QC Laboratory Analyst

We are searching for a QC laboratory Analyst to support the development and validation of methods to test new products manufactured at the site. Performs testing of experimental, confirmation and registration lots, stabilities and new supplier certifications. Participates in the transfer of analytical technology to the commercial laboratories with attention to details. Primary functions:

Receives and logs in samples, review analytical data and prepares certificate of analysis Prepares verification protocols and reports as required Revises SOPs and keeps track of daily schedule Performs test verifications when required and provides training to laboratory technologists as needed Keeps track of the reagents, standards and supplies inventory in the QC laboratory generate the purchase requisition request as needed Assures that files and records are maintained up to dateAttends QC or development meetings as needed Supports EHS program to assure compliance with safety policiesPerforms compendial test data verification under minimum supervisionInterprets results obtained during method development and troubleshoots tests as neededPerforms review of non-conventional testing of solid dosage forms, capsules and others forms, such as:

force degradation, tablet scoring, solubility, method validation, method development analysis, bioequivalence dissolution analysis with different medias, among others Performs tests review for API, raw materials, in-process samples, research samples, finished product and stabilities following analytical specifications, protocol specifications, procedures, and/or instructions as applicableRecords data in an orderly manner following laboratory rules and SOP's calculates results as required, compares results with specifications and seeks further direction when are not met Performs laboratory housekeeping always Prepares progress reports Assists in or carries out work of an experimental nature under limited supervisionWorks with instruments of an advanced and/or sophisticated nature and performs troubleshooting work when required Assists in data verification and informs supervisor if any discrepancy found Keeps records and files up to date and assures that information is available at all times.

NEnsures that any waste (hazardous, non-hazardous or special waste) generated as part of his/her responsibilities are handled in compliance with applicable environmental regulations and in accordance to establish SOP's for handling waste Documents on a timely manner in the corresponding laboratory logbooks and laboratory notebooks all the information regarding to the testing activitiesWrite/assist in laboratory protocols deviation reportPerforms other duties as assignedOther Functions: Supports revision of QC SOPs and preparation of analytical methods as needed for API, Excipients and Finished Product as neededMinimum Requirements:

Bachelor's Degree in ChemistryLicensed ChemistFive years (5) or more of experience in a cGMP regulated analytical laboratoryExperience in method validation (preparation of protocols and reports), analytical technology transfer and cleaning validationKnowledge in FDA, GMP, ICH and USP requirements for method, cleaning validation and transferComputer literateExcellent communication skills in English and SpanishOther Requirements: Flexible to work flexible shifts including weekendsWork under pressure and adapt to dynamic changes of working schedule and shift"Drug Free Workplace Policy:

In accordance with our commitment to maintaining a safe and productive work environment, all applicants for employment with our company are required to affirm their commitment to a drug-free workplace and consent to pre-employment drug testing as a condition of employment. "Share Tech Group is committed to being an equal opportunity employer, fostering a diverse and inclusive workplace where all individuals are treated with respect and provided with equal opportunities for employment and advancement. Powered by JazzHRpfUNQxXltz