Senior Manufacturing Technician, Consumables Manufacturing

Bruker Daltonics; Tucson (AZ); Vor Ort; USD 36.000 - 57.000; Vollzeit

Benefits dieser Stelle

401(k) with company match

Employee stock purchase plan

Medical and dental plans

Life insurance

Disability insurance

Paid time off

Zusammenfassung

Bruker Daltonics in Tucson, AZ, is seeking a Senior Manufacturing Technician to manufacture IVD consumable components and kits in a cGMP environment. You will be responsible for aseptic filling, equipment setup, and documentation to support Wave line production.

Responsibilities include maintaining equipment, training staff, and ensuring production records meet GDP standards while managing inventory and participating in process improvements.

Qualifikationen

• High school diploma or equivalent required.
• Associate degree in a technical, scientific, engineering technology, manufacturing technology, or related discipline preferred.
• Equivalent combinations of education, technical training, and related work experience will be considered in lieu of formal education.
• Minimum 5 years of experience in regulated manufacturing required.
• Experience with aseptic manufacturing processes, liquid filling operations, consumable manufacturing, or automated production equipment strongly preferred.

Aufgaben

• Manufacture IVD consumable components and kits in accordance with approved procedures, cGMP requirements, and quality standards.
• Perform consumable manufacturing activities including aseptic filling, component preparation, equipment setup, labeling, packaging, lot yield verification, and production record completion.
• Set up, operate, maintain, troubleshoot, and support filling equipment and associated manufacturing systems used in consumable production.
• Support manufacturing activities for existing and new products produced on the Wave card manufacturing line, including implementation of approved equipment modifications, process changes, and production readiness activities.
• Identify, document, and communicate manufacturing, equipment, and process-related issues; assist with troubleshooting activities; and support quality and manufacturing investigations and corrective action activities as required.
• Provide guidance to manufacturing personnel regarding established procedures, equipment operation, and manufacturing practices, and assist with training activities as assigned.
• Create, revise, and maintain manufacturing documentation including work instructions, equipment procedures, and production records in accordance with Good Documentation Practices (GDP).
• Manage manufacturing materials and inventory, including Kanban replenishment, material transactions, issuance activities, inventory reconciliation, and movement of materials through applicable business systems.
• Perform and support equipment maintenance activities including routine upkeep, preventive maintenance, calibration tracking, and maintenance documentation.
• Train and mentor technicians and other manufacturing personnel on established manufacturing processes, procedures, and equipment operation.
• Perform other duties as assigned.

Kenntnisse

cGMP knowledge

GDP knowledge

Aseptic manufacturing

Documentation skills

Cross-functional collaboration

Training others

Problem-solving

Attention to detail

Ausbildung

Associate degree in technical/engineering technology

High school diploma or equivalent

Equivalent combinations considered

Tools

ERP/MRP systems

Microsoft Office

Automation equipment

Jobbeschreibung

The Senior Manufacturing Technician is responsible for manufacturing in vitro diagnostic (IVD) consumable components and kits in a cGMP regulated environment. This position supports consumable production operations through aseptic filling, equipment setup and maintenance, production support, documentation, inventory management, and quality compliant manufacturing practices.

The role serves as an experienced manufacturing resource for consumable filling processes and supports production of new and existing products on the existing Wave card manufacturing line, including implementation of approved equipment and process changes required for manufacturing operations.

Responsibilities

Essential Functions

• Manufacture IVD consumable components and kits in accordance with approved procedures, cGMP requirements, and quality standards.
• Perform consumable manufacturing activities including aseptic filling, component preparation, equipment setup, labeling, packaging, lot yield verification, and production record completion.
• Set up, operate, maintain, troubleshoot, and support filling equipment and associated manufacturing systems used in consumable production.
• Support manufacturing activities for existing and new products produced on the Wave card manufacturing line, including implementation of approved equipment modifications, process changes, and production readiness activities.
• Identify, document, and communicate manufacturing, equipment, and process-related issues; assist with troubleshooting activities; and support quality and manufacturing investigations and corrective action activities as required.
• Provide guidance to manufacturing personnel regarding established procedures, equipment operation, and manufacturing practices, and assist with training activities as assigned.
• Create, revise, and maintain manufacturing documentation including work instructions, equipment procedures, and production records in accordance with Good Documentation Practices (GDP).
• Manage manufacturing materials and inventory, including Kanban replenishment, material transactions, issuance activities, inventory reconciliation, and movement of materials through applicable business systems.
• Perform and support equipment maintenance activities including routine upkeep, preventive maintenance, calibration tracking, and maintenance documentation.
• Train and mentor technicians and other manufacturing personnel on established manufacturing processes, procedures, and equipment operation.
• Perform other duties as assigned.

Qualifications

Formal Training / Education

• High school diploma or equivalent required.
• Associate degree in a technical, scientific, engineering technology, manufacturing technology, or related discipline preferred.
• Equivalent combinations of education, technical training, and related work experience will be considered in lieu of formal education.

Experience

• Minimum 5 years of experience in regulated manufacturing required. Experience in in vitro diagnostic (IVD), medical device, biotechnology, pharmaceutical, or other cGMP manufacturing environments preferred.
• Experience with aseptic manufacturing processes, liquid filling operations, consumable manufacturing, or automated production equipment strongly preferred.

Knowledge, Skills, And Abilities

• Working knowledge of Current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), manufacturing procedures, equipment operation, and safety requirements in a regulated manufacturing environment.
• Knowledge of basic biology and microbiology principles applicable to IVD, biotechnology, medical device, or life science manufacturing.
• Working knowledge of manufacturing troubleshooting techniques and the ability to assist with investigation of equipment, process, and product quality issues.
• Experience supporting process improvements, manufacturing investigations, and implementation of new products in a regulated manufacturing environment.
• Strong written and verbal communication skills, including the ability to prepare technical documentation, communicate effectively with cross-functional teams, and train others.
• Ability to perform assigned work with minimal day-to-day supervision while following established procedures, priorities, and departmental guidance.
• Ability to collaborate effectively with Quality, Engineering, Supply Chain, and external suppliers.
• Strong organizational, planning, time-management, and recordkeeping skills with a high level of attention to detail and accuracy.
• Basic mathematical skills required for manufacturing calculations, inventory transactions, and production record review.
• Ability to learn and adapt to new equipment, manufacturing processes, and technologies.
• Proficiency with Microsoft Office applications and manufacturing business systems such as ERP/MRP systems.

Physical Requirements

• Able to stand and walk for extended periods throughout the workday.
• Able to perform repetitive motions including grasping, reaching, bending, twisting, and lifting.
• Able to lift and carry up to 50 pounds.
• Able to wear required personal protective equipment (PPE) for extended periods.
• Able to work in laboratory, classified-area, and manufacturing environments.
• Able to move between multiple buildings and facilities as required.

Salary and Benefits

At Bruker, the base salary is part of our total compensation. The estimated hourly range for this full-time position is between $25.97/hr and $41.59/hr and provides an opportunity to progress as you grow and develop within a role. Please note this position is eligible for Overtime compensation. The base salary for the role will depend on several job-related factors, including, but not limited to, education, training, experience, the geographic location of the successful candidate, skills, competencies, job-related knowledge, and travel requirements for this position. Full-time employees may also be eligible for a performance-related incentive in addition to a full range of benefits, including 401(k) with company match, an employee stock purchase plan, medical and dental plans, life insurance, short-term and long-term disability insurance, employee assistance program and paid time off including vacation, sick time and holidays, and more.

Equal Opportunity Statement

Bruker is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, national origin, disability, veteran status, and other protected characteristics.

Export Control

Certain positions at Bruker require compliance with export control laws and as a result, all interviewed candidates for all positions will be screened pre-interview to determine their eligibility in light of export control restrictions.