Manufacturing Associate II (Team A)

20 Nov 2024

Vacancy expired!

With the support of Supervisors, Trainers, Quality Techs, and Engineering, a Manufacturing Associate II is essential to the manufacture of injection molded consumables for the use of Cepheid/Danaher Life Science Diagnostics finished goods. Associate II will be expected to provide guidance for Associate I while ensuring the successful completion and compliance in the initiation, maintenance, operation, packaging, inspection, environmental maintenance, and environmental control through injection molding. Manufacturing Associate II are the foundation to the Quality and Safety culture within the site and will be responsible to report as applicable, document when appropriate, and adhere to pertinent regulations and policies.ESSENTIAL JOB RESPONSIBILITIES: Responsible for the production of injection molded consumables within the Lodi facility controlled environments

Adherence to applicable health and safety procedures and will be required to wear appropriate Personal Protective Equipment

Recognizes when minor issues and defects and utilizes the processes in place to resolve the occurrence

Applies reasonable logical and rational reasoning to control contingency, gaps, or nonconformance in the process

Completes necessary documentation and/or escalates accordingly

Collaborates with cross functional teams on special projects and troubleshoots problems

Reports production units, job numbers, and labor hours

Monitors machine problems and informs the Supervisors and Leads of any issues

Responsible for following documentation compliance

Operates Manufacturing Equipment for Basic Start and restart functions of the robot, press trouble shooting, conveyor feeding trouble shooting, and basic injection alarm resolution

Responsible for auxiliary production devices to support production including scanners, pads, and removable equipment

Maintains cleanroom standards, practices, work equipment and housekeeping according to Standard Operating Procedures

Coordinates and confirms rework for a tote, bin, or lot

Applies basic lean principals for First in and First Out (FIFO), Kaizen, 5S, and Standard Work

Adherence of regulations and procedures pertaining to the manufacture of medical devices including basic Quality Assurance, Good Manufacturing Practices, Standard Work Instructions, 21 CFR Part 820

Understands QMS requirements for traceability

Responsible for traceability during the production of the lot

Documents inspections, operations, rework, or tests performed consistently and in real time

Responsible for quality, accuracy, and timeliness of information, data, and communication within the Device History Record or Electronic Batch Record production log

Executes line clearance during cavity changes

Provides training to other associates as needed

TRAINING RESPONSIBILITIES: (REQUIRED)

Complete all assigned and required training satisfactorily and on time

For people managers, ensure your associates attend and complete all required trainings satisfactorily and on time.

MINIMUM REQUIREMENTS:

Education or Experience (in years):

High school degree (or equivalent experience) with 1-2 years of relevant work experience

Knowledge and Skills:

Ability to comprehend verbal and written English to interpret documents such as safety rules, operating instruction, and procedure

Basic knowledge of Microsoft software (Word, PowerPoint, Excel, Outlook)

Ability to cooperate with co-workers in areas of safety, quality, production, maintenance, and engineering

Exhibits the ability to work calmly and accurately under varied conditions

Basic Knowledge of Quality Systems

Good Documentation Practices

Right First Time average greater than 99% effectively

Technical Knowledge and Skills:

Mechanical, Safety, Compliance, and Quality aptitude

Problem Solving, Quality Data, and Mathematics

General computation including addition, subtraction, multiplication, and division of all units of measure including whole numbers, common fractions, metric measurement, and decimals

Capable of using data to make determinations to resolve production related issues

Inspection and Inspection equipment

Ability to handle, interpret, and troubleshoot basic measuring devices such as a standard tape measurement, a micrometer, Caliper, pin gauges, drop gages, and height gages

Understands gage repeatability, gage resolution, and techniques for measurement

Recognizes and interprets measurements that are outside a specified range

Understands specifications, tolerance

Basic understanding of part drawings

Capability to understand the part control plan

Aptitude for interpreting the lot and tote acceptance criteria

Physical requirements/abilities required:

Ability to work in a clean room environment

Ability to visually determine minute geometrical quality characteristics

Skilled hand-eye coordination for handling critical parts

Must have appropriate vision to perform detailed quality inspection as outlined in the SOPs, WIs, control plans, visual aids, and product drawings

Ability to stand at workstation for extended periods of time (8 hours or more) operating equipment and packaging products while closely monitoring and visually inspecting products and process

Ability to lift or carry 25 lbs. totes

Moves freely around machine to assure all working mechanisms are operating properly

Able to reach parts in machine and make adjustments, set-ups, change overs, inspections, feeding and securing parts

Posture and Movement equal to but not less than requirement of the following:1-2 hours2-4 hours4-6 hours6-8 hoursStand☐☐☐☒Walk☐☒☐☐Sit☐☐☒☐Bend☒☐☐☐Reach☐☐☐☒Grasp☐☐☐☒Push/Pull☐☒☐☐Squat☒☐☐☐PREFERRED REQUIREMENTS: Minimum two years in Manufacturing Environment

Experience working in a clean room environment

When you join us, you’ll also be joining Danaher’s global organization, where 69,000 people wake up every day determined to help our customers win. As an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System (https://www.danaher.com/how-we-work/danaher-business-system) tools and the stability of a tested organization.Danaher Corporation and all Danaher Companies require all US and Puerto Rico employees to be fully vaccinated against COVID–19 as a condition of employment, subject to reasonable accommodation as required by law.Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.The EEO posters are available here (https://www.dol.gov/agencies/ofccp/posters) .We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at applyassistance@danaher.com to request accommodation. If you’ve ever wondered what’s within you, there’s no better time to find out.Operating Company: Cepheid

Full-time
  • ID: #23061669
  • State: California Newark 94560 Newark USA
  • City: Newark
  • Salary: USD TBD TBD
  • Showed: 2021-11-20
  • Deadline: 2022-01-19
  • Category: Et cetera