Manufacturing Associate Jobs in Mitchellville, MD

Key Responsibilities: Perform all tasks associated with the upstream portion of CAR-T manufacturing, including cell thaw, activation, transduction, and expansion in bioreactors or static culture systems. Operate and maintain single-use bioreactors, incubators, centrifuges, and other upstream equipment. Prepare and aliquot media, buffers, and other process-related solutions following aseptic techniques and SOPs. Execute cell culture operations in a cleanroom, maintaining strict adherence to GMP and aseptic processing standards. Accurately document all activities in batch records, logbooks, and electronic systems Collaborate with QA, QC, and MS&T teams to troubleshoot deviations and support process improvements. Participate in gowning qualification, environmental monitoring, and cleanroom maintenance. Assist in training of new team members and contribute to a positive, compliant, and efficient manufacturing environment. Qualifications: Bachelor's degree in Biology, Biotechnology, Biochemistry, or related field, or equivalent industry experience. 6 months or 1-3 years of experience in cell therapy, biologics, or pharmaceutical manufacturing in a GMP environment. Hands-on experience with cell culture, aseptic techniques, and bioreactor systems. Strong understanding of GMP regulations, cleanroom behavior, and safety practices. Ability to work a flexible schedule, including weekends or shift-based work as needed.

Biopharmaceutical Manufacturing Associate - Contract - Rockville, MD We are on the hunt for bold, innovative thinkers who are ready to help push the boundaries of science and make a tangible difference in the world. Proclinical is seeking a Biopharmaceutical Manufacturing Associate to join our client's team in Rockville, MD. Primary Responsibilities: The successful candidate will focus on supporting cell culture and purification operations with tasks such as preparing and sterilizing media, operating process equipment, and ensuring compliance with safety and documentation standards. This position requires attention to detail and the ability to work collaboratively within a team. Skills & Requirements: Basic understanding of ERP processes and continuous improvement systems. Ability to manage and use automation and digital platforms. Proficiency in Microsoft Office Applications (Excel, Word, Outlook). Ability to follow detailed instructions and document information accurately. Strong teamwork skills. The Biopharmaceutical Manufacturing Associate responsibilities will be: Prepare, clean, sterilize, batch, pasteurize, filter, and deliver media and solutions for cell culture and purification. Set up, operate, clean, and break down process equipment. Perform sampling procedures and operate filter integrity devices. Monitor and trend process operations, equipment, and instruments to identify and address issues. Set up processing equipment and parts for cleaning and sterilization. Follow SOPs, protocols, and batch records/logbooks for safe and compliant operations. Adhere to safety policies and actively correct unsafe behaviors and conditions. Communicate effectively in various situations. If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at j.cerchio@proclinical.com If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page. Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy. By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.proclinical.com/privacy-policy

Job Title : GMP Manufacturing Associate Duration : 12 months Shift timing : Initial shift for training will be from 8:00am - 5:00pm. Once they build the team it can be two options but will be assigned depending on business needs. 6:00 am - 6:00 pm OR 6:00 pm - 6:00 am Job Description : Preparation, cleaning, sterilization, batching, pasteurization or filtration and delivery of media and solutions for cell culture and purification operations. Follow appropriate standard operating procedures (SOPs), protocols and batch records/logbooks to safely perform process operations and document compliantly with good documentation and data integrity practices. Perform the set-up, operation, cleaning and break-down of process equipment. Perform sampling procedures on various analytical instruments to analyze cell culture, solution and/or product concentration characteristics. Operate Filter integrity devices to confirm the integrity of filters pre and post use. Perform process operations, equipment and instrument monitoring and trending to enable proactive identification of issues to escalate and correct with applicable departments.

This position requires performing a variety of operations for Elutia products including, but not limited to, Manufacturing activities, Shipping & Receiving, Inventory Control, as well as environmental monitoring & maintenance for a drug delivery device. The responsible individual will perform routine data entry in the MRP database, LHR releases, preparation of shipping documentation, etc. in compliance with internal procedures, FDA Quality Systems Regulations as well as ISO Standards. Essential Duties & Responsibilities: Manufacturing Issue, track and review Manufacturing Work Order (LHR) documentation for accuracy and component/product traceability. Manufacture, assemble products according to approved operating procedures. Perform label printing, initial packaging and final packaging as required to support operations functions. Prepare product samples for sterilization and lot release testing. Perform self-inspection on all assembly work performed to ensure adherence to workmanship standards. Maintain clean and orderly work station. · Follow all corporate, safety and production operating procedures. Perform environmental monitoring including viable & non-viable particulate counting, surface microbial testing as well as review and analysis of data for each test cycle. Other duties as required. Inventory, Receiving, & Distribution: Process incoming receiving and inventory transactions in the MRP system. Process transactions and documentation associated with product returns. Perform periodic cycle counting to monitor inventory levels and report inventory balances for financial reconciliation. Prepare shipments with appropriate documentation in compliance with procedures and all applicable export requirements, as applicable. Prepare and review inspection documentation and perform inspections as needed Education & Experience: High School diploma or equivalent (entry level position) 2+ years' experience in manufacturing and/or quality (production, packaging, labeling incoming and shipping, critical systems, etc.) preferred. Experience working in regulated work environment preferred - compliance to specifications and procedures as well as FDA QSR's (21 CFR 820) and ISO 1348

MUST BE A US CITIZEN (ITAR REQUIREMENT). Support a Fortune 500 Aero Defense company as a Manufacturing Technician. Responsibilities: • Performs functions associated with all manufacturing operations, including working with engineers in set-up and calibration tasks. • Performing rework and quality testing related to the production of parts, components, subassemblies and final assemblies. • Uses sophisticated programs to collect and evaluate operating data to conduct on-line adjustments to products, instruments or equipment. • Determines and may assist in developing methods and procedures to control or modify the manufacturing process. • Works with engineers in conducting experiments. Basic Qualifications for Manufacturing Technician 2 Minimum Requirements: • HS diploma or equivalent (education will be verified) • Minimum 2 years previous honeycomb panel fabrication or aerospace mechanical assembly experience. • Strong mechanical aptitude to include the ability to read and interpret drawings • Attention to detail with a focus on quality workmanship • Familiar with hand tools and good math/geometry skills. • Candidate must be able to read and follow written manufacturing instructions and technical procedures. • Operate equipment such as hand tools and power machinery for processing metals, composites and wood. • Must work closely with lead technicians and supervisor to meet build requirements and schedules within allotted budgets. • Ability to lift up to 50lbs.

An aerospace client is looking for a Manufacturing Technician who will perform functions associated with all manufacturing operations, including working with engineers in set-up and calibration tasks. Position: Manufacturing Technician Pay Rate: $24.58/hr. on W2 Duration: 6 months or longer Schedule: 9/80 A Shift: 1st shift ** Willing to work flexible schedules as needed to meet delivery dates.** RESPONSIBILITIES: • Performs functions associated with all manufacturing operations, including working with engineers in set-up and calibration tasks. • Performing rework and quality testing related to the production of parts, components, subassemblies and final assemblies. • Uses sophisticated programs to collect and evaluate operating data to conduct on-line adjustments to products, instruments or equipment. • Determines and may assist in developing methods and procedures to control or modify the manufacturing process. • Works with engineers in conducting experiments. BASIC QUALIFICATIONS: US Citizenship is required. HS diploma or equivalent (education will be verified). Minimum 2 years previous honeycomb panel fabrication or aerospace mechanical assembly experience. Strong mechanical aptitude to include the ability to read and interpret drawings. Attention to detail with a focus on quality workmanship. Familiar with hand tools and good math/geometry skills. Candidate must be able to read and follow written manufacturing instructions and technical procedures. Operate equipment such as hand tools and power machinery for processing metals, composites and wood. Must work closely with lead technicians and supervisor to meet build requirements and schedules within allotted budgets. Ability to lift up to 50lbs. Demonstrates high level of concern for safety of self and others. Willing to work flexible schedules as needed to meet delivery dates. Mechanical assembly, adhesive bonding experience. This is not electrical assembly work. Candidates must be local/able to come for on-site interviews if asked. PREFERRED QUALIFICATIONS: • Computer skills including MS Word and Excel are a plus. • Previous fabrication (honeycomb panel) experience in aerospace manufacturing environment. • Experience preparing/mixing epoxy and silicone adhesives for mechanical and thermal component installation in honeycomb panels and aluminum skins. • Experience handling of hazardous materials in accordance with OSHA and industry standards. Competencies for Success: • Successful candidates will need to be a team player with a strong desire to work in a fast-paced, professional environment • Ability to follow instructions, plan work, and manage time appropriately • Ability to follow safety procedures • Willing to work with a positive attitude • Detail oriented • Ability to be prompt for shift work. About our client: Our client is a world leader and premier innovator in aerospace, with over 100,000 top talent employees providing the most advanced products and technologies in the industry. With numerous awards and recognitions, they offer continuous growth, learning, and development for their employees. About APR: Since 1980 APR Consulting, Inc. has provided professional recruiting and contingent workforce solutions to a diverse mix of clients, industries, and skill sets nationwide. We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law. Don't miss out on this amazing opportunity! If you feel your experience is the match for this position please apply today and join our team. We look forward to working with you!

Manufacturing Technician / Sr. Manufacturing Technician Baltimore County, MD Responsibilities: Complete and maintain aseptic qualification training. Obtain basic understanding of a task, unit operation and/or document (forms and/or SOPs) while aiding with oversight from Manufacturing Technician III and above. Attain and maintain gowning qualification per appropriate SOPs. Follow SOPs, product batch record instructions, logbooks and forms, and corresponding quality documentation in detail. Prepare and maintain accurate documentation following cGMP and GDP principles. Ensure documentations are completed in real-time in accordance to CGMP and GDP principles. Adhere to all environmental, health, and safety policies and procedures and proactively identify unsafe conditions. Support QC sampling, equipment calibration, equipment/utility validation, and preventive maintenance as needed. Work collaboratively with internal teams to meet site goals and objectives as part of a team. Initiate and foster a spirit of cooperation within and between departments. Review documentation for accuracy, makes corrections and/or escalates to supervision/Manufacturing Quality Associate (MQA). Maintain all personal cGMP related training in a current state. Achieve and maintain cleaning and sanitization of cleanroom training. Participate in Aseptic media qualification per the appropriate qualification protocol. Support manufacturing in the investigation of deviations and performs required risk assessments. Participate in personnel monitoring as requested. Work closely with Operational Excellence to identify and implement process improvements. Set up and breakdown the filling equipment per appropriate SOPs. Transport equipment and components as needed. Interact with filling machines at the validated speeds and volumes. Perform volume checks. Perform and document inherent and non-inherent interventions. Ensure slow and purposeful movements appropriate for a Grade A/B GMP aseptic environment. Work with R&D and tech transfer team for successful transfer of Programs into the GMP area Perform all aseptic connections, respecting first air. Perform pre- and post-filter integrity testing as required. Aseptically sterile filter products into appropriate vessels. Complete routine and enhanced cleaning and sanitization of all controlled aseptic cleanrooms, as needed. Attain and maintain ability to perform environmental tasks as required. Perform other duties as assigned. Qualifications: High school diploma or equivalent with 1-3 years' experience, Bachelor's degree with a minimum of 1 year of experience, or equivalent combination of education, training and professional experience that provides the individual with the required knowledge, skills, and abilities. Senior Manufacturing Technician (minimum of 3 years of industry experience w/ fill finish experience) Prior experience in related field, preferred. cGMP manufacturing knowledge, preferred. Aseptic filling and general production knowledge, preferred. Demonstrate basic math skills. Demonstrate the ability to establish good working relationships with other departments, including vendors, colleagues, and subordinates. Demonstrates the appropriate technical knowledge necessary to make sound decisions on development issues with minimal supervision. Demonstrate the ability to analyze data and information and assess and resolve complex problems/issues as required. Must be able to comprehend and follow all applicable SOPs. Demonstrate knowledge and experience with electronic Quality Management Systems such as MasterControl and Trackwise. Demonstrate ability to acquire the appropriate knowledge from resources on the current federal, local, and international regulations regarding the production, testing, and release of drug substances and products. Good understanding of cGMPs, industry, and regulatory standards and guidelines. Demonstrate familiarity with Microsoft programs like Word, Excel, PowerPoint, Project, Teams, Outlook, etc. Demonstrate the ability to portray the appropriate level of integrity and professionalism. Demonstrate the ability to communicate effectively with management, staff, regulators, and client representatives in written and verbal formats. Demonstrate the ability to complete tasks accurately and according to established and shifting timelines. Demonstrate the ability to make quality scheduling, resource allocation, and priorities decisions. Energetic, execution-focused, self-motivated, and organized individual who is accustomed to working in a deadline-focused, high-pressure entrepreneurial environment. Results-oriented and efficient. Creative and open-minded who fosters an environment in which sharing of ideas is encouraged. Demonstrate the ability to work closely with a diverse customer and employee base (internally and externally). Demonstrate the ability to work well in a cross-functional team environment. Must communicate fluently in English and have legible handwriting.

Hourly Rate: $16.00/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.

RELOCATION ASSISTANCE: No relocation assistance available CLEARANCE TYPE: NoneTRAVEL: NoDescriptionAt Northrop Grumman, our employees have incredible opportunities to work on revolutionary systems that impact people's lives around the world today, and for generations to come. Our pioneering and inventive spirit has enabled us to be at the forefront of many technological advancements in our nation's history - from the first flight across the Atlantic Ocean, to stealth bombers, to landing on the moon. We look for people who have bold new ideas, courage and a pioneering spirit to join forces to invent the future, and have fun along the way. Our culture thrives on intellectual curiosity, cognitive diversity and bringing your whole self to work - and we have an insatiable drive to do what others think is impossible. Our employees are not only part of history, they're making history. Northrop Grumman Mission Systems is seeking Electronic Manufacturing Specialists for its Linthicum, MD location. The Electronic Manufacturing Specialist will perform all functions necessary for the complete manufacture of electronic assemblies. This is an IBEW Union represented position. Basic Qualifications: • High School graduate or recognized equivalent (GED). • Must be capable of successfully completing basic solder certification and pre-employment skills The application period for the job is estimated to be 20 days from the job posting date. However, this timeline may be shortened or extended depending on business needs and the availability of qualified candidates.Northrop Grumman is committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity/Affirmative Action Employer, making decisions without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability, or any other protected class. For our complete EEO/AA and Pay Transparency statement, please visit *********************************** U.S. Citizenship is required for all positions with a government clearance and certain other restricted positions.

Your Tasks: This position is responsible for manufacture of biologics (LV) under cGMP conditions. Staff must follow established procedures, execute batch production records using good documentation practices and adhere to gowning procedures required for work in cleanroom environment. Supports training new hires, trouble shooting, preparation of controlled documentation and other Manufacturing duties. Essential Duties and Responsibilities: Adhere to clean room Standard Operational Procedures (SOPs) for gowning, traffic flows, modes of operation. Preform process set up and operations, process monitoring, Filter Integrity Test (FIT), process sampling, system breakdown, and completion of production records Pass and maintain gowning and/or BSC qualifications. APQ are maintained as assigned. Follow batch record instruction and complete GMP documentation, review same for completeness and accuracy. Contribute to the development, writing, and review of Standard Operating Procedures (SOPs), Material Specifications (MSs), Standard Manufacturing Procedures (SMPs), Batch Production Records (BPRs) and other GMP documentation. Responsible for the proper maintenance and use of production equipment in strict accordance with cGMPs, SOPs and safety policies. Responsible for cleaning of equipment and work areas as required. Ensure and maintain inventory and restock supplies when needed. Complete Purchase Order Requests. Assist in troubleshooting processing issues, support investigation and establishing root cause and resolution/corrective action. Follow manufacturing schedules, ensuring adequate supplies and equipment are available and released for use. Participate in calibration and validation activities as needed. Able to support 24/7 process operations and shift schedule. Requirements: Bachelor's degree (B.S.) from a four-year college or university and at least 2 years of related experience; or equivalent combination of education and experience. Previous GMP experience is desired, as is good aseptic technique. Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to walk; use hands to finger, handle, or feel; reach with hands and arms, talk, and hear. The employee is required to stand; climb or balance and stoop, kneel, crouch. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, color vision, peripheral vision, depth perception and ability to adjust focus. Must have ability to handle more than one task at a time and must work at a rapid pace while maintaining attention to detail. Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. This job is performed in a temperature-controlled facility without exposure to extreme hot or cold temperatures. Generally, this job is performed in a sanitized laboratory setting and routinely uses standard medical and research equipment such as centrifuges, biosafety cabinets, chromatography devices and columns, tangential-flow filtration devices and filters, peristaltic pumps and metering fill pumps, pipettes and computers. While performing the duties of this job, the employee is frequently exposed to cultured human cells (immortalized, not primary) and lentivirus-derived vector particles. Employees entering and leaving the laboratory must wear appropriate clothing and protective equipment such as scrubs, coveralls, masks, glasses and gloves. The noise level in the work environment is usually moderate. The anticipated base salary range has been established at $24.95 - $33.75/hour. The salary of the finalist(s) selected for this role will be set based on a variety of factors, including but not limited to, internal equity, experience, education, specialization, skills, abilities, and training. The above salary range represents the Company's good faith and reasonable estimate of the range of possible compensation at the time of posting. In addition to your salary, the Company offers a comprehensive benefits package including health, vision, and dental insurance, plus a 401(k) plan. All benefits are subject to eligibility requirements. Certain positions are eligible for additional forms of compensation such as bonuses or commissions. Miltenyi Biotec is an EO Employer - M/F/Veteran/Disability/Sexual Orientation/Gender Identity. Miltenyi Biotec, Inc. participates in E-Verify. Are you ready to start revolutionizing biomedical research? When you join Miltenyi Biotec, you join a family that is passionate about making a real impact - one breakthrough at a time. One integral division of that Miltenyi Biotec family is Miltenyi Bioindustry - our contract development and manufacturing organization (CDMO). As a full-scale CDMO, we provide customers with services for the development and manufacturing of lentiviral vectors and cell and gene therapy products. This crucial arm of our enterprise bridges the gap between research and mass bioproduction, ensuring that our solutions are accessible on a global scale. Miltenyi Bioindustry plays a unique role as both the producer and the service provider, relying on our instruments and reagents for each workflow step, controlling the entire supply chain and thus delivering greater security and planning clarity to our customers.

Piper Companies has a Manufacturing Associate (Allstream) opportunity supporting one of our highly renowned pharmaceutical partners in the Gaithersburg, MD area. This role works with upstream and downstream biopharmaceutical manufacturing processes in a cGMP environment. Responsibilities for the Manufacturing Associate include: * Operates manufacturing equipment such as: incubators, stainless steel and disposable single-use bioreactors, depth filtration skids, chromatography skids, single-use mixers, centrifuges, washers, autoclaves, tanks and in-process testing instruments. * Performs cleaning/sanitization and basic calibration of equipment in accordance with SOPs. * Support process improvement initiatives and authors or revises standard operating procedures accordingly. * Records manufacturing activities clearly and accurately within approved current Good Manufacturing Practices (cGMP) documentation and regulatory requirements. * Reviews executed Production Records for accuracy and completion. Qualifications for the Manufacturing Associate include: * 1-2+ years of relevant biopharmaceutical manufacturing experience is required. * Bachelor of Science in Biology, Life Sciences, Pharmaceuticals, or similar degree is required. * Experience supporting both upstream and downstream/all-stream manufacturing processes is preferred. Compensation for the Manufacturing Associate includes: * Salary Range: approximately $25.00 - $30.00 hourly, commensurate with experience * Comprehensive Benefits: Cigna Medical, Dental, Vision, ADP 401k, PTO, Paid sick leave This job is open for applications on 5/8/2025. Applications for this role will be accepted at least 30 days from the posting date. Manufacturing, bioprocessing, upstream, downstream, allstream, biotech, biopharma, pharmaceutical manufacturing, drug, vaccine, medicine, bioreactor, autoclave, cleanroom, gmp, cgmp, gxp, gdp, fda, cell culture, filtration, chromatography, tff, purification #LI-CP1 #LI-ONSITE

Who we are: Maravai LifeSciences translates extraordinary science into everyday miracles, helping biotech, biopharma, and life sciences companies everywhere deliver novel vaccines, therapeutics, and diagnostics. We are global leaders in providing products and services within the fields of nucleic acid production and biologics safety testing to many of the world's leading biopharma, vaccine, diagnostics, and cell and gene therapy companies. At Maravai, we believe that diverse perspectives are the foundation of innovation. Through an inclusive and equitable culture where every team member is inspired to bring their best selves to work, we cultivate an environment in which we can lead together, providing differentiated value to our customers, and enabling the miracles of science. For over 35 years, Maravai's portfolio companies have served as a catalyst for innovative, lifesaving technology for humanity. Pioneering nucleotide research since its inception, we are now leading the way in the rapidly expanding mRNA market. Your next role as a Miracle Maker Maravai LifeSciences is seeking a #MiracleMaker to join our Manufacturing team as a Manufacturing Associate I, Dry Lab. In this role, you will be responsible for providing critical packaging support to our operations team. You will assist in the preparation and packaging of supports, phosphoramidites, and other non-hazardous materials essential for the synthesis and purification of DNA and RNA oligonucleotides. How you will make an impact: General laboratory maintenance and equipment maintenance Evaluation and cleaning of necessary production glassware Evaluation and assembly of support columns Distribution of products with correct documentation, using good documentation practices. Preparation and inspection of product labels Inspection of finished goods. Pull products from stock for customer orders Inspection of completed orders prior to shipment Ship products using automated software for FedEx Perform other functions and duties as required. The skills and experience that you will bring: Bachelor's Degree in Chemistry, Biology, or other science preferred. Prior experience in laboratory setting may be evaluated as an alternative to formal education. Must have good communication skills, written and verbal. Must be able to follow written Standard Operating Procedures (SOPs)/Work Instructions (WIs) as well as personalized instruction from leaders. Must be self-motivated and able to work both in a team setting as well as individually. Must be able to work in a fast paced environment without getting overwhelmed. Must be able to perform repetitive activities while maintaining accuracy. Must have excellent attention to detail and be able to perform work requiring fine motor skills. Must be a good timekeeper and ensure prompt arrival to work for each scheduled shift. Must have functional knowledge of Microsoft Office Suite. Experience with FileMaker database and NetSuite ERP software a plus. #LI-Onsite The benefits of being a #MiracleMaker: You have the potential to change, improve, and save lives around the world. You have the opportunity to be a part owner in Maravai through RSU grants and optional employee stock purchase plans. We offer comprehensive medical plans and HSA/FSA options. Fertility & family planning assistance. A variety of additional optional benefits and insurance options, including pet insurance. Retirement contributions. Holidays & Paid Time Off. Benefits may vary by region and employment type and do not apply to temporary employees or contractors. See a comprehensive list of benefits at our Benefits & growth site at **************************************************** To view more opportunities to become a #MiracleMaker, visit our career site at ******************************** Maravai LifeSciences is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation, and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law. Click here to view Maravai LifeSciences Privacy Notice HIRING SCAM ALERT Recently, individuals impersonating Maravai LifeSciences Human Resources members have offered fraudulent interviews and job offers to unsuspecting candidates. To help protect you from these scam artists, please be aware that: Maravai LifeSciences will never interview a candidate over RingCentral, similar messaging apps or social media (e.g. Telegram, Google Hangouts, WhatsApp, Facebook Messenger, etc.) Maravai LifeSciences will never send a company check or ask an applicant to pay a fee or purchase at home work/training materials in connection with an application for employment. Maravai LifeSciences will never provide excess money to an applicant and ask the applicant to write a check for repayment. If you have any doubt about a job offer or any other communication purporting to come from Maravai LifeSciences, please reach out to us directly at *****************. If you believe you have been a victim of fraud, you can report this activity at: *********** or

Who we are: Maravai LifeSciences translates extraordinary science into everyday miracles, helping biotech, biopharma, and life sciences companies everywhere deliver novel vaccines, therapeutics, and diagnostics. We are global leaders in providing products and services within the fields of nucleic acid production and biologics safety testing to many of the world's leading biopharma, vaccine, diagnostics, and cell and gene therapy companies. At Maravai, we believe that diverse perspectives are the foundation of innovation. Through an inclusive and equitable culture where every team member is inspired to bring their best selves to work, we cultivate an environment in which we can lead together, providing differentiated value to our customers, and enabling the miracles of science. For over 35 years, Maravai's portfolio companies have served as a catalyst for innovative, lifesaving technology for humanity. Pioneering nucleotide research since its inception, we are now leading the way in the rapidly expanding mRNA market. Your next role as a Miracle Maker Maravai LifeSciences is seeking a #MiracleMaker to join our Manufacturing team as a Manufacturing Associate I, Dry Lab. In this role, you will be responsible for providing critical packaging support to our operations team. You will assist in the preparation and packaging of supports, phosphoramidites, and other non-hazardous materials essential for the synthesis and purification of DNA and RNA oligonucleotides. How you will make an impact: * General laboratory maintenance and equipment maintenance * Evaluation and cleaning of necessary production glassware * Evaluation and assembly of support columns * Distribution of products with correct documentation, using good documentation practices. * Preparation and inspection of product labels * Inspection of finished goods. * Pull products from stock for customer orders * Inspection of completed orders prior to shipment * Ship products using automated software for FedEx * Perform other functions and duties as required. The skills and experience that you will bring: * Bachelor's Degree in Chemistry, Biology, or other science preferred. Prior experience in laboratory setting may be evaluated as an alternative to formal education. * Must have good communication skills, written and verbal. * Must be able to follow written Standard Operating Procedures (SOPs)/Work Instructions (WIs) * as well as personalized instruction from leaders. * Must be self-motivated and able to work both in a team setting as well as individually. * Must be able to work in a fast paced environment without getting overwhelmed. * Must be able to perform repetitive activities while maintaining accuracy. * Must have excellent attention to detail and be able to perform work requiring fine motor skills. * Must be a good timekeeper and ensure prompt arrival to work for each scheduled shift. * Must have functional knowledge of Microsoft Office Suite. * Experience with FileMaker database and NetSuite ERP software a plus. #LI-Onsite The benefits of being a #MiracleMaker: * You have the potential to change, improve, and save lives around the world. * You have the opportunity to be a part owner in Maravai through RSU grants and optional employee stock purchase plans. * We offer comprehensive medical plans and HSA/FSA options. * Fertility & family planning assistance. * A variety of additional optional benefits and insurance options, including pet insurance. * Retirement contributions. * Holidays & Paid Time Off. Benefits may vary by region and employment type and do not apply to temporary employees or contractors. See a comprehensive list of benefits at our Benefits & growth site at **************************************************** To view more opportunities to become a #MiracleMaker, visit our career site at ******************************** Maravai LifeSciences is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation, and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law. Click here to view Maravai LifeSciences Privacy Notice HIRING SCAM ALERT Recently, individuals impersonating Maravai LifeSciences Human Resources members have offered fraudulent interviews and job offers to unsuspecting candidates. To help protect you from these scam artists, please be aware that: * Maravai LifeSciences will never interview a candidate over RingCentral, similar messaging apps or social media (e.g. Telegram, Google Hangouts, WhatsApp, Facebook Messenger, etc.) * Maravai LifeSciences will never send a company check or ask an applicant to pay a fee or purchase at home work/training materials in connection with an application for employment. * Maravai LifeSciences will never provide excess money to an applicant and ask the applicant to write a check for repayment. If you have any doubt about a job offer or any other communication purporting to come from Maravai LifeSciences, please reach out to us directly at *****************. If you believe you have been a victim of fraud, you can report this activity at: *********** or ******************

Are you a skilled Process or Engineering Technician with chemical and mechanical experience who thrives in hands-on work and wants to contribute to the creation of high-quality sports surfaces? If so, we want to hear from you! We are seeking a Manufacturing Technician to join our dynamic team and play a key role in the manufacturing of industry-leading polyurethane-based sports surfaces. This is an exciting opportunity for someone with a passion for problem-solving, process improvement, and working in a fast-paced, hands-on environment.Responsibilities Assist in the manufacturing process of high-quality sports surfaces, applying your chemical and mechanical expertise. Provide hands-on support in the production of polyurethane-based products, ensuring safety, quality, and efficiency at every stage. Troubleshoot and solve problems related to equipment, processes, and production challenges. Operate and maintain equipment such as PLCs, HMIs, and DCS systems. Mentor and train team members on best practices for manufacturing processes. Analyze complex manufacturing issues, implement effective solutions, and make informed decisions under pressure. Ensure all products meet quality standards and customer specifications. Communicate effectively with team members and other departments to ensure smooth operations. Skills + Education Strong math acumen (percentages, ratios, algebra). Mechanical and chemical knowledge with the ability to apply to real-world manufacturing processes. Excellent communication, coaching, and mentoring skills. Ability to apply a hands-on approach to solve complex production problems. High School Diploma or equivalent required. Technical or Associate's degree in a related field preferred. $55,000 - $68,000 a year

Hydrasearch LLC is excited to announce an opening for a Manufacturing Technician Trainee at our state-of-the-art facility. This entry-level position is a unique opportunity for motivated individuals looking to launch their careers in the manufacturing sector! As a Manufacturing Technician Trainee, you will gain hands-on experience in various production processes and machinery while receiving guidance from experienced professionals in a fast-paced environment. This role is designed for individuals who are eager to learn, possess a strong work ethic, and are committed to producing high-quality products. You will be involved in all aspects of the manufacturing process, from understanding technical specifications to operating equipment safely and efficiently. As a trainee, you will also have the opportunity to collaborate with other team members and contribute to continuous improvement initiatives. We value safety, teamwork, and innovation, and we are dedicated to the professional development of our employees. If you have a passion for manufacturing and a desire to grow your skill set, we encourage you to apply and become part of our dynamic team. Proud Partner of DOD Skillbridge Our comprehensive benefits package is designed to support your well-being and professional growth. We offer medical, dental, and vision insurance for you and your family, competitive salary, bonus programs, and 401K retirement plan, training opportunities, tuition reimbursement, vacation and PTO, paid holidays, gym reimbursements, and more! The potential targeted range for this position is $18-24/hr. Join us and be a part of a team that values your contributions and supports your goals! Essential Functions: Assist in operating and maintaining manufacturing equipment Learn to read and interpret technical drawings and specifications Monitor production processes and report any issues Participate in quality control checks and inspections Support the implementation of manufacturing best practices Conduct routine safety checks and adhere to safety protocols Collaborate with team members to achieve production goals Qualifications: High school diploma or equivalent Strong attention to detail and good problem-solving skills Ability to work effectively in a team environment Basic math and measurement skills Willingness to learn and adapt in a fast-paced environment Good communication skills, both verbal and written Previous experience in a manufacturing or industrial setting is a plus The Dixon Group is an equal opportunity employer and complies with all applicable federal, state, and local fair employment practices and laws. Accordingly, to the fullest extent required by applicable law, The Dixon Group strictly prohibits and does not tolerate discrimination against employees, applicants, or any other covered persons. The Dixon Group is committed to protecting the privacy rights of its employees and job applicants to the fullest extent required by applicable law. To that end, personal information will be collected solely for those legitimate business purposes recognized by law, and then maintained in a manner consistent with all applicable laws and regulations pertaining to document retention requirements. The Dixon Group does not sell personal information to third parties, and does not share such personal information with third parties except when authorized by law to do so (e.g., in response to a lawful subpoena; mandatory tax reporting; etc.)

Join a growing Biotechnology company hiring an Upstream Manufacturing Associate I/II. Excellent work shift: 8am-5pm Monday-Friday standard business hours is Contract-to-Hire. Manufacture commercial-stage cell therapy products following batch records and standard operating procedures (SOPs). Perform upstream manufacturing activities according to SOPs in an Aseptic environment. Work as part of a team to execute GMP runs. Work in a clean room environment. Qualifications: Associates Degree OR Bachelors Degree in a science field 6 months or more of GMP manufacturing experience Hands-on training or experience in Upstream operations, including cell culture production, expansion etc. using bioreactor or similar production equipment. Cell Therapy production experience is a Plus (Masters and PhD degrees will not be considered) Extras: Contractor benefits include medical, dental, vision, 401K Once converted to internal company employee, company pays 100% of medical insurance costs

Your Tasks: This position is responsible for manufacture of biologics (LV) under cGMP conditions. The candidate must follow established procedures, execute batch production records using good documentation practices and adhere to gowning procedures required for work in cleanroom environment. You will also be required to work in a fast paced environment as part of a team. Essential Duties and Responsibilities: Follow established Standard Operational Procedures (SOPs), Batch Production Record, Logbooks etc. with the adherence to good documentation practices and safely perform daily process activities. Successfully complete GMP trainings and OJT's as required. Perform process set up and operations, process monitoring, filter integrity test (FIT), process sampling, system breakdown and completion of production records. Responsible for the proper use of production equipment in strict accordance with cGMPs, SOPs and safety policies. Responsible for cleaning of process equipment and work areas as required. Assist in the revision of established documentation (SOP's, BPR's, OJT). Maintain inventory and restock supplies when needed. Able to support 24/7 process operations and shift schedule. Adhere to company safety policies and procedures and actively contribute to identifying unsafe behaviors. Requirements: Associates degree with 2 years of GMP experience; or equivalent combination of education and experience. Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to walk; use hands to finger, handle, or feel; reach with hands and arms, talk, and hear. The employee is required to stand; climb or balance and stoop, kneel, crouch. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, color vision, peripheral vision, depth perception and ability to adjust focus. Must have ability to handle more than one task at a time and must work at a rapid pace while maintaining attention to detail. Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. This job is performed in a temperature controlled facility without exposure to extreme hot or cold temperatures. Generally, this job is performed in a sanitized laboratory setting and routinely uses standard medical and research equipment such as centrifuges, biosafety cabinets, chromatography devices and columns, tangential-flow filtration devices and filters, peristaltic pumps and metering fill pumps, pipettes and computers. While performing the duties of this job, the employee is frequently exposed to cultured human cells (immortalized, not primary) and lentivirus-derived vector particles. Employees entering and leaving the laboratory must wear appropriate clothing and protective equipment such as scrubs, coveralls, masks, glasses and gloves. The noise level in the work environment is usually moderate. The anticipated base salary range has been established at $21.68 - $29.37/hour. The salary of the finalist(s) selected for this role will be set based on a variety of factors, including but not limited to, internal equity, experience, education, specialization, skills, abilities, and training. The above salary range represents the Company's good faith and reasonable estimate of the range of possible compensation at the time of posting. In addition to your salary, the Company offers a comprehensive benefits package including health, vision, and dental insurance, plus a 401(k) plan. All benefits are subject to eligibility requirements. Certain positions are eligible for additional forms of compensation such as bonuses or commissions. Miltenyi Biotec is an EO Employer - M/F/Veteran/Disability/Sexual Orientation/Gender Identity. Miltenyi Biotec, Inc. participates in E-Verify. Are you ready to start revolutionizing biomedical research? When you join Miltenyi Biotec, you join a family that is passionate about making a real impact - one breakthrough at a time. One integral division of that Miltenyi Biotec family is Miltenyi Bioindustry - our contract development and manufacturing organization (CDMO). As a full-scale CDMO, we provide customers with services for the development and manufacturing of lentiviral vectors and cell and gene therapy products. This crucial arm of our enterprise bridges the gap between research and mass bioproduction, ensuring that our solutions are accessible on a global scale. Miltenyi Bioindustry plays a unique role as both the producer and the service provider, relying on our instruments and reagents for each workflow step, controlling the entire supply chain and thus delivering greater security and planning clarity to our customers.

Who we are: Maravai LifeSciences translates extraordinary science into everyday miracles, helping biotech, biopharma, and life sciences companies everywhere deliver novel vaccines, therapeutics, and diagnostics. We are global leaders in providing products and services within the fields of nucleic acid production and biologics safety testing to many of the world's leading biopharma, vaccine, diagnostics, and cell and gene therapy companies. At Maravai, we believe that diverse perspectives are the foundation of innovation. Through an inclusive and equitable culture where every team member is inspired to bring their best selves to work, we cultivate an environment in which we can lead together, providing differentiated value to our customers, and enabling the miracles of science. For over 35 years, Maravai's portfolio companies have served as a catalyst for innovative, lifesaving technology for humanity. Pioneering nucleotide research since its inception, we are now leading the way in the rapidly expanding mRNA market. Your next role as a Miracle Maker Maravai LifeSciences is seeking a #MiracleMaker to join Glen Research. As a Manufacturing I, you will support the formulation and testing of products used in DNA synthesis. This role requires a strong chemistry background, preferably with a Bachelor's degree in Chemistry or relevant experience. How you will make an impact: * Prepare catalog products using manufacturing instructions, procedures and protocols * Associated tasks include packaging, labeling, and storing of product; maintaining inventory of catalog products and raw materials * Conduct preventative maintenance * Prepare equipment and glassware; general inventory and organization of supplies * Assist with general shipping and receiving of hazmat products and materials * Maintain proper storage, handling, and disposal of organic solvents, hazardous chemicals, and waste is essential * Provide proper documentation and accountability of tasks performed * Maintain an organized work environment * Conduct general laboratory duties and other work as assigned * Assist with customer order fulfilment including preparing shipping documentation will be a priority. Receiving and processing incoming materials from vendors and suppliers is a key function * Provide General warehouse duties The skills and experience that you will bring: * BS in Chemistry or related science * 0-2 years of previous laboratory experience * Knowledge and experience in safely handling organic solvents and laboratory chemicals. * Ability to follow direction and work in a fast-paced work environment * This position requires the ability to lift cases, containers, and other laboratory materials using tools and equipment #LI-Onsite The benefits of being a #MiracleMaker: * You have the potential to change, improve, and save lives around the world. * You have the opportunity to be a part owner in Maravai through RSU grants and optional employee stock purchase plans. * We offer comprehensive medical plans and HSA/FSA options. * Fertility & family planning assistance. * A variety of additional optional benefits and insurance options, including pet insurance. * Retirement contributions. * Holidays & Paid Time Off. Benefits may vary by region and employment type and do not apply to temporary employees or contractors. See a comprehensive list of benefits at our Benefits & growth site at **************************************************** To view more opportunities to become a #MiracleMaker, visit our career site at ******************************** Maravai LifeSciences is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation, and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law. Click here to view Maravai LifeSciences Privacy Notice HIRING SCAM ALERT Recently, individuals impersonating Maravai LifeSciences Human Resources members have offered fraudulent interviews and job offers to unsuspecting candidates. To help protect you from these scam artists, please be aware that: * Maravai LifeSciences will never interview a candidate over RingCentral, similar messaging apps or social media (e.g. Telegram, Google Hangouts, WhatsApp, Facebook Messenger, etc.) * Maravai LifeSciences will never send a company check or ask an applicant to pay a fee or purchase at home work/training materials in connection with an application for employment. * Maravai LifeSciences will never provide excess money to an applicant and ask the applicant to write a check for repayment. If you have any doubt about a job offer or any other communication purporting to come from Maravai LifeSciences, please reach out to us directly at *****************. If you believe you have been a victim of fraud, you can report this activity at: *********** or ******************

We are seeking a skilled and reliable to join our team. The Manufacturing Technician will be responsible for performing preventative maintenance, troubleshooting, and repairing equipment, machinery, and facility systems. The ideal candidate should have strong technical knowledge, problem-solving skills, and a commitment to safety and efficiency. Responsibilities: Perform routine inspections, preventive maintenance, and repairs on facility equipment, HVAC systems, electrical, plumbing, and mechanical components. Diagnose and troubleshoot mechanical, electrical, and plumbing issues to ensure minimal downtime. Respond promptly to maintenance requests and emergency breakdowns. Maintain a clean and safe work environment, adhering to all company safety protocols and OSHA regulations. Maintain accurate records of maintenance work completed, including inspections and repairs. Provide support for facility improvements and special projects as needed. $24 - $30 an hour