Manufacturing Specialist

This is an onsite, in-office position at Geneoscopy HQ in St. Louis, Missouri.

The Manufacturing Specialist will be responsible for performing day-to-day manufacturing processes within the laboratory for Geneoscopy's In-Vitro Diagnostic products. These processes include manufacturing reagents and consumable specimen-collection kits.

RESPONSIBILITIES

• Complete and document manufacturing-related activities required to support the development and commercialization of new In-Vitro Diagnostic products.
• Maintain a high standard of product quality in accordance with Good Manufacturing Practices (GMP) and Geneoscopy's policies and procedures.
• Utilize problem-solving techniques to analyze issues at hand, identify the root cause, and develop/implement solutions.
• Accurately complete all required written documentation for batch records.
• Adhere to the laboratory's instrument calibration and maintenance procedures, and document all procedural maintenance and calibration performed.
• Monitor the production process and evaluate and analyze observations to ensure efficiency and quality.
• Cross-train and act as backup for receiving and preparing patient samples for testing, as well as general laboratory setup and maintenance activities
• Other duties as assigned.

EDUCATION REQUIREMENTS

• Bachelor's Degree required.

QUALIFICATIONS

• Ideally, possess 1-2 years' experience within a manufacturing environment.
• Demonstrate the ability to read and understand technical procedures and instructions.
• Exemplify the capability to carefully monitor production processes and document results.
• Exemplify the ability to communicate clearly, move quickly, and ability to make technical decisions with limited information.
• Possess a builder's mindset: proactive, collaborative, and comfortable wearing multiple hats.
• Demonstrate high integrity, accountability, and a desire to help shape both the technology and the team.
• Exemplify the ability to multitask and thrive in an agile, fast-paced, deadline-driven environment while remaining flexible, proactive, resourceful, and efficient.
• Possess proficient verbal and written communication skills, while willing to share and receive information and ideas from all levels of the organization to achieve the desired results.
• Possess high ethics and conduct business in the most professional manner.
• Seek inclusiveness and collaboration but step up to responsibility, make tough decisions, and be accountable for those decisions.
• Act as a results-oriented team player with strong interpersonal and communication skills, capable of working collaboratively with colleagues.
• Preferred Additional Experience:
  • Experience with cGMP processes.
  • Industry knowledge of diagnostics and/or life sciences.
  • Knowledge of biotech manufacturing processes and equipment.
  • Experience with manufacturing automation.

SCHEDULE
This is a salaried position, requiring at least 40 hours per week. There may be projects that require activities beyond the standard hours.

COMPENSATION & BENEFITS

• Base salary range: annually determined based on the candidate's experience, knowledge, and abilities.
• Bonus: discretionary annual bonus based on a percentage of the employee's base salary
• Benefits: health, vision, dental, life insurance, 401k (with employer match), and paid time off.
• Company stock options

ADDITIONAL INFORMATION

Geneoscopy's Core Values
Ability to embody Geneoscopy's beliefs, philosophies, and principles:

• Integrity - we do the right thing through our words, actions, and behaviors
• Courage - step up, speak up, stand out
• Agility - think and act fast, embracing change
• Passion - for our customers, our people, our work, and for excellence
• Collaboration - our differences are assets

Physical Demands

• Employees may be required to lift routine office supplies and use standard office equipment.
• Must possess the ability to sit and/or stand for long periods.
• Must possess the ability to perform repetitive motion.

Work Environment

• May have exposure to fumes and bio-hazardous material in the laboratory environment.
• May be required to handle blood-borne pathogens and general laboratory reagents.

By completing this online employment application, you certify that the information on this application is true and complete to the best of your knowledge. You understand that any misrepresentation or omission of fact in response to any inquiry made in this application may result in the rejection of the application or if hired, dismissal whenever it is discovered. You authorize and release all parties from any liability or damage that may result from seeking, furnishing, or using such information. You understand and agree that, if hired, your employment is for no definite period and may, regardless of the date of payment of compensation, be terminated by Geneoscopy at any time, for any or no reason, with or without notice. You understand that no representation to the contrary is valid unless in writing, setting a definite term of employment, and signed by the company's CEO. You further understand and agree that any job offer is contingent upon your passing, to the company's satisfaction, a criminal background check, reference checks, and other possible screenings. You understand that this application is active for 90 days only, and if you do not hear from the company but still wish to be considered for employment after 90 days, you will need to fill out a new application.