Manufacturing Associate Jobs in Sayreville, NJ

The Manufacturing Technician is responsible for the aseptic manufacturing of tissue-based (human and porcine) products for the regenerative market. This position involves operating simple processing equipment and manual handling of tissue to transform it into a finished product for our customers. To ensure product quality, this role much adhere to standard procedures and cGMP (Current Good Manufacturing Practices). Main Areas of Responsibilities • Works in a cleanroom or regulated area to process human and/or porcine tissue • Adheres to standard operating procedures and cGMP • Operates simple processing equipment including, but not limited to: heat sealers, biohazard laminar flow hoods, and mixers • Monitors the quality of pre-packaged finished goods during production • Records information on batch records, equipment and cleaning logs, and other documents. • Uses computers, barcode scanners, and SAP to enter data and generate reports • Maintains inventory of processing supplies • Responsible for the sanitization of the facility Qualifications The below skills are attributes that may not be mandatory but are desired in the ideal candidate. • High school diploma or equivalent required • Minimum 1-2 years of related manufacturing experience, preferred • Must have willingness to learn all equipment and jobs in the assigned processing area • Ability to maintain a safe working environment and practice safe working habits • Demonstrated attention to detail and adherence to procedures • Demonstrated oral and written communication, critical thinking, arithmetic and proper business etiquette skills • Must be willing and able to work with potentially biohazardous materials, including cadaveric tissue • Ability to work in a cleanroom environment with proper gowning attire • Ability to lift up to 30 pounds of boxes and materials off racks • The position involves frequently sitting, walking, reaching, stooping, squatting, crouching, kneeling, crawling and stair climbing and has the ability to use fine motor skills to operate equipment and or machinery Pay Range: $21-23/hr

Pay Range - $15.49 - $15.49/hour + Tips Our secret to leading the way in hospitality? We put our people first! At Shake Shack, our mission is to Stand For Something Good in all that we do. From our teams to our neighborhoods, we're committed to always doing the right thing. As one of the fastest-growing hospitality brands, we're all about crafting unforgettable experiences for our guests. We offer endless learning opportunities and the chance to make a lasting impact on our business, restaurants, and communities. As a member of the #ShackFam, you'll have access to hands-on mentorship, training, and growth potential, all in a fun and inclusive environment. Join us and Be a Part of Something Good. Job Responsibilities Embody enlightened hospitality by leading interactions with genuine warmth and care towards both team members and guests Prepare and assemble food orders according to Shake Shack's standards and recipes Master all stations and rotate through them, keeping each day fresh and exciting Follow all food safety and sanitation procedures to ensure the safety of guests and team members Stand for something good by aligning with Shake Shack's values of integrity, inclusivity, and community engagement Job Qualifications Ability to learn quickly in fast-paced, high-volume environment Adaptability to various roles within the restaurant Consistently demonstrates integrity by doing the right thing and taking accountability Flexible schedule availability, including evenings, weekends, and holidays 16 years or older Perks We take care our team members and support them in building successful futures through a variety of industry-leading benefits. Weekly Pay Medical, Dental, Vision Insurance & Flexible Spending Accounts* Supplemental Life Insurance and Short-Term Disability* 401(k) plan with Company Match* Paid Time Off/ Sick Time* Employer Assistance Program (EAP) Commuter Benefits Exclusive corporate discounts for travel, electronics, wellness, leisure activities and more Shake Shack Meal Discounts *Eligibility criteria applies Click the "Apply" button above to apply for this opening. About Us Beginning as a hot dog cart in New York City's Madison Square Park, Shake Shack was created by Danny Meyer, Founder and CEO of Union Square Hospitality Group and best-selling author of Setting the Table. Shack Fans lined up daily, making the cart a resounding success, and donating all proceeds back to the park beautification efforts. A permanent stand was eventually built…and the rest is Shack history! With our roots in fine dining and giving back to the community, we are committed to high quality food served with a high level of hospitality. Our team members enjoy a positive work environment that is deeply committed to the philosophy that we "Stand for Something Good." Shake Shack is an Equal Opportunity Employer All qualified applicants will receive consideration for employment without regard to any protected characteristic, including race, color, ancestry, national origin, religion, creed, age, disability (mental and physical), sex, gender identity, sexual orientation, gender expression, medical condition, genetic information, marital, military and veteran status.

Downstream Manufacturing Specialist Downstream Manufacturing Associate or Scientist to oversee the purification of 50L to 2000L volumes for engineering, clinical, and commercial batches in a cGMP environment. This role requires advanced technical expertise in downstream processes, including AKTA purification skids (or similar), tangential flow filtration (TFF), and comprehensive knowledge of batch records, protocols, investigations, and technical documentation. Essential Duties & Responsibilities Execute downstream purification processes at various scales (50L to 2000L) within a cGMP environment, including column packing, troubleshooting, and data analysis. Provide technical leadership in the development and execution of downstream purification processes. Utilize software systems to collect, monitor, and evaluate operational data, making real-time adjustments to downstream processes, instruments, or equipment. Ensure the timely and efficient execution of engineering and clinical batches. Establish specifications for downstream equipment and improve manufacturing techniques to enhance process efficiency. Collaborate with cross-functional teams and external vendors to address technical challenges and maintain downstream production equipment. Adhere to and enforce strict GMP and environmental health and safety (EHS) policies in the manufacturing environment. Lead investigations and implement corrective actions for downstream process deviations encountered during batch execution. Perform additional responsibilities as required, ensuring alignment with company policies and quality standards. Qualifications & Requirements A Bachelor's or Master's degree in chemical, biological, or biochemical sciences, with 4-5 years of relevant experience in the biopharmaceutical industry. Proven expertise in downstream purification within a cGMP and aseptic manufacturing environment. Hands-on experience with AKTA Process skids or equivalent systems, as well as familiarity with single-use manufacturing consumables (e.g., bags, tube sets, columns, and process manifolds). Comprehensive knowledge of GMP documentation and the ability to execute engineering and clinical batches. Strong troubleshooting and problem-solving skills specific to downstream processes and purification.

Looking for a lab technician to assist with the LPE (Liquid Phase Epitaxy) process of film growth. Available shifts: Shift A: Sun - Tues/Wed 5:00am-5:30pm, alternating Wednesdays off. Must be prepared to work up to a month Mon-Friday on first shift for training purposes. KEY FUNCTIONS OF JOB Recording and monitoring temperatures of furnaces Weighing chemicals for additions and new melts Mounting and etching substrates Loading and dipping wafers into furnaces Programming and terminating growth cycles Measuring weight/thickness/warp of wafers accurately Performing some data analysis Prepping furnaces for new melts Entering data using Access JOB REQUIREMENTS Education: Minimum: HS diploma or equivalent Preferred: Associate degree in a technical/engineering/scientific field Experience: Minimum 3 years' experience working in a technical, scientific, or mechanical field. Experience working in a laboratory environment and following good lab practices. Experience working with precision measurement methods and systems. Experience with PC based computers for programming LPE systems. Experience with Excel, Word, and Access. Experience with SAP is a plus. Experience working with fixtures, hand tools, and equipment controllers is a plus. Comfortable working with chemicals, acids, and a high temperature environment. Demonstrate the ability to read and follow directions while offering suggestions for continuous improvement. Safety Requirements All employees are required to follow the site EHS procedures and Coherent Corp. Corporate EHS standards. Quality and Environmental Responsibilities Depending on location, this position may be responsible for the execution and maintenance of the ISO 9000, 9001, 14001 and/or other applicable standards that may apply to the relevant roles and responsibilities within the Quality Management System and Environmental Management System. Culture Commitment Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent Corp.: Integrity - Create an Environment of Trust Collaboration - Innovate Through the Sharing of Ideas Accountability - Own the Process and the Outcome Respect - Recognize the Value in Everyone Enthusiasm - Find a Sense of Purpose in Work Coherent Corp. is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. If you need assistance or an accommodation due to a disability, you may contact us at ****************************** .

We at Global Life Science Hub are recruiting on behalf of an innovative biotech company based in Chicago, IL, that is experiencing rapid growth after securing two FDA approvals and developing a robust pipeline of assets. As the company transitions from R&D to full-scale commercial operations, they are scaling their manufacturing capabilities significantly, aiming to grow from 50L to 2000L by year's end and doubling their workforce within two years. We are seeking a Manufacturing Associate III to join their team during this exciting phase of expansion. This position will be instrumental in the production of mammalian-based biosimilars, focusing on purification processes ranging from 50L to 1000L in a cGMP environment. You will play a hands-on role in managing AKTA purification systems and tangential flow filtration (TFF) while overseeing batch records and compliance with regulatory standards. Key Responsibilities: Execute downstream processes in a cGMP environment, including troubleshooting and data analysis. Support the purification of mammalian cell cultures and recombinant protein production. Review and prepare quality management documents, such as deviations and change controls. Ensure timely execution of clinical and commercial batches. Collaborate with teams and vendors to maintain production equipment and resolve technical issues. Lead compliance with GMP and environmental health and safety policies. Qualifications: Bachelor's or Master's degree in Chemical, Biological, or Biochemical Sciences. 5+ years of experience in biopharmaceutical manufacturing with a focus on downstream processes. Proficiency with AKTA purification skids, TFF, and cGMP documentation. This role offers the chance to contribute to a company at the forefront of biotechnology, with opportunities for growth as they continue to expand through 2030.

Job Details Headquarters- New Jersey - PRINCETON, NJ Full Time Day PharmaceuticalResponsibilities: The Manufacturing Associate II-IV is responsible for the execution of production activities for early phase small molecule and/or biological programs within a GMP environment. The incumbent works cross-functionally with internal departments and external resources on manufacturing related issues. The Manufacturing Associate II-IV supports adherence to relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate. Performs manufacturing operations safely and compliantly in accordance with OSHA and cGMP guidelines. Manufacturing operations include but are not limited to, dispensing and sampling of raw materials, buffer preparation, column packing, UF/DF, chromatography, filtration, product sampling, and filling of bulk product or intermediate. Involved in biomanufacturing production of biologics, as well as with bioconjugation processes used in the manufacture of biologic drug substances such as mRNA therapeutics and Bioconjugates (ADCs, Oligoconjugates, etc.). Utilizes standard operating procedures and documents cGMP activities within batch records and logbooks applying good cGMP documentation and data integrity practices. May be asked to perform experiments for process development under supervision of senior personnel Performs oversight of process operations and monitors equipment and critical process parameters. Escalates any issues or abnormalities to management, senior associates and/or system matter experts. Participates in resulting troubleshooting activities as necessary. Completes set-up, use and cleaning (as necessary) of cGMP production equipment with accompanying recovery studies. Creates and revises SOPs (standard operating procedures) and MBRs (master batch records) as appropriate. Proactively works with senior associates, system matter experts, and management to achieve training competency in production operations. Maintains a clean and orderly production area. Positively engages and collaborates with other team members to ensure daily production tasks are completed in a timely manner. Participates in investigations of safety or quality issues as necessary. Participates and supports a culture of continuous improvement. Effectively collaborates with cross functional partners such as Engineering, Quality Assurance, Quality Control, Supply Chain, and Facilities Senior level may be involved in training associates I and II. Performs other tasks and assignments as needed and specified by management. Requirements: Required Knowledge, Skills and Abilities: Ability to follow detailed instructions and to maintain accurate records and notes. Ability to work effectively in a team environment. Energetic, motivated and dynamic individual. Proficiency with Microsoft Office Excellent verbal and written communication skills as well as interpersonal skills. Ability to work independently and collaboratively, as required, in a team environment consisting of internal and external team members. Analytical thinker with excellent problem-solving skills and the ability to adapt to changing priorities and deadlines. Excellent planning, organization and time management skills including the ability to support and prioritize multiple projects. Ability to work outside of normal business hours, including occasional nights, weekends or holidays, as needed to fulfil the business need. Education and Experience Requirements: BA/BS degree in a scientific discipline (Synthetic /Organic Chemistry/ Bioengineering/ Biochemistry/ equivalent) 2-11 years of cGMP experience. Strong desired background in science, technology, and manufacturing. Experience in HPAPI a plus. Physical Demands: Typically requires standing and walking for entire shift. Occasionally requires lifting of up to 20 pounds Frequently requires the use of a step stool Requires manual dexterity and visual abilities Working Conditions: Laboratory and office environment NJ Bio, Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to their race, color, sex, religion, age, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability or any other characteristic protected by applicable federal, state, or local laws.

Thank you for your interest in becoming part of the team at Legrand! If you'd like to work in a fun, creative, business-casual environment that offers a comprehensive benefit package, we encourage you to apply! Legrand is an equal employment opportunity employer. For California residents, please see the link for the Privacy Notice for Candidates. California law requires that we provide you this notice about the collection and use of your personal Information.

About Our Client - Enzene Enzene Inc. is an emerging Contract Development and Manufacturing Organization (CDMO) with a strong operational footprint in India. We are a subsidiary of Enzene Biosciences, a leading biotechnology company. Our mission is to provide high-quality biologics manufacturing services to our clients, contributing to the advancement of the pharmaceutical industry. Website: ************** Position Overview The Manufacturing Associate will be responsible (or lead, depending on level) for the day-to-day operations of upstream processing in a clean room environment. This role includes buffer and media preparation, cell culture, perfusion bioreactors, batch fed bioreactors, harvest operations, filtration, and aseptic processing. Key Responsibilities: · Buffer and Media Preparation: Prepare and maintain buffers and media required for downstream processes. Ensure accurate formulation and timely availability of all solutions. Maintain detailed records of preparation and usage. Cell Culture: Operate and maintain cell cultures in flasks, bioreactors and perfusion reactors. Monitor process parameters and ensure consistent product quality. Troubleshoot and resolve any issues that arise during vial thaw and cell expansion. Aseptic Processing: Perform aseptic processing in a clean room environment. Adhere to strict aseptic techniques to prevent contamination. Ensure compliance with Good Manufacturing Practices (GMP). · Clean Room Operations: Maintain a clean and organized work environment. Follow all clean room protocols and procedures. Participate in regular clean room maintenance and cleaning activities. · Documentation and Compliance: Maintain accurate and detailed records of all manufacturing activities. Ensure compliance with GMP and regulatory requirements. Participate in audits and inspections as needed. · Leadership (as appropriate for level of role): Lead daily manufacturing operations, ensuring production targets are met while maintaining high standards of quality and efficiency. Ensure team adherence to standard operating procedures (SOPs) and Good Manufacturing Practices (GMP) regulatory and safety regulations. Provide training, guidance, and performance feedback to team members. Lead and mentor members within your team, providing guidance, support and feedback to ensure overall effective performance and continuous improvement. Job requirements Qualifications Education and Experience: Bachelor's degree in biotechnology, Biochemistry, Chemical Engineering, or a related field with 0+ years of relevant experience. Individuals with 4+ years of relevant experience required for senior roles (H.S diploma with 4+ years of experience will be considered in lieu of Bachelors Degree). Skills: Ability to follow instructions and procedures. Experience with buffer and media preparation, chromatography, TFF, viral filtration, and aseptic processing a plus. Excellent problem-solving and analytical skills. Effective communication, leadership and teamwork abilities. Strong knowledge and experience working in a biopharmaceutical cGMP- regulated environment. This position requires the ability to stand for extended periods, bend, and lift objects weighing up to 50 pounds. Candidates must be physically capable of performing these tasks safely and effectively. Why Join Enzene? At Enzene, we foster a collaborative and innovative environment where science and business intersect. Our team is dedicated to pushing the boundaries of biosimilar manufacturing, and we are constantly striving to improve processes and patient outcomes. Joining Enzene means being part of a company that values integrity, innovation, and collaboration in pursuit of scientific excellence. We offer an environment of growth, learning, and opportunity in a sector that is driving change in healthcare. Equal Opportunity Employer Enzene is an equal opportunity employer, committed to fostering a diverse and inclusive work environment where all employees can thrive. All done! Your application has been successfully submitted! Other jobs

The HORIBA Group of worldwide companies provides an extensive array of instruments and systems for applications ranging from automotive R&D, process and environmental monitoring, in-vitro medical diagnostics, semiconductor manufacturing and metrology, to a broad range of scientific R&D and QC measurements. Proven quality and trustworthy performance have established widespread confidence in the HORIBA Brand. Inspired by our unique motto, “JOY and FUN,” we focus on social responsibilities by building state-of-the-art products for scientific advancement; especially for protecting health, safety, and the environment. “HORIBARIANs,” the HORIBA employees all over the world, look forward to working with additional creative and entrepreneurial self-starters. To learn more about our unique culture, visit our culture page. HORIBA is a global group of companies that develops, manufactures and provides an extensive array of analytical and measurement equipment to countries around the world. HORIBA Instruments Inc., a leading manufacturer of scientific instruments has an immediate opening for a CCD Lab Technician in the Piscataway, New Jersey facility. Duties/Requirements: Soldering skills, the ability to read mechanical and electrical drawings and schematics are a must Hands-on mechanical skills and familiarity with electronic test equipment such as meters and oscilloscopes. Two - Four-year degree related to mechanical or electrical engineering and or related work experience. Compensation Package: HORIBA Instruments offers a competitive compensation package that includes a 401(k) plan with match; employee group dental, vision, life, and disability (short and long-term) paid for by the company; medical insurance, family dental and vision insurance, and supplemental life insurance available with reasonable employee contributions; employee assistance program; paid holidays, vacation, and sick time; flexible spending accounts; and educational reimbursement and commuter benefit programs. If you are an individual with a disability and need an accommodation during the application/hiring process, please call ************* for assistance. HORIBA will provide reasonable accommodations, upon request, to support individuals with disabilities to be able to participate in the hiring process. HORIBA is committed to making our workplace accessible for individuals with disabilities. EEO/Affirmative Action/Veteran Status/Disabilities.

RequirementsEssential Duties & Responsibilities: Responsible to support manufacturing team with all kinds of documentation. Documentation includes reviewing executed batch records (both Upstream department and Downstream batch record). Responsible for filing change controls, deviation, CAPA for manufacturing department. For all critical / major investigation, will have to use investigation tools like 5why or 6M method. Attend daily meetings with both upstream and downstream process to get all the documentation requirement for the day. Meet weekly with QA to avoid any delay in the QMS closure. Author batch records, SOPs and associated forms / formats required for manufacturing process. Responsible for requesting / submitting all GMP documents to QA. Support manufacturing process (night shifts, weekends, holidays) during critical campaign. 10% wet lab work. Performs other functions as required or assigned. Complies with all company policies and standards. ? Requirements Education and Experience: A Minimum BA or BS in Biological Sciences or related technical field is required. Minimum 5 years of experience in Biopharmaceuticals. Knowledge in USP and DSP process Special Skills: Ability to work with other team members and independently - good interpersonal skills. Good communication skills: verbal and written, good computer and organization skills, detail oriented. Basic computer skills, including knowledge of Word, Excel, and spread sheet. Knowledgeable in GMP batch manufacturing and packaging documentation; audit and review. Knowledgeable in cleaning verification/validation.

Associate Production Technician Status: Fulltime (40 hours/week) Shift: 2nd shift US 2:00 - 10:30pm eastern time EUROIMMUN US is a MDSAP registered, ISO 13485:2016, 21 CFR 820 compliant Medical device company that manufactures, distributes, and performs service and installation activities of in vitro diagnostic test kits and instruments used in the detection of autoimmune status, allergies, infectious diseases and antigen detection. The Associate Production Technician is an essential role in Manufacturing, and will perform daily production and packaging activities of the medical device(s) manufactured in our facility. Day to day activities include and are not limited to inventory management, production planning, production, in-process QC, and packing. All work responsibilities to be performed carefully and accurately to meet the high quality standard of the company. The Production Technician will report to the Production Manager. KEY RESPONSIBILITIES Adhere to all company policies, procedures and comply with all safety and regulatory requirements. Operate production machines, participate in day to day production activities accurately following detailed work instructions, processes and procedures. Identify quality and defects within process, product, or equipment. Maintain a clean and safe work environment. Maintain appropriate records and complete other production related paperwork. Provide training to coworkers as required. Contribute to continuous improvement initiatives. Perform all other duties and tasks as assigned. Perform other delegated tasks as required. Nothing in this job description restricts management's right to assign or reassign duties and responsibilities of this job at any time. Skills: Medical device manufacturing experience. Understanding and experience with Quality Systems. Ability to read and comprehend procedures written in English. Good oral or written communication skills. Keen attention to details and problem solving skills; deadline driven work ethic. Team players who perform well in a steady or fast paced environment. Well-organized, ability to work efficiently and independently with minimum supervision. Proactive, planning and exhibits high level of critical thinking abilities. Education: . High school diploma or GED and 0-1 years of manufacturing experience in a regulated industry Skills: Required MEDICAL DEVICE PACKING MANUFACTURING TECHNICIAN INVENTORY MANAGEMENT PROBLEM SOLVING Additional ISO ADME PACKAGING SCHEDULING * Job details *

Come create your career with Volt! Volt is immediately hiring for Warehouse Production Workers in Flemington, New Jersey Perks: Weekly Pay Occasional Over Time Onsite HR Support Great Benefits Great company culture As a Warehouse Production Worker, you will: Assemble/package products in warehouse manufacturing environment. Perform all quality checks on inventory/parts prior to assembly. Receive, process, locate parts/product/shipments in warehouse. Meet/Exceed production standards, hitting goals and working safely at every point in the manufacturing process. The ideal Warehouse Production Worker Candidate will have: High school diploma or GED Ability to lift to 30 lbs. throughout shift. Ability to stand and work throughout shift. This is a Full-time contract position. Location: FLEMINGTON, New Jersey 08822 Available Shifts: 7:00am - 3:30pm 3:00pm-11:30pm 3:30pm-11:30pm Pay Rate: $20.50 - $23.50 per hour. *Pay range offered to a successful candidate will be based on several factors, including the candidate's education, work experience, work location, specific job duties, certifications, etc. Qualified candidates should APPLY NOW for immediate consideration! Please hit APPLY to provide the required information, and we will be back in touch as soon as possible. Benefits: Volt offers benefits (based on eligibility) that include the following: health, dental, vision, term life, short term disability, AD&D, 401(k), Sick time, and other types of paid leaves (as required by law), Employee Assistance Program (EAP). Volt is an Equal Opportunity Employer and prohibits any kind of unlawful discrimination and harassment. Volt is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment on the basis of race, color, religion or belief, national origin, citizenship, social or ethnic origin, sex, age, physical or mental disability, veteran status, marital status, domestic partner status, sexual orientation, or any other status protected by the statutes, rules, and regulations in the locations where it operates. If you are an individual with a disability and need a reasonable accommodation to assist with your job search or application for employment, please click here or call (866) -###-####. Please indicate the specifics of the assistance needed. Volt does not discriminate against applicants based on citizenship status, immigration status, or national origin, in accordance with 8 U.S.C. § 1324b. The company will consider for employment qualified applicants with arrest and conviction records in a manner that complies with the San Francisco Fair Chance Ordinance, the Los Angeles Fair Chance Initiative for Hiring Ordinance, and other applicable laws. Qualified candidates should APPLY NOW for immediate consideration! Please hit APPLY to provide the required information, and we will be back in touch as soon as possible Benefits: Volt offers benefits (based on eligibility) that include the following: health, dental, vision, term life, short term disability, AD&D, 401(k), Sick time, and other types of paid leaves (as required by law), Employee Assistance Program (EAP). Volt is an Equal Opportunity Employer and prohibits any kind of unlawful discrimination and harassment. Volt is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment on the basis of race, color, religion or belief, national origin, citizenship, social or ethnic origin, sex, age, physical or mental disability, veteran status, marital status, domestic partner status, sexual orientation, or any other status protected by the statutes, rules, and regulations in the locations where it operates. If you are an individual with a disability and need a reasonable accommodation to assist with your job search or application for employment, please call (866) -###-####. Please indicate the specifics of the assistance needed. Volt does not discriminate against applicants based on citizenship status, immigration status, or national origin, in accordance with 8 U.S.C. § 1324b. The company will consider for employment qualified applicants with arrest and conviction records in a manner that complies with the San Francisco Fair Chance Ordinance, the Los Angeles Fair Chance Initiative for Hiring Ordinance, and other applicable laws

Upstream Processing Manufacturing Associate / Scientist To support our next growth phase, we are hiring seven Upstream Manufacturing Scientists/Associates at various experience levels to meet the increasing demands of our Upstream and Downstream Manufacturing teams. These teams are gearing up to scale from pilot manufacturing to full-scale commercial production at our new NJ facility. Positions Available: Manufacturing Scientist I - III - from 1 years of experience + USP Manufacturing Scientists: Execute mammalian cell culture processes to produce recombinant proteins for biologics, managing cell culture batches up to 2000L. Operate bioreactors, establish equipment specifications, and enhance manufacturing techniques. Collaborate with manufacturing associates and engineers, providing clear instructions and guidance. Initiate batch records, protocols, and oversee investigations in a cGMP environment to ensure compliance. Review and document manufacturing and packaging batch records, ensuring adherence to safety standards and GMP guidelines. Experience/Qualifications: Upstream: At least 1-2 years of experience in cell culture and bioreactor operations, including GMP and aseptic manufacturing experience. Proficiency with single-use manufacturing consumables (e.g., bags, tube sets, columns) and experience in scale-up manufacturing activities.

Looking for a lab technician to assist with the LPE (Liquid Phase Epitaxy) process of film growth. Available shifts: Shift A: Sun - Tues/Wed 5:00am-5:30pm, alternating Wednesdays off. Must be prepared to work up to a month Mon-Friday on first shift for training purposes. KEY FUNCTIONS OF JOB * Recording and monitoring temperatures of furnaces * Weighing chemicals for additions and new melts * Mounting and etching substrates * Loading and dipping wafers into furnaces * Programming and terminating growth cycles * Measuring weight/thickness/warp of wafers accurately * Performing some data analysis * Prepping furnaces for new melts * Entering data using Access JOB REQUIREMENTS Education: * Minimum: HS diploma or equivalent * Preferred: Associate degree in a technical/engineering/scientific field Experience: * Minimum 3 years' experience working in a technical, scientific, or mechanical field. * Experience working in a laboratory environment and following good lab practices. * Experience working with precision measurement methods and systems. * Experience with PC based computers for programming LPE systems. * Experience with Excel, Word, and Access. * Experience with SAP is a plus. * Experience working with fixtures, hand tools, and equipment controllers is a plus. * Comfortable working with chemicals, acids, and a high temperature environment. * Demonstrate the ability to read and follow directions while offering suggestions for continuous improvement. Safety Requirements All employees are required to follow the site EHS procedures and Coherent Corp. Corporate EHS standards. Quality and Environmental Responsibilities Depending on location, this position may be responsible for the execution and maintenance of the ISO 9000, 9001, 14001 and/or other applicable standards that may apply to the relevant roles and responsibilities within the Quality Management System and Environmental Management System. Culture Commitment Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent Corp.: Integrity - Create an Environment of Trust Collaboration - Innovate Through the Sharing of Ideas Accountability - Own the Process and the Outcome Respect - Recognize the Value in Everyone Enthusiasm - Find a Sense of Purpose in Work Coherent Corp. is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. If you need assistance or an accommodation due to a disability, you may contact us at ******************************.

Job Details Headquarters- New Jersey - PRINCETON, NJ Full Time Day PharmaceuticalResponsibilities: The Manufacturing Associate I is responsible for the execution of production activities for early phase small molecule and/or biological programs within a GMP environment. The incumbent works cross-functionally with internal departments and external resources on manufacturing related issues. The Manufacturing Associate I supports adherence to relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate. Performs manufacturing operations safely and compliantly in accordance with OSHA and cGMP guidelines. Manufacturing operations include but are not limited to, dispensing and sampling of raw materials, buffer preparation, column packing, UF/DF, chromatography, filtration, product sampling, and filling of bulk product or intermediate. Assists in biomanufacturing production of biologics, as well as assisting with bioconjugation processes used in the manufacture of biologic drug substances such as mRNA therapeutics and Bioconjugates (ADCs, Oligoconjugates, etc.). Utilizes standard operating procedures and documents cGMP activities within batch records and logbooks applying good cGMP documentation and data integrity practices. Performs oversight of process operations and monitors equipment and critical process parameters. Escalates any issues or abnormalities to management, senior associates and/or system matter experts. Participates in resulting troubleshooting activities as necessary. Completes set-up, use and cleaning (as necessary) of cGMP production equipment. Creates and revises SOPs (standard operating procedures) and MBRs (master batch records) as appropriate. Proactively works with senior associates, system matter experts, and management to achieve training competency in production operations. Maintains a clean and orderly production area. Positively engages and collaborates with other team members to ensure daily production tasks are completed in a timely manner. Participates in investigations of safety or quality issues as necessary. Participates and supports a culture of continuous improvement. Effectively collaborates with cross functional partners such as Engineering, Quality Assurance, Quality Control, Supply Chain, and Facilities Performs other tasks and assignments as needed and specified by management Requirements: Required Knowledge, Skills and Abilities: Ability to follow detailed instructions and to maintain accurate records and notes. Ability to work effectively in a team environment. Energetic, motivated and dynamic individual. Proficiency with Microsoft Office Excellent verbal and written communication skills as well as interpersonal skills. Ability to work independently and collaboratively, as required, in a team environment consisting of internal and external team members. Analytical thinker with excellent problem-solving skills and the ability to adapt to changing priorities and deadlines. Excellent planning, organization and time management skills including the ability to support and prioritize multiple projects. Ability to work outside of normal business hours, including occasional nights, weekends or holidays, as needed to fulfil the business need. Education and Experience Requirements: BA/BS degree in a scientific discipline (synthetic /organic chemistry) 0-2 years of cGMP experience. Physical Demands: Typically requires standing and walking for entire shift. Occasionally requires lifting of up to 20 pounds Frequently requires the use of a step stool Requires manual dexterity and visual abilities Working Conditions: Laboratory and office environment NJ Bio, Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to their race, color, sex, religion, age, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability or any other characteristic protected by applicable federal, state, or local laws.

Provide daily support for all cGMP manufacturing activities. Includes preparation of all solutions, buffers and all activities associated with an aseptic production area, such as room and equipment cleaning and moving equipment as needed. Follows cGMP guidelines at all times. Takes responsibility to be properly trained and helps to ensure that all training records are kept up-to-date. Requirements Essential Duties: Assist in preparation of solutions and buffers for the manufacturing process. Complies with all pertinent SOPs and/ or master batch record following GMP guidance. Must have a strong working knowledge and complies with cGMP guidance as applicable. Must have experience working with in ISO 8, 7 environments. Strong background in Single-Use technology. Familiar with Downstream manufacturing, depth filtration, TFF, and Final Fill. Assist with production process steps as needed. Assist with the cleaning/ sanitizing of manufacturing vessels, equipment and other process related items. Assist with cleaning/ sanitizing of rooms and fixed equipment in the aseptic production area. Must be able to write SOPs and other GxP documents. Must be able to assist/ write and implement deviations, investigations, and CAPAs Daily visual and physical checks/ calibrations of all in-process equipment. Review and document data with accuracy. Must be able to setup and execute projects independently. Must be able to troubleshoot and maintain process equipment. Must display leadership characteristics. Must have strong communication skills internal and external to the department. Must be able to work well with a team. Must be able to follow written and or verbal direction. Education: Associate degree or equivalent professional experience. Bachelor's degree a plus. Experience: 8-10 years of relevant work experience in Pharma company. High attention to detail. Proven documentation skills. Dedication to production quality. Experience with production planning. Family with equipment calibration techniques.

The appointed Manufacturing Associates will help meet the increasing demands of Upstream and Downstream Manufacturing teams. The appointed candidates will run and pack chromatography columns, execute TFF processes, and run cell-culture programmes to scale up bioreactor operations in a cGMP commercial environment. Positions Available: Manufacturing Associate I: 1-2 years of USP/DSP Manufacturing experience Manufacturing Associate II: 2-5 years of USP/DSP Manufacturing experience Manufacturing Associate III: 6+ years of USP/DSP Manufacturing experience Key Responsibilities: Weighing and dispensing materials Operating filtration systems Inoculating mammalian or cytokine cell cultures Conducting fermentation and harvest processes Managing chromatography columns and TFF procedures Performing in-process tests, including pH, conductivity, spectrophotometry, osmometry, cell counts, etc. Preparing media and buffer solutions Completing Batch Records and other cGMP documents accurately and promptly Removing and disposing of used materials from the manufacturing area Ensuring that cleanroom standards are consistently met within manufacturing spaces Reporting any non-conformance or incidents to the Supervisor during shifts Assisting with technology transfer from Process Development to cGMP Manufacturing Adhering to safety, cGMP, and company policies and procedures Carrying out additional tasks as assigned

Looking for a lab technician to assist with the LPE (Liquid Phase Epitaxy) process of film growth. Available shifts: Shift B: Wed/Thurs - Sat 5:30am - 6:00pm, alternating Wednesdays off Must be prepared to work a minimum of one to two months Mon-Friday on first shift for training purposes. KEY FUNCTIONS OF JOB * Recording and monitoring temperatures of furnaces * Weighing chemicals for additions and new melts * Mounting and etching substrates * Loading and dipping wafers into furnaces * Programming and terminating growth cycles * Measuring weight/thickness/warp of wafers accurately * Performing some data analysis * Prepping furnaces for new melts * Entering data using Access JOB REQUIREMENTS Education: * Minimum: HS diploma or equivalent * Preferred: Associate degree in a technical/engineering/scientific field Experience: * Minimum 3 years' experience working in a technical, scientific, or mechanical field. * Experience working in a laboratory environment and following good lab practices. * Experience working with precision measurement methods and systems. * Experience with PC based computers for programming LPE systems. * Experience with Excel, Word, and Access. * Experience with SAP is a plus. * Experience working with fixtures, hand tools, and equipment controllers is a plus. * Comfortable working with chemicals, acids, and a high temperature environment. * Demonstrate the ability to read and follow directions while offering suggestions for continuous improvement. Safety Requirements All employees are required to follow the site EHS procedures and Coherent Corp. Corporate EHS standards. Quality and Environmental Responsibilities Depending on location, this position may be responsible for the execution and maintenance of the ISO 9000, 9001, 14001 and/or other applicable standards that may apply to the relevant roles and responsibilities within the Quality Management System and Environmental Management System. Culture Commitment Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent Corp.: Integrity - Create an Environment of Trust Collaboration - Innovate Through the Sharing of Ideas Accountability - Own the Process and the Outcome Respect - Recognize the Value in Everyone Enthusiasm - Find a Sense of Purpose in Work Coherent Corp. is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. If you need assistance or an accommodation due to a disability, you may contact us at ******************************.

Requirements Assist in preparation of solutions and buffers for the manufacturing process. Complies with all pertinent SOPs and/ or master batch record following GMP guidance. Must have a strong working knowledge and complies with cGMP guidance as applicable. Must have experience working with in ISO 8, 7 environments. Strong background in Single-Use technology. Familiar with Downstream manufacturing, depth filtration, TFF, and Final Fill. Assist with production process steps as needed. Assist with the cleaning/ sanitizing of manufacturing vessels, equipment and other process related items. Assist with cleaning/ sanitizing of rooms and fixed equipment in the aseptic production area. Must be able to write SOPs and other GxP documents. Must be able to assist/ write and implement deviations, investigations, and CAPAs Daily visual and physical checks/ calibrations of all in-process equipment. Review and document data with accuracy. Must be able to setup and execute projects independently. Must be able to troubleshoot and maintain process equipment. Must display leadership characteristics. Must have strong communication skills internal and external to the department. Must be able to work well with a team. Must be able to follow written and or verbal direction. Education: Associate degree or equivalent professional experience. Bachelor's degree a plus. Experience: 8-10 years of relevant work experience in Pharma company. High attention to detail. Proven documentation skills. Dedication to production quality. Experience with production planning. Family with equipment calibration techniques.