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Manufacturing Technician II, Inspection (Nights)

National Resilience

United StatesFull-time$21.5–32/hrPosted 5mo agoStill listed 1 day ago

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At a glance

Compensation
$21.5–32/hr
Location
United States
Schedule
Full-time
Work Authorization
US work authorization required

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Requirements

Credentials this posting asks for.

Visual Inspection QualificationAcquire And Maintain All Required CertificationsBachelor's degree

Job overview

Resilience is hiring a Manufacturing Technician II, Inspection (Nights). The Manufacturing Technician II performs equipment operation, visual, cosmetic and physical inspections, line clearances, data collection and batch record entries while supporting 5S and process improvement activities in a cGMP environment.

Key focus areas include Operate assigned machinery and service automated inspection equipment, Perform manual visual, cosmetic, and physical inspection of materials, and Escalate concerns to lead and manager as needed.

Successful candidates bring Visual Inspection Qualification, Experience In Pharmaceutical Or cGMP Regulated Environment, and Effectively Understand, Read, Write, Communicate And Follow Instructions In English. Important skills include Operating Assigned Machinery, Servicing Automated Inspection Equipment, Monitoring Equipment Status, Reintroduction Of Materials, Manually Palletizing Inspected Materials, and Manual Visual Inspection. Preferred (not required): cGMPs, 5S, Problem-Solving, and Manual Tracking Of Performance Data.

Skills & qualifications

RequiredNice to have

Skills

Operating Assigned MachineryServicing Automated Inspection EquipmentMonitoring Equipment StatusReintroduction of MaterialsManually Palletizing Inspected MaterialsManual Visual InspectionCosmetic InspectionPhysical InspectionStarting Up EquipmentMinor Adjustments to MachineryRemoving JamsMinor TroubleshootingMinor Assembly/Disassembly for CleaningMotorized Pallet JacksManual Pallet JacksNon-Motorized LiftsHousekeepingLine Clearance ActivitiesBatch Record EntriesGMP Documentation EntriesMaintaining RecordsMaintaining LogsMathematical ComputationProduct Security ControlsMaterial Handling EquipmentOutgoing Quality LevelJob-Related Safety ProceduresPPEsErgonomicsLOTOHuman SafetyWaste HandlingChemical HandlingSpill ControlsSOPscGMPsOSHA RequirementsMaterial Safety Data SheetsLearning New SkillsDeveloping New CapabilitiesCollaborationAdaptabilityAttention to DetailKeeping Accurate Records5SProblem-SolvingManual Tracking of Performance DataReview Process DocumentsIdentify Process Improvement SuggestionsMaintain QualityManual Cosmetic InspectionManual Physical InspectionEscalate ConcernsStart Up EquipmentRemove JamsUse Material Handling EquipmentMaintain RecordsMaintain LogsReport DiscrepanciesWork in Accordance With SOPsWork in Accordance With cGMPsWork in Accordance With Established Safety ProceduresPrint SOPs/Forms via ECMSLearn New SkillsDevelop New CapabilitiesWork Effectively in a Team EnvironmentAdapt to a Changing/Demanding EnvironmentUnderstand EnglishRead EnglishWrite EnglishCommunicate in EnglishFollow Instructions in EnglishSupport Lean Activities

Qualifications

Visual Inspection QualificationAcquire and Maintain All Required CertificationsExperience in Pharmaceutical or cGMP Regulated EnvironmentPrior Production ExperienceExperience Working in a LEAN Manufacturing EnvironmentPrior Inspection Experience in a Pharmaceutical Manufacturing Environment

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match
Paid Time Off
Tuition Assistance
Parental Leave
Relocation Assistance

Full job description

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 www.resilience.com

Brief Job Description

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, participate in problem-solving and Kaizen events, manual data collection) in accordance with cGMPs.

Primary Responsibilities

  • Perform the duties of operating assigned machinery consisting of servicing automated inspection equipment, monitoring equipment status, reintroduction of materials, manually palletizing inspected materials, and assuring a smooth flow of product.

  • Perform manual visual, cosmetic, and physical inspection of material. Promptly escalate concerns to Lead and Manager/Supervisor as needed. Must obtain and maintain visual inspection qualification.

  • Be able to start up equipment, make minor adjustments to machinery, remove jams, minor troubleshooting, and minor assembly/disassembly for cleaning purpose.

  • Ability to use material handling equipment such as motorized and manual pallet jacks, non-motorized lifts.

  • Perform cleaning, housekeeping and line clearance activities for assigned areas as required to maintain a cGMP environment.

  • Perform batch record and GMP documentation entries. Maintain records and/or logs as required in the performance of job responsibilities. This will include mathematical computation where needed.

  • Knowledge of product security controls and material handling equipment.

  • Responsible for outgoing quality level.

  • Be familiar with job-related safety procedures and hazards including PPEs, ergonomics, LOTO, human safety, material handling, waste handling, chemical handling, and spill controls. Report all discrepancies to process facilitator.

  • Perform work requirements in a responsible manner, in accordance with SOPs, cGMPs and established safety procedures in accordance with OSHA requirements and guidelines. Be familiar with “Material Safety Data Sheets” for area chemicals.

  • Obtain knowledge to be able to print off SOP’s/Forms via ECMS.

Other Responsibilities

  • Support lean activities and process improvement work such as performing 5S in the work area, participating in problem-solving, and manual tracking of performance data for OEE and process improvement analysis.

  • Review process documents such as operational SOPs, forms and batch records for accuracy. Identify and provide suggestions for process improvement while maintaining quality and cGMP compliance as opportunities arise.

  • 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 as needed.

Optional Training / Responsibilities

  • Obtain cold room training/access to be able to transfer materials in and out of the cold rooms.

  • Take proper training to become certified trainer on assigned equipment and process tasks. Train and conduct evaluations on other team members for training qualifications.

  • Obtain a novice to intermediate level of knowledge of SAP inventory movements and inventory management such as moving items from one storage location to another and goods issuing items to process orders as required.

Competencies & Job Requirements:

  • Acquire and maintain all required certifications and qualifications for the assigned work area

  • Capable and motivated to learn new skills and develop new capabilities on an on-going basis to contribute to the success of the Process Execution Team

  • Ability to work effectively in a team environment

  • Candidate should possess the 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

  • Must have the ability to effectively understand, read, write, communicate and follow instructions in the English language.

  • Good attention to detail is required. Individual must be 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, or 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. Excited about Resilience? We encourage you to apply and start a conversation with one of our recruiters.

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