Director of Research & Development

at  LaMotte Chemical Products Company

Newark, DE 19702, USA -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate23 Jan, 2025Not Specified24 Oct, 2024N/AMicroprocessors,Chemicals,Formulation Chemistry,Electronics,Laboratory Skills,Optics,Operating Systems,Data AnalysisNoNo
Add to Wishlist Apply All Jobs
Required Visa Status:
CitizenGC
US CitizenStudent Visa
H1BCPT
OPTH4 Spouse of H1B
GC Green Card
Employment Type:
Full TimePart Time
PermanentIndependent - 1099
Contract – W2C2H Independent
C2H W2Contract – Corp 2 Corp
Contract to Hire – Corp 2 Corp

Description:

Description:
Job Title: Director of Research & Development
Department: R&D
Reports To: Vice President of Technology


POSITION SUMMARY:

The Director of Research & Development will lead the R&D team in developing innovative reagents and products, ensuring alignment with company objectives as well as manage and coordinate with outside engineering resources. This role requires a strong background in chemistry and formulation, alongside managerial experience, to drive the successful execution of projects through the Phase Gate method. The position can be based out of either Newark, DE or Chestertown, MD and reports in to the Vice President of Technology.

QUALIFICATIONS:

An advanced degree in chemistry or pharmaceutical chemistry from an accredited institution. Extensive experience in chemistry or formulation chemistry, particularly in analytical reagent systems and novel delivery systems. Good color perception is a plus.

TECHNICAL SKILLS:

o Basic knowledge of electronics, circuit boards, microprocessors, and optics.
o Proficient in data analysis and familiar with relevant software, firmware, operating systems, and serial communication.
o Laboratory skills for safe handling of chemicals and instruments.
Proven experience in managing teams effectively.

ABOUT US:

LaMotte Company is a 100+ year-old global industry and technology leader in developing and manufacturing premier water testing solutions. LaMotte operates from two manufacturing sites in Chestertown, MD and Newark, DE. Both facilities have production, research and development, and administrative capabilities, with the Newark site operating 24/7. LaMotte sells their products globally through direct and indirect sales channels into a variety of end market applications.
LaMotte offers paid time off including vacation, sick leave and paid holidays. Full-Time employees, who regularly work at least 30 hours per week, are eligible for employer-provided insurance including health, dental, vision, disability, life insurance and supplemental insurance. Full-time employees are eligible to contribute to our 401(k) plan with employer match available.
LaMotte is committed to a policy of Equal Employment Opportunity and will not discriminate against an applicant or employee on the basis of race, color, religion, creed, national origin or ancestry, sex, age, disability, military status, genetic information, sexual orientation, or any other legally recognized protected basis under federal, state, or local laws

Responsibilities:

  • Product Development: Direct the development of new and improved reagents, including tableted, powdered, and liquid formulations, as well as test strip reagents.
  • Team Leadership: Manage and mentor a team of chemists, chemical engineers, and technicians; hold weekly meetings to ensure project alignment and progress.
  • Production Support: Oversee production support for various product lines and ensure effective collaboration with Customer Service and Marketing teams.
  • Technical Problem Solving: Address and resolve technical issues, providing support to Quality Control (QC) and Quality Assurance (QA).
  • Regulatory Compliance: Direct interactions with regulatory agencies (e.g., EPA) and certification bodies (e.g., NSF, ASTM, PHTA) to ensure compliance.
  • Contractor Oversight: Supervise R&D contractors, including electrical engineers and industrial designers, to support project needs.
  • Market Analysis: Conduct performance evaluations of products versus competitors and provide technical insights for quotations and product costs.
  • Documentation Management: Maintain accurate laboratory records, including electronic notes, Safety Data Sheets (SDS), and product labels.
  • Phase/Gate Management: Track new product development products through the phase/gate process.
  • Other Duties assigned (such duties may or may not be essential functions of the job).
    Requirements:


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Chemistry

Proficient

1

Newark, DE 19702, USA