Neotech Employment
Work hard. Have fun. Make a Difference. That’s the culture of Neotech and we’ve been doing it that way for over 30 years.
Describe your ideal workplace and you’ll likely be describing Neotech, where we value and support a good work-life balance. And we believe life during work is pretty good too. We enjoy great food with several company lunches, BBQs and potlucks. We’ve been known to partake in foosball tournaments, cornhole tournaments, eating contests, and more. We really get into Halloween and other holidays. The highlight of the year? Our holiday pajama day potluck brunch.
On the business side of things, Neotech Products is an equal opportunity employer that values diversity. We foster a culture of advancement supported by our mentor program. We offer a competitive salary and comprehensive benefits package including healthcare, dental, vision, 401(k) with company match, paid vacation, paid sick time, bonus plan and much more.
Neotech Products is also a Certified B Corporation®.
What We Do
We design, develop and manufacture high-quality, innovative medical products that Make a Difference in the quality of treatment for neonatal and pediatric patients, their parents, and the clinicians who attend to them.
Current Job Listings
See our listings below. If you are interested in joining the Neotech family, please fill out the inquiry form.
Account Manager
Join Neotech’s dynamic sales team! This close-knit group works together to provide the best in customer service.
We’re looking for the right candidate to join our sales team. This is a full time position, 7:00 AM – 3:30 PM, Monday-Friday. This position reports to the Sales Manager. This position has no direct reports.
Responsibilities
- Outbound phone calls and email communication to Healthcare Personnel to develop and grow sales
- Watch/analyze key accounts and buying patterns
- Work with clinical educators and consultants to coordinate on-site education and product introductions
- Customer service, answer phones, take orders, and process sample requests
- Maintain accurate records of calls and follow-up activity within CRM software
- Work with Microsoft Office, Fishbowl, QuickBooks and various other programs or systems
- Provide backup support to other Account managers when needed
- Provide monthly reports of activity within a given territory
- Processes & Procedures subject to change as needed.
- Other duties as assigned by Management
- Some travel to Trade Shows (local & throughout the US) – non essential
Qualifications
- High School Diploma or GED required.
- 2 years previous customer service and sales experience.
- CRM program (Salesforce, Sugar or Goldmine, etc.) experience required.
- Call center experience a plus.
- Proficient in Microsoft Word and Microsoft Excel.
- Fishbowl, QuickBooks & other software and reporting experience a plus.
- Excellent communication skills both written and verbal.
- Highly motivated and self-starter with a positive attitude.
- Ability to learn new skills, processes and procedures as the role dictates.
- Ability to sit or stand for long periods at a time.
- Ability to work on computer or typing for long periods at a time.
Pay range: Level II – $40k-$55k annually BOE, non-exempt.
As a Manufacturer of Medical Devices we are considered an essential business during this “Safer at Home” time. All applicants will undergo extensive pre-screening which includes: health & recent travel screening questions as well as pre-employment drug screening. NO WALK-IN applicants accepted.
Quality Assurance Engineer
Join Neotech to help maintain our extremely high quality standards!
The Quality Assurance Engineer is to implement Standard Operating Procedures to assist Quality Manager in verity aspects of Quality Management System such as design control, V&V, risk management, supplier control in relation with Class I and Class II medical devices. This is a full time position, 7:00 AM – 3:30 PM, Monday-Friday.
Duties
- Support company goals and objectives, policies and procedures through Good Manufacturing Practices GMP, US-FDA/Europe medical device regulations and ISO 13485.
- Develop risk management plans/reports and FMEAs through collaboration with design team.
- Develop and execute verification and validation protocols, analyze data and write engineering test reports.
- Assist in production and maintenance of technical documentation in compliance with domestic and international medical device regulations. (US and EU)
- Routine Inspection of products and assembly line. Create/manage Non-Conformance-Reports (NCR) and host the material review board, MRB.
- Perform statistical analysis, work with complex spreadsheets, and charts and presentations.
- Mange CAPAs through a comprehensive documentation and collaborative process.
- Create/update/Release documents such as procedures, plans and engineering specifications.
- Recognize problems, analyze, summarize and interpret data, draw conclusions and make appropriate recommendations, write reports and give oral presentations.
- Experience assisting in internal and external audits (e.g., FDA, Notified Body, Supplier)
Qualifications
- Superior customer service skills and a “Can Do” attitude for a culturally diversified work place.
- Dedicated engineer with BS/MS degree in Engineering with minimum of 2 years of experience in Quality/Regulatory Department of a US
- Medical Device company.
- Excellent technical writing and oral communication skills.
- Exceptional attention to details. Strong organizational and time management skills.
- Knowledge and experience of Design Control, CAPA, Complaint and Risk management.
- Medical Device Quality System Knowledge Including 21 CFR Part 820 (QSR) & ISO 13485.
- Strong MS Office skills. Experience with SolidWorks and Minitab is a plus but not required.
- Working knowledge of 5S, Lean, Root Cause Analysis and Supplier Control. ASQ certificates preferred.
- Ability to sit, stand, type or use computers for long periods of time.
- Ability to lift, move or carry up to 50 lbs. (occasionally).
Pay range: Level III – $60k-$80k annually BOE, non-exempt.
As a Manufacturer of Medical Devices we are considered an essential business during this “Safer at Home” time. All applicants will undergo extensive pre-screening which includes: health & recent travel screening questions as well as pre-employment drug screening. NO WALK-IN applicants accepted.
Product Assembler
Join our assembly team and build products that save lives.
Neotech Products LLC is looking for a qualified candidate to join their team of talented people in their Valencia, CA headquarters. This is a full time position, 7:00 AM – 3:30 PM, Monday-Friday. Subject to change as needed.
Essential Functions
- Complete daily assembly of medical products
- Clean and maintain all work areas
- Perform production as needed
- Communicate effectively with other employees
- Back up for other employees in the Assembly Area
- Other duties assigned by Management
- Reports to the Assembly Supervisor
- Understand and abide by all safety procedures and PPE requirements
Qualifications
- High School Diploma/ G.E.D. required2 years’ minimum of assembly experience a plus
- Ability to sit or stand for long periods at a time
- Ability to lift or carry up to 10 lbs.
- Proficient with fine motor skills and repetitive movements for long periods of time
- Strong attention to detail
- Ability to read, write and/or communicate effectively
- Bilingual English and Spanish a plus
- Health & Safety Screening is REQUIRED due to COVID-19 restrictions
Starting Pay: $15.00 per hour
As a Manufacturer of Medical Devices we are considered an essential business during this “Safer at Home” time. All applicants will undergo extensive pre-screening which includes: health & recent travel screening questions.
No WALK-IN or IN-PERSON applications will be accepted
Join our Clinical Consultant team - click for more info
Neotech has a very successful Clinical Consultant program and we are looking for professionals to cover specific geographic areas.
Our objective is to have licensed RNs and RTs throughout the country who have the ability to teach other clinicians how to properly use Neotech products. The consultant will travel to hospitals in their geographic zone.
Requirements
- Must be licensed in your respective areas of expertise
- Must have prior knowledge or experience using Neotech products (particularly the NeoBar)
- Must complete all necessary paperwork prior to beginning work for Neotech
- Prior experience educating/training other professionals on the use of medical devices is beneficial
In-service Duties
- Contact hospitals to confirm need for services and schedule appointment(s) for in-servicing
- Contact Neotech for sample product requirements and request approval of estimated in-service hours before commencing
- Visit hospital and train staff appropriately on the use of Neotech products
- Complete summary report and return to Neotech
Additional Potential Duties
- Attend trade shows and work the Neotech booth as needed
- Attend one-day seminars at hospitals as needed
- Look for new product ideas while in the field
- Introduce new Neotech products to hospitals
- Provide Neotech with input on new products
- Undertake clinical investigations of new or existing products