Chemist I.US-PBF.423
3.
3 Full-time 4 hours ago Full Job Description Overview:
Integra LifeSciences is a global leader in regenerative technologies and neurosurgical solutions dedicated to limiting uncertainty for clinicians, so they can focus on providing the best patient care.
Founded in 1989, Integra develops, manufactures, sells and supplies best-in-class products to regenerate tissue, remove brain tumors, prevent infection and much more.
And over the last three decades, we've evolved into one of the world's leading global medical technology companies with more than 4,000 dedicated employees who deliver innovative medical technology solutions.
But that's just the beginning.
Integra is growing at an unprecedented rate.
We're at a moment in time where the experience you'll gain is more robust than the experience you bring.
And we're out to invest in your future because it's the best way to maximize ours.
At Integra, we firmly believe our people are our greatest asset and the foundation of our success.
Our comprehensive Global Total Rewards program provides competitive compensation and benefits designed to keep our people healthy, motivated and engaged.
Investing in our people through these programs is possible because of Integra's ongoing commitment to our values and our shared success.
Integra's health as a company begins with the well-being of our people.
Benefit programs vary by country, whether provided through company-sponsored insurance and programs, through statutory government programs, or a combination of both.
Regardless of geographic location, our commitment is to offer the following, whenever possible:
Benefit plans that meet all local statutory requirements A range of programs that reflect typical local market practices An opportunity for employees to tailor benefits to their specific needs Benefits that balance employee's short-term and long-term needs Click HERE for more information regarding our benefits and total rewards program
Responsibilities:
SUMMARY DESCRIPTION The Chemist I will provide support to the QC Analytical Laboratory for the testing of in-process and finished good products, raw materials, water, stability studies, and validation studies.
This position is responsible for operating in compliance with all applicable procedures and policies.
SUPERVISION RECEIVED Under direct supervision of Supervisor, QC Analytical SUPERVISION EXERCISED None ESSENTIAL DUTIES AND RESPONSIBILITIES To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
Ensure compliance with all company policies and procedures and appropriate regulations, including FDA and ISO 9001, ISO 13485, CMDR and the Medical Device Directive.
Perform and document instrumental (e.
g.
, UV-VIS, HPLC) and wet chemistry techniques/analyses.
Perform laboratory testing, as well as general laboratory maintenance, including in-process and final product release testing and stability testing.
Ensure timely testing and result reporting.
Submit samples for shipment to third-party labs when necessary.
Maintain GMP/GLP laboratory notebooks and documentation relevant to the duties and responsibilities assigned.
Maintain laboratory instrumentation required for testing.
Assist as needed in test method validation, implementation, and execution.
Report any equipment and testing deviations to the Supervisor.
Assist with proper execution of laboratory Out-of-Specification (OOS) investigations.
Complete data entry for trending reports for In-process and Finished Goods Quality Control Testing, as well as Stability Testing.
Train team members in Analytical department as assigned.
Handle and dispose of biohazard material in compliance with OSHA and Standard Operating Procedures.
Demonstrate organizational and time management skills.
Perform other related duties as required.
TOOLS AND EQUIPMENT USED Analytical Instrumentation (GC, HPLC, UV-Vis, FT-IR), wet chemistry techniques, computers, along with new and existing manufacturing and test equipment.
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 speak and write in English.
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 50lbs.
The employee requires visual acuity and color perception adequate to perform job duties.
Eyesight correctable to 20/25 to detect the presence of defined defect classifications in/on product/materials.
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.
Adverse exposure may result from the handling of hazardous and biohazardous materials that include, but are not limited to, flammable and corrosive liquids, compressed gases, sharps, and medical wastes
Qualifications:
DESIRED MINIMUM QUALIFICATIONS The requirements listed below are representative of the knowledge, skill, and/or ability required for this position.
Bachelor's degree, in Chemistry or biological sciences preferred 0-3 years of relevant GMP/GLP laboratory experience in regulated industry preferred Capable of effective written and verbal communication Must be able to work independently with minimal supervision Knowledge of MS Office Suite In an effort to minimize the spread of the coronavirus and to protect our employees, all new hires in the US and Puerto Rico will need to be fully vaccinated for COVID-19 in order to be considered for employment with Integra LifeSciences, unless eligible for an accommodation as provided by law.
.
Estimated Salary: $20 to $28 per hour based on qualifications.
3 Full-time 4 hours ago Full Job Description Overview:
Integra LifeSciences is a global leader in regenerative technologies and neurosurgical solutions dedicated to limiting uncertainty for clinicians, so they can focus on providing the best patient care.
Founded in 1989, Integra develops, manufactures, sells and supplies best-in-class products to regenerate tissue, remove brain tumors, prevent infection and much more.
And over the last three decades, we've evolved into one of the world's leading global medical technology companies with more than 4,000 dedicated employees who deliver innovative medical technology solutions.
But that's just the beginning.
Integra is growing at an unprecedented rate.
We're at a moment in time where the experience you'll gain is more robust than the experience you bring.
And we're out to invest in your future because it's the best way to maximize ours.
At Integra, we firmly believe our people are our greatest asset and the foundation of our success.
Our comprehensive Global Total Rewards program provides competitive compensation and benefits designed to keep our people healthy, motivated and engaged.
Investing in our people through these programs is possible because of Integra's ongoing commitment to our values and our shared success.
Integra's health as a company begins with the well-being of our people.
Benefit programs vary by country, whether provided through company-sponsored insurance and programs, through statutory government programs, or a combination of both.
Regardless of geographic location, our commitment is to offer the following, whenever possible:
Benefit plans that meet all local statutory requirements A range of programs that reflect typical local market practices An opportunity for employees to tailor benefits to their specific needs Benefits that balance employee's short-term and long-term needs Click HERE for more information regarding our benefits and total rewards program
Responsibilities:
SUMMARY DESCRIPTION The Chemist I will provide support to the QC Analytical Laboratory for the testing of in-process and finished good products, raw materials, water, stability studies, and validation studies.
This position is responsible for operating in compliance with all applicable procedures and policies.
SUPERVISION RECEIVED Under direct supervision of Supervisor, QC Analytical SUPERVISION EXERCISED None ESSENTIAL DUTIES AND RESPONSIBILITIES To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
Ensure compliance with all company policies and procedures and appropriate regulations, including FDA and ISO 9001, ISO 13485, CMDR and the Medical Device Directive.
Perform and document instrumental (e.
g.
, UV-VIS, HPLC) and wet chemistry techniques/analyses.
Perform laboratory testing, as well as general laboratory maintenance, including in-process and final product release testing and stability testing.
Ensure timely testing and result reporting.
Submit samples for shipment to third-party labs when necessary.
Maintain GMP/GLP laboratory notebooks and documentation relevant to the duties and responsibilities assigned.
Maintain laboratory instrumentation required for testing.
Assist as needed in test method validation, implementation, and execution.
Report any equipment and testing deviations to the Supervisor.
Assist with proper execution of laboratory Out-of-Specification (OOS) investigations.
Complete data entry for trending reports for In-process and Finished Goods Quality Control Testing, as well as Stability Testing.
Train team members in Analytical department as assigned.
Handle and dispose of biohazard material in compliance with OSHA and Standard Operating Procedures.
Demonstrate organizational and time management skills.
Perform other related duties as required.
TOOLS AND EQUIPMENT USED Analytical Instrumentation (GC, HPLC, UV-Vis, FT-IR), wet chemistry techniques, computers, along with new and existing manufacturing and test equipment.
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 speak and write in English.
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 50lbs.
The employee requires visual acuity and color perception adequate to perform job duties.
Eyesight correctable to 20/25 to detect the presence of defined defect classifications in/on product/materials.
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.
Adverse exposure may result from the handling of hazardous and biohazardous materials that include, but are not limited to, flammable and corrosive liquids, compressed gases, sharps, and medical wastes
Qualifications:
DESIRED MINIMUM QUALIFICATIONS The requirements listed below are representative of the knowledge, skill, and/or ability required for this position.
Bachelor's degree, in Chemistry or biological sciences preferred 0-3 years of relevant GMP/GLP laboratory experience in regulated industry preferred Capable of effective written and verbal communication Must be able to work independently with minimal supervision Knowledge of MS Office Suite In an effort to minimize the spread of the coronavirus and to protect our employees, all new hires in the US and Puerto Rico will need to be fully vaccinated for COVID-19 in order to be considered for employment with Integra LifeSciences, unless eligible for an accommodation as provided by law.
.
Estimated Salary: $20 to $28 per hour based on qualifications.
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