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Integrated Resources, Inc ( IRI )

Chemist

Integrated Resources, Inc ( IRI ), Los Angeles, California, United States, 90079

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Integrated Resources, Inc ( IRI ) provided pay range This range is provided by Integrated Resources, Inc ( IRI ). Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range $39.56/hr - $39.56/hr

Recruitment Delivery Leader | Expert in Scientific & Clinical Hiring | Performance Mentor | Pharma/Biotech Talent Strategist Top Needs:

Analytical chemistry lab experience

LC, LC-MS

GC-MS

ICP-MS

We are seeking a Chemist II with hands‑on experience in analytical techniques including FTIR, ICP‑MS, LC‑UV/LC‑MS, and GC‑FID/MS.

The candidate will perform qualitative and quantitative analyses on a variety of sample types to support new product development. Responsibilities also include assisting in method development, maintaining laboratory instrumentation, and ensuring compliance with laboratory protocols. The Chemist II will contribute to protocol and report writing, data interpretation, and general laboratory support activities.

Position responsibilities: Analytical Testing & Method Development

Performs routine and non‑routine qualitative and quantitative analyses of raw materials, in‑process samples, and finished products using techniques such as FTIR, ICP‑MS, LC‑UV/LC‑MS, GC‑FID/MS, and others.

Develops and improves analytical methods; validates methods in compliance with regulatory standards.

Supports product development activities by executing analytical testing, compatibility studies, and development plans.

Applies a strong understanding of underlying chemistry to method development, data interpretation, and troubleshooting analytical challenges.

Documentation & Compliance

Prepares and reviews technical documents including protocols, reports, and data sheets for analytical parameters.

Conducts analytical work in compliance with cGMP, regulatory standards, and safe laboratory practices; documents any variances appropriately.

Frequently applies regulatory standards to drug and device testing.

Collaboration & Technical Communication

Maintains a collaborative environment across cross‑functional teams within the Drug Delivery Systems group.

Contributes to multiple projects simultaneously, including the preparation of scientific presentations and research articles.

Plays an integral role in the strategic and tactical operations of the analytical department.

Laboratory Operations & Problem Solving

Independently investigates and resolves analytical issues and proposes preventive solutions.

Prepares reagents and solutions, performs general lab duties including equipment maintenance, cleaning, sample/standards preparation, and housekeeping.

Outlines and implements effective solutions for laboratory investigations and supports continuous improvement initiatives.

Education Required:

Requires broad theoretical job knowledge typically obtained through advanced education. Requires a Baccalaureate degree in science from a four‑year college or university (or for degrees earned outside of the United States, a degree which satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A)).

Years of Experience: 2+ years of related experience with a bachelor’s degree, 0+ years of experience with a master’s degree.

Specialized Knowledge Required:

Demonstrated experience in developing analytical methods and performing material or product characterization using a range of chemical analysis techniques in academic or industry settings.

Proficient in applying advanced analytical instrumentation, including FTIR, LC‑UV/LC‑MS, GC‑FID/MS, and ICP‑MS.

Strong background in analytical chemistry with hands‑on laboratory experience.

Skilled in interpreting complex analytical data and applying mathematical concepts relevant to quantitative and qualitative laboratory analyses.

Preferred qualifications (optional):

Bachelor’s or advanced degrees in Biochemistry, Chemistry, or Analytical Chemistry.

Hands‑on experience working in a chemistry laboratory environment.

Familiarity with ISO 10993 standards for biological evaluation of medical devices.

Strong problem‑solving skills with a practical, hands‑on approach to troubleshooting laboratory issues.

Proven ability to thrive in a collaborative, fast‑paced research setting.

Excellent time management and prioritization skills for handling multiple concurrent projects effectively.

Seniority level Associate

Employment type Contract

Job function Other

Industries Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing

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