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Bio Manufacturing Jobs (NOW HIRING)

Bio Manufacturing Operator

Elwood, KS

$17 - $20.25/hr

Execute and monitor core mAb manufacturing processes (media/buffer prep, upstream/downstream processing, formulation, fill/finish, secondary packaging). * Maintain cGMP compliance in a regulated ...

Manufacturing Engineer

Waunakee, WI · On-site

$69K - $85K/yr

This is a great opportunity for an early-career engineer looking to develop hands-on experience in a fast-paced, bio-manufacturing environment while contributing to meaningful work within animal ...

Execute and monitor core mAb manufacturing processes (media/buffer prep, upstream/downstream processing, formulation, fill/finish, secondary packaging). * Maintain cGMP compliance in a regulated ...

Opportunity - To be part in building a company focused on a future increasingly reliant on bio-manufacturing and making a sustainable and positive impact in the world. * Accountability - You will ...

Opportunity - To be part in building a company focused on a future increasingly reliant on bio-manufacturing and making a sustainable and positive impact in the world. * Accountability - You will ...

This person will be expected to play an integral part of Manus Bio's manufacturing and process development team located in Augusta, GA. The Downstream Processing Operator is responsible for the ...

The Specialist, Logistics ensures the secure and timely transport of donor cells and drug products between Orca Bio's manufacturing sites and transplant centers. This role owns real-time coordination ...

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Showing results 1-20

Bio Manufacturing information

See salary details

$35.5K

$79.8K

$112.5K

How much do bio manufacturing jobs pay per year?

As of Aug 1, 2026, the average yearly pay for bio manufacturing in the United States is $79,845.00, according to ZipRecruiter salary data. Most workers in this role earn between $71,000.00 and $89,000.00 per year, depending on experience, location, and employer.

What is the job of a biotechnician?

A biotechnician assists in laboratory and manufacturing processes related to biotechnology, including preparing samples, operating equipment, and maintaining lab environments. They often follow strict safety protocols and may need technical certifications or training in biotechnology techniques.

What biology jobs pay over $100k?

In the field of bio manufacturing, roles such as senior bioprocess engineers, regulatory affairs managers, and research directors often have salaries exceeding $100,000 annually. These positions typically require advanced degrees, specialized skills in bioprocessing or quality assurance, and experience managing large-scale production or research projects.

What are the key skills and qualifications needed to thrive in Bio Manufacturing, and why are they important?

To thrive in Bio Manufacturing, you need a solid background in biology, chemistry, or engineering, often supported by a relevant degree or certification. Familiarity with Good Manufacturing Practices (GMP), bioprocessing equipment, and quality control systems is typically required. Attention to detail, problem-solving abilities, and strong teamwork skills help individuals excel in this environment. These competencies are crucial for ensuring product quality, regulatory compliance, and efficient production in the biotechnology industry.

What are some common challenges faced by professionals working in bio manufacturing, and how can they be addressed?

Professionals in bio manufacturing often encounter challenges such as maintaining strict quality control standards, adapting to rapidly evolving technologies, and ensuring compliance with regulatory requirements. Addressing these challenges involves continuous training, staying updated on industry best practices, and fostering strong communication within cross-functional teams. Many companies also encourage ongoing professional development and provide resources to help employees stay current with regulations and technological advancements.

What is bio manufacturing?

Bio manufacturing, also known as biomanufacturing, is the process of using biological systems like cells or enzymes to produce commercial products such as medicines, vaccines, biofuels, and food ingredients. This field combines biology, engineering, and technology to create products in a controlled and scalable way, often using fermentation or cell culture techniques. Biomanufacturing plays a critical role in the pharmaceutical, biotechnology, and food industries, enabling the production of complex molecules that are difficult to synthesize chemically. Professionals in this field work on developing, optimizing, and scaling up these biological processes to ensure high-quality and cost-effective product output.

What is the difference between Bio Manufacturing vs Bioprocess Technician?

AspectBio ManufacturingBioprocess Technician
CredentialsTypically requires a Bachelor's degree in Biotechnology, Biology, or related fieldOften requires a diploma or associate degree in Biotechnology or related field
Work EnvironmentManufacturing facilities, laboratories, cleanroomsProduction floors, laboratories, cleanrooms
Industry UsageUsed broadly across biotech, pharmaceutical, and biopharmaceutical companiesPrimarily in biotech and pharmaceutical manufacturing
Job FocusOversees entire manufacturing processes, quality control, and compliancePerforms specific tasks in bioprocessing, equipment operation, and sample testing

Bio Manufacturing involves overseeing the entire production process in biotech and pharmaceutical industries, often requiring higher-level degrees and responsibilities. Bioprocess Technicians focus on executing specific bioprocessing tasks, typically with technical diplomas. Both roles work in similar environments but differ in scope and qualifications.

Is biotech a high paying job?

Bio manufacturing jobs in the biotech industry often offer competitive salaries, especially for roles requiring specialized skills or advanced education. Entry-level positions may have moderate pay, but experienced professionals with certifications or technical expertise can earn higher wages. Overall, biotech careers can be financially rewarding compared to many other manufacturing or laboratory roles.

How much does biomanufacturing pay?

Biomanufacturing technicians and specialists typically earn between $50,000 and $80,000 annually, depending on experience, education, and location. Entry-level roles may start around $40,000, while experienced professionals or those with advanced certifications can earn over $100,000. The field often requires knowledge of GMP standards, bioprocessing equipment, and quality control procedures.
More about Bio Manufacturing jobs
What cities are hiring for Bio Manufacturing jobs? Cities with the most Bio Manufacturing job openings:
What states have the most Bio Manufacturing jobs? States with the most job openings for Bio Manufacturing jobs include:
Infographic showing various Bio Manufacturing job openings in the United States as of July 2026, with employment types broken down into 60% Full Time, 20% Part Time, and 20% Contract. Highlights an 100% In-person job distribution, with an average salary of $79,845 per year, or $38.4 per hour.

Bio-Manufacturing Support Tech I

Xtant Medical Holdings Inc

Belgrade, MT • On-site

$24/hr

Full-time

Re-posted 10 days ago


Job description

Classification: Full Time, Non-Exempt

Reports to: Bio-Manufacturing Support Team Lead

  1. Job Summary

This position will perform activities related to donor tissue processing while maintaining quality and regulatory compliance within their department. This person reports to and will support the activities of the Bio-Manufacturing Support Team Lead and Supervisors. This position interacts with employees in the Tissue Processing Department and may interact with other department supervisors, team leads, and personnel as necessary.

  1. Supervisory Responsibilities
    • This position does not supervise others or teams
  2. Duties and Responsibilities
    • Develop and maintain an understanding of relevant industry standards and regulations including but not limited to 21 CFR 820, 21 CFR 1271, AATB, MDSAP (per jurisdictional requirements), and ISO 13485, ensuring compliance with these requirements across the organization.
    • Actively contribute to the fulfillment of Xtant Medical’s mission, values and quality policy
    • Maintain a safe, clean work environment and ensure proper disposal of hazardous and non-hazardous waste according to OSHA guidelines and Xtant Medical standard operating procedures (SOP)
    • Develop and maintain an understanding of Xtant Medical products
    • Understand the interaction of departmental activities with the Quality System and their impact on the production of medical devices and human cells, tissues, and cellular and tissue-based products (HCT/Ps)
    • Adhere to Xtant Medical SOPs, Good Documentation Practices (GDP), and safety protocols
    • Responsible for decontamination, cleaning, and environmental monitoring of the cleanroom areas and non-sterile equipment used to process donor tissue
    • Responsible for maintaining inventory of processing supplies/reagents and other materials within the cleanroom environment and other areas throughout the processing facility
    • Ensure supplies are acceptable for processing use and stock is rotated using the First-In First-Out (FIFO) method. Aseptically transfer supplies into the cleanroom environment to maintain adequate inventory and whenever needed
    • Obtain environmental samples for surface, air, and water monitoring in conjunction with laboratory testing protocols
    • Assist with error investigations, and resolution, within the quality system
    • Assist in the preparation and transportation of soiled processing instruments, equipment, cleanroom garments, and biohazardous waste throughout the processing facility
    • Operate, monitor, and maintain lyophilizers (freeze-dryers) in accordance with the manufacturer’s recommendations and equipment-specific SOPs
    • Operate, monitor, and maintain autoclaves in accordance with the manufacturer’s recommendations and equipment-specific SOPs
    • Transport unprocessed donor tissue across campus
    • Know the appropriate storage conditions, locations, and tissue handling methods for unprocessed and processed donor tissue
    • Provide facility cleaning support to areas outside of the cleanroom environment
    • Responsible for decontamination, disinfection, cleaning, and sterilization (where appropriate) of all non-disposable processing instruments and equipment
    • Manually wash processing instruments and equipment according to Xtant SOPs
    • Ensure all reusable tissue processing equipment and instruments are suitable for use, including inspection and assembly if applicable
    • Prepare relevant donor processing documentation, labels, and other consumable supplies for sterilization
    • Aseptically introduce equipment and supplies into the cleanroom environment
    • Safely operate, monitor, and maintain cleaning and sterilization equipment in accordance with manufacturer recommendations and equipment-specific SOPs when applicable
    • Safely prepare and handle cleaning reagents and solutions according to SDS and SOPs and follow OSHA bloodborne pathogen standards, Universal Precautions, and current Good Tissue Practices (cGTP) when handling biological material
    • Provide facility cleaning support to areas outside of the cleanroom environment
    • Collect and prepare soiled cleanroom garments for shipment to vendor
    • Collect and prepare solid biohazardous waste for shipment in accordance with OSHA standards and Xtant SOPs
    • Aid and support other teams, departments, team leads, and supervisors as requested
    • Other duties as assigned
  3. Financial Responsibilities
    • Submit timely expense reports and abide by the Expense Reimbursement Policy
  4. Training
    • Complete required training, including but not limited to initial orientation and environmental health and safety training prior to performing tasks
    • Participate in training programs, ensuring timely completion and accurate, up-to-date training records
    • Complete annual SOP review and safety training (i.e. OSHA, bloodborne pathogens) as applicable
    • Complete Document Read Training (DRT) within required deadlines whenever a document within the Quality System undergoes revision
    • May require OSHA (bloodborne pathogen) training, SDS, and other safety training as applicable
    • May require experience or training in the routine handling of chemicals and biohazards
  5. Document Control and Record Control
    • Complete all documentation accurately and legibly per GDP, retain records according to Xtant Medical’s procedures, and review others’ documentation as needed
    • Maintain information in physical and electronic files as required
    • Train on and demonstrate proficiency in Xtant Medical’s document control system
    • Participate in the completion of Donor Processing Records as applicable
    • Participate in changes to documents and to products and processes
    • Complete document corrections in a timely manner and maintain error rates at or below departmental benchmarks
  6. Performance of Duties
    • Perform duties and responsibilities to the highest standards with efficiency, professionalism, and attention to detail; adapt to job changes and contribute to team success
    • Perform all duties according to established procedures and follow appropriate safety precautions and measures
    • Conduct himself/herself in a professional and courteous manner in all aspects of interaction with fellow employees, surgeons, staff, and end users
    • Maintain confidentiality of donor and recipient information according to HIPAA
  7. Required Skills/Abilities
    • Must be willing to acquire knowledge of FDA, ISO, and AATB regulations, as applicable
    • Develop an understanding of aseptic techniques and practices
    • Demonstrate capability to communicate effectively both orally and in writing
    • Ability to multitask and manage time efficiently
    • Ability to analyze information to draw relevant conclusions
    • Adapt to quickly changing priorities and schedules
    • Must possess excellent organizational skills and strong attention to detail
    • Must be able to reason independently and work with minimal guidance
    • Basic computer skills are required, such as knowledge of MS Word, Excel, PowerPoint, Outlook, and other software as necessary
    • Some experience with records maintenance and document control preferred
  8. Education & Experience
    • High school diploma required
    • Willing to acquire Certified Tissue Bank Specialist (CTBS) certification
    • Some familiarity with basic laboratory techniques and equipment, aseptic practices is preferred, but not required
    • Experience working in sterile environments, healthcare or medical device production is preferred, but not required
  9. Working Conditions
    • This position is based in an office/cleanroom/warehouse environment
    • Standard work hours are Monday - Thursday (2 pm - 1 am), with occasional overtime or weekend work based on project/production needs
    • Shift times may vary depending on the needs of the department and employee shifts can be subject to change
    • This position is based on-site in Belgrade, MT
    • Working conditions will include environmentally controlled areas (ECA), cleanrooms, and other sterile environments with varying temperatures
    • Duties will include contact with human tissue, blood, bone, and fluids. Working in PPE such as cleanroom suites, with face shields and masks as necessary
    • This position will require frequent use of personal protective equipment (PPE), including scrubs, gloves, etc.
    • Hepatitis B vaccine is highly recommended and provided to employees who may have contact with human tissue at no cost to the employee. Any employee who declines a Hepatitis B vaccine will be required to sign a waiver
  10. Physical Requirements
    • Ability to sit, stand, and work at a computer for prolonged periods
    • Ability to lift, carry, push or pull items of varying weight, typically up to 60 lbs.
    • May require 4+ hours of continuous standing
    • Ability to move, bend, or twist the body in various ways
    • Ability to perform repetitive motions, such as reaching, grasping, bending, squatting, and stooping
    • Requires hand-eye coordination and manual dexterity for tasks such as typing, using hand tools or equipment, and assembling or handling small components with precision
    • Ability to see clearly, whether with or without corrective lenses
    • Ability to hear and understand safety signals, alarms, and requests in a noisy environment

Note: This Job Description is not designed to include a detailed listing of the activities, duties or responsibilities that may be required of the employee. This job description does not constitute an employment contract, implied or otherwise, and is subject to change by the employer as the needs of the employer and requirements of the job change.

Xtant Medical provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.



Monday - Thursday (2 pm - 1 am)