34 Manufacturing jobs in Longmont

Are you humble, hungry, and smart?

Have production/manufacturing experience?

M eet Forefront Health .

We are a small and fast-growing natural health company based out of beautiful Boulder, Colorado and we’re on a mission to advance the education of thyroid health, formulate simple solutions, and empower a lifestyle that restores thyroid health and a life without limitations.

Our work currently touches the lives of hundreds of thousands of thyroid sufferers worldwide. Yet, with more than 20 million thyroid sufferers in the US alone, we have a lot of work to do.

And, we can’t do it without you .

It’s simple really.

Step one is to join our team with this full-time opportunity.

Step two is to fast-track your advancement as we’re continuously identifying new roles and opportunities for which you may be a great fit.

Step three is to start living your dream.

If that sounds like a plan for you, then Apply Now and experience what it’s like to actually be excited to come to work, enjoy the people you work with, and feel fulfilled in what you do.

Or, you can keep doing what you’re doing and hope that one day something will change.

Don’t let your potential and value go to waste.

You can keep dreaming, or you can come work with us and start living your dream .

Job Description:

• Title: Production Associate
• Job Type: Full-time, Monday - Friday
• Pay: Starting at $27 - $30 an hour
• Benefits: Bonus Potential, Health Insurance (full-time), Dental/Vision/Life Insurance, On-the-Job Training, Opportunities for Advancement, Paid Time Off, Referral Program, and more.

Overview:

The Manufacturing Coordinator works within the Manufacturing & Production Department where they help support the production and manufacturing of health supplements under a cleanroom production environment. They are responsible for supporting lab operations and ensuring operational efficiencies to help produce finished products that are pure, clean, effective, and that help our customers feel their best.

Requirements:

• Lab experience is required.
• Familiarity with GMP compliance and QA/QC processes.
• Ability to Follow Procedures (SOPs) Accurately
• Strong Attention to Detail & Organizational Skills
• Excellent Time Management & Project Management Skills
• Comfortable Standing for 8 hrs & Capable of Lifting up to 75 lbs
• Excellent Communicator (Written & Verbal)
• Interest in Working for a Health & Wellness Company

This Opportunity is Perfect for You if You Enjoy…

• Staying busy - You and your team will be engaged during the entire work day.
• Team environment - You enjoy working in small teams that support each other.
• Casual work environment - You enjoy listening to music, dress is almost always casual, and there’s always someone laughing or telling a good story.
• Career advancement - You are looking for a small, fast-growing company with lots of growth potential, encourages a variety of training & development programs, and has opportunities to move around within the different departments.

• Performs non-routine and complex Electrical & Mechanical Assembly tasks
• Read and work from assembly drawings, wiring diagrams, parts list
• Performing rework and repairs of materials to IPC standards
• Populate PCBAs, both through-hole and surface mount and the masking and conformal coating of boards
• Perform work and assembly processes that meet or exceed IPC standards
• Perform tasks in a timely manner which meets or exceeds time standards
• Perform construction and in-process inspection on box builds, PCBAs, and cables
• Work to production schedules and timelines
• Successfully pass IPC-610 certification training within 3 months
• Perform duties in a safe, non-hazardous manner in compliance with safety standards
• Maintaining a clean working area
• May perform non-established, non-routine testing or troubleshooting of components, devices, modules or products
• Successfully pass J-STD-001 certification training within 6 months
• Perform rework and repairs of materials including multilevel boards to IPC standards
• Identify and recommend disposition of defective components
• May assist in the training of less experienced technicians
• May rework products to meet customer specs
• May Inspect incoming material, including custom sheet metal, PCBAs and Cables

• Wellness & Medical Benefits effective on your First Day of Employment
• Gold Standard in Medical, Prescription Drug, Dental & Vision Benefits
• Quarterly Employee Cash Bonus Plan
• Restricted Stock Grant
• Employee Stock Purchase Plan
• Tuition Reimbursement
• 401K Retirement Savings Plan
• Spending Accounts
• Life Insurance
• Long Term Care
• Legal
• Employee Assistance Plan

• Vacation Pay
• Absence Time - "Sick Pay"
• 10 Paid Holidays

• Ability to multi-task while paying careful attention to detail
• Prior success working both individually and in a team environment
• Good written and verbal communication skills
• Ability to follow written and verbal communication skills
• Ability to read, comprehend and follow detailed work specifications
• Excellent listening skills
• Adaptability to frequent changes and improvements
• Regular and predictable attendance is essential
• Ability to wear the required Protective Equipment
• Basic computer, math and reading comprehension skills
• You must be 18 years old with a high school diploma or GED

• Minimum of 2 years of experience and a proven track record of excellence in Electrical Assembly
• Minimum of 2 years of experience and a proven track record of excellence in Mechanical Assembly
• Demonstrated ability to multi-task and remain highly organized in a high-volume production environment
• Comfortable working with cross functional teams
• Ability to learn quickly and adapt to fast pace environment
• Strong commitment to teamwork and process

• Active IPC 610, 620 and J-STD certifications
• Experience in Microsoft Office. (Excel, Word, Access)
• 2+ years of experience in related field
• Prior Mil-Std Workmanship experience a plus
• Desire to continually learn new skills

• This job operates in an environment employing a variety of manufacturing and test techniques. This role routinely uses standard manufacturing and test equipment in addition to application specific systems.

• Incumbent may sit in a stationary position for a long period of time
• Frequent use of manufacturing and test equipment and exposure to computer screens
• This position requires the ability to occasionally lift 25-50 pounds
• Must have the ability to multi-task, often performing multiple functions simultaneously

Ursa Major was founded to address a critical shortfall in the U.S. industrial base and bring a new model to aerospace and defense systems: we design and manufacture the world's leading propulsion systems for space, hypersonic applications, and missile systems. Our products and technologies require an extraordinary team - a team that will mold tomorrow's technologies while deploying today's best. We are an intrinsically motivated team that has a passion for solving problems and empowering each other every day to develop our skills, knowing that there is always room for growth.The Quality Control Inspector's primary focus will be ensuring on-time delivery of high-quality products that meet our customer's expectations. Supporting the manufacturing and design teams to ensure the parts and materials used in the manufacture of our products meet the specification requirements and aerospace standards.This role reports to the Inspection Lead with support from manufacturing planning and other Quality roles, such as Quality Management, Quality Engineers, and Supplier Quality Engineers.Responsibilities:Perform electrical, dimensional, and/or visual inspections as appropriate for procured or manufactured parts and subassembliesOperate manual and automated test and inspection equipmentReview submitted supplier documentation as required (material and/or special process) for accuracy and completenessPerform part and subassembly inspection or testingRecord legible, complete, and accurate inspection results and other documentationAuthor Discrepancy Reports (DR) as neededSupport MRB inventory and clearance activitiesAssist in calibration and maintenance of inspection equipment and update the calibration recall tracking systemOther duties as assigned by Quality ManagementRequired Qualifications:High School degree (technical school preferred)Quality control/inspection experience in a precision machining or aerospace environment (3+ years)Ability to read drawings and standardsKnowledge of the background and application of Geometric Dimensioning and Tolerancing (GD&T)Skill using standard inspection tools, methods, and reporting requirementsPrevious experience with various types of metrology equipment used in performing dimensional or electrical inspections including their capabilities and limitationsExperience in a moderate volume and mix manufacturing environmentDesired Experience:Experience operating automated inspection equipment such as comparators, height stands, surface profilometers, CMM, or similarAerospace industry or machine shop experienceASQ CQI CertificationAssociate's or Bachelor's degreeColorado law requires us to tell you the base compensation range of this role, which is $25.00 - $35.00 per hour, determined by your education, experience, knowledge, skills, and abilities. What we can't quantify for you are the exciting challenges, supportive team, and amazing culture we enjoy. Click here for more information about our awesome benefits.Classification: Full-time Non-ExemptBenefits Include:Unlimited PTO - Vacation, Sick, Personal, and BereavementPaid Parental and Adoptive LeaveMedical, Dental and Vision InsuranceTax Advantage Accounts (HSA/FSA)Employer Paid Short and Long Term Disability, Basic Life, AD&DAdditional Benefit Options Including Voluntary Life and Emergency Medical TransportEAP ProgramRetirement Savings Plan - Traditional 401(k) and a Roth 401(k)Equity Grants in the CompanyNOTE: Research suggests that women and BIPOC individuals may self-select out of opportunities if they don't meet 100% of the job requirements. We encourage anyone who believes they have the skills and the drive necessary to succeed here to apply for this role.US CITIZENSHIP, PERMANENT RESIDENCY, REFUGEE OR ASYLUM STATUS IS REQUIRED.We're an equal-opportunity employer. You will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.No outside recruiters, please.

The Manufacturing Technician position is designed as an introduction to the industry of cGMP manufacturing.

This position is a 2 on, 2 off , 3 on "pitman" Day shift schedule with working hours from 6:00 AM to 6:30 PM.

This position executes a large amount of material wipe in a movement into cGMP areas, performs routine/non-routine cleaning of equipment, glass wash of misc. parts, assembles setups and filters, autoclaves media/materials, tests filter integrity, manages process waste flows and material movement, and executes inventory management tasks at the cGMP facility to support continuous manufacturing operations. This position requires a shift schedule and gowning into a clean room environment. This position requires PPE.

Must be able to document, record activities in electronic systems and comply with regulatory requirements, cGMPs, Policy Documents and SOPs. Must be able to maintain training at 95% or greater. Must always wear proper PPE and follow all safety guidelines outlined by the SOP and site policies when working in the facility.

Must be able to perform general tasks as assigned by Management to support manufacturing, i.e., staging materials, discarding waste, moving equipment, and other general clean room tasks.

Responsibilities:

Cleaning of equipment, glass wash of misc. parts, assembles setups and filters, autoclaves medias/materials, tests filter integrity, manages process waste flows and material movement, and executes inventory management tasks.

Handling and discarding of hazardous and nonhazardous waste.

Computer: Includes maintaining training and job-related functions. Ordering and stocking general supplies in the manufacturing production areas.

Performing other various task as assigned by the Supervisor/Manager

Due to non-routine cleanings and the need to adhere to the manufacturing schedule, it is required, if necessary, to stay past the assigned shift to complete such requests. This position requires standing for long periods of time. For cleaning, this position also requires bending, kneeling, and reaching above head. This position is considered "Essential Personnel" which requires 7 days a week work coverage even though the company closes (i.e., inclement weather). This position is required to ensure cGMP production tasks are completed every day.

Salary Range: $21.63/hour-$27.40/hour

Salary range provided per current averages and expectations. The salary and job title for this opening will be based on the selected candidate's qualifications and experience and may be outside this range. KBI has a robust total rewards strategy which includes an annual bonus structure for all employees, medical, dental, and vision coverage, paid PTO and holidays, 401K matching with 100% vesting in 60 days and employee recognition programs.

"Please note: Our pre-employment drug screening includes substances that are legal in Colorado but remain illegal under federal law, such as marijuana. A positive result for these substances may result in disqualification from employment consideration."

About KBI:
KBI Biopharma, Inc., a JSR Life Sciences company, is a global contract development and manufacturing organization
(CDMO) providing fully integrated and accelerated drug development and biologics manufacturing services to life
science companies. KBI supports its 500+ customers in advancing more than 160 drug candidates from preclinical and
clinical stages to market, including the manufacture of ten commercial products. Recognized for quality manufacturing, KBI delivers robust process development and cGMP manufacturing services across its six global locations in the USA and
Europe. For more information, visit
KBI is a proud EEO/AA employer dedicated to building a diverse and inclusive workforce. We believe that innovation
thrives in an environment where all voices are heard and valued. That's why we actively seek individuals from all
backgrounds - regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age,
disability, or veteran status - and strongly encourage all qualified candidates to apply and bring their unique
perspectives to our team.

KBI Biopharma is committed to providing a safe and healthy workplace. Any employee entering a KBI site located in the US must inform KBI Biopharma of their vaccination status and must submit their vaccination status. All vaccinated employees are required to provide proof of their COVID-19 vaccination, with a COVID-19 vaccination which has been granted FDA approval or Emergency Use Authorization.

KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply.

I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.

I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.

The Manufacturing Technician position is designed as an introduction to the industry of cGMP manufacturing.

This position is a 2 on, 2 off , 3 on "pitman" Night shift schedule with working hours from 6:00 PM to 6:30 AM.

This position performs all routine/non-routine cleaning of equipment, prepares buffers/medias, glass wash of misc. parts, assembles setups and filters, autoclaves media/materials, tests filter integrity, manages process waste flows and material movement, and executes inventory management tasks at the cGMP facility to support continuous manufacturing operations. This position requires a shift schedule and gowning into a clean room environment. This position requires PPE.

Must be able to document, record activities in electronic systems and comply with regulatory requirements, cGMPs, Policy Documents and SOPs. Must be able to maintain training at 95% or greater. Must always wear proper PPE and follow all safety guidelines outlined by the SOP and site policies when working in the facility.

Must be able to perform general tasks as assigned by Management to support manufacturing, i.e., staging materials, discarding waste, moving equipment, and other general clean room tasks.

Responsibilities:

Cleaning of equipment, glasswash of misc. parts, assembles setups and filters, autoclaves medias/materials, tests filter integrity, manages process waste flows and material movement, and executes inventory management tasks.

Handling and discarding of hazardous and nonhazardous waste.

Computer: Includes maintaining training and job-related functions. Ordering and stocking general supplies in the manufacturing production areas.

Performing other various task as assigned by the Supervisor/Manager

Due to non-routine cleanings and the need to adhere to the manufacturing schedule, it is required, if necessary, to stay past the assigned shift to complete such requests. This position requires standing for long periods of time. For cleaning, this position also requires bending, kneeling, and reaching above head. This position is considered "Essential Personnel" which requires 7 days a week work coverage even though the company closes (i.e., inclement weather). This position is required to ensure cGMP production tasks are completed every day.

Salary Range: $21.63/hour-$27.40/hour

*There is an additional 15% shift differential for nightshift positions.

Salary range provided per current averages and expectations. The salary and job title for this opening will be based on the selected candidate's qualifications and experience and may be outside this range. KBI has a robust total rewards strategy which includes an annual bonus structure for all employees, medical, dental, and vision coverage, paid PTO and holidays, 401K matching with 100% vesting in 60 days and employee recognition programs.

KBI Biopharma is committed to providing a safe and healthy workplace. Any employee entering a KBI site located in the US must inform KBI Biopharma of their vaccination status and must submit their vaccination status. All vaccinated employees are required to provide proof of their COVID-19 vaccination, with a COVID-19 vaccination which has been granted FDA approval or Emergency Use Authorization.

KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply.

I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.

I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.

• Connect on LinkedIn

Company Information

You Matter to Cambrex.

Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance, drug product, and analytical services across the entire drug lifecycle. With more than 40 years of experience and a growing team of over 2,400 professionals servicing global clients, Cambrex is a trusted partner in branded and generic markets for API and dosage form development and manufacturing.

Your Work Matters.

At Cambrex, we strive to build a culture where all colleagues have the opportunity to:

• engage in work that matters to our customers and the patients they serve
• learn new skills and enjoy new experiences in an engaging and safe environment
• strengthen connections with coworkers and the community

• Properly sets up, operates, breaks down and cleans production equipment per written procedures.
• Maintains cGMP suites to be tour/audit ready and prepared for manufacturing activities.
• Functions independently on basic to intermediate scale-up operations of drug substance in assigned manufacturing area.
• Understands and follows written procedures.
• Consistently, clearly, and accurately documents activities for production records and manufacturing equipment in accordance with ALCOA, GMP, and Good Documentation Practices (GDP).
• Performs routine equipment maintenance/preventative maintenance activities. Basic mechanical aptitude and able to repair production equipment with guidance as needed.
• Clean production suites, hoods, and equipment in accordance with standard operating procedures using good chemical hygiene practices.
• Works with or around hazardous waste. It is expected that you will receive and maintain Resource Conservation and Recovery Act (RCRA) training annually.
• Identifies and stocks equipment/parts as needed for manufacturing processes.

• Basic understanding of cGMP and GDP requirements for drug substance manufacturing operations.
• Able to apply learned knowledge of equipment and facility maintenance for the GMP and non-GMP production areas. Good mechanical aptitude preferred.
• Basic to intermediate knowledge of manufacturing equipment operations including batch reactors, filters, dryers, and pumps, as well as handling glass lab equipment.
• Basic chemical processing skills, including weighing, calculations, GMP documentation, vacuum, pressure, and filtration techniques.
• Ability to wear respirators and various types of PPE while promoting a safe work environment.
• Able to read and comprehend detailed written instructions. Provides feedback to ensure instructions are accurate and can be performed as written.
• Must adhere to the Cambrex attendance policy. Employee should be punctual, reliable, and willing to work outside of normal working hours as requested.
• Effectively communicates both verbally and in writing.
• Able to perform basic to intermediate mathematical calculations including inventory reconciliation.
• Able to work independently or within a team environment with minimal supervision.
• Shows initiative, high attention to detail and performs tasks with minimal supervision.
• Able to troubleshoot and communicates potential roadblocks to management.
• Flexibility and time management skills to perform other duties as assigned without hindering obligations.

• High school diploma or equivalent with 3+ year of laboratory experience in a regulated environment.

• Opportunity for advancement!
• Competitive pay structure!
• Excellent benefits package!
• Great company culture!

• Optimize and refine manufacturing processes to ensure consistent, high-quality output.
• Analyze production data to reduce variation and increase efficiency through scientific and data-driven methods.
• Lead tooling validations and support new equipment or product introductions.
• Troubleshoot equipment, tooling, and automation systems to reduce downtime and improve throughput.
• Create and maintain standardized process documentation for consistency across shifts.
• Contribute to continuous improvement initiatives using Lean, Six Sigma, and DOE methodologies.
• Enhance and maintain automation systems, including programming and supporting robotic tools.
• Collaborate closely with engineering, quality, and operations teams to align on production goals.

• Bachelor's degree in Engineering (Mechanical, Manufacturing, or related field preferred).
• 5+ years of hands-on experience in a high-volume manufacturing or process engineering environment.
• Strong understanding of process development, validation, and optimization methods.
• Experience working with CAD software, CNC equipment, and industrial robotics.
• Ability to interpret and work from technical drawings, specs, and process documentation.
• Familiarity with ISO standards, quality systems, and structured process control.
• Proven analytical and problem-solving skills in technical environments.
• Must be able to work onsite in Erie, CO and engage in occasional customer-facing interactions.