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Assistant Scientist AR&D

Perrigouk

Allegan (MI)

Hybrid

USD 55,000 - 95,000

Full time

30+ days ago

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Job summary

Join a forward-thinking company dedicated to enhancing health and wellness through innovative solutions. This role focuses on creating analytical methodologies and generating high-quality data for drug products. You'll work with advanced analytical tools and contribute to cross-functional teams, ensuring efficient product development cycles. Enjoy a hybrid working approach that promotes flexibility while collaborating in a vibrant office environment. If you're passionate about making a difference in self-care, this opportunity is perfect for you.

Benefits

Competitive compensation
Career development opportunities
Hybrid working model
Inclusive culture
Flexible work arrangements

Qualifications

  • 2+ years of relevant experience in analytical methodology and instrument use.
  • Hands-on experience in a cGMP laboratory setting is essential.

Responsibilities

  • Generate high-quality analytical data on various samples using analytical equipment.
  • Research and prepare technical documents for testing protocols and validation.

Skills

Analytical methodology
Liquid chromatography
Gas chromatography
Spectroscopy
Mass spectrometry
Statistical analysis
Documentation of experiments
Customer service
cGMP laboratory experience

Education

Bachelor’s degree in Chemistry
Master's degree in Chemistry

Tools

HPLC
UPLC
GC
MS
USP dissolution apparatus
Moisture analyzers
Electronic laboratory notebook software

Job description

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At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill, Compeed, Solpadeine, NiQuitin, ACO, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.

Join us on our One Perrigo journey as we evolve to win in self-care.

Description Overview

Our primary focus is the creation of analytical methodology to promote research and the characterization of new and reformulated drug products. Principal techniques include liquid and gas chromatography with a variety of separation chemistries and detection mechanisms, USP-based dissolution, spectroscopy, solid-state technologies, and mass spectrometry, along with introduction of various new analytical tools as needed.

Scope of the Role
  • Generate high quality analytical data on raw materials, in-process, and finished product developmental and stability samples using a variety of analytical equipment.
  • Research, prepare and review technical documents, including but not limited to: testing protocols, material specifications, analytical methods, certificates of analysis, validation reports, and regulatory responses/submissions.
  • Dedication to continuous improvement and expedient customer service.
  • The ability to learn quickly and adapt to changing customer and business needs.
  • Commitment to meet or exceed project milestones for efficient product development cycle times.
  • Eventually develop, validate and transfer analytical methods of varying complexity.
  • Contribute to cross-functional teams at project-related meetings and technical discussions.
Experience Required
  • Knowledge of analytical instruments and associated software for physical and chemical analyses including, but not limited to, analytical balances, pH meters, HPLC, UPLC, GC, MS, USP dissolution apparatus, and moisture analyzers.
  • Familiarity with a variety of compendial references including the United States and European Pharmacopeia.
  • Understanding and expertise with statistical analysis, chromatography acquisition, and electronic laboratory notebook software platforms.
  • Demonstrated ability to precisely execute and clearly and accurately document complex analytical experiments.
  • Hands-on experience in a cGMP laboratory setting.
  • The skills required for this role are normally acquired through completion of a:
  • Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences or other related field with 2+ years of relevant experience OR a
  • Master's degree in Chemistry, Biochemistry, Pharmaceutical Sciences or other related field

Benefits
We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.

Hybrid Working Approach
We love our offices and the setting they provide for in-person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles.

We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more here

Applicants please note: To apply to this position please click the APPLY button at the bottom of the application. (The SAVE button will only save your profile information but not submit an application for this open position.) Thank you.

We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law. #weareperrigo

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