Explore 5 batch processing operator jobs from 2 hiring companies in Newark, NJ, US. Filter by remote, salary, experience, and company, then open any listing to apply.

batch-processing-operator

Batch Processing Operator

New York City

Brooklyn

Manhattan

East Orange

Queens

Irvington

The Bronx

Elizabeth

Bloomfield

Union

Staten Island

Clifton

Paterson

Yonkers

Batch Processing Operator Jobs

Integra LifeSciences

Thermo Fisher Scientific

Onsite

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.This Clean Room Manufacturing Operator role will include processes such as enzymatic treatment of collagen, alkali treatment of collagen, tendon collagen prep, dispersion preparation, and lyophilization. It is essential to perform these tasks meticulously to ensure the quality of our products. Additionally, you will be responsible for the setup, operation, and cleaning of all clean room manufacturing equipment. This entails working in ISO Class 5 or ISO Class 7 areas and adhering to Clean Room gowning protocols. All operations must be conducted in compliance with Good Manufacturing Practices (GMP), Quality Systems Regulations, Standard Operating Procedures (SOPs), and Health and Safety requirements. Operating in a team environment, we emphasize daily achievements and maintaining high-quality standards in our production processes. Your dedication and attention to detail will play a valuable role in our success.ESSENTIAL DUTIES AND RESPONSIBILITIES To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.<ul><li>Operate, maintain, and troubleshoot process equipment utilized in the collagen business, and can make minor equipment adjustments as needed.</li><li>Responsible for performing precise measurements and using measurement equipment to accurately add chemicals to batches.</li><li>Blend, mix, pour, and load collagen prepped material into lyophilizing equipment.</li><li>Pass and maintain gowning qualification to perform Gowning Requirement for ISO Class 5 Clean room operations or ISO Class 7 Clean room operations.</li><li>Responsible for accurately maintaining legible and accurate records, required logs, books, 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.</li><li>Interface with QA/QC/Material departments during course of work to coordinate inspections and efficient flow of subassemblies and completed product.</li><li>Enter and record production activities in Oracle MRP systems to issue material and labor hours to specific work orders.</li><li>Follow applicable Standard Operating Procedures, Quality System Regulations and ISO 13485 requirements.</li><li>Responsible for handling, decontamination, and cleaning of production supplies, instruments, and equipment to support all cleanroom production related activities</li><li>Responsible for reporting all discrepancies to the Supervisor or Group Leader.</li><li>Support department and plant Safety goals by continuously demonstrating safe behavior.</li><li>Maintain a clean and orderly work area.</li></ul><ul><li>Ability to work flexible shifts, and flexible days within the week to meet batch milestone requirements.</li><li>Perform other manufacturing activities as assigned by the department leadership</li></ul>DESIRED MINIMUM QUALIFICATIONSThe requirements listed below are representative of the knowledge, skill, and/or ability required for this position.<ul><li>High School diploma or equivalent.  Degree in related science a plus.</li><li>0 - 2 years of chemical processing experience or batch mixing in Medical Device or Pharmaceutical manufacturing industry.   Production experience in a clean room environment is highly desirable.</li><li>Basic computer skills for email and data entry.</li></ul><ul><li>Must read, write and speak in English, and communicate clearly and concisely.</li><li>Fundamental understanding of mathematics and chemistry.</li><li>Able to participate in a team-oriented environment, willingness to assist and train others</li><li>Able to work independently with minimal supervision</li><li>Ability to operate, maintain and troubleshoot process equipment, and make minor adjustments as needed.</li><li>Ability to gown to ISO Class 5 and 7 Clean Room standards.</li><li>Able to work overtime</li></ul>TOOLS AND EQUIPMENT USED<ul><li>Lyophilizers, autoclave, homogenizers, grinder, vacuum pump, pH meters, thermometers, balances (scales), water bath circulators, sonicators, humidity cabinet, mixers, centrifuge, blenders, air gun, drop indicator, Filamatic filling machines, slicer machines, scalpels, temperature recorders, crosslinking chamber, humidification chamber, compression unit, cutting table, sealing machines, shrink wrap machines.</li></ul>PHYSICAL REQUIREMENTSThe physical requirements listed in this section include but are not limited to the motor/physical abilities and skills required of this position 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, speak, and write/type. The employee must be able to stand for 8 hours, lift up to 60lbs and climb ladders without assistance. The employee is required to go to all areas of the company.<ul><li>Must be able to bend and lift 30 to 60 lbs without assistance on a daily basis.</li><li>Ability to gown to ISO Class 5 Clean Room standards and/or additional Clean room clothing</li><li>Ability to gown to ISO Class 7 Clean Room standards and/or additional Clean room clothing</li><li>Ability to stand for 8 hours</li><li>Must be able to climb step ladders, without assistance</li><li>Vision: Requires eye sight correctable to 20/25 to detect any defect in product/materials. Visual acuity adequate to perform job duties, including meeting all the quality reclassification. Requires normal color perception</li></ul>Salary Pay Range:$19.19 - $25.43 USD HourlyOur 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 <a target="_blank" href="https://jobs.integralife.com/total-rewards/">https://jobs.integralife.com/total-rewards/</a>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&#39;d like more information on your rights under the law, please see the following notices: <a href="https://www.eeoc.gov" target="_blank">EEO Is the Law</a> | <a href="https://www.eeoc.gov/eeoc/publications/ada_veterans_employers.cfm" target="_blank">EOE including Disability/Protected Veterans</a> 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 <a href="https://www.eeoc.gov/eeoc/publications/fs-ada.cfm" target="_blank">ADA</a>. If you have difficulty using our online system due to a disability and need an accommodation, please email us at careers&#64;integralife.com.Unsolicited Agency SubmissionIntegra 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.<a target="_blank" href="https://player.vimeo.com/video/265760526">Integra - Employer Branding from Integra LifeSciences on Vimeo</a>

Manufacturing Operator 1

Manufacturing Operator

High school diploma; 0-2 years chemical processing/batch mixing in medical device/pharma; clean room experience preferred; English proficiency; able to operate GMP equipment.

High school diploma; 0-2 years chemical processing/batch mixing in medical device/pharma; clean room exp preferred; basic computer skills; English proficiency; able to lift up to 60 lbs; overtime.

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 Manufacturing Operator II will perform pre and post-formulation processing such as blending, mixing, pouring, loading, product cutting, inspection, defect identification, packaging, machine packaging operations, labeling, and boxing in order to produce the finished good. Also performs sub assembly post chemical processing such as crosslinking required to produce collagen-based products. All work streams include responsibility for the setup, operation and cleaning of all cleanroom manufacturing equipment. All chemical processing operations are performed in ISO Class 5 or ISO Class 7 areas and require proper Cleanroom gowning. All processing is performed in compliance with Good Manufacturing Practices (GMP), Quality Systems Regulations (QSR), Standard Operating Procedures (SOP’s) and Health and Safety requirements. Operate in a team environment focused on daily milestones and quality throughout. This is a first shift (7:00 a.m. - 3:30 p.m.), Monday through Friday role. •  Operate, maintain, and troubleshoot process equipment utilized in the collagen business, and can make minor equipment adjustments as needed.  •  Responsible for performing precise measurements and using measurement equipment to accurately add chemicals to batches.  •  Blend, mix, pour, and load collagen prepped material into lyophilizing equipment.  •  Pass and maintain gowning qualification to perform Gowning Requirement for ISO Class 5 Clean room operations or ISO Class 7 Clean room operations.  •  Responsible for accurately maintaining legible and accurate records, required logs, books, 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.  •  Interface with QA/QC/Material departments during course of work to coordinate inspections and efficient flow of subassemblies and completed product.  •  Enter and record production activities in Oracle MRP systems to issue material and labor hours to specific work orders.  •  Follow applicable Standard Operating Procedures, Quality System Regulations and ISO 13485 requirements.  •  Responsible for handling, decontamination, and cleaning of production supplies, instruments, and equipment to support all cleanroom production related activities  •  Responsible for reporting all discrepancies to the Supervisor or Group Leader.   •  Support department and plant Safety goals by continuously demonstrating safe behavior.  •  Support training as required by the department management.•  Ability to work flexible shifts, and flexible days within the week to meet batch milestone requirements.DESIRED MINIMUM QUALIFICATIONS<h2></h2><h2>The requirements listed below are representative of the knowledge, skill, and/or ability required for this position. </h2>•  High School diploma or equivalent.  Degree in related science a plus.  •  2&#43;  years of chemical processing experience or batch mixing in Medical Device or Pharmaceutical manufacturing industry.   Production experience in a clean room environment is highly desirable.   •  Basic computer skills for email and data entry.  •  Must read, write and speak in English, and communicate clearly and concisely.  •  Fundamental understanding of mathematics and chemistry.  •  Able to participate in a team-oriented environment, willingness to assist and train others  •  Able to work independently with minimal supervision  •  Ability to operate, maintain and troubleshoot process equipment, and make minor adjustments as needed.  •  Ability to gown to ISO Class 5 and 7 Clean Room standards.  •  Able to work overtime  TOOLS AND EQUIPMENT USED Lyophilizers, autoclave, homogenizers, grinder, vacuum pump, pH meters, thermometers, balances (scales), water bath circulators, sonicators, humidity cabinet, mixers, centrifuge, blenders, air gun, drop indicator, Filamatic filling machines, slicer machines, scalpels, temperature recorders, crosslinking chamber, humidification chamber, compression unit, cutting table, sealing machines, shrink wrap machines.  PHYSICAL REQUIREMENTS The physical requirements listed in this section include but are not limited to the motor/physical abilities and skills required of this position 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, speak, and write/type. The employee must be able to stand for 8 hours, lift up to 60lbs and climb ladders without assistance. The employee is required to go to all areas of the company.    OTHER REQUIREMENTS •  Must be able to bend and lift 30 to 60 lbs without assistance on a daily basis.  •  Ability to gown to ISO Class 5 Clean Room standards and/or additional Clean room clothing  • Ability to gown to ISO Class 7 Clean Room standards and/or additional Clean room clothing  • Ability to stand for 8 hours  • Must be able to climb step ladders, without assistance  • Vision: Requires eye sight correctable to 20/25 to detect any defect in product/materials. Visual acuity adequate to perform job duties, including meeting all the quality reclassification. Requires normal color perception.Salary Pay Range:$21.12 - $27.98 USD HourlyOur 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 <a target="_blank" href="https://jobs.integralife.com/total-rewards/">https://jobs.integralife.com/total-rewards/</a>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&#39;d like more information on your rights under the law, please see the following notices: <a href="https://www.eeoc.gov" target="_blank">EEO Is the Law</a> | <a href="https://www.eeoc.gov/eeoc/publications/ada_veterans_employers.cfm" target="_blank">EOE including Disability/Protected Veterans</a> 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 <a href="https://www.eeoc.gov/eeoc/publications/fs-ada.cfm" target="_blank">ADA</a>. If you have difficulty using our online system due to a disability and need an accommodation, please email us at careers&#64;integralife.com.Unsolicited Agency SubmissionIntegra 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.<a target="_blank" href="https://player.vimeo.com/video/265760526">Integra - Employer Branding from Integra LifeSciences on Vimeo</a>

Clean Room Manufacturing Operator 2

High school diploma; 2+ years chemical processing/batch mixing in medical device/pharma; cleanroom GMP/QSR/SOP; English required; ability to use measurement equipment; overtime; team-oriented.

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 Manufacturing Operator level II performs post-formulation processing such as product cutting, inspection, defect identification, packaging, machine packaging operations, and labeling and boxing to produce the finished good. Also performs sub assemble post chemical processing such as cross linking required to produce collagen-based products. All work streams include responsibility in the setup, operation, and cleaning of all clean room manufacturing equipment. All chemical processing operations are performed in ISO Class 5 or ISO Class 7 areas 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. Operate in a team environment focused on daily milestones and quality throughout.Shift works Monday - Thursday 1st shift, 10 hour days<ul><li>Performs the setup, operation, and cleaning of all clean room manufacturing equipment. All chemical processing operations are performed in ISO Class 5 or ISO Class 7 areas 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. Operate in a team environment focused on daily milestones and quality throughout.</li><li>Blend, mix, pour, and load collagen prepped material into lyophilizing chambers.</li><li>Operate, maintain, and troubleshoot process equipment utilized in the collagen business, and be able to make minor equipment adjustments as needed.</li><li>Responsible for performing precise measurements and using measurement equipment to accurately add chemicals to batches.</li><li>Responsible for the cross linking, cutting, packaging, and boxing of the product in its finished goods form, which includes performing visual product and component inspections to identify and remove defects.</li><li>Pass and maintain gowning qualification to perform Gowning Requirement for ISO Class 5 Clean room operations or ISO Class 7 Clean room operations.</li><li>Responsible for accurately maintaining legible and accurate records, required logs, books, records, 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.</li><li>Interface with QA/QC/Material departments during course of work to coordinate inspections and efficient flow of subassemblies and completed product.</li><li>Enter and record production activities in Oracle MRP systems to issue material and labor hours to specific work orders.</li><li>Follow applicable Standard Operating Procedures, Quality System Regulations, and ISO 13485 requirements.</li></ul>DESIRED MINIMUM QUALIFICATIONS<ul><li>High School diploma or equivalent. Degree in a related science a plus.</li><li>0 - 2 years of chemical processing experience or batch mixing in Medical Device or Pharmaceutical manufacturing industry.   Production experience is highly desirable.</li><li>Basic computer skills for email and data entry.</li><li>Must read, write, and speak in English, and communicate clearly and concisely.</li><li>Fundamental understanding of mathematics and chemistry.</li><li>Able to participate in a team-oriented environment, willingness to assist and train others.</li><li>Able to work independently with minimal supervision.</li><li>Ability to operate, maintain and troubleshoot process equipment, and make minor adjustments as needed.</li><li>Ability to gown to ISO Class 5 and 7 Clean Room standards.</li><li>Able to work overtime.</li><li>Support department and plant Safety goals by continuously demonstrating safe behavior.</li><li>Maintain a clean and orderly work area.</li><li>Ability to work flexible shifts, and flexible days within the week to meet batch milestone requirements.</li><li>Perform other manufacturing activities as assigned by the department leadership.</li></ul>TOOLS AND EQUIPMENT USEDLyophilizers, Autoclave, homogenizers, grinder, vacuum pump, pH meters, thermometers, balances (scales), water bath circulators, sonicators, humidity cabinet, mixers, centrifuge, blenders, air gun, drop indicator, Filamatic filling machines, slicer machines, scalpels, temperature recorders, Crosslinking chamber, humidification chamber, compression unit, cutting table, sealing machines, shrink wrap machines.PHYSICAL REQUIREMENTS<ul><li>The physical requirements listed in this section include, but are not limited, to the motor/physical abilities and skills require of position 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.</li><li>While undertaking the essential duties and responsibilities of the position, the employee must repeatedly sit, listen, speak, and write/type. The employee must be able to stand for 8 hours, lift to 60lbs and climb ladders without assistance. The employee is required to go to all areas of the company.</li><li>Must be able to bend and lift 30 to 60 lbs without assistance daily.</li><li>Ability to gown to ISO Class 5 type Clean Room standards and/or additional clean room clothing.</li><li>Ability to gown to ISO Class 7 type Clean Room standards and/or additional clean room clothing.</li><li>Ability to stand for 8 hours.</li><li>Must be able to climb step ladders without assistance.</li><li>Vision: Requires eyesight correctable to 20/25 to detect any defect in product/materials.  Visual acuity adequate to perform job duties, including meeting all of quality reclassification.  Requires normal color perception.</li></ul>Salary Pay Range:$21.12 - $27.98 USD HourlyOur 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 <a target="_blank" href="https://www.integralife.com/careers/total-rewards">Total Rewards | Integra LifeSciences</a>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&#39;d like more information on your rights under the law, please see the following notices: <a href="https://www.eeoc.gov" target="_blank">EEO Is the Law</a> | <a href="https://www.eeoc.gov/eeoc/publications/ada_veterans_employers.cfm" target="_blank">EOE including Disability/Protected Veterans</a> 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 <a href="https://www.eeoc.gov/eeoc/publications/fs-ada.cfm" target="_blank">ADA</a>. If you have difficulty using our online system due to a disability and need an accommodation, please email us at careers&#64;integralife.com.Unsolicited Agency SubmissionIntegra 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.<a target="_blank" href="https://player.vimeo.com/video/265760526">Integra - Employer Branding from Integra LifeSciences on Vimeo</a>

Manufacturing Operator II

High School diploma or equivalent; 0-2 years chemical processing or batch mixing experience; basic computer skills; fluent in English; able to work overtime; able to gown to ISO Class 5/7 clean rooms; team-oriented; capable of standing for long periods and lifting up to 60 lbs.

Work ScheduleFirst Shift (Days)Environmental ConditionsAble to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Loud Noises (Equipment/Machinery), No contact lens allowed; prescriptive glasses will be provided, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Various outside weather conditions, Will work with hazardous/toxic materialsJob Description<div></div><div><div><div><div><div><div><div><div><div>Compensation Range: $26.51 - 35.35/hr Shift: 1st Shift  <h2>Discover Impactful Work:</h2>The Distillation Technician – Liquids supports the Operations Manager and Production Supervisor in achieving daily production targets prioritized by Safety, Quality, Delivery, and Cost. Following the priorities set by leadership ensures that distillation columns operate safely per procedures and meet daily production goals established by the supply chain.<h2></h2><h2>A Day in the Life:</h2><ul><li>Operates distillation columns, related receiver tanks, &amp; batch formulation in liquids department. Operates facility equipment (pumps, compressors, condensers, safety equipment, etc.). Performs sampling and testing of product per procedure</li><li>Focuses on distillation and related operations &amp; operator oversight to maintain a high safety standard.</li><li>Oversee operator activities &amp; daily operator rounds to improve safety and quality in the proves areas.</li><li>Assists maintenance department with maintenance activities and related work permits when needed.</li><li>Manages truck intake and outbound &amp; related communication with liquids planner and truck driver to minimize impact on distillation productivity. Enters data related to all inbound and outbound raw materials and products.</li><li>When needed, acts as a packaging team lead or supervisor in achieving daily production targets.</li><li>Lead daily tier meeting for distillation process &amp; batch formulation with operators.</li><li>Performs all required liquids manufacturing processing required to product and assess safe and effective products.</li><li>Meet distillation goals laid out by the Liquids planner’s weekly schedule and/or requests.</li><li>Participate in safety and quality incident investigations, Process Hazard Analysis (PHA), Job Hazard Analysis (JHAs), etc. to drive root cause of the issues &amp; help with implementation of action items and upgrade of procedures and batch records</li><li>Work with the Lab &amp; QA department in investigating any issues that arise during testing of receiving tanks.</li><li>Distribute work orders as required for meeting production schedule.</li><li>Identify missing/unprinted jobs and work closely with label department and Fair Lawn Liquids planner to obtain these work orders.</li><li>Complete work order and perform label reconciliation at end of jobs to comply with QA requirements.</li><li>Assist in customer and internal audits as necessary.</li><li>Record daily production as work orders are returned to Liquids Pack Office and, when needed, any quality inspections required for kegs.</li><li>Support and participate in the company’s efforts in Practical Process Improvement, LEAN, standard work, and 5s.</li><li>Serve as primary back up when supervisor or manager not present.</li><li>Enforce rules and regulations of Company and Department.</li><li>Other duties as assigned</li></ul><h2></h2><h2>Keys to Success:</h2><h3>Education</h3><ul><li>High school diploma or equivalent required.</li></ul>Experience<ul><li>Administrative experience, 1-2 years preferred. Exposure to a production and/or chemical environment a plus.</li><li><h3>Knowledge, Skills, Abilities</h3></li><li>Knowledge of and operating experience of Distillation processes, batch formulation and adjustments or equivalent is preferable</li><li>PC literate with a working knowledge of Databases, Access, Work, Outlook, and Excel.</li><li>Knowledge of various documentation and procedures related to manufacturing, shipping and receiving. Diligence in batch-record and log keeping.</li><li>Ability to effectively communicate with different levels of the organization.</li><li>Analytical ability to detect and solve problems.</li><li>Must be capable of multitasking in a rapid-paced manufacturing environment.</li><li>GLP and GDP experience a plus.</li><li>Must be capable of organizing time to effectively perform the necessary daily tasks.</li><li>Ability to quickly learn basic reconciling and inventory control practices and procedures.</li><li>Excellent organizational skills and attention to detail.</li><li>Good verbal and written communication skills.</li><li>Strong team-oriented interpersonal skills are essential.</li></ul><h2></h2><h2>Physical Requirements / Work Environment</h2><h2></h2>What We Offer: Compensation:<ul><li>Competitive Hourly Pay Rate!</li><li>Additional shift differential for 2nd shift and 3rd shift positions</li><li>Annual performance-based bonus</li><li>Annual merit performance-based increase</li></ul> Excellent Benefits:<ul><li>Benefits &amp; Total Rewards | Thermo Fisher Scientific</li><li>Medical, Dental, &amp; Vision benefits-effective Day 1</li><li>Paid Time Off &amp; Designated Paid Holidays</li><li>401K</li><li>Tuition Reimbursement</li><li>Employee Referral Bonus</li></ul></div></div></div></div></div></div></div></div></div>Compensation and BenefitsThe hourly pay range estimated for this position based in New Jersey is $26.51–$35.35.This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:<ul><li>A choice of national medical and dental plans, and a national vision plan, including health incentive programs</li><li>Employee assistance and family support programs, including commuter benefits and tuition reimbursement</li><li>At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy</li><li>Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan</li><li>Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount</li></ul>For more information on our benefits, please visit: <a href="https://jobs.thermofisher.com/global/en/total-rewards" target="_blank">https://jobs.thermofisher.com/global/en/total-rewards</a>

Distillation Technician - 1st Shift

Distillation Technician

Experience with distillation processes and liquids operations; high school diploma; 1-2 years production/administrative exposure; familiarity with batch records and QA processes.

Batch Processing Operator Jobs in Newark, NJ, US

Batch Processing Operator Jobs market signals in Newark, NJ, US

Companies appearing in this market

Work location mix in visible results

Related browse hubs