What are the responsibilities and job description for the Clean Room Inspector/Packaging Operator - 1st Shift position at Integra LifeSciences?
Changing lives. Building Careers.
Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what’s possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care.
SUPERVISION RECEIVED: Under the direct supervision of the Production Manager
SUPERVISION EXERCISED: NA
ESSENTIAL DUTIES AND RESPONSIBILITIES
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
- Responsible for accurately maintaining accurate records, required logs and other procedures to comply with regulatory requirements, Good Manufacturing Practices (GMP), Quality Systems Regulations, Standard Operating Procedures (SOP’s), and Health and Safety requirements.
- Performs and supports daily manufacturing operations inclusive of Cutting, Product Inspections, Packaging of product and cleaning of manufacturing equipment.
- Enter and record production activities in Oracle MRP systems to issue material and labor hours to specific work orders.
- Able to work independently with minimal supervision.
- Supports equipment evaluations and validation activities associated with the developed manufacturing processes
- Communicate with team members and support teams to ensure continuous production of the correct product at high quality levels with minimal wasted time and materials
- Responsible for performing precise measurements and using measurement equipment to accurately inspect product.
- Support department and plant Safety goals by continuously demonstrating safe behavior.
- Able to participate in a team-oriented environment, willingness to assist and train others.
- Interface with QA/QC/Material departments during course of work to coordinate inspections and efficient flow of subassemblies and completed product.
- Maintain a clean and orderly work area.
DESIRED MINIMUM QUALIFICATIONS
The requirements listed below are representative of the knowledge, skill, and/or ability required for this position.
- High School diploma or equivalent.
- 0-2 years working in Medical Device or Pharmaceutical manufacturing industry. Production experience is highly desirable.
- Basic computer skills for email and data entry.
- Must work and collaborate as part of a team.
- Ability to operate, maintain and process equipment, and make adjustments as needed.
- Must read, write, and speak in English, and communicate clearly and concisely.
- Able to work independently with minimal supervision.
- Ability to gown to ISO Class 7 Clean Room standards.
- Able to participate in a team-oriented environment, willingness to assist and train others.
- Able to work independently with minimal supervision.
TOOLS AND EQUIPMENT USED
- Cutting Machines, sealing machines, Printers, Crosslink chambers, Drop gauges.
- Oracle MRP System
PHYSICAL REQUIREMENTS
The physical requirements listed in this section include, but are not limited, to the motor/physical abilities and skills require of this position in order to successfully undertake the essential duties and responsibilities of this position. In accordance with the Americans with Disabilities Act (ADA), reasonable accommodations may be made to empower individuals with disabilities to undertake the essential duties and responsibilities of the position.
While undertaking the essential duties and responsibilities of the position, the employee must repeatedly
sit, listen, and speak. The employee is required to go to all areas of the company. The employee may be required to periodically lift and/or move up to 25 pounds.
ADVERSE WORKING CONDITIONS
The adverse working conditions listed in this section include, but are not limited to, those environmental conditions to which the employee may be exposed while undertaking the essential duties and responsibilities of this position, which is that of a general plant environment.
- Daily interaction with hazardous materials used in a controlled environment.
SELECTION GUIDELINES
Formal application, rating of education and experience; oral interview and reference check; job related tests may be required.
DISCLAIMER
The duties listed above are intended only as illustrations of the various types of work that may be performed. The omission of specific statements of duties does not exclude them from the position if the work is similar, related, or a logical assignment to the position.
The job description does not constitute an employment agreement between the employer and employee and is subject to change by the employer as the needs of the employer and requirements of the job change.
Integra LifeSciences is an equal opportunity employer, and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status.
This site is governed solely by applicable U.S. laws and governmental regulations. If you'd like more information on your rights under the law, please see the following notices:
Integra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the
This site is governed solely by applicable U.S. laws and governmental regulations. If you'd like more information on your rights under the law, please see the following notices:
EEO Is the Law
| EOE including Disability/Protected Veterans
Integra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the
ADA
. If you have difficulty using our online system due to a disability and need an accommodation, please email us at careers@integralife.com or call us at 855-936-2666.
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