Skip to main content
Tallo logoTallo logo

Find Jobs

Find Jobs Near You – Available Work in Your Location

Skip to job details

Back to Results

Apply for this opportunity

To apply for this job, you'll continue to an external website or email application.

Oxoid Remel Microbiology

Process Engineer II

Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
68
out of 100
Average of individual scores

Were these scores useful?

Job Description

Process Engineer II Oxoid Remel Microbiology Lenexa, KS Job Details 3 hours ago Qualifications Technical engineering Content creation for technical audiences Technical documentation ISO standards Spreadsheets Technical writing experience within manufacturing Project management experience in manufacturing Manufacturing facility experience Quality standards in production Biomedical regulatory compliance Productivity software Manufacturing company experience Data analysis software Full Job Description Job Number Job Number
R-01362783
Highlights Location Lenexa, Kansas Start Date Immediately Work Location On-Site Work Only Skills Lean Manufacturing Description Workday ID:
R-01362783
Joining our team, you'll play an active part in helping to deliver meaningful impact. At Oxoid Remel Microbiology, acquired from Thermo Fisher Scientific, we play a crucial role in accurate identification and targeted treatment for diseases, ensuring food and beverage safety, and supporting pharmaceutical manufacturing integrity. Our products and services are designed to meet the highest standards of quality and performance, helping our customers achieve their objectives efficiently and effectively. Company Information About the Role The process engineering role is responsible as the subject matter expert over site's products and processes. The role is responsible for resolving product and process deviations and maintaining efficient processes in the manufacturing of in vitro diagnostic and lab use culture media. Key Responsibilities Review and investigate all non-conforming culture media, track results using Excel spreadsheets (Pivot Tables, PowerBI) and identify trends for RCA. Drives special projects to drive business growth, cost savings, and profitability. Perform historical product batch and literature reviews to resolve product performance (engineering, microbiology, chemistry, equipment) Drives practical process improvements in manufacturing through Six Sigma and Lean manufacturing techniques. Develop and improve processing methods (aseptic and non aseptic dispensing, dry blending, mixing, cooling, solubility, freeze drying, dispensing, thermal processing, formulation) Implement engineering controls for equipment. Resolves critical issues without affecting productivity. Utilization of good judgment on short term versus long term goals. Author protocols to complete engineering studies on products and processes. Work with industrial processing equipment (boiling tanks, blenders, dispensers, labellers, etc) to test processes, investigate issues, and build work instructions. Proficient in statistical and data analysis (ex. MiniTab). Use Statistical DoE, Process Control, GR&R, Regression, and ANOVAs to determine process capability. Author and lead investigations within QMS; deviation investigations (planned and unplanned), CAPAs, and customer complaints. Strong collaboration skills, working with department supervisors and other departments using verbal and written communication. Update documentation such as batch records or SOPs, as required. Performs additional duties as needed. Minimum Requirements & Qualifications Possess a BS in Engineering (preferred) or other STEM degree. Analytical skills, good problem-solving technique and data analysis skills with Excel and statistical software Technical Writing Experience with ISO 9001 and
ISO 13485
Excellent communication skills, both written and verbal Ability to handle and plan multiple projects Outgoing and collaborative in nature Detail Oriented Six Sigma or Lean manufacturing experience Ability to Work on Manufacturing Floor 1-5 years technical experience that includes process engineering, process development, project management. 1-5 years experience within the medical device, food, or pharmaceutical industry Preferred to have 1-5 years direct microbiology experience within the medical device, food, or pharmaceutical industry
Non-Negotiable Hiring Criteria:
Bachelor's Degree
ACCESSIBILITY/DISABILITY ACCESS
This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response. This is an exciting time to join us as we continue to build on more than 100 years of microbiology excellence. With a broad portfolio of instruments, services, and global resources, we're steadfast in our commitment to helping you succeed. Together, we can cultivate a thriving microbiology culture that supports you today, tomorrow, and for life. Oxoid Remel Microbiology, acquired from Thermo Fisher Scientific, is now under the ownership of Astorg, a leading private equity firm with deep healthcare sector expertise and proven track record in diagnostics. With the continuity of trusted brands, established expertise and a long-standing reputation in microbiology, we're looking for talented people to join us as we enter our next chapter of growth. Come and be part of what's next for our company.

Benefits

  • Dental Insurance