Manufacturing Specialist

Geneoscopy, Inc.•Maryland Heights, MO

7d•Onsite

About The Position

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.

Requirements

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 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.

Nice To Haves

Experience with cGMP processes.
Industry knowledge of diagnostics and/or life sciences.
Knowledge of biotech manufacturing processes and equipment.
Experience with manufacturing automation.

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.