Job ID: 1794062
Reference Code: MKMSD1JP00003277
Job Summary
We are seeking a motivated Bioprocess Manufacturing Technician for a contract opportunity in De Soto, KS. This role is ideal for a reliable manufacturing or production professional who is interested in gaining hands-on experience in bioprocessing, sterile processing, and regulated production operations.
As a Bioprocess Manufacturing Technician, you will support antigen processing through centrifugation, equipment preparation, cleaning, sterilization, and accurate production documentation. Aseptic procedures can be taught on the job, making this a strong opportunity for candidates with solid attention to detail, a strong work ethic, and an interest in building skills in a highly regulated manufacturing environment.
This position offers a steady Monday through Friday daytime schedule, structured training, supportive leadership, and the opportunity to contribute to critical production work where quality, safety, and consistency matter every day. Candidates who enjoy teamwork, routine accuracy, and learning specialized manufacturing processes can thrive in this role.
Key Responsibilities
- Operate centrifuges to process, concentrate, and support antigen batch production.
- Follow aseptic processing techniques to help maintain sterile conditions and prevent contamination.
- Prepare, clean, set up, and sterilize processing equipment according to established procedures.
- Complete production records accurately using Good Documentation Practices.
- Follow Standard Operating Procedures, safety requirements, quality standards, and regulated manufacturing guidelines.
- Assist with downstream production, cleaning, preparation, and material handling activities as needed.
Compensation and Benefits
- Pay rate: $20 per hour.
- Schedule: Monday through Friday, 7:00 AM to 3:30 PM.
- Contract/temporary position.
- Recruiting and retention bonus available up to $1,000 total.
- $500 after 2 weeks of employment.
- $500 after 90 days of continuous employment.
Equal Opportunity Employer / Disabled / Protected Veterans
The Know Your Rights poster is available here:
https://www.eeoc.gov/sites/default/files/2023-06/22-088_EEOC_KnowYourRights6.12.pdf
The pay transparency policy is available here:
https://www.dol.gov/sites/dolgov/files/ofccp/pdf/pay-transp_%20English_formattedESQA508c.pdf
For temporary assignments lasting 13 weeks or longer, AppleOne is pleased to offer major medical, dental, vision, 401k and any statutory sick pay where required.
We are committed to working with and providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation for any part of the employment process, please contact your staffing representative who will reach out to our HR team.
AppleOne participates in the E-Verify program in certain locations as required by law. Learn more about the E-Verify program.
https://e-verify.uscis.gov/web/media/resourcesContents/E-Verify_Participation_Poster_ES.pdf
We also consider for employment qualified applicants regardless of criminal histories, consistent with legal requirements, including, if applicable, the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance. Pursuant to applicable state and municipal Fair Chance Laws and Ordinances, we will consider for employment-qualified applicants with arrest and conviction records, including, if applicable, the San Francisco Fair Chance Ordinance. For Los Angeles, CA applicants: Qualified applications with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
Required Qualifications and Skills
- Operate centrifugation equipment to support bioprocess manufacturing activities.
- Maintain sterile processing practices while handling antigen batches and production materials.
- Prepare, clean, sterilize, and document production equipment and process steps.
- Follow SOPs, GDP, safety guidelines, and quality standards in a regulated manufacturing environment.
- High School Diploma or GED required.
- 1 to 3 years of manufacturing, production, or related hands-on work experience preferred.
- Strong attention to detail and commitment to product quality, safety, and process accuracy.
- Basic computer skills for documentation and production recordkeeping.
- Strong communication skills and the ability to follow written and verbal instructions.
- Basic troubleshooting skills and ability to work through repetitive tasks with consistency.
- Ability to lift and move containers weighing up to 25 lbs., with occasional lifting up to 20 kg.
- Ability to work in a manufacturing environment while following strict procedures and cleanliness requirements.
- Understanding of aseptic processing, Good Documentation Practices, and Standard Operating Procedures.
Preferred Qualifications
- Bachelor’s degree in Biology or a related science field.
- Prior experience in bioprocessing, pharmaceutical manufacturing, laboratory production, or regulated manufacturing.
- Knowledge of quality improvement processes.
- Familiarity with USDA regulations or other regulated production standards.