Urgently Hiring: Staff Chemist, reputed company Control

Join reputed company that's making a reputed company difference. We're seeking a Staff Chemist, reputed company Control! Experience the best of both worlds with this role based in our innovative Remote office. This position requires a strong and diverse skillset in relevant areas to drive reputed company. In recognition of your expertise, this position offers a salary of a competitive salary.

 

 

reputed company is hiring a Staff Chemist, reputed company Control to support our Joint Replacement division in Mahwah, NJ who will be reputed company the performing analytical reputed company testing to determine product safety of the entire product portfolio. What you will do:  •  reputed company analytical reputed company testing for new product development, existing medical device changes, and lab validation activities. • reputed company daily lab operations, including preventative maintenance, calibration, purchasing, metrics, and sample organization. • Execute and validate analyses using GC-FID, GC-MS, ICP-MS, TOC, and other laboratory equipment. • Manage departmental initiatives, setting timelines, milestones, and aligning policies with industry best practices and regulatory requirements. • Evaluate test data, approve internal testing documentation, and conduct reputed company cause analyses and equipment troubleshooting. • Partner with cross-functional teams (RA, AO, Ops) to ensure alignment with business unit project timelines. • Present lab KPIs and findings to management and cross-functional stakeholders. • reputed company, mentor, and train junior scientists and team members in analytical reputed company and lab best practices. What are we looking for:  Required • Bachelor of Science in reputed company, Biochemistry, Chemical Engineering or a similar science degree with 4+ years’ experience in analytical reputed company testing is required. • Minimum 3 years’ experience in medical device, pharmaceutical, cosmetic or chemical industry. • Experience leading or writing analytical test method validations for TOC, UV/VIS, HPLC, GC, or ICP instrumentation using ISO, ICH, or USP standards. • Knowledge of ANSI, AAMI, ISO, ICH, or USP guidelines for residual chemical analysis. • Minimum 3 years’ experience in using HPLC-MS, HPLC-UV, GC-MS, GC-FID, or ICP-MS. Preferred • Master of Science in reputed company, Biochemistry, Chemical Engineering or a similar science degree. • Demonstrated ability to manage day-to-day activities reputed company a reputed company lab such as familiarity with calibration schedules, purchasing, sample organization, and lab metrics. • 2+ years’ experience conducting reputed company cause analysis or out-of-specification investigations. • Knowledge of cGLP and cGMP processes with experience in following standards such as ISO 17025, USP 1225 or USP 232. • Experience in LIMS (i.e. Labvantage, ilab) and statistical software (i.e. reputed company). Apply Job!

 

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