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Distek, Inc., a leader in the scientific instrumentation field, is currently seeking a Bioprocessing Field Validation Specialist in the Ohio area. This is a great opportunity to join our growing bioprocessing team.
As a Bioprocessing Field Validation Specialist, you will be responsible for ensuring the quality and compliance of our bioprocessing equipment. Your expertise will contribute to the validation and optimization of our scientific instruments, ensuring they meet industry standards and regulations.
If you have a strong background in bioprocessing validation and are seeking a rewarding career in the scientific instrumentation field, we invite you to apply for the Bioprocessing Field Validation Specialist position.
Responsibilities
This position reports to the Bioprocessing Service Manager. The major responsibilities of the position are described below.
- Technical Responsibilities
- Perform Bioprocessing Validation/Repair Services at customer sites
- Lead and perform BIOne equipment installations
- Perform IQ / PM / OQ validation services on Distek bioprocessing instruments
- Perform related installations on non Distek equipment
- Perform repair services on Distek Bioprocessing Instruments
- Troubleshoot and perform minor maintenance / repair service for Distek instruments
- Participate in training of new Validation Specialists
- Administrative Responsibilities
- Complete and submit service reports in a timely and efficient manner
- Accurately complete and submit expense statements and supporting documents in a timely manner
- Store, maintain, and use all tools, validation tools, support instruments, electronic devices, and other Company issued items safely, properly and with the utmost care
- Sales Support Responsibilities
- Provide product familiarization to customers
- Respond to customer inquiries regarding validation/repair services
- Provide instrument and service sales leads to Sales department
- Product Development / Continuous Improvement Responsibilities
- Provide feedback to all Service Manager for continuous improvement in the level of service and instrument performance
- Identify recurring problems and bring them to the attention of Management, Production, and Engineering
- General Responsibilities
- Perform all required work in adherence to ISO standards
- Participate in projects and special assignments as needed
Requirements
The qualified candidate must have:
- Life Science B.S. Degree (Biology, Cell Biology, Biochemistry) OR previous bioprocessing experience
- Ability and willingness to travel at least 50-75% throughout the United States and Internationally
- High self-motivation, the ability to work independently, requiring minimal supervision
- Ability to successfully prioritize and handle multiple tasks simultaneously
- Ability to handle interruptions and adjust to quick changes in priorities
- Proficiency in Microsoft Office – Word, Excel, Outlook
- Excellent interpersonal, organizational; oral and written communication skills
- Proven ability to work well in a team environment
- Ability to lift up to 60 lbs. unassisted
Preferred knowledge and skills:
- Upstream bioreactor experience (mammalian/insect cell culture or fermentation)
- Familiarity with cGMP/cGLP regulations
- Familiarity with common laboratory layouts
- Prior experience in the authoring of technical documentation and procedures
Contact info
Benefits
- Base Salary
- Medical & Dental Insurance
- 401(k) Retirement Plan
- Paid Vacation
EEO policy
Distek, Inc. is an Equal Employment Opportunity employer. Thank you for your interest, however, only candidates selected for interviews will be contacted.
Please note that all offer of employment is subject to a satisfactory background check and passing a 10 Panel Drug test.