Bench Scientist I

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.

Job Description:

Responsible for the lifecycle of regulated and clinical samples of bio therapeutics in various matrices to be tested in ligand binding assays on various instrument platforms.

Responsible for the routine and non-routine maintenance of lab equipment (e.g. plate washers, plate readers) used in support of regulated and clinical studies.

Assist with quality control of operational procedures and software applications in accordance with departmental SOPs and bio analytical methods.

Sample lifecycle management and lab equipment maintenance to be governed per departmental SOP. Attention to detail to ensure accurate execution and documentation of these processes in a regulatory compliant manner. Knowledge of GLP/GCP and working in a regulated environment is highly desirable.

Implement various processes needed to manage a sample’s lifecycle which includes accession, check-in and disposal within a laboratory management system (LIMS). Become proficient in LIMS to conduct these activities in a dynamic environment. Collaborate with external groups to resolve sample discrepancies. Assist in the transmission and formatting of clinical files for the importation/exportation of clinical data from LIMS.

Execute routine maintenance of lab instrumentation as required per departmental SOPs.

Education experience:

BSc with at least 1+ year relevant experience, with a focus on sample management / ligand binding assay validation/sample testing; preferably in a GLP/GCP laboratory.

· Industry experience with a focus in bio therapeutics; familiarity with LIMS and instrumentation used in execution of ligand binding assays.

· Skills in GLP/GCP compliant laboratory including following SOP and provision of quality regulatory documents is highly desirable.

Additional Skills:

· Knowledge and hands-on experience with sample management in a LIMS as well as lab equipment used in support of ligand binding assays.

· Knowledge and hands on experience working under GLP/GCP regulations is highly desirable

· Ability to execute tasks with high quality against challenging time lines

· BSc with at least 1+ year relevant experience, with a focus on sample management / ligand binding assay validation/sample tesing; preferably in a GLP/GCP laboratory;

· Industry experience with a focus in bio therapeutics; familiarity with LIMS and instrumentation used in execution of ligand binding assays.

· Skills in GLP/GCP compliant laboratory including following SOP and provision of quality regulatory documents is highly desirable.

Technical/Functional Competencies:

· Proven ability to deliver quality sample management within tight timelines.

· GLP/GCP knowledge desirable.

· Bio hazardous Agent work (such as menigiditis, staph aureus, Lenti Virus, streph pneumoniae)

· NHP cells or tissues

· Unscreened blood, human tissue or human cell lines

Feel free to forward my email to your friends/colleagues who might be available. We do offer referral Bonus.

Thank you.

Kind Regards,

Harris Kaushik

Clinical Recruiter

Integrated Resources, Inc.

IT Life Sciences Allied Healthcare CRO

DIRECT # - (650)-399-0891

Gold Seal JCAHO Certified ™ for Health Care Staffing

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