Production Operator Jobs in Collingswood, NJ

Our large home building client is currently hiring for 2 Production Workers to join their team in Morrisville PA. These individuals will be responsible for working on the production of interior and exterior doors. Specifically, they will be building and assembling these doors, lifting them onto the table, ensuring accurate measurements, and getting them built properly. This individual should have a background within the residential construction space and experience/comfortability working day in and day out with their hands. The ideal candidate will have experience working with a tape measure, as well as using tools such as nail guns, screw guns, and chop saws. This individual will be required to lift the doors on a daily basis so ability to lift 80lbs is required. This is a full-time onsite position working 4, 10-hour shifts, Monday through Thursday. Hours are 6AM-4:30PM Compensation: $8.85/hr - $31.25/hr Exact compensation may vary based on several factors, including skills, experience, and education. Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.

At this company we believe in passionately working toward helping patients Do More, Feel Better, and Live Longer. We do this by supporting our energetic, dynamic teams. Under the direction of senior personnel, you will perform production operations including cell culture operations, preparation of media and buffer solutions, chromatographic separation, sterile filtration, and concentration operations. Work with various equipment including: bioreactors, tanks, chromatography columns, agitators, filtration devices, centrifuges, autoclaves, washers, computers and software, and other instrumentation. Time management skills, clear communication, self-motivation, and team work will be required for this position. • Being able to work a flexible shift schedule which includes coverage every other weekend. Includes possible placement on AM or PM shifts. • Completing daily manufacturing tasks per cGMPs, standard operating procedures, and batch document instructions • Monitoring critical process parameters • Documenting all manufacturing activities clearly and accurately. • Active participation in effective troubleshooting of equipment and processing issues • Ensuring all processing equipment and materials necessary are adequate and available to set the team up for success • Maintaining a high level of mechanical and technical aptitude and training • Ensuring all production activities are completed in a safe and compliant manor. • Joining a diverse shift team that will rely on consistent contributions to be successful QUALIFICATIONS: Required: • This is a HANDS-ON manufacturing role. Ability to work scheduled hours on-site. • HS Diploma or equivalent • Strong desire for science & technology Preferred: • Experience in manufacturing • Experience in science & technology • 4 year degree in biological/life science

Machine Operator Clearance Requirements: N/A Open Pay Rate: $17/hr on W2 **Shift time(B): 2pm - 10pm • At least 18 years of age • Mobile Equipment Operator Exam completion & medically cleared to work by Altria required criteria through Concentra • Legally eligible to work in the United States and for John Middleton Company • Available to work any shift, and must be willing to work mandatory overtime, weekends, and holidays • Possess manufacturing experience, operator experience, or relevant military experience preferred • Basic computer skills including Microsoft office preferred • Regular, reliable, and predictable attendance Your job duties/responsibilities may include, but are not limited to: • Operating machines and processing product to meet all quality requirements as a skilled machine operator • Understanding and following safety rules and practices and ensuring the safety of self and others • Reviewing and following written instructions, work procedures, and safety procedures and requirements • Assisting area team members in ensuring operational procedures are being maintained according to company standards • Monitoring and inspecting equipment, materials, or products • Identifying and resolving problems in processes or equipment • Ability to train and qualify on all HMI's • Listening to others, asking questions, and explaining and sharing information with your team to solve problems • Reviewing, interpreting, or entering data on paper and computers • Using or cleaning machines, equipment, or tools • Completing tasks that require manual work and some level of physical effort such as lifting to 50 pounds, carrying, pushing, pulling, climbing ladders, bending, stooping, crawling, and walking or standing most of your shift • Some of the working conditions are not climate controlled, so you may be working in hot or cold conditions and in dusty or dirty work environments About Seneca Resources: Seneca Resources is a client driven provider of strategic Information Technology consulting services and Workforce Solutions to government and industry. Seneca Resources is a leading IT services provider with offices in Virginia, Alabama, Georgia, Florida and Texas that service clients throughout the United States. We are an Equal Opportunity Employer and value the benefits of diversity in our workplace.

We are seeking a skilled and reliable Machine Operator to join our team, The ideal candidate will be responsible for operating machines, processing products, and maintaining high-quality standards in our manufacturing environment. Job Title: Machine Operator Payrate: $18.50/hr on W2 Bill Rate: $26 Schedule: M-F 6AM-2PM Location: 418 W Church Rd King of Prussia, PA 19406 Duration: 12+ months Job Description: Your job duties/responsibilities may include, but are not limited to: • Operating machines and processing product to meet all quality requirements as a skilled machine operator • Understanding and following safety rules and practices and ensuring the safety of self and others • Reviewing and following written instructions, work procedures, and safety procedures and requirements • Assisting area team members in ensuring operational procedures are being maintained according to company standards • Monitoring and inspecting equipment, materials, or products • Identifying and resolving problems in processes or equipment • Ability to train and qualify on all HMI's • Listening to others, asking questions, and explaining and sharing information with your team to solve problems • Reviewing, interpreting, or entering data on paper and computers • Using or cleaning machines, equipment, or tools • Completing tasks that require manual work and some level of physical effort such as lifting to 50 pounds, carrying, pushing, pulling, climbing ladders, bending, stooping, crawling, and walking or standing most of your shift • Some of the working conditions are not climate controlled, so you may be working in hot or cold conditions and in dusty or dirty work environments Required Qualifications are: • At least 18 years of age • Legally eligible to work in the United States and for John Middleton Company and have high school diploma or equivalent. • Available to work any shift, and must be willing to work mandatory overtime, weekends, and holidays • Possess manufacturing experience, operator experience, or relevant military experience preferred • Basic computer skills including Microsoft office preferred • Regular, reliable, and predictable attendance

*Work Schedule* Standard (Mon-Fri)*Environmental Conditions* Office** Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission - to enable our clients to make the world healthier, safer, and cleaner. Within our Analytical Services team, we have a functional service provider solution, which is an outstanding partnership that allows our customers to use the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits. Perform all tasks assigned per Sterile Manufacturing Operator job description which includes, but is not limited to: • Able to perform all technical operations in area of assignment at a high level of proficiency, such as logging in materials, inspection for damage and cold chain compliance, maintaining inventory records, sampling of raw materials, and updating materials in conformity to GMP standards. • Store materials in appropriately identified manner in suitable environment. • Maintain inventory records. • Performs packaging of materials for shipment with minimal supervision. • Contributes to the creation and revision of Material specifications, accession control forms and SOPs. • Maintains housekeeping of the area and restocking of general supplies. • Coordinates transfer of excipients, components, and samples to support clinical and pre-clinical manufacture and component processing orders. • Manage inventories and schedule activities appropriately. • Contributes to relevant investigations. • Assist in the preparation of metrics and key KPIs for the area. • Able to identify and coordinate implementation of safety, quality, and business improvements. • Employee will participate in department consumables storage and stocking programs. • Employee may be asked to perform administrative tasks such as procedure revision, template revision, records filing, records archiving, and other tasks as needed. • All job functions will be performed according to procedure and in accordance with cGMPs, Standard Operating Procedures, and safety codes and regulations. • Identifies risks to business for consideration by management. • Assist and contribute to GMP and safety self-inspection activities. • Accountable for reporting and maintaining metrics as appropriate. • Zero instances of data falsification or data integrity issues by PPD staff. • Employee has basic computer skills including Word, Outlook, and ability to navigate simple website interfaces. • When performing manufacturing operations, employee will be expected to wear appropriate gowning (scrubs, hair net, beard cover, gloves, safety glasses, safety shoes), stand for periods of time, and operate standard pharmaceutical manufacturing equipment. • Employee must have good hygiene, practice good hand-washing behaviors, and be comfortable frequently using hand sanitizing agents. *Education and Experience:* * Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0-1+ years). *In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. * *Knowledge, Skills and Abilities: * * Knowledge of applicable regulatory authority, compendia and ICH guidelines * Ability to understand and independently apply GMPs and /or GLPs to everyday work with regard to documentation and instrument use * Ability to utilize Microsoft Excel and Word to perform tasks * Ability to independently optimize analytical methods * Good written and oral communication skills * Time management and project management skills * Problem solving and troubleshooting abilities * Ability to work in a collaborative work environment with a team Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role: * Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner. * Able to work upright and stationary and/or standing for typical working hours. * Able to lift and move objects up to 25 pounds. * Able to work in non-traditional work environments. * Able to use and learn standard office equipment and technology with proficiency. * May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments. * Able to perform successfully under pressure while prioritizing and handling multiple projects or activities. We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

Our client is currently seeking a Central Processing Department Technician! 2 shifts available: 7a-3:30p -OR- 3p-11:30p This position is responsible for ensuring that all reusable surgical supplies, instruments, and equipment are properly decontaminated, inspected, assembled, packaged, sterilized, stored, inventoried, and appropriately tracked in accordance with the established departmental and or hospital policies and procedures. Qualifications & Requirements: 2 years Central Processing Department Technician (CPD Tech) experience in an Inpatient Hospital setting Certified Registered Central Service Technician (CRCST) Certification Certified Endoscope Reprocessor (CER) Thank you for your time, we look forward to working with you!

As this person will be a key member of the autologous cell therapy manufacturing program, a background in cell culture, aseptic gowning and qualification, and ISO class 5 cleanroom operations is required. Specific Responsibilities Develop a comprehensive understanding of and be able to proficiently execute current cell therapy manufacturing process. Complete training sessions and ensure training documentation is maintained. Understands and complies with quality standards and requirements as documented. Provides operational support functions including materials stocking, kit preparation, reagent preparation, cleaning activities, and equipment maintenance. Supports technical transfer and additional research level testing activities. Adheres to Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs), including Good Documentation Practices (GDP). Completes recording of data to comply with regulatory requirements. Support documentation needs, which may including drafting and approval of SOPs, Batch Records, Deviations, CAPAs, etc. Perform basic revisions as needed to accurately reflect current procedures. Attends the daily lab meeting and escalates issues/concerns at that forum to Area Management for further investigation. Ability to work in a team environment and independently as required. Works on routine assignments per written procedures, where ability to recognize deviation from accepted practice is required. Other duties as assigned. Qualifications Minimum B.S. degree in biology, biochemistry, bioengineering, or related technical field, or equivalent industry experience. 0-5 years of experience in biopharmaceutical based GMP manufacturing operations, including experience in cell culture and associated downstream processing. Demonstrated technical knowledge of aseptic processing in cleanroom environments is a must. Ability to mentor and provide best practices to other members of the team. Ability to build relationships quickly and credibly. Ability to accurately and reproducibly perform arithmetic calculations including fractions, decimals and percentages and basic algebraic and geometric calculations. Proactive, results oriented, self-starter with experience in a complex manufacturing environment. Ability to work successfully in a fast-paced team-oriented environment. Quality mindset, familiar with 21 CFR Part 11 and standard GxP best practices and FDA regulations. Must adhere to core values, policies, procedures and business ethics. Need to be able to read, write and understand English, and be proficient in Microsoft (Excel, Word, Outlook). May require up to 5% travel, based on business need. Physical Requirements Must be able to work in environment with variable noise levels Must be able to work in Lab setting with Biohazards /various Chemicals Clarity of vision at near and mid-range, depth perception, ability to identify and distinguish colors. Must be able to wear appropriate clean room attire and all Personal Protective Equipment (PPE), i.e. scrubs, gowning coverall, masks, gloves, etc. Works in production environment with exposure to latex and bleach. Potential exposure to noise and equipment hazards and strong odors. Ability to stand/sit/walk for long periods of time Ability to crouch, bend, twist, reach, and perform activities with repetitive motions Ability to lift 20 lbs Shifts: Wednesday - Saturday or Sunday - Wednesday (4 Days a week / 10 hours each) 616604

Job Title- Production Supervisor Pay Rate: $36.15/hr on W2 (US Citizen and GC only) 2nd Shift and Alternate Sat working At our client and through their businesses, They create innovative climate solutions for buildings, homes, and transportation that challenge what's possible for a sustainable world. We're a team that dares to look at the world's challenges and see impactful possibilities. We believe in a better future when we uplift others and enable our people to thrive at work and at home. We boldly go. Job Summary: Clients, Trenton, New Jersey is hiring a Plant Supervisor. In this role you will supervise and coordinate daily operation of production shift with responsibility for achieving quality and cost effectiveness in an on time and efficient manner. Responsible for implementing and driving change in a high volume, fast-paced, lean manufacturing environment. Interacts daily with department supervisors/leaders in Operations, Quality, Human Resources, Finance, Materials, Engineering, and Continuous Improvement. Responsibilities: • Responsible for overall performance of assigned work group, including safety, quality, cost and output schedule performance. • Supervises the activities of production or plant associates to achieve objectives with regard to quality, cost and time. Evaluates the performance of associates and completes necessary reports. Recommends merit increases and training/development needs. • Supervises the utilization of materials to assure an appropriate amount of parts are available to maintain smooth production flow; identifies wasteful practices and methods; reports any problems/concerns with viable solutions to the Manager, Production; and, reports suggestions recommended by associates for procedure change, etc. • Actively support plant programs and goals, including but not limited to: units per man hour, safety and 5S, quality, customer availability, TAKT attainment, and cost as measured by overall plant performance. • Identify opportunities for improvement; implement improvement plans, lead daily problem-solving activities within teams for process improvements, develop department budgets and ensure they are to plan. • Provide for effective associate relations within manufacturing by ensuring that employment practices are fair and consistent. Ensure adherence to standard work, including plant work rules, collective bargaining agreement and payroll compliance (if applicable) • Implement plant wide communication plans and initiatives with employees in area of responsibility. Serve as primary communication vehicle between leadership team and production employee. Qualifications: • Bachelor's Degree or business degree preferred. • 1 to 3 years of manufacturing experience. • Must possess sound interpersonal skills and demonstrated ability to work effectively in a team environment. • Excellent problem solving and conflict management skills. • Lean or Six Sigma Experience Preferred • Supervisory experience preferred. • Experience in a union environment preferred About Acro: Acro Service Corporation is a global professional services and contract staffing company that has provided IT, Engineering, and Professional services/ personnel to major corporations. Acro values diversity in our workforce and is an Affirmative Action & Equal Opportunity Employer. Acro is also committed to hiring veterans and offers sponsorship opportunities

Responsible for various tasks, such as cleaning, sanitization, preparation, and fulfilling products for commercial and clinical use. Perform document review, including executed Batch Records and Logbooks. Support documentation needs, which include a review of SOPs, Batch Records, Deviations, CAPAs, etc. Supports technical transfer and additional research-level testing activities as needed May support training sessions as a qualified trainer, ensuring training documentation is maintained. Qualifications: Minimum 2 years of experience in biopharmaceutical-based GMP manufacturing operations, including experience in cell culture and associated downstream processing. Quality mindset, familiar with 21 CFR Part 11 and standard GxP best practices and FDA Preferably with experience in cell culture, aseptic gowning and qualification, and ISO class 5 cleanroom operation

Avo Photonics is a dynamic contract engineering services company that designs, develops, and manufactures custom opto-electronic products for a large customer base. We seek a diligent, dedicated, and meticulous person who will help further our success and reputation in the industry. The successful candidate will have at least three years of manufacturing experience. Responsibilities: Support Process Engineering team by assembling prototypes and provide critical feedback on process viability for manufacturing Perform directed design of experiments; record structured data against controlled experiments and generate reports on procedure and results Perform documented performance checks, calibrations, and preventative maintenance on equipment including laser welders, seam sealers, die bonders, wire bonders, and more Collect measurements to ensure workstations are meeting ESD and cleanroom standards Review work instructions and provide training on developed processes to Manufacturing team Troubleshoot equipment and optical workstations to quickly resolve authorized production-impacting issues Requirements: A.S. (B.S. preferred) in the Sciences or Engineering 3 years of manufacturing experience 2 years experience in an engineer facing role Excellent communication skills and willingness to learn Avo Photonics offers competitive salaries and a comprehensive benefits package. Avo Photonics is not accepting unsolicited assistance from search firms for this employment opportunity. All resumes submitted by search firms to any employee of Avo Photonics by any method without a valid written contract in place with Avo Photonics will be deemed the sole property of Avo Photonics. No fee will be paid in the event the candidate is hired by Avo Photonics as a result of the referral or through any other means.

Under supervision and guidance, the Process Technician of Upstream Operations will be responsible for hand-on executing the routine operation, maintenance, and periodically requalification of cell culture based upstream production equipment and production suites in a cGMP biopharmaceutical pilot plant. In addition, the individual will execute and participate in the execution activities for scale-up and system operations supporting the manufacture of preclinical, clinical, and commercial biologics drug substances, including operation of cell culture bioreactors and harvest equipment, GMP documentation, and ensuring compliance to relevant regulations. Responsibilities Work in a hands-on capacity in the operation of upstream equipment for the manufacture of preclinical, clinical, and commercial biologics drug substances. Ability to follow oral and written instructions, maintain neat, accurate, and current training and cGMP records. Performs all work duties via automated systems or manual operations in compliance with safe operating procedures, company and government regulations, and good manufacturing practices. Perform process performance sampling/ in process testing supporting the manufacturing. Maintains, inventories, and transports all required equipment, materials, supplies and products. Some heavy lifting is expected. Participate and contribute in the validation maintenance, re-qualification of upstream (cell culture and harvest) production equipment. Assist and contribute in the commissioning of new equipment for upstream manufacturing. Participation in other areas within the facility may be added at the company's discretion. Assist in equipment maintenance and calibration with appropriate internal departments. Provide cross-functional support for other departments within the pilot plant at the discretion of management. The individual will play a hand-on execution role in the routine operation of the Biological pilot plant whose purpose is to produce material for preclinical, clinical, and commercial biologics drug substance to support Company's pipelines. Execution of manufacturing in the GMP production suites including documenting data compliantly. Specifically, this person will participate and contribute to the success of the cell culture and harvest equipment operation and processes for the manufacture of materials for global clinical supplies. The individual will also participate in monitoring and maintaining the production area processes to remain compliant to regulations. The individual may also supporting a campaign and may provide cross-functional support for other departments within the pilot plant at the discretion of management. Education: Two-year Associate degree or Four-year BS in Biotechnology or (Bio) Chemical Engineering or Engineering or Biological Sciences or equivalent job experience/degree is strongly preferred. Experience: Minimum of 2-5 year (Associate degree) or 1-3 year (BS) practical scientific experience. Ability to follow direction, work under supervision, and demonstrate capability in organizing complex activities in a cGMP production process. Basic skills in executing routine production, maintenance, and operation of upstream cell culture and harvest equipment. Must have a Mechanical aptitude. Good aseptic technique in maintaining process sterility. Good written, communication, and interpersonal skills with the ability to work in a team environment required. Capabilities in the operation of all area-specific production equipment such as large scale stir tank and/or single-use disposable bioreactors, centrifuge, micro-filtration, and CIP/SIP operations is a plus. Previous exposures to cGMP, EMEA, and JP regulations as a plus.

Ecolab, the global leader in premium cleaning, sanitizing and maintenance products and services for the hospitality, institutional and industrial markets is seeking a Chemical Mixer. This role is responsible for mixing chemical batches by following standard formulas, applicable instructions and current standard operating procedures. What's in it For You: The opportunity to take on some of the world's most meaningful challenges, helping customers achieve clean water, safe food, and healthy environments The ability to make an impact and shape your career with a company that is passionate about growth The support of an organization that believes it is vital to include and engage diverse people, perspectives and ideas to achieve our best Comprehensive benefits package starting day one of employment including medical, dental, vision, matching 401k, company paid pension, stock purchase plan, tuition reimbursement and more! Click Here to see our benefits. What You Will Do: Review daily mix schedules and ensures the raw materials required are available Follow mix instructions and accurately adds raw materials to the mixes manually, using pumps or mixing systems Mix batches using variable agitation Perform routine observation of product during the mixing and filling process to ensure batch quality. Report any out-of-spec raw material, premixes or mixed batches and consults with Quality personnel on any batch adjustments. Properly cleans out all mix tanks Operate fork trucks, palletizers, scales, pumps and other material handling equipment to transport raw material and finished product Perform building and equipment preventative maintenance Perform other duties as assigned Position Details: Plant location: King of Prussia, PA Work week and shift: 12-hour fixed schedule (Day shift and night shift available) Minimum Qualifications: High School diploma or equivalent Ability to work safely and efficiently Ability to understand systems, pumps, read meters, basic Quality Control data and to track mixing and quality information (mix logs, batch adjustments, etc.) Ability to perform basic Quality Control tests (take samples, perform pH tests) Excellent attention to detail; must be able to simultaneously mix several tanks and accurately complete related documents Ability to read and match numbers on shipping records, labels, raw materials and finished goods No Immigration Sponsorship available for this opportunity Preferred Qualifications: Previous experience working in a chemical and/or manufacturing environment Basic knowledge of chemistry Ability to work in a fast-paced environment Excellent organizational skills and ability to multitask Excellent communication skills and the ability to work as part of a team Physical Requirements: Must be able to lift/carry 50lbs Must be able to participate in respirator fitness, if required Must be able to pass a drug screen and physical exam Annual or Hourly Compensation Range: $27.00-$33.00 per hour Many factors are taken into consideration when determining compensation, such as experience, education, training, geography, etc. We comply with all minimum wage and overtime laws. Benefits Ecolab provides the following benefits: medical, dental, vision, life insurance, accident insurance, critical illness insurance, hospital indemnity insurance, auto insurance, home insurance, pet insurance, identity theft protection, short-term and long-term disability, 401k, pension plans, retirement health care benefits, short-term incentives, vacation (12 days), holidays, parental leave, employee stock purchase plans (Full-Time Associates), discount on day care services and caregiver services, adoption assistance, group legal services, employee assistance program, employee discount program, and education assistance program, on-Site childcare and fitness facilities may be available at select Ecolab locations. Click here for additional benefits information. If you are viewing this posting on a site other than our Ecolab Career website, view our benefits at jobs.ecolab.com/working-here . Potential Customer Requirements Notice To meet customer requirements and comply with local or state regulations, applicants for certain customer-facing roles may need to: - Undergo additional background screens and/or drug/alcohol testing for customer credentialing. - Be fully vaccinated for COVID-19, including a booster if eligible, unless a religious or medical accommodation is requested by the applicant and approved by Ecolab. Americans with Disabilities Act (ADA) Ecolab will provide reasonable accommodation (such as a qualified sign language interpreter or other personal assistance) with our application process upon request as required to comply with applicable laws. If you have a disability and require accommodation assistance in this application process, please visit the Recruiting Support link in the footer of each page of our career website.

Machine Operator **DNA Recruitment** - Mordialloc, VIC Trades & Services Source: ***Kingston Jobs*** JOB DESCRIPTION **temp to perm** opportunity with day and afternoon shifts available and a chance to grow within a cutting-edge industry. **What You'll Do:** * Operate cutting-edge machinery * Perform preventive maintenance to ensure smooth operations * Maintain top-quality standards across all products * Drive efficiency, minimizing waste and maximizing processes * Keep the plant and work areas clean and organized * Prioritize safety by following strict safety protocols **What You'll Need:** * Valid forklift license (essential) * A sharp eye for detail and a strong commitment to safety * Thrive in a fast-paced, high-energy environment * A mechanical mindset to anticipate needs and resolve issues * Adaptability and a strong willingness to learn * Ability to work independently or as part of a collaborative team * Excellent communication skills **What's in It for You:** * Temp to perm opportunity for the right candidate * Ongoing training to grow your skills * Immediate start available! * Competitive pay: $31.23 per hour (day shift) | $35.91 per hour (afternoon shift) **Shifts Available:** * **Day Shift:** 10 AM to 6 PM * **Afternoon Shift:** 2 PM to 10 PM We can't wait to hear from you! **Job Types:**

This position is responsible for inspecting and packing quality product in a safe, efficient and quality manner. Essential Duties Include: · Respond to /and operate machines · Identify serious problems for maintenance · Assemble and pack boxes with light-weight packaging components consisting of lids and tubs · Place boxes of finished goods on skids approximately 24 times per hour · On occasion (up to approximately 6 times per hour) lift cases weighing up to 30lbs. to a height of 6 ft. to put on skids · Push boxes into case sealer · Deliver materials to machines (inserts, film, color, resin, etc.) · Inspect product as per quality standards and pack boxes · Apply proper labels and identification codes to boxes of product · Complete traceability forms and record production data, enter data into computer, verify that correct labels are applied to boxes and production information is correct. · Perform online quality checks · Maintain a clean and organized work area · Perform c/o in a timely manner following procedures and work instructions. · Follow procedures and guideline as defined by the Good Manufacturing Practices (GMP) and the Master Cleaning Schedule Double H offers competitive pay and benefits! 2nd Shift: 3:00pm-11:30pm

Overview: GEON is actively looking for experienced individuals on our night shift. Hours are 7:00 PM - 7:30 AM. Benefits: Our Experienced Operator base pay range is $21.55 to $27.50 per hour. In addition to competitive pay, we also currently offer $1,500 Sign-On and Referral bonuses, manufacturing incentive bonus, and paid time-off plans. Benefits include medical, dental, vision, life insurance, disability, spending accounts and 401(k) that all start on your first day. As a member of GEON Nation, you will join a team of associates whose daily contributions drive our rich culture and legacy forward. With global operations spanning the U.S., Canada, Mexico, and China, we celebrate our rich diversity and invite you to share in our core values of Win Together, Create Opportunities and Pay it Forward. Your Career at GEON Performance Solutions: Your career at GEON Performance Solutions will be full of rewarding challenges and professional growth in a culture of respect, tolerance, and continuous improvement. Your journey on GEON's manufacturing team will start based on your experience in manufacturing, specifically with PVC and CPVC compounds. We're looking for people to join our team who are excited and energized inventing the future in polymer compounding and process technology. We offer cross-training and help you develop additional skills to ensure your future success and advancement at GEON Performance Solutions Job Summary: GEON Performance Solutions has an excellent opportunity for an experienced Production Operator for the Croydon, PA facility. Under the direction of the Production Supervisor, the Production Operator is responsible for the setup and operation of equipment that blends/mixes/extrudes/ packages/transports the liquid or dry chemicals that comprise our customer products. The Production Operator ensures the highest quality product at the lowest possible costs while meeting customer specifications and delivery requirements per GEON Performance Solutions' policies and procedures. Essential Functions * Sets up and starts all machines, checking all controls for adherence to procedures. * Weighs ingredients to meet recipe specifications and inserts into machinery. * Monitors production and equipment to ensure safe and efficient operation. Troubleshoots equipment and processing issues. * Operates machinery to mix, discharge or handle materials according to operating procedures. * Examines materials visually or physically to ensure conformance with established standards. * May take samples of materials to lab for evaluations and instructions. * Refers issues/problems to lead/supervisor for disposition. * Performs all required machine cleaning * Completes and maintains all required computer inputs. Responsible for data integrity. * Documents work completed as required including logs, data reports, procedures, etc. * Participates in training, retraining and continual improvement processes and methods. * Maintains departmental housekeeping standards. * Follows all rules, laws and procedures related to HS&E, ISO, and other regulations. * Other duties as assigned. Education and Experience * US High School diploma or GED equivalency * Six (6) to ten (10) years of Manufacturing Machine Operation Experience * Experience with Polymer Process Experience (Extrusion, Injection Molding, Milling) or Lead Operator or Shift Leader Experience in Manufacturing a plus Additional Qualifications * Must successfully complete assessment of mechanical skills and applications * Must proficiently communicate in writing and verbally in English. * Basic competency in computer and PC software including email, internet, and MS office. * Must have superior manual dexterity for hand tools of various types. * Must be able to safely operate a forklift. * Must have problem-solving skills and mechanical aptitude. * Must have flexibility to work overtime coverage as required and weekend work. Physical Demands While performing the duties of this job, the employee is regularly required to stand; walk; stoop, kneel, crouch or crawl; use hands to finger, handle or feel objects, tools, or controls; talk and/or hear. Occasionally required to sit. The employee must frequently lift and/or move up to 55 pounds and occasionally handle up to 250 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus. Requires the use of safety equipment as dictated by the work area such as safety glasses and shoes, dust mask, hard hat, respirator, face shield, hearing protection, chemical suit, gloves, aprons, etc. The noise level in the work environment is usually moderate except for high noise areas. Proper personal safety equipment needs to be used while performing this job and that equipment is dictated by the plant safety guidelines. While performing the duties of this job, the employee is regularly exposed to wet and/or humid conditions, moving mechanical parts, dust, fumes, airborne particles, chemical dust, vibration, non-hazardous chemical agents, and outside weather conditions. GEON Performance Solutions is a drug-free workplace. GEON Performance Solutions is an equal opportunity employer. We maintain a policy of non-discrimination in providing equal employment to all qualified employees and candidates regardless of race, sex, sexual orientation, gender identity, age, color, religion, national origin, disability, genetic information, protected veteran's status, or other legally protected classification following applicable state and local law.

in Cherry Hill NJ. In accordance with Hikma SOP's and cGMP's, the Production Operator II is responsible for the inspection, labeling and packaging of finished drug product. The Production Operator II position will execute these tasks manually, or will be responsible for operating equipment that performs these functions. Performs visual inspection of drug product in accordance with SOP's and cGMP's. Performs manual packaging functions as required. Sets up, maintains and operates various pieces of computerized and manual inspection/packaging equipment. Performs line clearance of assigned production lines as required. Adheres to cGMP's and internal SOP's as required. Responsible for maintaining the quality of machine output and product integrity. Responsible for maintaining a clean production environment during shift. Completes and maintains applicable log book and batch record paperwork as required. Reports both machine and manual deviations to area supervisor or designee. Performs other related production functions, such as: Inspector, Packer, Catching, etc. as determined by supervisor and/or management. H.S. Diploma or equivalent is required. Some college and/or college degree preferred. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. A close visual acuity (eye exam) is required. Employee may be required to lift 5 - 40 pounds. Employee may be required to stand continually throughout the shift. Job involves frequent bending, twisting, pushing, pulling and lifting. The noise level of the job environment is moderate. Hearing protection is provided and may be required at times.

Company: AmeriGas Propane, Inc. Remote Options: Requistion Number: 25176 When you work for AmeriGas, you become a part of something BIG! Founded in 1959, AmeriGas is the nation's premiere propane company, serving over 1.5 million residential, commercial, industrial and motor fuel propane customers. Together, over 6,500 dedicated professionals will deliver over 1 billion gallons of propane from 1,800+ distribution points across the United States. ****Posting**** Job Summary (Purpose): The Utility Worker primarily works in the outside production area of the AmeriGas Cylinder Exchange facility. The employee is responsible for the processing of cylinders (20 lb. barbeque grill cylinders). Key Characteristics: * Models a commitment to safety through his/her own day-to-day behavior; follows company safety procedures and policies * Demonstrates high professional and personal standards; has a commitment to quality, timeliness, and continuous improvement * Ability to function effectively as a member of a production team Duties and Responsibilities: * Sort, inspect, clean, paint, label, and refill empty cylinders. * Maintain a safety focus at all times and wear the proper PPE * Ensure the consistent quality of cylinders are being processed * Load filled cylinders onto the truck(s) for the next day's shipments. * Ability to stand and walk 8 - 12 hours per day. * Ability to lift 50 pounds repeatedly throughout the day. * Perform general housekeeping duties. Knowledge, Skills and Abilities: * Ability to follow processes, procedures, and instructions * Ability to function effectively as a member of a production team * Willingness to grow and learn * Basic mechanical aptitude * Basic computer knowledge * Work in a fast-paced environment * Be able to stand 8-10 hours per day * Ability to obtain required state licensing * Ability to be forklift certified Education and Experience Required: * 1 - 2 years work experience in manufacturing is preferred * High School Diploma or GED Working conditions: * Environmental conditions such as wind, rain, ice, and snow may affect this job, as the production area where the employee spends most of the workday is not enclosed. AmeriGas is an Equal Opportunity and Affirmative Action Employer. The Company does not discriminate on the basis of race, color, sex, national origin, disability, age, gender identity, sexual orientation, veteran status, or any other legally protected class in its practices. AmeriGas is a Drug Free Workplace. Candidates must be willing to submit to a pre-employment drug screen and a criminal background check. Successful applicants shall be required to pass a pre-employment drug screen as a condition of employment, and if hired, shall be subject to substance abuse testing in accordance with AmeriGas policies. As a federal contractor that engages in safety-sensitive work, AmeriGas cannot permit employees in certain positions to use medical marijuana, even if prescribed by an authorized physician. Similarly, applicants for such positions who are actively using medical marijuana may be denied hire on that basis. **Nearest Major Market:** New Jersey **Job Segment:** Behavioral Health, Substance Abuse, Industrial, Forklift, Warehouse, Healthcare, Manufacturing Provider Description Enabled SAP as service provider * "route" is used for session stickiness * "career SiteCompanyId" is used to send the request to the correct data center * "JSESSIONID" is placed on the visitor's device during the session so the server can identify the visitor * "Load balancer cookie" (actual cookie name may vary) prevents a visitor from bouncing from one instance to another

**GBP3750.00** **Production Operator Needed for Building Materials in Gloucester** Offered by: Ad ID: **Contact** Press to display the phone number (0************** **Post this ad on** **Description** Join our team as a Production Operator in Gloucester and play a key role in the manufacturing of high-quality building materials. As a member of our production team, you will operate machinery, monitor production processes, and ensure product quality. We are looking for candidates with experience in manufacturing and a strong attention to detail. Salary: £3,750.00. Contact Lucas at (0************** for more information! **Note** While using our platform to contact advertisers, we encourage you to exercise caution and prudence. It's important to note that the platform does not guarantee or control user behavior. When interacting with advertisers, we advise you to: - Verify the details provided in the ad before making any commitments. - Be wary of any requests for personal or financial information and avoid sharing sensitive details unless necessary. - Meet in a safe and public place if arranging in-person meetings. - Trust your instincts and report any suspicious activity immediately. Your safety and security are important to us. By remaining vigilant and exercising good judgment, you can help ensure a positive experience for yourself and other members of our community. **Safe Trading** Experience peace of mind with webmall.uk - where trust meets seamless transactions!

To monitor flow of incoming materials (bottles or cans) and outgoing finished goods and correct any disturbance in flow, working with maintenance as necessary. REPRESENTATIVE RESPONSIBILITIES: The following responsibilities are general duties that a particular employee in this position may or may not be required to perform. The actual duties required of this position will vary. Operate and monitor line. Remove or shift materials and/or finished product as necessary. Expedite repairs to line; working with maintenance as necessary. Communicate with laboratory and/or supervisor regarding product change and cut-off. Performs other job-related duties as assigned. Required: 3+ years Production Operator experience. Has knowledge of commonly-used concepts, practices, and procedures within a particular field. Preferred: Related training or certification. Experience working in a team environment. PHYSICAL DEMANDS: Lift/Carry 12lbs or less Occasionally 13-25lbs Frequently 26-40lbs Occasionally 41-100lbs Occasionally Push/Pull 12lbs or less Frequently 13-25lbs Frequently 26-40lbs Occasionally 41-100lbs Occasionally Other Bend Frequently Squat/Kneel Occasionally Twist/Turn Frequently Climb Frequently Crawl Occasionally Reach above Shoulder Occasionally Reach Outward Frequently Stand/Walk Constantly Sit Occasionally Drive Auto/Stand Occasionally Type/Keypunch Occasionally * We do not provide application status due to overwhelming volume. If your skills meet our needs, we will contact you to move forward in the process.* **EOE without regard to race, color, religion, creed, affectional or sexual orientation or sex, national origin, ancestry, age, disability, genetics, veteran status, gender, gender identity, citizenship status, marital status, VEVRAA Federal Contractor.** ***If you have a disability and you need an accommodation to apply, please contact the Sr. Director of Talent and Development at ************ ext. 2975***