דרושים Qc Chemist ב-Ge Healthcare ב-ארהב

You will be responsible for in-process and release testing of Injectable pharmaceutical finished products produced on site. The chemist participates in the development of new procedures and is involved in validation studies as they pertain to analytical testing. Work is technical and specialized, requiring accuracy and attention to detail.

Key responsibilities/essential functions include

• Performs required analytical testing on in-process and final products.
• Testing using HPLC, FTIR, ICP-OES, UV/VIS, Liquid Scintillation, and Gamma Spectrometer.
• Participates in the performance of investigations of OOS results.
• Tracking and trending of analytical data.
• Participates in validation projects requiring analytical support.
• Contributes to process improvement through Lean and 5S.
• Assists in the stocking and supplying of the QC lab.
• Performs visual inspection of finished product.

Quality Specific Goals:

• Knowledge and understanding of acceptance activity requirements for incoming, in-process, and final inspection requirements (as associated with job type/position) to ensure the product conforms to its specification and out of specification items are properly handled.
• Basic knowledge and understanding of Stop Orders, Concessions, CAPA, Calibration, Preventative Maintenance, Material Identification & Segregation, documentation configuration control practices; documentation & disposition of non-conforming material, and Good Documentation Practices requirements, Part 11 compliance as associated with this job type/position
• Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position
• Complete all planned Quality & Compliance training within the defined deadlines
• Identify and report any quality or compliance concerns and take immediate corrective action as required

Required Qualifications:

• Bachelor’s degree in chemistry (preferred) or related science field.
• Proficient with software applications applicable to the job.
• Must be available for nights and weekends as needed.
• Must have the ability to distinguish color.
• Ability to lift 25lbs

Preferred Qualifications:

• Waters Empower Experience or similar software.
• Equipment experience with HPLC, ICP, UV/Vis, FT-IR.
• Experience working with radioactive material including the use of gamma spectrometers, Ion Chambers and liquid scintillation analyzers.
• Visual inspection experience Working knowledge of USP Experience in a FDA regulated QC environment
• Background in Math or Chemistry

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities.
Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.

We will not sponsor individuals for employment visas, now or in the future, for this job opening.

The Microbiologist is responsible for in-process and release testing of injectable pharmaceutical finished products. The role includes final product microbiological testing, maintenance of controlled areas, environmental monitoring, analysis of results, raw material testing, growth promotion testing and performing microbiological identification. The Microbiologist I participates in the periodic review of procedures and supports validation studies as they pertain to microbiology.
functions include:

• Perform required bioburden, sterility and bacterial endotoxin testing on final products and raw materials utilizing specialized equipment

• Perform viable and non-viable environmental monitoring

• Operate non-viable particle counter/facility monitoring systems

• Monitor sterility and environmental media for microbiological growth and perform incoming growth promotion testing

• Participate in validation projects requiring microbiology support

• Perform required procedures to initiate isolate identification from environmental samples and sterility tests

• Perform computer data entry with programs such as Microsoft Excel and MODA

• Maintain accurate records of environmental data and finished product/raw material testing

• Perform sample collection and testing of the Reverse Osmosis system that feeds the production autoclaves; operate a Total Organic Carbon analyzer

• Prepare supplies for sterilization (autoclave) and depyrogenation (dry heat oven)

• Perform requalification testing for gown and aseptic qualified operators

• Evaluate documentation and GMPs as they relate to microbiological issues

• Contribute to process improvement through Lean, 5S and six sigma tools

• Understand maintenance and use of biological indicators

• Create/perform unscheduled work orders and preventative maintenance records for laboratory upkeep

Quality Specific Goals:

• Knowledge and understanding of acceptance activity requirements for incoming, in-process, and final inspection requirements (as associated with job type/position) to ensure that product conforms to its specification and out of specification items are properly handled

• Knowledge and understanding of Shop Orders, Concessions, Calibration, Preventative Maintenance, Material Identification & Segregation, documentation configuration control practices; documentation & disposition of non-conforming material, Part 11 compliance and Good Documentation Practices requirements, as associated with this job type/position

• Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position

• Complete all planned Quality & Compliance training within the defined deadlines

• Identify and report any quality or compliance concerns and take immediate corrective action as required

Required Qualifications:

• Bachelor’s degree in Microbiology or related Science degree

• Ability to speak, understand, read and write in local language

• Proficiency with Microsoft Office Suite (including Access)

• Availability for early shifts and weekends as needed

• Ability to distinguish color

• Knowledge of microbiological techniques (gram stain/microbial ID, aseptic, gowning, etc.)

• Ability to lift 25lbs

• Legal authorization to work in the U.S. is required. We will not sponsor individuals for employment visas, now or in the future, for this job opening.

Preferred Qualifications:

• Cleanroom experience

• Experience with electronic data tracking systems such as MODA

• Experience with bioburden, sterility and bacterial endotoxin testing

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.

We will not sponsor individuals for employment visas, now or in the future, for this job opening.

You will be responsible for in-process and release testing of Injectable pharmaceutical finished products produced on site. The chemist participates in the development of new procedures and is involved in validation studies as they pertain to analytical testing. Work is technical and specialized, requiring accuracy and attention to detail.

Keyresponsibilities/essentialfunctions include

• Performs required analytical testing on in-process and final products.
• Testing using HPLC, FTIR, ICP-OES, UV/VIS, Liquid Scintillation, and Gamma Spectrometer.
• Participates in the performance of investigations of OOS results.
• Tracking and trending of analytical data.
• Participates in validation projects requiring analytical support.
• Contributes to process improvement through Lean and 5S.
• Assists in the stocking and supplying of the QC lab.
• Performs visual inspection of finished product.

Quality Specific Goals:

• Knowledge and understanding of acceptance activity requirements for incoming, in-process, and final inspection requirements (as associated with job type/position) to ensure the product conforms to its specification and out of specification items are properly handled.
• Basic knowledge and understanding of Stop Orders, Concessions, CAPA, Calibration, Preventative Maintenance, Material Identification & Segregation, documentation configuration control practices; documentation & disposition of non-conforming material, and Good Documentation Practices requirements, Part 11 compliance as associated with this job type/position
• Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position
• Complete all planned Quality & Compliance training within the defined deadlines
• Identify and report any quality or compliance concerns and take immediate corrective action as required

Required Qualifications:

• Bachelor’s degree in chemistry (preferred) or related science field.
• Proficient with software applications applicable to the job.
• Must be available for nights and weekends as needed.
• Must have the ability to distinguish color.
• Ability to lift 25lbs

Preferred Qualifications:

• Waters Empower Experience or similar software.
• Equipment experience with HPLC, ICP, UV/Vis, FT-IR.
• Experience working with radioactive material including the use of gamma spectrometers, Ion Chambers and liquid scintillation analyzers.
• Visual inspection experience Working knowledge of USP Experience in a FDA regulated QC environment
• Background in Math or Chemistry

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities.
Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.

We will not sponsor individuals for employment visas, now or in the future, for this job opening.

You will be responsible for in-process and release testing of Injectable pharmaceutical finished products produced on site. The chemist participates in the development of new procedures and is involved in validation studies as they pertain to analytical testing. Work is technical and specialized, requiring accuracy and attention to detail.
Key responsibilities/essential functions:

• Performs required analytical testing on in-process and final products.

• Testing using HPLC, FTIR, ICP-OES, UV/VIS, Liquid Scintillation, and Gamma Spectrometer.

• Participates in the performance of investigations of OOS results.

• Tracking and trending of analytical data.

• Participates in validation projects requiring analytical support.

• Contributes to process improvement through Lean and 5S.

• Assists in the stocking and supplying of the QC lab.

• Performs visual inspection of finished product.

Quality Specific Goals:

• Knowledge and understanding of acceptance activity requirements for incoming, in-process, and final inspection requirements (as associated with job type/position) to ensure the product conforms to its specification and out of specification items are properly handled.

• Basic knowledge and understanding of Stop Orders, Concessions, CAPA, Calibration, Preventative Maintenance, Material Identification & Segregation, documentation configuration control practices; documentation & disposition of non-conforming material, and Good Documentation Practices requirements, Part 11 compliance as associated with this job type/position

• Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position

• Complete all planned Quality & Compliance training within the defined deadlines

• Identify and report any quality or compliance concerns and take immediate corrective action as required

Required Qualifications:

• Bachelor’s degree in chemistry (preferred) or related science field.

• Proficient with software applications applicable to the job.

• Must be available for nights and weekends as needed.

• Must have the ability to distinguish color.

• Ability to lift 25lbs

• Legal authorization to work in the U.S. is required. We will not sponsor individuals for employment visas, now or in the future, for this job opening.

Preferred Qualifications:

• Waters Empower Experience or similar software.

• Equipment experience with HPLC, ICP, UV/Vis, FT-IR.

• Experience working with radioactive material including the use of gamma spectrometers, Ion Chambers and liquid scintillation analyzers.

• Visual inspection experience Working knowledge of USP Experience in a FDA regulated QC environment Background in Math or Chemistry

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.

You will be responsible for in-process and release testing of Injectable pharmaceutical finished products produced on site. The chemist participates in the development of new procedures and is involved in validation studies as they pertain to analytical testing. Work is technical and specialized, requiring accuracy and attention to detail.
Key responsibilities/essential functions:

• Performs required analytical testing on in-process and final products.

• Testing using HPLC, FTIR, ICP-OES, UV/VIS, Liquid Scintillation, and Gamma Spectrometer.

• Participates in the performance of investigations of OOS results.

• Tracking and trending of analytical data.

• Participates in validation projects requiring analytical support.

• Contributes to process improvement through Lean and 5S.

• Assists in the stocking and supplying of the QC lab.

• Performs visual inspection of finished product.

Quality Specific Goals:

• Knowledge and understanding of acceptance activity requirements for incoming, in-process, and final inspection requirements (as associated with job type/position) to ensure the product conforms to its specification and out of specification items are properly handled.

• Basic knowledge and understanding of Stop Orders, Concessions, CAPA, Calibration, Preventative Maintenance, Material Identification & Segregation, documentation configuration control practices; documentation & disposition of non-conforming material, and Good Documentation Practices requirements, Part 11 compliance as associated with this job type/position

• Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position

• Complete all planned Quality & Compliance training within the defined deadlines

• Identify and report any quality or compliance concerns and take immediate corrective action as required

Required Qualifications:

• Bachelor’s degree in chemistry (preferred) or related science field.

• Proficient with software applications applicable to the job.

• Must be available for nights and weekends as needed.

• Must have the ability to distinguish color.

• Ability to lift 25lbs

• Legal authorization to work in the U.S. is required. We will not sponsor individuals for employment visas, now or in the future, for this job opening.

Preferred Qualifications:

• Waters Empower Experience or similar software.

• Equipment experience with HPLC, ICP, UV/Vis, FT-IR.

• Experience working with radioactive material including the use of gamma spectrometers, Ion Chambers and liquid scintillation analyzers.

• Visual inspection experience Working knowledge of USP Experience in a FDA regulated QC environment Background in Math or Chemistry

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.