Instrument assembler job description

Job DescriptionHiring Manager is Ellen Felzemburg-Chang

Pay rate *** hr
Hours 6 am to 2:30 pm

Instrument Assembly Associate II
Performs electro-mechanical assembly of flow cytometers, sub-assemblies and related medical device products. Follows established methods and procedures in performing, assembly of optical, mechanical, fluidic and electronic components and
assemblies. Employs high standards of workmanship to ensure high quality products are produced on schedule.

Performs instrument assembly by following released procedures
Must be able to read and understand: assembly instructions, work orders, Bills of Materials, Standard Operation Procedures, and all other documentation used to control our products and processes.
Confers with engineers, technicians, production personnel, and others regarding assembly procedures.
Must have the ability to create and maintain productive working relationships within the work team and with other functions. Collaborates with peers to achieve shared departmental goals.
Keep work area clean organized and safe
Fill out time sheets and all other required paperwork accurately and on time. Keeps training file up to date at all times.
Other duties may be assigned.

Ability to effectively communicate information and respond to questions both verbally and in writing.
Good mechanical aptitude, dexterity and hand/eye coordination. Must be able to reach, bend and lift 35 lbs on a daily basis
PC or MAC user, familiar with: Word, Excel, and Windows.

Must be willing to be trained in other areas of production where the skill level requirements may be lower
Knowledge and adherence to safety procedures and programs

Minimum Requirements (Must Haves):
Typically requires an High school or GED degree.
Ability to effectively communicate information and respond to questions both verbally and in writing.
Good mechanical aptitude, dexterity and hand/eye coordination. Must be able to reach, bend and lift 35 lbs on a daily basis
Experienced PC or MAC user, familiar with: Word, Excel, Windows and/or MAC OS
Knowledge of PCs and networking environments
Must be able to follow established methods and procedures in performing ex: assembly of optical, mechanical, fluidic and/or electronic components, assemblies and testing.

Desirable Qualifications (Nice to Have):
Experience working in a medical device manufacturing organization.
3+ years related experience in a high tech, manufacturing environment
Experience with Excel, Visio, Power Point
Knowledge of ISO 9000, cGMP 21 CFR part 820 or FDA
Performs electro-mechanical assembly and sub-assemblies for medical device products.
SAP experience preferred

Job DescriptionHiring Manager is Ellen Felzemburg-Chang

Pay rate *** hr
Hours 6 am to 2:30 pm

Instrument Assembly Associate II
Performs electro-mechanical assembly of flow cytometers, sub-assemblies and related medical device products. Follows established methods and procedures in performing, assembly of optical, mechanical, fluidic and electronic components and
assemblies. Employs high standards of workmanship to ensure high quality products are produced on schedule.

Performs instrument assembly by following released procedures
Must be able to read and understand: assembly instructions, work orders, Bills of Materials, Standard Operation Procedures, and all other documentation used to control our products and processes.
Confers with engineers, technicians, production personnel, and others regarding assembly procedures.
Must have the ability to create and maintain productive working relationships within the work team and with other functions. Collaborates with peers to achieve shared departmental goals.
Keep work area clean organized and safe
Fill out time sheets and all other required paperwork accurately and on time. Keeps training file up to date at all times.
Other duties may be assigned.

Ability to effectively communicate information and respond to questions both verbally and in writing.
Good mechanical aptitude, dexterity and hand/eye coordination. Must be able to reach, bend and lift 35 lbs on a daily basis
PC or MAC user, familiar with: Word, Excel, and Windows.

Must be willing to be trained in other areas of production where the skill level requirements may be lower
Knowledge and adherence to safety procedures and programs

Minimum Requirements (Must Haves):
Typically requires an High school or GED degree.
Ability to effectively communicate information and respond to questions both verbally and in writing.
Good mechanical aptitude, dexterity and hand/eye coordination. Must be able to reach, bend and lift 35 lbs on a daily basis
Experienced PC or MAC user, familiar with: Word, Excel, Windows and/or MAC OS
Knowledge of PC s and networking environments
Must be able to follow established methods and procedures in performing ex: assembly of optical, mechanical, fluidic and/or electronic components, assemblies and testing.

Desirable Qualifications (Nice to Have):
Experience working in a medical device manufacturing organization.
3+ years related experience in a high tech, manufacturing environment
Experience with Excel, Visio, Power Point
Knowledge of ISO 9000, cGMP 21 CFR part 820 or FDA
Performs electro-mechanical assembly and sub-assemblies for medical device products.
SAP experience preferred

Executes a variety of tasks that includes receipt and verification of materials, calibration and operation of equipment, assembly of components and kits, performing calculations, and completing required documentation
following Good Documentation Practices.

Responsibilities

* Performs basic manufacturing tasks and basic maintenance of semiautomatic and/or automated assembly equipment and tools for both instruments and consumables.
* Performs calibration and operation of equipment, dispensing or packaging dry and/ or wet products, capping and torqueing of bottles, assembly of components and kits, performing calculations
* Completing required documentation following Good Documentation Practices.
* Verifies required materials against the process order and prepares work area for production operation.
* Strictly follow work instructions to execute production tasks.
* Performs in-line quality inspection and weighs finished products to confirm it meets specifications.
* Inspects product using visual, automated, electronic and mechanical inspection procedures.
* Performs line clearance.
* Completes required documentation in an accurate and timely manner following Good Documentation Practices (GDP).
* Ensures scrap and waste are disposed of properly.
* Operates motorized and non-motorized equipment to move materials, supplies and equipment as instructed.
* Adheres to all policies and procedures relating to Good Manufacturing Practices (GMP/Quality Systems).
* Complies with 5S requirements.
* Completes special projects and other duties as assigned.
* Trains other employees.
* Basic troubleshooting as needed.
* Completes and maintains quality records.
* Cross train on 1-2 production lines.
* Strictly follows PPE procedures.
* Monitors and maintains inventory at their work areas.
* Keeps supervisor appraised of any abnormal production issues.
* May work on different shifts.

Qualifications

* High school diploma or equivalent preferred.
* 0-3 plus years related experience or equivalent combination of education and experience.
* Ability to read, to write, to comprehend, and follow written instructions.
* Basic math, problem solving and computer skills.
* Transaction in SAP a plus.
* Experience operating manual, semi-auto and automatic production machinery, preferred.
* Must be able to lift up to 50 lbs and sit or stand for long periods of time
* Must be able to stoop, squat, reach, push and lift frequently.
* Utilize basic technical skills to troubleshoot equipment.
* Ability to prioritize work.
* Accurate and detail-oriented.
* Team player/ flexible/ attentive to detail and quality minded.
* Possesses positive attitude with ability to lead team to achieve department goals and objectives.
* Ability to work a flexible schedule, with overtime as needed.
* Ability to train others.
* Basic computer skills are desirable.

Vaccination Requirement:

Ability and consent to upload proof of completed Covid-19 vaccination into our secure database within 3 days of start date.

About Bio-Rad:

Bio-Rad is a global leader providing a broad array of clinical diagnostics and life science research products. With a team of more than 8,000 employees and a global network of operations serving our customers, we help people live longer, healthier lives.

Bio-Rad was founded over six decades ago and has continued to provide the healthcare industry with innovative and useful products that help life science researchers accelerate the discovery process and medical diagnostic labs obtain faster, better results.

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Agency Non-Solicitation:

Bio-Rad does not accept agency resumes, unless the agency has been authorized by a Bio-Rad Recruiting Representative. Please do not submit resumes unless authorized to do so. Bio-Rad will not pay for any fees related to unsolicited resumes.