Manufacturing Specialist

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.

• 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.

• Bachelor's Degree required.

• 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 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.

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

• 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.

• 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.
• 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.