Quality Control Chemist

2 weeks ago

Iowa City, Iowa, United States Bureau Veritas Full time
Position Title: Analytical Chemist

Company Overview:

Bureau Veritas is a leading professional services organization dedicated to providing comprehensive support for FDA-regulated products and companies globally. Our expertise spans scientific, engineering, and regulatory laboratory services, ensuring we meet the needs of the consumer goods, pharmaceutical, and medical device sectors.

With our headquarters in Cincinnati, Ohio, we pride ourselves on being a dynamic and profitable organization, employing nearly 500 skilled professionals across the United States.

Our mission is to deliver exceptional value to our clients throughout every phase of the product life cycle, establishing ourselves as the preferred partner for Fortune 500 companies.


Work Schedule:
12-hour rotating day/night shifts, including every other weekend.

Position Summary: The Analytical Chemist will operate both autonomously and under managerial guidance, ensuring access to support for inquiries. The primary responsibility of this role is to conduct quality assessments on raw materials, in-process samples, and finished products.

Duties & Responsibilities:
  • Conduct various sample preparation, extraction, and analytical techniques.
  • Perform serial dilutions to establish standards and quality control samples according to established protocols.
  • Execute identification, gravimetric, qualitative, and physical testing regularly.
  • Carry out titration testing, chromatography (GC and/or HPLC), and atomic absorption (AA).
  • Utilize basic instrumentation for routine testing.
  • Adhere to testing deadlines and maintain accurate documentation of all analyses.
  • Conduct method validations and verifications.
  • Complete DIR/OOS/CAPA documentation as required.
  • Review SOPs and methods, suggesting and implementing changes as necessary.
  • Assist in audit preparations.
  • Maintain a clean and safe laboratory environment through routine maintenance.
  • Perform additional tasks as assigned.

Education & Experience:
  • Bachelor's Degree in Chemistry or a related scientific field.
  • Strong interpersonal skills, including relationship building, initiative, and teamwork.
  • Effective communication skills for presenting facts and recommendations.
  • Ability to prioritize tasks and manage time efficiently.
  • Capability to work independently and collaboratively.
  • Proficient data management skills, including sorting and interpretation.
  • Able to thrive in a fast-paced, agile work environment.
  • Proficient in Microsoft Office applications.
  • 0-1 years of experience with GC, HPLC, or Atomic Absorption (AA) preferred.
  • Experience in an FDA or cGMP regulated setting preferred.
  • Understanding of instrumentation and methodology, including method validation, preferred.
  • Experience in consumer products, pharmaceuticals, or personal care industries preferred.

Physical & Travel Requirements:
  • Frequent standing for up to 12 hours.
  • Regular walking within a large manufacturing facility.
  • Frequent fine manipulation with hands.
  • Occasional lifting of up to 10 lbs.
  • 0% travel required.

Bureau Veritas is an Equal Opportunity Employer committed to fostering a diverse workplace. We do not discriminate in recruitment, hiring, training, promotion, or other employment practices based on race, color, religion, gender, sexual orientation, national origin, age, marital or veteran status, medical condition or disability, or any other legally protected status.

We strongly support diversity in the workplace.

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