Qc Inspect I Jobs in Florida

Read test results and notify Lab Management of results that are out of specification;

Reporting and evaluating results and data entry using Labware (LIMS);

Knowledge of chemistry and analytical chemistry fundamentals as related to quality control;

Strong functional and technical skills, strong analytical instrumentation background in quality control and in a production environment;

Excellent written and oral communication skills;

Good organizational skills and great attention to detail;

Medical Dental & Vision coverage (Available first day of employment)

Company supply PPE (Personal Protection Equipment)

Perform chemical, physical, and organoleptic analysis of raw products based on written procedures.

Perform daily verification of the equipment. Perform minor maintenance on test equipment as assigned.

Assure all retained samples are identified and properly stored.

Laboratory housekeeping based on Good Lab Practices.

o Assist with inventory management:

o Maintain all qualification and validation requirements for entering ISO classified area.

o Perform radiation safety duties according to SOFIE’s Corporate Radiation Compliance Program and site licensing requirements.

o Technical experience with computer-controlled automation preferred.

o Perform FDG and NaF synthesis according to SOFIE Standard Operating Procedures (SOPs):

o Ensure all materials/reagents are accepted according to SOPs and within expiry

Judgement is required in resolving complex problems based on experience.

02-04 years related experience required.

Occasional business travel required, Valid driver's license and passport, Ability to work non-stand schedule as needed, On-call hours as needed.

Occasionally:Reaching upward and downward, Push/pull, Visual Acuity with or without corrective lenses

Occasionally: Proximity to moving parts

Occasionally: Production/manufacturing environment, Warehouse environment

Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/210/211).

Oversee and execute analytical method qualifications, validations and transfers including drafting technical protocols, reports and assay troubleshooting.

Author, revise and review SOPs, qualification/validation protocols and reports.

Strong knowledge of GMP, SOP’s and quality control process

Strong written and verbal communication skills.

Experience in the biotech and/or pharmaceutical industry.

Fulfill requests from management for assistance in other matters as needed.

In addition to competitive compensation, we offer a comprehensive benefits package including:

Perform instrument/equipment calibration or preventative maintenance according to written procedures.

Participate in material and reagent receipt for the QC Microbiology Laboratory

Assist in the generation of work order requests

Assist in performing inventory and ordering, as needed