards, work rules, and efficient operation of equipment
· Report potential production downtime, scrap production, and quality of each machine and summarize data from shift
· Maintain a clean and safe work environment
· Follow company packing procedures and standards
· Handle inventory with care and attention to detail
· Adhere to safety programs and OSHA compliance for a safe work environment
· Ensure product orders are packed and moved carefully
· Perform other job duties or administrative tasks as needed by Supervisor
Skills and Abilities:
· Great communication skills
· Basic computer skills
· Strong work ethic and organizational skills, attention to detail
· Ability to lift up to 50 pounds and work on foot for extended periods of time
· Able to work in 40°ree; F refrigerated facility
Education/Experience:
· High school diploma or GED certificate (preferred)
· Previous experience a plus but not required
Comprehensive Benefits: Comprehensive insurance benefits, including medical, dental, vision, ensuring financial security and well-being for employees and their families
Time-off: Competitive time off including sick leave and site closures for selected holidays
Corporate Discounts: Get discounts on travel, subscriptions and more!
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HJGART7vnH
Production Worker
Production worker job in South River, NJ
Job Description
Paragon Staffing, LLC is a company that specializes in connecting job seekers with employers who are seeking temporary, contract, or permanent positions.
Responsibilities:
Line Leader
Caping
Palletizing
Apply Labels
Forklift Experience
Pallet Loading/ Combining
Scanner
Pay Rate :
$18/HR
Schedule
7:30 AM - 4:00 PM
Monday to Friday
Location:
South River, NJ
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Production Operator - Mon - Fri Day Shift (7am - 3:30pm)
Production worker job in Flemington, NJ
Job DescriptionLuxfer MEL Technologies is a global leader in the development, manufacture and supply of Magnesium and Zirconium based products and services to technology industries worldwide. We provide innovative products and solutions to customers worldwide for use in a broad range of markets including Aerospace, Automotive, Oil & Gas, Ceramics and Healthcare. We have a wide range of products, including Hazardous, Non-Hazardous and Export shipments. We are an innovative technology driven business where we have a relentless drive and a passion to achieve high standards. At Luxfer Customer First, Integrity, Accountability, Innovation, Personal Development and Teamwork are our core values.
The main purpose of the role is to work as part of a team with responsibilities on the production line reporting to the Team Leader. You will also be required to work flexibly and may be required to work on other related activities when the business need requires.
Benefits
Medical, Dental, Vision Insurance, eligible on the 1st of the month following hire
Disability and Life Insurance
401k Plan with Company Match
Tuition Reimbursement
Career Advancement Opportunities
Hourly rate $20-$25
Main responsibilities:
Understanding the basic chemistry involved in the process in order to effectively monitor and troubleshoot. Operators are expected to continually upgrade their skills until they fully understand the entire plant process flow in addition to the basic chemistry of all the plant processes.
Maintaining the work area in a safe and tidy condition. Adhering to Health & Safety policy and procedures.
Monitors processes, performs required measurements and tests, monitors the operation of equipment and sets equipment controls in maintain right-first time quality products.
Maintains production line operation by following SOP's, solving production process problems and reporting to others to achieve the short-term manufacturing plans.
Understands the basic mechanical operations of the process in order to effectively monitor and troubleshoot. Through continuous improvement, Operators upgrade their skills until they understand the basic mechanical aspects of the entire plant.
Monitors equipment operation on a day-to-day basis. Performs basic troubleshooting, notifying Team Leader and Maintenance when a situation is beyond limits. Assists in the repairs to equipment and other simple maintenance tasks. Participates in equipment PM and project installation as necessary.
Documents production and production processes by completing production log sheets, recording the receipt and usage of raw materials, and calculating material usage.
Understands customer and product requirements, monitors and adjusts processes to ensure compliance.
Understands environmental regulations and complies fully.
Requirements and Qualifications:
High school diploma or GED
2-5 years working in a manufacturing environment
Experience working in a team
Ability to work in a logical organized manner
Able to work safely using tools and equipment
Ability to work effectively, efficiently and safely to schedules and deadlines
Chemical manufacturing experience Desired
Lean manufacturing (including 5S) Desired
Familiarity with SAP S4 Hana or equivalent ERP system is beneficial
Skills & Knowledge:
Must have the ability to prioritize tasks and work well under pressure
Computer literate - Experience using MS Office; Excel, Word & Outlook
Basic mathematics
Accurate data entry
Forklift truck license desired
Boiler license desired
Luxfer MEL Technologies is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status. Women, minorities and veterans are encouraged to apply.
This position requires access to our export-controlled commodities, technical data, technology, and services. These items are restricted under the International Traffic in Arms Regulations (ITAR) to U.S. Citizens, Lawful Permanent Residents of the U.S., and properly licensed foreign persons. To conform to U.S. Government export regulations, applicant must be a i) a U.S. citizen or national, ii) U.S. lawful permanent resident (aka green card holder), iii) refugee under 8 U.S.C. §1157, or iv) asylee under 8 U.S.C. § 1158, or be a properly licensed foreign person. Therefore, employment is contingent on compliance with ITAR regulations and successfully obtaining and maintaining the necessary export authorization license from the U.S. Department of Commerce Bureau of Industry and Security (BIS) or U.S. Department of State Directorate of Defense Trade Controls (DDTC). Candidates must be authorized to work in the US.
We are committed to a safe, drug-free work environment and pre-employment drug screening and background checks are required.
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UOIv4MsGZ0
Production Operator - Mon - Fri Night Shift (11pm - 7:30am)
Production worker job in Flemington, NJ
Luxfer MEL Technologies is a global leader in the development, manufacture and supply of Magnesium and Zirconium based products and services to technology industries worldwide. We provide innovative products and solutions to customers worldwide for use in a broad range of markets including Aerospace, Automotive, Oil & Gas, Ceramics and Healthcare. We have a wide range of products, including Hazardous, Non-Hazardous and Export shipments. We are an innovative technology driven business where we have a relentless drive and a passion to achieve high standards. At Luxfer Customer First, Integrity, Accountability, Innovation, Personal Development and Teamwork are our core values.
The main purpose of the role is to work as part of a team with responsibilities on the production line reporting to the Team Leader. You will also be required to work flexibly and may be required to work on other related activities when the business need requires.
Benefits
* Medical, Dental, Vision Insurance, eligible on the 1st of the month following hire
* Disability and Life Insurance
* 401k Plan with Company Match
* Tuition Reimbursement
* Career Advancement Opportunities
* Hourly rate $20-$25
Main responsibilities:
* Understanding the basic chemistry involved in the process in order to effectively monitor and troubleshoot. Operators are expected to continually upgrade their skills until they fully understand the entire plant process flow in addition to the basic chemistry of all the plant processes.
* Maintaining the work area in a safe and tidy condition. Adhering to Health & Safety policy and procedures.
* Monitors processes, performs required measurements and tests, monitors the operation of equipment and sets equipment controls in maintain right-first time quality products.
* Maintains production line operation by following SOP's, solving production process problems and reporting to others to achieve the short-term manufacturing plans.
* Understanding the basic mechanical operations of the process in order to effectively monitor and troubleshoot. Through continuous improvement, Operators upgrade their skills until they understand the basic mechanical aspects of the entire plant.
* Monitors equipment operation on a day-to-day basis. Performs basic troubleshooting, notifying Team Leader and Maintenance when a situation is beyond limits. Assists in the repairs to equipment and other simple maintenance tasks. Participates in equipment PM and project installation as necessary.
* Documents production and production processes by completing production log sheets, recording the receipt and usage of raw materials, and calculating material usage.
* Understands customer and product requirements, monitors and adjusts processes to ensure compliance.
* Understands environmental regulations and complies fully.
Requirements and Qualifications:
* High school diploma or GED
* 2-5 years working in a manufacturing environment
* Experience working in a team
* Ability to work in a logical organized manner
* Able to work safely using tools and equipment
* Ability to work effectively, efficiently and safely to schedules and deadlines
* Chemical manufacturing experience Desired
* Lean manufacturing (including 5S) Desired
* Familiarity with SAP S4 Hana or equivalent ERP system would be beneficial
Skills & Knowledge:
* Must have the ability to prioritize tasks and work well under pressure
* Computer literate - Experience using MS Office; Excel, Word & Outlook
* Basic mathematics
* Accurate data entry
* Forklift truck license desired
* Boiler license desired
Luxfer MEL Technologies is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status. Women, minorities and veterans are encouraged to apply.
This role may involve access to Controlled Unclassified Information (CUI) and export-controlled data subject to the International Traffic in Arms Regulations (ITAR). Employees are expected to follow company policies and security protocols for handling, storing, accessing, and transmitting sensitive information. Compliance training will be required after hire.
Due to federal export control requirements, access to certain information is limited to U.S. Citizens, U.S. Lawful Permanent Residents, and individuals lawfully admitted as asylees or refugees, unless a valid export authorization is obtained. Employment is contingent upon meeting these eligibility requirements and adhering to applicable CUI and ITAR policies.
We are committed to a safe, drug-free work environment and pre-employment drug screening and background checks are required.
Production Operator
Production worker job in Cranbury, NJ
Job DescriptionLocationCranburyJob Purpose
Responsible for the execution of all aspects of solid-dosage manufacturing which includes, but is not limited to, the dispensing, granulation, sifting, milling, drying, encapsulation, coating, compression, and cleaning related activities. Must be able to interact daily with all site support personnel as required. Must be able to complete all required batch record documentation in a thorough, accurate, and legible manner in English. Must be capable of reading and understanding all documented Standard Operating Procedures in English plus demonstrate competency through action and written evaluation.
Essential Duties and Responsibilities
Assist Production Management with all scheduled and requested activities in an efficient and smooth operation.
Ensure all scheduled commercial and non-commercial manufacturing activities are completed on time.
Become proficient in the setup, operation, and cleaning of all cGMP equipment used during production operations.
Participate in all Quality Investigations as required.
Adhere to all approved Standard Operating Procedures, Batch Records, and Safety Procedures as written when performing all daily activities.
Ensure the cGMP area is cleaned and maintained following all SOPs and good housekeeping practices.
Must use required PPE during cGMP activities as specified in the Batch Records and Safety Data Sheets.
Requirements to Perform the Job Successfully
Familiarity with working in a regulated pharmaceutical solid dosage facility.
Ability to read and write documents written in English.
Excellent written communication skills.
Familiarity with various cGMP solid dosage pharmaceutical manufacturing equipment. Able to setup, operate, clean, and troubleshoot the solid dosage pharmaceutical manufacturing equipment being used.
Able to work with minimal supervision.
Able to stand on feet throughout an eight-hour workday.
Able to lift up to 30 lbs (14 kgs) without assistance.
Maintain personal hygiene habits consistent with working in a cGMP environment.
Be capable of wearing all required PPE, including partial and full facepieces based on OSHA guidelines.
Education
High School Diploma or GED Equivalent.
Bachelors degree in Physical Sciences or Pharmaceutical Life Sciencerelated field of study.