Quicksilver Scientific® is a leading manufacturer of advanced nutritional systems with a focus on detoxification. We specialize in superior liposomal delivery systems and heavy metal testing to support optimal health. Our advanced liposomal supplements are highly absorbable and support the body in the elimination of the broad range of toxins we’re exposed to, helping you restore the full expression of your health. At Quicksilver Scientific, we are passionate about health and well-being and are committed to improving the lives of everyone we touch.

Quicksilver is a pioneer in the natural health industry. Our mission is to deliver on the promise of natural medicine, delivering products that help individuals achieve mind and body health through nature inspired innovation. Our growth is fueled by individuals who share our passion. Currently, we have an opening for a Manufacturing Manager in our Lafayette, CO location.

The Manufacturing Manager will be responsible for overseeing the day-to-day operations of the organization’s manufacturing facilities, planning, coordinating, and directing the activities (processes) that result in products (goods).

 Core Responsibilities include:

• Manage the respective activities related to cGMP manufacturing with direct guidance and in conjunction with VP of Operations; develop and implement manufacturing methods, processes, and operations for manufactured products.
• Meet regularly with VP of Operations to understand the business needs and manage production accordingly.
• Ensure the efficient use of material, equipment and personnel while producing products at high quality levels, ensuring that manufacturing stays on schedule and within budget.
• Direct corrections (Corrective Action) of any manufacturing problems that may arise; work with Quality Manager in development and implementation of corrective and preventive actions (CAPA).
• Provides day to day management of the manufacturing team.
• Hire, train, and evaluate manufacturing workers; monitor workers to ensure they meet performance and safety requirements.
• Manage daily schedules of production activities, outline staff assignments, material and equipment requirements, and training needs. Assist staff with execution of production tasks.
• Participate in design and implementation of new manufacturing space.
• In cooperation with management personnel, look for opportunities to improve operations. Closely coordinate potential process improvements with quality and regulatory to assure cGMP compliance.
• Implement quality control programs that ensure the finished product meets a certain standard.
• As needed, implement new training programs, reorganize the manufacturing process.

Qualifications:

Qualified candidates must have a Bachelor’s degree in Chemical Engineering, Life Sciences, or related sciences. Must have 5+ years of manufacturing experience in a cGMP-regulated environment. Must be able to walk, bend, stoop, repeatedly lift up to 35lbs and withstand a manufacturing environment. Must be proficient in MS Office with intermediate proficiency in Excel.

Ideal Candidates have the following traits:

• 2+ years of experience in a food, pharmaceutical, or dietary supplement manufacturing.
• 2+ years of experience managing personnel in a production environment.
• Knowledge and application of Lean Manufacturing principles.
• ERP software experience.
• High level of initiative and ability to work effectively with minimal supervision.
• Demonstrated track record of problem solving, team building, planning and decision making.
• Demonstrated ability to lead, motivate, and manage change.
• Excellent oral and written communication skills – ability to communicate clearly and effectively with a variety of stakeholders.
• Flexible to quickly adjust to the changing needs of the company.