Process Technician jobs at Management Recruiters International(MRI) - 3453 jobs

Swing Shift Manufacturing Technician in Newburyport, MA. This is for a company I represent design, manufacturing, and servicing of equipment and solutions for the semiconductor and display industries, which are crucial for producing chips and screens for electronics like smartphones, computers, and TVs. The company's work is focused on advanced material engineering and is a key part of the supply chain for modern technology. Swing Shift or Second Shift 3:30 pm to 12:00 am (Midnight) Monday through Friday 18-month contract with a chance of going permanent. Pay Rate is $23.00 to $25.00 per hour with a 10 % differential bringing the hourly rate $25.30 to $27.50 Overview Join a dynamic team in a hands-on role where you'll build, test, and troubleshoot complex electro-mechanical systems. This position is ideal for individuals who thrive in a fast-paced, physically active environment and are committed to safety and precision. Key Responsibilities Assemble, repair, and test electrical, electro-mechanical, vacuum, and pneumatic components using schematics, wiring diagrams, and work orders. Perform troubleshooting and corrective actions on assemblies and subassemblies. Operate test fixtures, electronic measurement equipment, leak detectors, and vacuum pumps. Document progress, labor details, and work expenses using computer systems. Inspect incoming parts for defects and ensure all necessary components are available. Audit and improve processes to enhance quality and efficiency. Maintain a clean, safe, and secure work environment in compliance with health and safety standards. Report safety hazards, injuries, or emergencies promptly. Use appropriate PPE and follow clean room protocols when required. Physical & Environmental Requirements Ability to stand, walk, bend, squat, kneel, twist, reach, and climb stairs/ladders for extended periods. Capable of lifting and operating heavy machinery including forklifts. Comfortable working in noisy environments and tight spaces. Must be able to distinguish between colors. Willingness to wear PPE such as coveralls, hoods, booties, safety glasses, gloves, respirators, chemical aprons, and face shields. Qualifications Prior experience in electro-mechanical assembly or testing preferred. Ability to read and interpret technical documents and schematics. Strong attention to detail and commitment to safety. Basic computer skills for data entry and documentation. Experience working in clean room environments is a plus. What's In It for You? We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh's network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh's extensive talent community that will provide you with access to Yoh's vast network of opportunities and gain access to this exclusive opportunity available to you. Medical, Dental & Vision Benefits 401K Retirement Saving Plan Life & Disability Insurance Direct Deposit & weekly epayroll Employee Discount Program's Referral Bonus Program's All offers are contingent to passing all pre-employment screenings and background check. Estimated Min Rate: $23.00 Estimated Max Rate: $25.00 What's In It for You? We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh's network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh's extensive talent community that will provide you with access to Yoh's vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include: Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week) Health Savings Account (HSA) (for employees working 20+ hours per week) Life & Disability Insurance (for employees working 20+ hours per week) MetLife Voluntary Benefits Employee Assistance Program (EAP) 401K Retirement Savings Plan Direct Deposit & weekly epayroll Referral Bonus Programs Certification and training opportunities Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply. Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Visit ************************************************ to contact us if you are an individual with a disability and require accommodation in the application process. For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh's hiring clients' preferences. To learn more about Yoh's privacy practices, please see our Candidate Privacy Notice: **********************************

Trident Consulting is seeking a " Production Technician (Aseptic/Pharmaceutical)" for one of our clients. A global leader in business and technology services. Job Title: Production Technician (Aseptic/Pharmaceutical) Category: Supply Chain Labor Type: Industrial Pay Rate: $27-$30/hr on w2 Type: Contract Job Description The role supports aseptic pharmaceutical manufacturing operations, requiring significant training and demonstrated expertise. Responsibilities include: Operations & Equipment Set up, calibrate, and operate equipment according to specifications Adjust filler and labeler equipment with proper parts/settings Assemble containers and components for portioning Portion materials into containers safely Set up, operate, and troubleshoot automated labeling and bagging equipment Conduct housekeeping, disinfection, and autoclaving as required Maintain accurate records of tests, measurements, calibrations, and conversions Monitor inventory and stock necessary supplies Compliance & Safety Wear appropriate PPE (steel-toed shoes, other safety equipment) Follow FMP, SOPs, UOPs, and safety rules Maintain cleanliness of equipment and work areas Report safety or quality concerns immediately Maintain certification for entry into the Aseptic Core Independently make important decisions during processing Oversee work of other Manufacturing team members Process Improvement Suggest improvements to save cost or improve efficiency Participate in testing and implementation of changes Qualifications Education: High School Diploma, GED, or HSED required; college coursework in chemistry desirable Experience: Minimum 2 years in pharmaceutical aseptic manufacturing (food industry aseptic experience not accepted) Experience in Clean Room/Aseptic environments, Equipment Preparation, Stopper Preparation, Semi-automated/manual Inspection, Packaging Operations, Sanitization, Autoclave operation Skills & Knowledge: Basic math including metrics/conversions Mechanical aptitude and eye-hand coordination Ability to use hand/air tools, pumps, electronic scales, and material handling equipment Strong communication, teamwork, problem-solving, and documentation skills Ability to train others About Trident: Trident Consulting is an award-winning IT/engineering staffing company founded in 2005 and headquartered in San Ramon, CA. We specialize in placing high-quality vetted technology and engineering professionals in contract and full-time roles. Trident's commitment is to deliver the best and brightest individuals in the industry for our clients' toughest requirements. Some of our recent awards include 2022, 2021, 2020 Inc. 5000 fastest-growing private companies in America 2022, 2021 SF Business Times 100 fastest-growing private companies in Bay Area

Kodak is looking for Technicians to join our team in Kodak's Advanced Materials and Chemicals Division onsite in Rochester, NY. Technicians work in a variety of roles, all of which are involved in manufacturing the highest-quality light-sensitive coated products in the world. Components Testing: Kodak's legacy is the production of the finest coated film products in the world. This starts with testing all the components that go into our films and ensuring that they meet our tight standards. Technicians test our liquid components - from gel to sensitized emulsion layers - for chemical concentrations, particle size, density, viscosity, and light sensitivity, etc. Materials of unknown origin, such as dust, and components with unexpected results are also subjected to special testing to determine root cause and origin. As a technician, you will: • Work in both light and dark room conditions. • Work 12-hour rotating shifts (days one week, nights the next). • Work overnights. • 2-5 years of employment experience. Required skills and experience: • Must be a detail-orientated team player. • Must have the ability to be flexible between multiple positions, sometimes multi-tasking or moving within a shift. • Must work effectively with minimal supervision. • Ability to prioritize work to meet business needs. • Ability to express oneself communicate clearly, both written and verbal, and comprehend a variety of work requests • Willing to work overtime or adjust work schedule for business needs. • Must be willing and able to lift and move objects up to 50 pounds. • Must maintain a clean work area. • Must maintain strict adherence to safety procedures and quality standards. • Computer proficiency including navigating screens and data entry. • Involvement in product quality and process improvement activities. • Interaction with operators, engineers, and maintenance personnel. Preferred skills and experience: • Associate's degree, technical certifications or equivalent • At least 2 years of hands-on experience in a manufacturing environment. • Understanding of film photography. • Understanding of thin-film coating processes. • Strong problem solving, data analysis, and computer abilities (Excel, Word, etc.). • Knowledge of Outlook, One-LIMS, Felix, and the SAP system. We recommend watching the following videos to learn more about the manufacturing process at Kodak: A tour of our PET film base manufacturing plant: How Does Kodak Make Film? (Kodak Factory Tour Part 1 of 3)  *********************************** A tour of our film sensitizing plant: How Does Kodak Make Film? (Kodak Factory Tour Part 2 of 3)  ***********************************

Rangam is seeking candidates for a Direct Hire role as a Sterile Manufacturing Operator with our client Pfizer, one of the world's largest pharmaceutical companies. Applicants cannot be allergic to penicillin or amoxicillin Seeking candidates on-site in Rochester, MI 48307 First shift | Full Time | Hourly Rate: $26.57 *This position is being offered as part of a disability/neurodiversity hiring program which is designed to provide a more inclusive and supportive hiring process and work environment for job seekers with physical and cognitive disabilities, which includes, but is not limited to autism, ADD/ADHD, PTSD, OCD, Anxiety Disorder, Dyslexia, Bipolar, and Tourette's Syndrome* Use Your Power for Purpose At Pfizer, we believe that every role contributes to our mission of improving patients' lives. Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is crucial to ensuring customers and patients receive the medicines they need, precisely when they need them. By collaborating with our forward-thinking engineering team, you'll play a pivotal role in accelerating the delivery of medicines to the world. What You Will Achieve In this role, you will: Provide technical and business support to engineers on various tasks. Prepare detailed engineering documentation, reports, and drawings. Conduct preliminary analyses of trajectory adequacy data and ensure model dimensional consistency. Make quantitative judgments on technical data and conduct tests to assist in engineering evaluations. Take responsibility for individual contributions to achieve team deliverables, working effectively as a team member and coordinating with others. Manage personal time and professional development, being accountable for results. Follow standard procedures to complete tasks of varying scope, sequence, and complexity within the agreed timeframe. Identify and solve moderately routine problems. Complete assignments with moderate supervision using established procedures, referring deviations from standard procedures to the supervisor. Ensure work is reviewed for accuracy, quality, and adherence to standards. Here Is What You Need (Minimum Requirements) High School Diploma or GED with 2+ years of experience Understanding basic problem-solving methods, mathematics, and reading skills Good Manufacturing Practices (also cGMP) and Batch Record comprehension Strong communication and leadership skills Ability to contribute to department success in a team environment Performing tasks at a productive level under demanding conditions Solid understanding of procedures, techniques, tools, materials, and equipment Bonus Points If You Have (Preferred Requirements) Experience in a pharmaceutical or manufacturing environment Proficiency in engineering software and tools Knowledge of regulatory requirements and quality standards Strong analytical and problem-solving skills Excellent organizational and time management skills Demonstrated ability to prioritize tasks and manage multiple projects simultaneously Familiarity and basic understanding of common AI tools and a curiosity for learning how they can be used to enhance productivity Essential Duties and Responsibilities: The essential duties for this position include but are not limited to: Performs all tasks as outlined in the Batch Card, SOPs, and/or Job Aids. Effectively demonstrates and understands the SOPs and Job Aids pertinent to all assigned tasks. Inspects filled syringes to established criteria and sort defects into the appropriate receptacle for reconciliation. Performs manual packaging operations as assigned by the supervisor according to the appropriate SOP or Job Aid. Observes all SOPs and Safety and Health Regulations. Re-stocks packaging supplies from line stock as required to maintain packaging operation. Notifies supervisor, PMO and/or Quality Specialist of unusual or recurring defects in syringe products or packaging materials. Maintains work area in a clean and orderly manner. Assists in training new colleagues as required. If required, verifies packaging supplies and product against product board or Batch Card to assure correctness. Signs pertinent forms as required. Participates in all required training programs to maintain required level of cGMP compliance. Performs off-line inspection of product, such as media reading, as required. Performs other miscellaneous duties as assigned by supervisor. PHYSICAL/MENTAL REQUIREMENTS This position is in a Penicillin Facility. The candidate cannot be allergic to Penicillin, and will be required to undergo Penicillin allergy testing. This department requires the SMO to bend, reach, lift and stand for extended periods of time. The SMO must be able to grasp from 4 - 5 filled syringes at a time in one hand while manipulating them with the other hand for overall evaluation for defects. All SMOs must have corrected 20/20 vision and must be able to pass a routine inspection test using seeded syringes. The Penicillin Inspection/Packaging department is currently operating on a one-shift basis, five days per week. However, SMOs must be available for extended hours and six to seven day operations, if required. In order to maintain the required delivery schedule, overtime may be required. The hourly rate is $26.57 per hour. In addition, this position offers eligibility for overtime, weekend, holiday and other pay premiums depending on the work schedule and the Company's policies. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site - U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire.

100% ONSITE WORCESTER MA Pay: $29-$32/hr based on shift Required: Recent Graduate with a BS in Biotechnology, Biology, Biological Engineering, Bioengineering, or other relevant science degree. Familiarity with GMP Drug production, following SOPs, Aseptic techniques Job Description: As a Manufacturing Technician, you'll collaborate with our talented engineers, quality experts, and cross-functional teams to execute crucial functions that drive our operations. You'll have the opportunity to leverage state-of-the-art programs such as LIMS, SAP, automated control systems, DCS, PLC, PI, and more. One of the unique advantages of joining this team is our comprehensive 6-week onboarding training program exclusively designed for our manufacturing technicians. You'll receive the support and resources needed to excel in your role right from the start. As a key member of our team, you'll take on a diverse range of responsibilities that encompass Upstream, Downstream, and Core Support functions. Your key responsibilities may include: Following precise verbal and written procedures in a controlled cGMP environment while prioritizing safety regulations. Meticulously documenting processes in corresponding batch records and log sheets, adhering to cGMP and established Standard Operating Procedures. Collaborating with our team to determine innovative process methods and procedures, actively contributing to the continuous improvement of our operations. Demonstrating a strong commitment to safety by diligently wearing personal protective equipment, such as gowning, safety glasses, gloves, and safety shoes. Proactively completing and maintaining training requirements to stay up to date with the latest industry standards. Occasionally going above and beyond by working overtime to meet project deadlines and deliver exceptional results. Managing inventory levels and actively participating in the shipping of finished materials. Conducting sampling and performing in-process analytical testing to guarantee product quality and integrity. Skillfully preparing equipment for operation, including cleaning and sterilization processes (CIP/SIP). Performing pH and conductivity measurements, crucial parameters for process control and optimization. Operating manufacturing equipment, such as glass washers and autoclaves. Contributing to the preparation of buffers and media, vital components of our production activities. Engaging in cell culture activities, ranging from vial thaw to production scale. Responsible for performing key column operations, Tangential Flow Filtration (TFF), and load line setup. Requirements: Bachelor's Degree in a science discipline is highly preferred with 1 year + manufacturing experience. Knowledge of cGMP operations is preferable. The ability to exercise considerable judgment and initiative, as you'll be working on assignments that require critical decision-making. A deep understanding of the implications of your work and the capacity to make well-informed recommendations for effective solutions. The capability to determine appropriate methods and procedures when faced with new assignments, showcasing your adaptability and problem-solving skills. Strong written and verbal skills, enabling effective communication. The ability to read written instructions and/or numbers at close and far ranges. Comfortable working with a computer or tablet for 50-60% of scheduled work time. The ability to thrive in a manufacturing environment with a constant sound level of 75 decibels, which is comparable to the sound of a washing machine. Occasional use of hearing protection may be required to ensure your well-being. Adaptability to spending 50% of your scheduled work time in a stationary position, where your focus and attention to detail will be paramount. Frequently move and position yourself to observe equipment readings, ensuring accurate monitoring and data collection. Work with your team to transport/move equipment weighing up to 50 lbs., with support from appropriate safety equipment. Your safety is our top priority.

Pride Health is seeking a Process Technician for an American multinational conglomerate operating in the fields of industry, worker safety, healthcare, and consumer goods. Job Title: Process Technician Job Type: Contract Length: 12-Months Hours: 40 hours/week, 8 hours/day Pay Rate: $21.00 - $23.40 per hour Overview: The successful candidate will apply strong mechanical aptitude and problem‐solving skills to develop specialized nonwovens process technology and equipment. The role requires working on lab‐line equipment as well as larger roll‐to‐roll web processing systems. Experience with roll‐to‐roll or similar heavy industrial equipment in production or pilot‐plant settings is highly desirable. Strong communication skills and the ability to remain comfortable with changing priorities and run plans in a high‐speed, team‐based environment are critical to success. Responsibilities: Configuring, operating, and maintaining process equipment, including lab‐line systems Measuring and characterizing the properties of nonwoven materials off the production line Keeping detailed records and communicating technical work and results Following and developing standard operating procedures while adapting to changing priorities and evolving run plans Maintaining a safe and organized work environment Handling materials, including lifting pails, moving pallets, and completing other assigned duties The role requires the ability to lift 50 lbs. The work environment requires steel‐toe shoes, hearing protection, and respiratory protection. Minimum Requirements: High school diploma, GED, or higher At least one (1) year of technician or operator experience in an industrial setting Additional Qualifications: Associate degree or two‐year technical program certificate in mechanical, materials, or process engineering, or a similar field Two (2) or more years of experience in nonwovens or fiber processing, web processing, or roll‐to‐roll processing Two (2) or more years of experience in process development using 5S, Six Sigma, SPC, or similar methodologies Strong mechanical aptitude and problem‐solving ability Proficiency in Microsoft Office Strong written and verbal communication skills Ability and desire to excel in a highly interdisciplinary, team‐oriented work environment, including frequent work on lab‐line equipment and regular adaptation to shifting operational priorities Benefits that Pride Health offers: Pride Health offers eligible employee's comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance and hospital indemnity), a 401(k)-retirement savings, life & disability insurance, an employee assistance program, identity theft protection, legal support, auto and home insurance, pet insurance, and employee discounts with some preferred vendors. Apply Today! If you are interested in the position, please email your resume to **************************** for immediate consideration.

Trident Consulting is seeking a " Production Technician for one of our clients in " Indianapolis IN”. A global leader in business and technology services Job Title: Production Technician Type: Contract 1st shift (0700 - 1530), Mon to Fri Rate: $27 - $30 per hour Interviews: virtual or onsite ***Must have previous isolator experience. ***HM seeks a candidate with Pharmaceutical manufacturing experience. Position Overview: This is a mid-level position in the aseptic filling group within the Manufacturing department. It utilizes those with experience and the training needed to manufacture pharmaceuticals in a strictly controlled GMP environment. The employee will progress through a number of job functions and be required to demonstrate increasing skill levels while demonstrating leadership capabilities. NOTE: This position has exposure to SIP100 PPE will need to be worn, which is provided by EMD Major Position Activities & Responsibilities: • Become certified for entry into the GMP cleanroom space to be able to perform sanitization, stock/replenish supplies, equipment setup, and all related aseptic filling operations. • Execute aseptic fill processes using batch records and SOPs. • Responsible for verifying the calibration of all related equipment and sanitization of supplies to support production • Increasing level of competency in the manufacturing area procedures. Assigned job duties will include Aseptic and clean room areas, Component Preparation, Filling and Capping • Learn the functions necessary to work in the Fill suite. This will include the operation of the associated equipment. • Ability to perform tasks with minimal supervisor direction. • Provide training for new team members. • Able to understand the manufacturing schedule and coordinate tasks to achieve the schedule. • Provide floor leadership in the absence of a supervisor or PT3 technicians. • Transport and/or dispose of hazardous chemicals. • Perform all other duties as assigned. • Must immediately notify supervisor if affected by an infectious disease or open lesions on the body, as individuals are not permitted to enter manufacturing areas or handle products if these conditions exist. Scope: • This position has no direct reports. Background Qualifications: • High school diploma or the equivalent. College coursework preferred • Minimum 3-5 years, including relevant aseptic filling experience in a cGMP pharmaceutical manufacturing facility. • Must possess working knowledge and understanding of GMP compliance regulations. • Must possess knowledge and experience in the aseptic filling process, along with equipment cleaning, preparation, and assembly. Experience in stopper prep, capping, and packaging preferred. • As persons in this role are engaged in the open manufacture of medicinal products, individuals must not be affected by an infectious disease nor have open lesions on any exposed surface of the body. • Must be able to comprehend and follow detailed procedural instructions in written and verbal form. • Must possess adequate working knowledge of arithmetic functions to accurately perform or check calculations required in the product documentation. • While performing the duties of this job, the employee is regularly required to use their hands and arms. The employee is frequently required to stand. The employee is occasionally required to sit, walk, stoop, kneel, bend, crouch, or crawl, talk or hear. The employee must regularly lift and /or move up to 10 pounds, and frequently lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, and peripheral vision. • Must possess fluent English (written and verbal) skills in order to read, comprehend, and communicate GMP compliance documentation as well as Standard Operating Procedures. • Computer skills in Microsoft Office, such as Word and Excel are a plus. Trident Consulting is a premier IT staffing firm providing high-impact workforce solutions to Fortune 500 and mid-market clients. Since 2005, we've specialized in sourcing elite technology and engineering talent for contract, direct hire, and managed services roles. Our expertise spans cloud, AI/ML, cybersecurity, and data analytics, supported by a 3M+ candidate database and a 78% fill ratio. With a highly engaged leadership team and a reputation for delivering hard-to-fill, niche talent, we help organizations build agile, high-performing teams that drive innovation and business success. Learn more: tridentconsultinginc.com. Some of our recent awards include: Trailblazer Women Award 2025 by Consulate General of India in San Francisco. Ranked as the #1 Women Owned Business Enterprise in the large category by ITServe. Received the TechServe Excellence award

Hi, This is Dinesh and I'm an IT recruiter at Trident Consulting, one of the fastest-growing IT staffing and services firms in the nation. We are currently seeking a Packaging Operator (Chemical Packaging Consultant for one of our industry leading clients. 📌 Job Description - Packaging Operator 1 (Chemical Packaging Technician) Location: 3500 Dekalb Street, St. Louis, MO 63118 Shift: Monday-Friday | 6:00 AM - 2:30 PM Duration: Feb 16, 2026 - Feb 15, 2027 Pay Rate: $22.50/hour on W2 Role Overview We are seeking an experienced Packaging Operator / Chemical Packaging Technician to support chemical product packaging operations in a regulated manufacturing environment. This role involves hands-on filling, labeling, and over-packing of chemical products while strictly following safety, quality, and ISO procedures. Key Responsibilities Stage materials and perform manual or semi-automatic filling of chemical products Cap, label, and over-pack liquid, powder, or lyophilized products Follow approved packaging specifications, SOPs, and ISO procedures Complete accurate packaging documentation and basic data entry Transport finished goods to inventory locations Comply with all safety, quality, and regulatory requirements Wear required PPE including respirator, Tyvek suits, gloves, and eye protection Support quality systems and assist in training team members Work collaboratively within the packaging team Required Experience & Skills 5-6 years of experience in chemical, pharmaceutical, biotech, or industrial packaging Hands-on experience with: Mixing chemicals Filling, capping, labeling, and over-packing Handling liquid, powder, or lyophilized products Strong knowledge of chemical safety procedures Basic math skills (measurements, counts, weights) Basic computer skills and data entry experience Ability to stand for extended periods and perform repetitive tasks Ability to lift up to 50 lbs (with lifting equipment) High School Diploma or GED Must be clean-shaven daily (respirator requirement) Nice to Have SAP experience or familiarity Experience working in ISO-regulated environments Pharmaceutical or biotech manufacturing background Physical & Safety Requirements Mandatory use of respirator/air helmet and full PPE Physical exam and respirator fit testing required post-offer Exposure to chemicals in a controlled environment Vision required for both close and distance work Interview Process Onsite interview Physical exam and respirator fit test after offer About Trident: Trident Consulting is an award-winning IT/engineering staffing company founded in 2005 and headquartered in San Ramon, CA. We specialize in placing high-quality vetted technology and engineering professionals in contract and full-time roles. Trident's commitment is to deliver the best and brightest individuals in the industry for our clients' toughest requirements. Some of our recent awards include: 2022, 2021, 2020 Inc. 5000 fastest-growing private companies in America 2022, 2021 SF Business Times 100 fastest-growing private companies in Bay Area

Qualifications: Education: • Associate's or bachelor's degree in engineering, science, or a related technical field. Relevant certifications may be considered. Experience: • 1-3 years of experience in equipment qualification or a related role. • Technical Skills: • Knowledge of equipment qualification protocols (IQ, OQ, PQ). • Familiarity with regulatory requirements (e.g., ISO, OSHA) • Proficiency with diagnostic tools and calibration equipment. • Industrial equipment operation and troubleshooting. Soft Skills: • Strong analytical and problem-solving skills. • Excellent written and verbal communication. • Attention to detail and ability to follow procedures precisely. • Other Requirements: • Ability to work independently and as part of a team. • Willingness to travel to different sites when necessary. • Physical ability to handle equipment and perform inspections.

Our Client a technology company that specializes in providing mission-critical communication systems and analytics for public safety, is looking for someone to join their team as a Manufacturing Technician! **This is an onsite 6-month contract with long term potential, that takes place in Elgin, IL ** Required Skills &Experience Mechanical & Electrical Repair: Strong hands-on skills in pneumatics, hydraulics, soldering, and fixture maintenance. Preventative Maintenance: Experience maintaining warehouse and production equipment (e.g., printers, forklifts, scanners). Troubleshooting: Ability to diagnose and fix mechanical/electrical issues independently. Basic Computer Skills: Turning on and navigating a computer, using USB tools, and accessing digital manuals. Email & Communication Tools: Outlook, Teams, or similar for internal communication and reporting. Spreadsheet Software: Microsoft Excel or Google Sheets for logging maintenance tasks or calibration data. What You Will Be Doing Ensure Operational Continuity Through Preventative Maintenance. Impact: Minimize equipment downtime and maintain smooth warehouse and production operations. Troubleshoot and Repair Complex Mechanical and Electrical Systems. Impact: Improve equipment reliability and reduce repair turnaround time. Build and Optimize Production Infrastructure. Impact: Enhance production efficiency and safety through custom-built and well-maintained fixtures You will receive the following benefits: Medical Insurance - Four medical plans to choose from for you and your family Dental & Orthodontia Benefits Vision Benefits Health Savings Account (HSA) Health and Dependent Care Flexible Spending Accounts Voluntary Life Insurance, Long-Term & Short-Term Disability Insurance Hospital Indemnity Insurance 401(k) Paid Sick Time Leave Legal and Identity Protection Plans Pre-tax Commuter Benefit 529 College Saver Plan Motion Recruitment Partners (MRP) is an Equal Opportunity Employer. All applicants must be currently authorized to work on a full-time basis in the country for which they are applying, and no sponsorship is currently available. Employment is subject to the successful completion of a pre-employment screening. Accommodation will be provided in all parts of the hiring process as required under MRP's Employment Accommodation policy. Applicants need to make their needs known in advance.

The Equipment Qualification Technician is responsible for verifying, qualifying, and maintaining the quality and performance of manufacturing equipment (not finished products). This role focuses on ensuring machines and production systems operate reliably, meet qualification standards, and comply with regulatory requirements in a manufacturing environment. Key Responsibilities: Perform IQ, OQ, and PQ on manufacturing equipment Verify machine performance, functionality, and compliance (not product inspection) Document qualification results, deviations, and corrective actions Work hands-on on the manufacturing floor / shop environment Support equipment setup, troubleshooting, and issue resolution Work around production lines, machines, and industrial systems Partner with Engineering, Quality, and Operations teams Participate in root cause analysis, audits, and process improvement activities Train operators and provide technical support once equipment is qualified Experience Prior experience in a manufacturing environment (required) Experience working with machines, equipment, or production lines Experience in regulated environments (GMP / ISO preferred) Technical Skills Equipment qualification or validation exposure (IQ/OQ/PQ preferred) Mechanical aptitude with hands-on troubleshooting and equipment setup Ability to follow and document technical procedures

We're Hiring: Manufacturing Technician Job Type: Temp; upto 6 months Shift: 3:30pm-2am About the Role We are seeking a detail-oriented and motivated Manufacturing Technician to support our manufacturing operations. This role is ideal for early-career professionals who want hands-on experience working closely with engineers, equipment, and production teams in a regulated manufacturing environment. Key Responsibilities Perform functions associated with all manufacturing operations, including production, rework, and quality testing of parts, components, subassemblies, and final assemblies Work closely with engineers on equipment setup, calibration, process development, and experimentation Install, validate, and maintain equipment and manufacturing processes to improve yield and reduce cycle time Perform corrective, preventive, and calibration maintenance on production equipment Evaluate operating data and make on-line adjustments to products, instruments, or equipment Participate in the Material Review Board (MRB) decision-making process Identify manufacturing-related issues and implement corrective actions Develop, revise, and follow manufacturing documents and procedures Certify manufacturing associates on production processes Evaluate and order necessary equipment, tools, and fixtures Compliance & Safety Ensure compliance with all Corporate and Divisional policies and procedures Strictly follow all safety rules and regulations, including QSR and ISO standards Qualifications High School Diploma or equivalent required 0-3 years of manufacturing or technical experience preferred Ability to work effectively with cross-functional teams Strong attention to detail and problem-solving skills Comfortable working in a regulated manufacturing environment

GMP Manufacturing/Laboratory Technician Onsite in Chapel Hill, NC Contract for 1 year GMP Manufacturing Technician The Good Manufacturing Practices (GMP) facility focused on expansion and manipulation of human cells for clinical phase 1 applications, specifically including applications involving chimeric antigen receptor (CAR) T cells. The Client Facility also manufactures Master Cell Banks (MCBs) used in the production of clinical grade gamma retrovirus vector for use in CAR T clinical trials. Activities include cell culture work within an ISO 7 clean room environment. Working aseptically in a Biological Safety cabinet. Follow SOPs and execute cell counting, making manufacturing decisions as needed to support patient products being manufactured. Know when to ask questions and look for support in manufacturing when questions should arise. Helping to maintain inventory stock in clean rooms and release space. Supporting variety of other manufacturing duties as they come up as needed. Will be required to lead or support projects for validations of manufacturing systems.

Required Skills: Degree in Industrial Maintenance related field. 1+ years of Client PE Seibi experience. 3+ years of Automotive experience. Experience with mentoring and/or technical training. Responsibilities: The primary responsibility of this role is to inspect and confirm new or modified equipment and to prepare that equipment for manufacturing production. On-site robot programming and interlocking. Confirm that the new model equipment meets set standards and performs as intended. Prepare and confirm new Body Weld equipment at the vendors. Support weld machine Seibi activity at North American Manufacturing Companies from installation to start of production. Develop equipment countermeasures during setup/trials.

Great opportunity for a Process Controls Technician to work for an innovative paper manufacturing company located in Wabash, IN. This Process Controls Technician will be responsible for boots on the ground troubleshooting & repairs of plant control systems, primarily I/O, DCS, & QCS. Responsibilities Lead and supervise process control activities with a strong focus on safety and housekeeping Standardize control system practices Develop and monitor strategic goals for process control performance Research and implement new technologies to improve system reliability Manage, program, and maintain all process control hardware and software Oversee system backups, documentation, and change records Support vendor installations and commissioning Maintain parts inventory and maintenance records Provide emergency troubleshooting and off‑shift support as needed Qualifications High school diploma or GED required; technical degree preferred 7+ years of experience in process control, automation, or industrial systems Experience training others in PLC, drive, and network systems Knowledge of NFPA, OSHA, and NEMA electrical safety standards Strong logic, troubleshooting, and problem‑solving skills Ability to design and implement industrial control strategies

Job Title: QC Environmental Monitoring Technician Department: Quality Control The QC Environmental Monitoring Technician is responsible for supporting parenteral manufacturing operations through routine environmental monitoring of classified manufacturing areas, as well as conducting clean utility sampling and analysis within both manufacturing and QC laboratory facilities. This role plays a critical part in ensuring compliance with cGMP requirements and maintaining a controlled manufacturing environment to support the production of safe and effective pharmaceutical products. Key Responsibilities: Adhere to and promote compliance with all cGMP procedures, Quality Systems, and Good Documentation Practices (GDP). Perform routine environmental monitoring of classified manufacturing areas to support both standard operations and Environmental Monitoring Performance Qualification (EMPQ) activities. Conduct clean utility sampling and analysis, including but not limited to: Compressed air Potable water Purified water Water for Injection (WFI) Clean steam Support manufacturing and laboratory activities by providing timely and accurate environmental monitoring data. Enumerate, review, and document sampling results in LIMS or other laboratory data systems. Perform Second Person Verification (SPV) of environmental monitoring results on a routine basis. Participate in continuous improvement projects and quality initiatives. Assist with authoring and updating Standard Operating Procedures (SOPs) and Work Instructions as required. Adhere to and promote compliance with all site safety standards. Minimum Requirements: High School Diploma or equivalent required; Associate degree preferred. 2+ years of experience performing Environmental Monitoring in a GMP pharmaceutical manufacturing environment, preferably supporting aseptic or parenteral production. Demonstrated experience with environmental monitoring techniques, including: Viable surface monitoring Viable air monitoring Non-viable air monitoring Compressed air sampling Water and clean utility sampling and analysis Experience with laboratory systems such as LIMS, LES, and/or MODA. Preferred Qualifications: Strong understanding of cGMP requirements and regulatory compliance. Experience performing environmental monitoring within filling isolators or restricted access barrier systems (RABS). Ability to train and mentor junior Environmental Monitoring Technicians. Strong verbal and written communication skills. Ability to work effectively with cross-functional teams. Physical & Work Environment Requirements: Ability to work in laboratory and cleanroom environments while wearing appropriate PPE. Ability to gown into facility-dedicated cleanroom attire as required. Ability to stand or walk for extended periods and perform repetitive tasks. Ability to lift, push, pull, and carry up to 30 pounds. Work Schedule & Travel: Ability to work 12-hour shifts. Flexibility to work day or night shifts as required, especially during training and startup phases. Role may initially support project/startup activities and transition into a routine operational support role.

Hands-on technician to assist with production troubleshooting and support projects to improve manufacturing methods. Assist manufacturing engineers to address equipment and tooling needs to reduce costs and improve product quality on fans, wheels, blower packages, and corresponding component parts. Responsibilities: Under technical direction, troubleshoot and analyze manufacturing problems and implement corrective actions for high quality, efficient manufacturing solutions. Support workflow analysis, work methods, plant and department layouts for improved product flow in production. Help identify required tools, jigs and fixtures, or other new or special equipment required for new production or improvements to existing production lines. Assist in the development of justifications for the purchase of manufacturing equipment. Assist with the installation and debugging of production equipment. Update and maintain visual and written work guidelines. Update and maintain manufacturing routings. Perform time studies. Perform other manufacturing tasks as assigned. Qualifications: Associates Degree in Manufacturing or Mechanical Engineering Technology. Proficient in Solidworks or similar 3D modeling package Must have a good mechanical aptitude of general machinery. Excellent communication and organizational skills Ability to develop data-driven solutions in a manufacturing environment

NOVA Engineering & Environmental is seeking a highly organized and detail-oriented Permit Technician in the Westlake, FL area. This role serves as a critical point of contact for the public, city staff, inspectors, plans examiners, and the Building Official. The ideal candidate will demonstrate exceptional customer service skills, strong organizational abilities, and the capacity to manage multiple priorities in a fast-paced environment. Key Responsibilities: Permit Processing: Review and process permit applications, collect and record payments/fees, and conduct permit audits to ensure compliance. Documentation & Records Management: Maintain accurate and organized files, including permits, inspection reports, blueprints, and reference materials. Customer Service: Provide professional assistance to contractors, homeowners, and the public regarding permitting requirements and building department services. Inspection Coordination: Schedule inspections for building code compliance and assist inspectors with administrative support. Contractor Registration: Maintain and update contractor registration records. Data Management: Perform data entry tasks, manage fee details, and maintain Excel spreadsheets (e.g., tax logs). Communication: Answer phones, respond to inquiries, and ensure timely resolution of customer needs. Additional Duties: Support the Building Official and department staff with related tasks as assigned. Minimum Qualifications High School diploma or equivalent; Associate's or Bachelor's degree preferred. Previous experience in permitting with a municipality or building department highly preferred. Strong understanding of construction permitting processes and building codes. Proficiency in Microsoft Office Suite (Word, Excel, Outlook). Valid State Driver's License. Preferred Qualifications: International Code Council (ICC) Permit Technician Certification (not required but strongly preferred). Experience with permitting software systems and electronic document management. Familiarity with Florida Building Code and related regulations. Core Competencies: Exceptional customer service and interpersonal skills. Strong attention to detail and organizational abilities. Ability to multi-task and prioritize in a deadline-driven environment. Effective written and verbal communication skills. NOVA is an Equal Opportunity Employer. All qualified candidates are encouraged to apply. NOVA does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, ancestry, marital status, veteran status or any other characteristic protected by law. About Nova: Established in 1996, NOVA was originally founded to provide Environmental Consulting, Geotechnical Engineering, and Construction Materials Testing and Inspection services to the design and construction community, largely in the southeastern United States. Since our founding, NOVA has added additional service lines such as Facilities and Building Envelope, Forensics, Municipal and more. We are dedicated to providing a wide variety of projects and services with an emphasis on collaboration and safety. We offer a stimulating and inspiring work environment where our employees are recognized for their efforts and achievements and are mentored for professional growth. Currently, NOVA employs 650+ personnel in 20 offices serving clients throughout the southeastern United States and beyond. Our firm has professional and administrative support staff that includes registered professional engineers, registered professional geologists, environmental scientists, registered roof observers, LEED accredited professionals, soil/foundation engineers, laboratory specialists, materials technicians, ICC-certified inspectors, NICET-certified technicians, and AWS-certified welding inspectors. NOVA's facilities include AASHTO-accredited laboratories in soils, concrete, aggregate and hot-mix asphalt testing/inspection. We also have CCRL-inspected laboratories for concrete sampling, curing, and testing. NOVA will continue to expand its reach and reputation as a leader in the testing, inspection, and consulting fields with a strong legacy of quality and integrity by promoting our best internal resources and recruiting a diverse culture of valued and exceptional talent.

Technician II (NO C2C) Santa Clara, CA (Onsite) 6 Months contract with possible extension 25-29.00/hr on W2 , DOE Key Responsibilities: Build Test Racks and Setups: Assemble and maintain test racks and test setups for electrical testing (RF, digital, and antenna). Test Execution: Conduct tests on electrical, RF components, and antennas. Analyze results and troubleshoot any issues that arise during testing. Documentation & Reporting: Maintain accurate records of test results, generate detailed reports, and provide feedback on performance and improvements. Lab Organization & Cleanliness: Ensure the lab environment is safe, organized, and compliant with safety regulations. Problem-Solving: Identify and troubleshoot issues with test setups, hardware, and software to ensure smooth operations. Required Qualifications: Technical degree in Engineering or a related field (preferred). Minimum of 3 years of experience working in an R&D lab performing light assembly work and electrical testing. Technical Skills: Using hand tools to perform assembly tasks of mechanical and electrical systems. Proficient in using oscilloscopes, spectrum analysers, signal generators, network analysers, and other common test equipment. Strong focus on accuracy and precision in assembly work, test setup, execution, and documentation. Ability to work autonomously, manage tasks, and meet deadlines in a fast-paced environment. Excellent troubleshooting skills for identifying and resolving issues.