Work Schedule

First Shift (Days)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

Excellent Benefits Package

Review our company’s Total Rewards

Medical, Dental, & Vision benefits-effective Day 1

Paid Time Off & Holidays

401K Company Match up to 6%

Tuition Reimbursement – eligible after 90 days!

Employee Referral Bonus

Employee Discount Program

Recognition Program

Charitable Gift Matching

Company Paid Parental Leave

Career Advancement Opportunities

Discover Impactful Work:

Your expertise will help us maintain our world-class standards while driving growth and expansion. In this role you will lead a team to successfully Formulate, Fill, Label and Package Immunological and Biological Assays.

A day in the Life:Set departmental level priorities and key performance indicators in alignment with the site and corporation.Supervise and develop colleagues ranging from entry-level associates to professional tract Formulators and Manufacturing Managers.Use customer and internal forecasts to build manufacturing strategies and staffing patterns to enable Class A Order Fulfillment.Identify and implement site-level efficiency and quality improvement projects within the area of responsibility.Lead professional engineers and teams (direct and indirect reporting) to meet the quality compliance needs of an ISO 13485 Medical Device Site.Learn and understand financial reporting and the contributions of your value stream to the overall success of the site (Revenue, EBITA, Productivity, Utilization, Efficiency, Scrap).Guide and encourage others to promote standard processes both within and outside of your team.Keys to Success:

Education

Bachelor Degree in Chemical Engineering, Biochemistry, Biology, Chemistry, or other related field with 10 years of experience required.Master Degree in Business Management or a Science related field preferred, but equivalent experience will also be considered.ExperienceExperience in a regulated industry, preferably ISO 13485 or pharmaceuticals, strongly desired.Minimum 5 years of people leadership experience required.Knowledge, Skills, AbilitiesAbility to communicate (verbally, written) with customers concisely and effectively required.Understanding of Immunological and Biological Assay manufacturing helpful.Ability to lead and develop team members at all levels (career entry-level to degreed professional track) required.