Labs FSP - Sterile Manufacturing Operator

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission – to enable our clients to make the world healthier, safer, and cleaner. Within our Analytical Services team, we have a functional service provider solution, which is an outstanding partnership that allows our customers to use the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits.   Perform all tasks assigned per Sterile Manufacturing Operator job description which includes, but is not limited to: • Able to perform all technical operations in area of assignment at a high level of proficiency, such as logging in materials, inspection for damage and cold chain compliance, maintaining inventory records, sampling of raw materials, and updating materials in conformity to GMP standards. • Store materials in appropriately identified manner in suitable environment. • Maintain inventory records. • Performs packaging of materials for shipment with minimal supervision. • Contributes to the creation and revision of Material specifications, accession control forms and SOPs. • Maintains housekeeping of the area and restocking of general supplies. • Coordinates transfer of excipients, components, and samples to support clinical and pre-clinical manufacture and component processing orders. • Manage inventories and schedule activities appropriately. • Contributes to relevant investigations. • Assist in the preparation of metrics and key KPIs for the area. • Able to identify and coordinate implementation of safety, quality, and business  improvements. • Employee will participate in department consumables storage and stocking programs. • Employee may be asked to perform administrative tasks such as procedure revision, template revision, records filing, records archiving, and other tasks as needed.  • All job functions will be performed according to procedure and in accordance with cGMPs, Standard Operating Procedures, and safety codes and regulations. • Identifies risks to business for consideration by management. • Assist and contribute to GMP and safety self-inspection activities.  • Accountable for reporting and maintaining metrics as appropriate. • Zero instances of data falsification or data integrity issues by PPD staff. • Employee has basic computer skills including Word, Outlook, and ability to navigate simple website interfaces. • When performing manufacturing operations, employee will be expected to wear appropriate gowning (scrubs, hair net, beard cover, gloves, safety glasses, safety shoes), stand for periods of time, and operate standard pharmaceutical manufacturing equipment.  • Employee must have good hygiene, practice good hand-washing behaviors, and be comfortable frequently using hand sanitizing agents.

High school diploma or GED Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0-1+ years). In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.   Knowledge, Skills and Abilities: Knowledge of applicable regulatory authority, compendia and ICH guidelines Ability to understand and independently apply GMPs and /or GLPs to everyday work with regard to documentation and instrument use Ability to utilize Microsoft Excel and Word to perform tasks Ability to independently optimize analytical methods Good written and oral communication skills Time management and project management skills Problem solving and troubleshooting