Jobs in Manufacturing

Electronic Technician /Assembler 25
E Talent Network    02-14-2020 North Charleston, SC, USA

Position: Electronic Technician /Assembler

Location: North Charleston, SC 29418

Duration: 12+ months

 

Job Description:

 

  • Ability to select correct parts, materials, tools, assemblies, standards, hardware, etc. to Install, fit, fasten, align, adjust and perform the necessary pre-installation assembly work to accomplish the installation of wire provisions, wire bundles and harnesses, power feeders, signal data lines, and fiber optic harnesses requiring the use of production and engineering prints to determine exact locations.
  • Install cables and wire bundles when similar in complexity and incidental but necessary to the expeditious accomplishment of work assignment.
  • Report job constraints such as: errors caused by workmanship, defects in parts, materials, assembly procedures, tools, sequences, etc., in accordance with Boeing procedures.
  • Perform any repairs, rework, functional checks and the incorporation of authorized changes, etc., as outlined by Lead. Remove and/or replace installed components and any related parts.
  • Ability to read and understand blueprints, drawings, schematics, engineering dispositions and instructions.
  • Be safety conscious; employ the use of safety glasses, safety harnesses, respirators, boot socks, and other pertinent safety equipment 100% of the time. Exhibit exemplary housekeeping and Foreign Object Debris (FOD) standards.
  • Maintain clean, neat, organized and FOD free work area. Possess understanding and knowledge of basic computer systems and programs.
  • Ability stand for long periods of time, and work in elevated and/or confined spaces as required. Frequent overhead work may be required. Frequent overtime may be required.

 

Ability to perform the following requirements:

 

  • Lift less than 25 pounds (Occasional lifting of 21-35 pounds), bend and twist at the waist, walk, crawl, crouch, stand for long periods, kneel, reach, climb/balance, flexion/extension
  • Contact with sealants and solvents, exposure to noise, working on elevated platforms
  • Use personal protective gear for face, eyes, ears, hand, and arms as required.
  • Pass visual acuity and color perception tests
  • Obtain & maintain training certifications as required to support assignment responsibilities
  • Occasional (1 to 3 hrs) finger manipulation
  • On occasion, a 2-person lift may be necessary for weights greater than 50 lbs
  • Frequent reaching overhead (3 to 6 hrs)
  • Frequent balancing on a ladder, steps, or uneven surfaces
  • Occasional climbing on 3-12 ft ladders or stands
  • Rotation of head/neck, sitting, crawling, squatting, bend/stoop, lying down, and operate foot controls
  • Frequent exposure to noise
  • Candidates must be able to be moved as needed to the evening, afternoon, or morning shifts if necessary for the business need.

 

Education / Experience:

  • High school diploma or GED and typically 1 or more years' related experience or an equivalent combination of education and experience. (HS Diploma or GED required)
General Worker 9
Integrated Resources, Inc    02-14-2020 Cleveland, MS 38732, USA

Title  General Worker

Location – Cleveland, MS

Contract 12 months

 

Job Duties:
• Must clean and setup sub-assembly equipment.
• Must startup and verify readiness of machine and support equipment prior to
production
• Must monitor equipment and perform minor adjustments.
• Must have quality checker training to perform and document in-process quality
Inspections
• Must verify correctness of material
• Must supply parts to operation.
• Must perform general housekeeping duties.
• Must complete production release documentation associated with the operation.
• Must stack boxes on pallets.
• Must perform line clearances
• Must pull parts and stage batches per B.O.M.
• Must have knowledge of both plant and departmental health and safety regulations and comply with said regulations accordingly.
• Must perform all other duties and responsibilities as determined by supervision/management.

Qualifications:
• Ability to lift, push, pull up to 50 pounds repetitively
• Must stand for long periods of time and walk frequently.
• Audiometric testing required
• Hearing protection required
• Ability to climb ladders
• Must be able to work without direct supervision.
• Ability to read, write, count, use maintenance tools and calculator.
• Must have minor mechanical troubleshooting ability.
• Must be able to work overtime as required.
• Must be able to work during plant shutdown and holidays as needed.
• High School diploma or equivalent.

 

 

Manufacturing Operator 18
Integrated Resources, Inc    02-12-2020 Lenexa, KS, USA

Title: Manufacturing Operator

Location: Lenexa, KS

Duration:6 months

 

Job responsibilities:

Performs production procedures in accordance with Standard Operating Procedures (SOP), resulting in quality product.

Formulation Tasks:

  • Gather chemicals from different storage locations (i.e. room temperature, coolers and freezers)
  • Use designated weights from 1 gm to 250 kg to verify scales.
  • scoop and dump chemicals into containers up to 1,000 kg.
  • place finished containers on a scale to verify gross weight.
  • Use a computer to capture production information.
  • Approve related reports and complete related documentation.

Blending and Milling Tasks:

  • Check rooms and equipment for cleanliness and damage prior to use.
  • locate formulated chemicals for charging into blenders.
  • setup and operate blenders in accordance with required specifications.
  • setup and operate pin mill system in accordance with required specifications.
  • setup and operate nitrogen conveying system.
  • setup and operate clean-in-place (CIP) systems.
  • control and monitor processes with an operator interface terminal (OIT).
  • use a computer to capture production information.
  • approve related reports and complete related documentation.

Packaging Tasks:

  • Use designated weights from 1 gm to 25 kg to verify scales are in specification.
  • Confirm material and supplies are staged.
  • Set up and operate automated packaging equipment within specified tolerances.
  • Fill powder into final containers up to 100 kg in weight.
  • Perform label reconciliation to ensure proper package labeling.
  • Move pallets of product to finished goods storage.
  • Approve related reports and complete related documentation.
  • Must be able to properly gown and comply with all cGMP and PPE guidelines
  • Set-up equipment ensuring operations are consistent with current operating procedures.
  • Equipment components can weigh up to 50 kg and have critical tolerance requirements.
  • Report equipment failures and work with repair personnel to correct problems
  • Performs procedures resulting in the cleaning of manufacturing equipment and facilities.
  • Continually increases proficiency and understanding of manufacturing processes and systems.
  • Able to Read and Understand all written procedures as outlined in SOP's,
  • Work Instructions and Master Batch Records (MBR).
  • Completes all documentation in accordance with current Good Manufacturing Practices (cGMP) and SOP.
  • Perform operations in compliance with rules and in a safe, orderly manner.
  • Participates in training programs as directed by the Department Supervisor.
  • This may include monthly safety meetings, internal safety audits of operations, respirator training, and skill-based pay.
  • Follow production procedures and safety policies at all time.
  • Maintain good housekeeping in working areas.
  • Reports any unsafe working conditions or safety concerns through the corporate Medgate system.
  • Reports any property damage to the shift supervisor immediately Takes part in and contributes to a safe working environment by following corporate and departmental safety regulations.
  • Use, clean, and store all personal protective gear appropriately
  • Makes recommendations for continuous process improvements in the manufacturing area.
  • Actively participates in Quality systems practices.

 

Education

  • High school diploma or equivalent with good math and reading skills.
  • Experience
  • Experience in a manufacturing environment preferably with cGMP or regulatory compliance practices.
  • Demonstrated mechanical aptitude including previous maintenance experience with process equipment or mechanical systems.
  • Dry product processing and packaging experience.

 

Knowledge and Skills

  • Ability to read and follow written and verbal instructions.
  • Ability to perform basic metric and other mathematical calculations.
  • Ability to work independently and as part of a team.

 

Soft Skills

  • Works as a productive member of a team
  • Ability to effectively communicate with others.
  • Basic mechanical aptitude
  • Basic problem solving

 

Skills Required:

  • Must be able to lift 5 pounds for a six-hour period, or as required.
  • Occasionally required to lift up to 50 pounds.
  • Must be able to maneuver and position mechanical components up to 50 kg.
  • Must be able to stand for long periods of time
  • Must be able to work within a controlled space without excessive perspiration

 

 

Manufacturing Associate 39
Integrated Resources, Inc    01-13-2020 Brooklyn Park, MN, USA

Title: Manufacturing Associate/Lab Associate

Location: Brooklyn Park, MN

Duration: 12 Months+

 

Description:
*TEMP TO PERM ROLES*


OBJECTIVES:

  • Perform and document daily manufacturing operations according to SOP’s in a cGMP environment
    • Operate biologics production equipment (bioreactors, filtration units, chromatography systems and fixed/portable vessels)
    • Execute validation protocols
    • Create or revise cGMP documents

    ACCOUNTABILITIES:
  • With general supervision or guidance will assemble and/or operate biologics production equipment, such as bioreactors, filtration units, chromatography systems and fixed/portable vessels.
    • Perform basic trouble shooting
    • Performs/assists with processing steps and/or manufacturing support activities by monitoring process parameters in batch record and control systems
    • Documents cGMP data and information for processing steps and/or equipment activities while following standard operating procedures. Key documentation includes batch records, work orders, and equipment logbooks.
    • Executes batch records and validation protocols under supervision/direction of others
    • Author and review equipment use logs
    • Performs inventory transactions in SAP
    • Performs data entry into LIMS
    • Accountable for completing assigned trainings within required timeline and actively participate in training activities.
    • Stock production and cleaning supplies
    • Perform cleaning/sanitizing production rooms and equipment
    • Other duties as assigned

    EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS:

Preferred combination of education and experience:
• Bachelor’s degree in Science or Engineering; or
• Associate’s degree in science-related area and 1 or more years of relevant experience; or
• High school diploma or GED and 3 or more years of relevant experience.
• Experience in a regulated environment preferred

Knowledge, competencies and skills:
• Understanding of current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP) preferred
• Familiar or experience with cGMP within Biotech or Pharmaceutical operations preferred
• Knowledge of non-manufacturing functions such as QC, Regulatory, QA, and/or Materials Management a plus
• Prior experience with lab equipment a plus
• Knowledge of mathematical calculations (addition, subtraction, division, multiplication) and rounding.
• Must have excellent written and oral communication skills
• Must be team and detail-oriented and able to work in a fast-paced environment.
• Ability to perform basic computer operations, such as ability to navigate in MS Office, use email, and complete training using Web Based Training (WBT)
• Must be able to read and understand English

PHYSICAL DEMANDS:
• Stand and Walk - Required to stand/walk while operating manufacturing/computer equipment for several hours at a time daily
• Carrying weight, Pushing, Pulling Lifting - Required to carry, lift, push, and/or pull up to 50 pounds several times a day for 15-minute durations while handling production equipment and/or materials
• Climb - Required to climb (use of stepladders/stairs in production areas, or stairwells in work campus) several times a day for 15-minute durations.
• Bend and Kneel - Required to bend, kneel, or crawl several times a day for 15-minute durations
• Overhead work - Required to perform overhead reaching during handling of production materials/files/supplies several times a day for 15-minute durations
• Moving Head and Neck – Required movement of head/neck while using computer applications and handling of production equipment and materials several times a day for several hours at a time
• Twisting - Required movement of twisting waist while setting up equipment several times a day for several hours at a time
• Repetitive Use - Required repetitive use of arms and wrists while setting up equipment several times a day for several hours at a time


Manufacturing Engineer I 29
TekWissen LLC    12-20-2019 Goleta, CA, USA

Job Description: 

  • Candidates will be responsible for manufacturing engineering support for focal plane fabrication for both engineering/development and production programs.  
  • Duties include planning sequence of operations and specifies procedures for the fabrication of tools and equipment and other functions that affect product performance. 
  •  Evaluates product nonconformances.  
  • Develops rework procedures for non-conforming parts.  
  • Inspects performance of machinery, equipment, and tools to verify their efficiency, and investigates and initiates corrective action of problems and deficiencies to ensure product quality.  
  • Develops manufacturing processes that are applicable to statistical process control, and may develop those techniques.  
  • Provides guidance to engineering regarding design concepts and specification requirements to best utilize equipment and manufacturing techniques.  
  • Assist production teams in meeting production goals through the day to day production support and process improvements. 

Additional Job Details:

 Required Skills: 

  • Excellent communication skills within a cross-functional team environment, both written and oral.  Demonstrated critical thinking skills including the ability to quickly recognize and resolve problems.  Must be organized with the ability to plan and coordinate multiple tasks.  
  •  Able to work independently with minimal supervision.  
  •  Good mechanical aptitude and/or chemical handling ability  

Desired Skills: 

  •  Familiarity with semiconductor processing equipment, methods, and processes  
  •  Familiarity with a cleanroom work environment (Class 100)  
  •  Previous work experience or internship in a professional engineering firm  
  • Ability to read and interpret technical drawings or schematics  

Required Education:  

  •  Bachelor of Science degree in engineering or science.
Manufacturing Support Coordinator 28
TekWissen LLC    12-20-2019 Carlsbad, CA, USA
Job Description:
  • You will work in a team-based environment within a manufacturing department responsible for producing molecular biology reagents for use in research in the life sciences industry.
Responsible for:      
  • Works in a laboratory environment.
  • The primary responsibilities will be to wash and sterilize labware.
  • Proper technique for cleaning glassware and plasticware from the labs.
  • Operating dishwashers, autoclaves, pH meters, scales, and mixers.
  • Picking up glassware and non-hazardous waste in MGF and R&D labs.
  • Learning and following all departmental SOPs, guidelines, and procedures
  • Entering data into manufacturing batch records, open Problem Notifications if needed.
  • Manufacturing of solutions, media and agar plates using aseptic technique.
  • Ability to maintain production standards and efficiencies.
  • Performing job duties with high attention to detail.
  • Maintaining accurate inventory.
  • Complying with all company safety regulations and procedures and report non-compliance.
  • Serving as an effective safety steward by ensuring accurate reporting of near misses and attending safety training.
  • Knowledge of MSDS for relevant products.
  • Operating in a safe work environment through continuous safety awareness and full compliance with all EH&S programs and activities.
  • Provide assistance to adjacent groups after daily duties have been achieved.
  • Perform other related duties as assigned by the supervisor.
  • This position requires working in a timely and efficient manner to perform lab support duties for the client facility in Carlsbad.
Education:
  • High school diploma or equivalent required.
  • Experience in a related field (i.e. working in a lab environment), preferably a manufacturing environment; or equivalent combination of education and experience is preferred
  • Must be able to work safely with chemicals and hazardous materials.
  • Demonstrates strong communication skills.
  • Must be able to adapt and be flexible in a fast-paced manufacturing environment.
  • Must be able to follow verbal and written instructions.
  • Well organized, detail-oriented and proficient at multitasking.
  • Works well in a team environment and individually.
  • Displays a positive attitude toward the job and others.
  • Must be highly motivated and dedicated.
Working Conditions:
  • While performing the duties of this job, the employee is regularly required to sit, stand, walk, talk and hear; use hands to finger, handle or feel; and reach with hands and arms.
  • May be required to stand for long periods of time while performing duties.
  • Close vision and ability to adjust focus required.
  • Regularly required to lift up to 30 pounds.
  • May be required to lift the weight of 45 pounds or more, with assistance and/or with equipment on occasion.
Questions:
  • Experiences working in a laboratory environment
  • Education
  • Manufacturing Environment Experiences
Manufacturing Support Coordinator 24
TekWissen LLC    12-20-2019 Carlsbad, CA, USA
Job Description:
  • You will work in a team-based environment within a manufacturing department responsible for producing molecular biology reagents for use in research in the life sciences industry.
Responsible for:      
  • Works in a laboratory environment.
  • The primary responsibilities will be to wash and sterilize labware.
  • Proper technique for cleaning glassware and plasticware from the labs.
  • Operating dishwashers, autoclaves, pH meters, scales, and mixers.
  • Picking up glassware and non-hazardous waste in MGF and R&D labs.
  • Learning and following all departmental SOPs, guidelines, and procedures
  • Entering data into manufacturing batch records, open Problem Notifications if needed.
  • Manufacturing of solutions, media and agar plates using aseptic technique.
  • Ability to maintain production standards and efficiencies.
  • Performing job duties with high attention to detail.
  • Maintaining accurate inventory.
  • Complying with all company safety regulations and procedures and report non-compliance.
  • Serving as an effective safety steward by ensuring accurate reporting of near misses and attending safety training.
  • Knowledge of MSDS for relevant products.
  • Operating in a safe work environment through continuous safety awareness and full compliance with all EH&S programs and activities.
  • Provide assistance to adjacent groups after daily duties have been achieved.
  • Perform other related duties as assigned by the supervisor.
  • This position requires working in a timely and efficient manner to perform lab support duties for the client facility in Carlsbad.
Education:
  • High school diploma or equivalent required.
  • Experience in a related field (i.e. working in a lab environment), preferably a manufacturing environment; or equivalent combination of education and experience is preferred
  • Must be able to work safely with chemicals and hazardous materials.
  • Demonstrates strong communication skills.
  • Must be able to adapt and be flexible in a fast-paced manufacturing environment.
  • Must be able to follow verbal and written instructions.
  • Well organized, detail-oriented and proficient at multitasking.
  • Works well in a team environment and individually.
  • Displays a positive attitude toward the job and others.
  • Must be highly motivated and dedicated.
Working Conditions:
  • While performing the duties of this job, the employee is regularly required to sit, stand, walk, talk and hear; use hands to finger, handle or feel; and reach with hands and arms.
  • May be required to stand for long periods of time while performing duties.
  • Close vision and ability to adjust focus required.
  • Regularly required to lift up to 30 pounds.
  • May be required to lift the weight of 45 pounds or more, with assistance and/or with equipment on occasion.
Questions:
  • Experiences working in a laboratory environment
  • Education
  • Manufacturing Environment Experiences
Manufacturing Technician I 24
TekWissen LLC    12-17-2019 Frederick, MD, USA

Job Summary: 

  • To support the Fill/Finish Department by Filling, capping, labeling, and assembling both sub-assemblies and finished good products 

Job Responsibilities: 

  • Fill, cap, and label vials, bottles, and tubes working both individually or as part of a team in accordance with established standard operating procedures to ensure customers receive a product that meets or exceeds quality specifications. 
  • Effectively communicate and interface with workgroups to ensure the completion of daily production. 
  • Work in both standard and cleanroom environments while adhering to room-specific PPE requirements. 
  • Safely operate both manual and automated filling equipment, as required. 
  • Satisfactorily complete client training requirements on time and operate within all ISO and FDA standards pertaining to Frederick Site Manufacturing. 

Nature and Scope: 

  • This position largely interacts with equivalent levels of internal personnel.
  • That interaction requires good communication skills and customer service skills.
  • Effectiveness in this role also requires some knowledge of biology, chemistry and basic manufacturing principals as well as the ability to understand and interpret team metrics.
  • The job encounters recurring work situations of a routine nature where the ability to recognize a deviation from accepted practice is required.
  • Attention to detail and accuracy is required in performing all functions of this position as errors in work could cause customers to receive a non-conforming product.
  • This position requires the individual to be ready to start work on-time daily and maintain strong attendance performance.
  • Training will be provided through one on one instruction following process-specific on-the-job-training (OJT's) until the operator is proficient to work individually.
  • The incumbent normally receives general instruction on routine work and detailed instruction on new assignments. 

Minimum Qualifications: 

  • Associate or bachelor degree 
  • Minimum of 0-2 years related experience 
  • Proven ability to consistently and independently follow policies and procedures, instructions, and to meet schedules 
  • Ability to work in a fast-paced environment with changing priorities 
  • Basic computer skills such as proficiency with Microsoft Office Suite to support the operation in its daily functions 
  • Ability to lift up to 40 pounds 

Preferred Qualifications: 

  • Experience in a manufacturing life science company 
  • Biology or chemistry background 

 
 
 
TekWissen® Group is an equal opportunity/affirmative action Employer (m/f/d/v) supporting workforce diversity.   

  

Questions:

experience as a Manufacturing Technician?
Experience in Filling, capping, labeling, and assembling both sub-assemblies and finished good products ?
Associate or bachelor's degree?
Robotic Welder/Welder Fabricator 64
TekWissen LLC    12-16-2019 Euless, TX, USA

Description:

JOB SUMMARY:

Produce and maintain quality product using robot fixtures, and gauges required by manufacturing. Perform various functions such as editing programs, and insure weld processes are followed. Assist in designing and fabricating fixtures for robotic welder.

DUTIES & RESPONSIBILITIES:

  • Set up and operate robotic welder. Record machinery operation variances from normal settings and results. Complete basic preventive maintenance on machinery and equipment. Performs visual safety checks for machine wear, damage to tooling and correct positioning of safety guards.
  • Operates overhead hoists and forklifts to move material and necessary equipment to perform machine operations. Arranges parts as needed for production. Delivers raw stock, partially completed work, and completed jobs to appropriate storage or production areas.
  • Examine weld fixtures to determine whether repair, modification or replacement is required. Collaborate with production, engineering and planning to develop improvements in parts or changes in operation or maintenance to reduce setup time or extend tool life.
  • Develop, load, and maintain programs that follow the established welding process. Make appropriate adjustments necessary to the machine, tooling and/or program to produce the highest quality product.
  • Inspects own parts as well as those of others using tools such as tape measures, scales, calipers and possibly various computerized measuring devices. Reads and completes production, QA and manufacturing documentation as required.
  • Work with engineering, designers on future product for robotic welder. Assists in the design of engineering prototypes and manufacturing jobs. Devises methods to fabricate models for engineering. Investigates/recommends new methods, processes, and equipment to improve throughput within the department.
  • Determine the best method of repairing defective or damaged fixtures. Troubleshoot and remedy the situation by designing, repairing or fabricating the necessary parts in the most efficient manner to minimize downtime and restore production.
  • Maintain work area in a safe and professional manner. Clean, maintain robotic welder to maximize operating reliability, precision, and equipment life. Understand and comply with our ISO standards and environmental management system.
  • Train new personnel on operating robotic welder the proper loading and unloading of parts, highlighting the quality requirements and maintenance requirements of the robot.

QUALIFICATIONS:

  • High school diploma or equivalent preferred but not required.

Experience:

  • One (1) to three (3) years of related machine operating experience required – equivalent education background may be substituted for experience in some areas
  • At least One (1) year of robotic welding experience.
  • One (1) to Two (2) years welding experience.
  • Requires a thorough knowledge of welding theory, welding symbols, and procedures (GMAW).
  • Must have ability to read and interpret average to complex welding drawings and must be able to work from prints, sketches and verbal instructions.
  • Requires a working knowledge of using a teach pendant controller for NC/CNC robotic programming.
  • Must be proficient with computers.
  • Computer Aid Drawing and CAD CAM experience is preferred
  • Must pass visual acuity test. (color blindness)
  • Welder certification (AWS / CWB)
  • Ability to regularly lift and/or move up to 25 pounds, frequently lift and/or move up to 50 pounds, and occasionally lift, with assistance, up to 100 pounds.
Validation Engineer 58
TekWissen LLC    12-11-2019 West Hills, Los Angeles, CA, USA
Position Summary:
  • This position will mainly be focused on writing and executing equipment validations associated with the manufacture of In Vitro Diagnostic (IVD) Medical Devices during the preparation and transfer of operations from one facility to another.
  • This move is scheduled to start in Q4 2019.
  • The candidate will also work closely with cross-functional teams (R&D, Manufacturing, Quality Control) to help prepare their equipment, materials, and laboratories for the move.  
  • The main function of this position is to support the physical move of the business, so it will require flexibility and motivation to help with “other duties as assigned”.
  • Position requires working knowledge and proven experience with Installation Qualification (IQ), Operational Qualification (OQ), performance qualification (PQ), cleaning validation in support of the processes and equipment validations.  
  • This will all be done under the guidance of the Technical Operations Group.
Key Responsibilities: 
  • The Client is an Equal Employment Opportunity and Affirmative Action Employer
  • Write new validation (IQ/OQ/PQ) protocols for existing equipment
  • Transfer existing validation (IQ/OQ/PQ) protocols to new standard templates
  • Execute IQ/OQ/PQ protocols
  • Write IQ/OQ/PQ reports
  • Write new EQ (Equipment Specification) documents for existing equipment
  • Update existing EQ documents, where needed
  • Work with the Technical Operations team to help R&D, Operations, and Quality Control prepare equipment & materials prior to the move.
  • Willingness to be flexible and participate in other activities, as assigned, to help the business prepare for the move.  
  • This may include, but not limited to:
  • Updating non-validation type documents
  • Set-up of materials, equipment at the destination site
  • Organization/coordination of equipment movement
  • Assistance with cleaning validations
  • Other duties as assigned
  • Willingness to participate or lead PPI Business System Kaizen and 5S events
  • Preferred – Lean or Six Sigma exposure
  • Mindset for continuous improvement
  • Adhere to relevant Medical Device / pharmaceutical regulations and current interpretations affecting the product, process, equipment, and cleaning validation.
  • This position requires a high level of organization
  • Promote a collaborative team environment that fosters creativity, innovation, and high performance.
 
Minimum Requirements:
  • Bachelor’s degree (or higher) required, with majors in Engineering or Natural/Life Sciences.
  • At least 3 years’ relevant experience in IVD/medical device arena required
  • Working knowledge & proven to experience with equipment qualification (IQ/OQ/PQ), cleaning validation, and computer/automation systems.
  • Strong project management and organizational skills.
  • Excellent verbal and written communication skills.
  • Excellent use of Microsoft Office Suite.
  • Must work well with a cross-functional team, and be ready to serve our internal “Customers” (Operations, Research, Quality Control departments) on a daily basis
  • Performs all job duties in a safe manner, consistent with the Code of Ethics

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