Manufacturing Technician II - Inspection (Nights)

A career at Resilience is more than just a job – it’s an opportunity to change the future. Resilience is a technology-focused biomanufacturing company that’s changing the way medicine is made. We’re building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need. For more information, please visit The Manufacturing Technician II reports to a Manager/Supervisor in the Inspection Process Execution Team (PET) operations. This position will require working in various Controlled/Non-Classified areas. The Technician performs a variety of manufacturing tasks (operates equipment, performs visual, cosmetic, and physical inspection, line clearances, OEE data collection and completes batch record entries) and supports improvement activities (5S, participation in problem-solving and Kaizen events, manual data collection) in accordance with cGMPs. Primary Responsibilities Operate assigned machinery: servicing automated inspection equipment, monitoring equipment status, reintroduction of materials, manually palletizing inspected materials, ensuring a smooth flow of product. Perform manual visual, cosmetic, and physical inspection of material; promptly escalating concerns to Lead and Manager/Supervisor as needed; maintain visual inspection qualification. Start up equipment, make minor adjustments, remove jams, perform minor troubleshooting, and conduct minor assembly/disassembly for cleaning purposes. Use material handling equipment such as motorized and manual pallet jacks and non-motorized lifts. Perform cleaning, housekeeping, and line clearance activities for assigned areas to maintain a cGMP environment. Perform batch record and GMP documentation entries; maintain records and logs; conduct mathematical computations as required. Apply knowledge of product security controls and material handling equipment. Ensure outgoing quality level. Familiar with job‑related safety procedures and hazards including PPE, ergonomics, LOTO, human safety, material handling, waste handling, chemical handling, and spill controls; report all discrepancies to the process facilitator. Execute work in accordance with SOPs, cGMPs, OSHA requirements, and guidelines; be familiar with Material Safety Data Sheets for area chemicals. Print off SOPs and forms via ECMS. Other Responsibilities Support lean activities and process improvement work such as performing 5S, participating in problem‑solving, and manually tracking performance data for OEE and process improvement analysis. Review process documents including operational SOPs, forms, and batch records for accuracy; identify and provide suggestions for process improvement while maintaining quality and cGMP compliance. Be flexible and support other work areas as needed. Perform all other assigned duties with minimal supervision under the direction of the process facilitator or designee. Optional Training / Responsibilities Obtain cold‑room training/access to transfer materials in and out of cold rooms. Complete training to become a certified trainer on assigned equipment and process tasks; train and conduct evaluations on other team members. Acquire a novice to intermediate level of knowledge of SAP inventory movements and inventory management such as moving items between storage locations and issuing goods to process orders. Competencies & Job Requirements Acquire and maintain all required certifications and qualifications for the assigned work area. Be capable and motivated to learn new skills and develop new capabilities on an ongoing basis to contribute to the success of the Process Execution Team. Ability to work effectively in a team environment. Ability to work in and adapt to a changing/demanding environment. Some overtime may be required with minimal advance notice to support business needs. Minimum Qualifications Experience in a pharmaceutical or cGMP regulated environment. Ability to effectively understand, read, write, communicate, and follow instructions in the English language. Good attention to detail; capable of keeping accurate records and performing mathematical calculations. Preferred Qualifications Prior production experience. Experience working in a LEAN manufacturing environment. Knowledge of cGMPs and FDA policies/procedures. Prior inspection experience in a pharmaceutical manufacturing environment. Sponsorship or support for work authorization, including visas, is not available for this position. Resilience is an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, physical or mental disability, genetic information, characteristic, or other non‑job‑related characteristics or other prohibited grounds specified in applicable federal, state, and local laws. Requests for reasonable accommodation can be made at any stage of the recruitment process. Resilience offers employees a robust total rewards program including an annual cash bonus program, a 401(k) plan with a generous company match and our benefits package which is thoughtfully designed to support our employees with great healthcare (including medical, dental and vision), family building benefits, life and disability insurance, paid vacation, paid holidays, other paid leaves of absence, tuition reimbursement and support for caregiving needs. Our target base pay hiring range for this position is $21.50‑$32.00 per hour. Actual base pay is dependent upon a number of factors, including but not limited to, the candidate’s geographical location, relevant experience, qualifications, skills and knowledge. #J-18808-Ljbffr