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Description

We are seeking a highly skilled and experienced Senior Chemist to join our R&D team supporting combination medical device development. This role is ideal for a seasoned professional with a strong background in analytical chemistry, method development, and instrument troubleshooting within regulated environments. You will play a key role in both new product development and sustaining engineering efforts, contributing to the advancement of life-saving technologies.

Key Responsibilities

Lead and execute analytical method development and validation for combination products using techniques such as HPLC, GC, dissolution, and bioassay.

Conduct formulation and performance testing of adhesives and cyanoacrylates used in device assemblies.

Operate, troubleshoot, and maintain analytical instrumentation including HPLC-DAD, GC-FID/MS, GPC, Karl Fischer, FT-IR, UV-Vis, and USP dissolution apparatuses.

Design and conduct exploratory research to support product innovation and process improvements.

Analyze complex datasets using statistical tools and provide actionable insights.

Collaborate cross-functionally with R&D, Quality, Regulatory, and Manufacturing teams.

Prepare technical documentation, protocols, and reports in compliance with GLP/GMP and internal SOPs.

Mentor junior scientists and contribute to project leadership as needed.

Qualifications

Required Qualifications

Advanced degree (MS or PhD preferred) in Chemistry, Chemical Engineering, or a related technical field.

Minimum 5 years of experience in R&D within the medical device or pharmaceutical industry.

Proven expertise in combination product testing, method development, and instrument troubleshooting.

Proficiency with Empower and MassHunter chromatography software.

Experience with electronic documentation systems such as MAP, Agile, or equivalent.

Strong problem-solving, communication, and project management skills.

Ability to work independently and manage multiple priorities in a fast-paced environment.

Nice to Have

5 years of experience in RampD within medical device or pharmaceutical industries

Experience with new product development and sustaining project support

Strong problem-solving capabilities

Solid oral and written communication skills

Ability to manage and prioritize multiple tasks and lead projects

Formulation and testing experience with adhesives cyanoacrylates preferred

Expertise in analytical test method development and validation: HPLC and GC

Expertise with analytical instrumentation: HPLC-DAD GPC GC-FID/MS Karl Fischer FT-IR and UV-Vis

Experience in moderate and complex data analyses using statistical techniques

Experience with equipment troubleshooting

Experience of using chromatography software: Empower and MassHunter

Experience using common electronic documentation software e.g. MAP Agile or equivalent.

Pay and Benefits

The pay range for this position is $35.00 - $50.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Plymouth,MN.

Application Deadline

This position is anticipated to close on Jul 17, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] (%[email protected]) for other accommodation options.