Job Description
Qualifications
Education: Bachelor’s degree in Chemistry, Biology, Biochemistry or science related field
Experience: 5 years of related/applicable lab experience; minimum 1 year of supervisory experience
Familiarity with MS Office (Word, Excel, Access)
Strong interpersonal and organizational skills
Ability to work in a team environment
Ability to identify and resolve issues
Strong decision making skills
Ability to lead a team and provide guidance
Strong attention to detail
Strong communication skills
Benefits
Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor
Responsibilities
Responsible for providing supervision of inspection process and staff
Ensure staffing levels and work assignments meet facility requirements
Assist in the administration of the Quality Assurance (QA) and Quality Control (QC) programs and ensure compliance with the Quality Manual as well as all applicable regulations and standards for which Therapak/VWR is certified to
Perform acceptance activities as required to ensure Company objectives are met
May provide oversight to lower-level supervisor(s)
This position reports into the Sr
Quality Control Manager and sits at our Solon, OH location
Directly supervises the quality control staff, monitor individual skills and abilities for most efficient operation; follow progress of work; anticipate or investigate delays or inadequate performance; take corrective action within limits of established practice; provide assistance to other departments as needed
Provides on the floor and technical support to quality control associates
Support and enforce the quality system, regulatory policies and work instructions
Maintain quality and quantity of output; arrange for equipment, materials and supplies to be available for work assignments; see that equipment is given proper care; troubleshoot faulty operations to determine cause and arrange for required repair and maintenance
Provide or arranges for training and cross training to employees in the performance of duties; assist and instruct personnel as necessary to insure proper flow of work through department
Provide guidance to all level Technicians including test methods, analytical technique, good laboratory practice, paperwork completion, equipment, schedule interpretation, and LIMS support
Review and approval of controlled Quality Control documents including but not limited to: specifications, procedures, work instructions, validation protocols and validation reports
Ensure department documents and procedures are up to date and reflect current practice; revising procedures & processes when needed
Performs investigations for laboratory out of specification results, safety related incidents and/or processes related to the QC laboratory
Work with customers, regulatory agents and vendors during audits and site visits
Understands regulatory requirements for 21 CFR820, GLP, GMP including USP/EP general practices and procedures
Proactively maintains current industry and regulatory knowledge for medical devices, , GMP principles and current analytical technology
Assist in determining priority of urgent items and appropriate action plan to effectuate priority
Approve rejections and rework actions as recommended by Quality Control Technicians
Enforce prescribed safety rules and regulations; insure that work areas are maintained in a neat and orderly condition; perform safety and security procedures to open and close buildings and facilities
Performs other duties as assigned
Environmental Working Conditions & Physical Effort
Typically works in a lab environment with adequate lighting and ventilation and a normal range of temperature and noise level
At times, may be exposed to a variety of different chemicals including flammables, corrosives, oxidizers and others
It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle
It enables medical devices that help a little boy hear his mom's voice for the first time
Job description
The Opportunity:
At Avantor, people are the most important part of our success because they drive our global performance. That’s why our Operations, Lab Services, Sales, and many other Avantor teams rely on our talent acquisition initiatives to attract, engage and hire the right talent. Avantor’s Quality Assurance & Quality Systems vertical is a crucial part of this mix, enabling all our internal teams worldwide to grow beyond their limits.
Responsible for providing supervision of inspection process and staff. Ensure staffing levels and work assignments meet facility requirements. Assist in the administration of the Quality Assurance (QA) and Quality Control (QC) programs and ensure compliance with the Quality Manual as well as all applicable regulations and standards for which Therapak/VWR is certified to. Perform acceptance activities as required to ensure Company objectives are met. May provide oversight to lower-level supervisor(s).
This position reports into the Sr. Quality Control Manager and sits at our Solon, OH location.
What we’re looking for:
• Education: Bachelor’s degree in Chemistry, Biology, Biochemistry or science related field
• Experience: 5 years of related/applicable lab experience; minimum 1 year of supervisory experience
• Familiarity with MS Office (Word, Excel, Access)
Who you are
• Strong interpersonal and organizational skills
• Ability to work in a team environment
• Ability to identify and resolve issues
• Strong decision making skills
• Ability to lead a team and provide guidance
• Strong attention to detail
• Strong communication skills
How you will create an impact
• Directly supervises the quality control staff, monitor individual skills and abilities for most efficient operation; follow progress of work; anticipate or investigate delays or inadequate performance; take corrective action within limits of established practice; provide assistance to other departments as needed.
• Provides on the floor and technical support to quality control associates
• Support and enforce the quality system, regulatory policies and work instructions.
• Maintain quality and quantity of output; arrange for equipment, materials and supplies to be available for work assignments; see that equipment is given proper care; troubleshoot faulty operations to determine cause and arrange for required repair and maintenance.
• Provide or arranges for training and cross training to employees in the performance of duties; assist and instruct personnel as necessary to insure proper flow of work through department.
• Provide guidance to all level Technicians including test methods, analytical technique, good laboratory practice, paperwork completion, equipment, schedule interpretation, and LIMS support.
• Review and approval of controlled Quality Control documents including but not limited to: specifications, procedures, work instructions, validation protocols and validation reports.
• Ensure department documents and procedures are up to date and reflect current practice; revising procedures & processes when needed.
• Performs investigations for laboratory out of specification results, safety related incidents and/or processes related to the QC laboratory.
• Work with customers, regulatory agents and vendors during audits and site visits.
• Understands regulatory requirements for 21 CFR820, GLP, GMP including USP/EP general practices and procedures.
• Proactively maintains current industry and regulatory knowledge for medical devices, , GMP principles and current analytical technology.
• Assist in determining priority of urgent items and appropriate action plan to effectuate priority.
• Approve rejections and rework actions as recommended by Quality Control Technicians.
• Enforce prescribed safety rules and regulations; insure that work areas are maintained in a neat and orderly condition; perform safety and security procedures to open and close buildings and facilities.
• Performs other duties as assigned.
Environmental Working Conditions & Physical Effort
• Typically works in a lab environment with adequate lighting and ventilation and a normal range of temperature and noise level.
• At times, may be exposed to a variety of different chemicals including flammables, corrosives, oxidizers and others.
Disclaimer:
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer.
Why Avantor?
Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science.
The work we do changes people's lives for the better. It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor.
We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world. Apply today!
EEO Statement:
We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, ****** orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law.
If you need a reasonable accommodation for any part of the employment process, please contact us by email at [email protected] and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address.
For more information about equal employment opportunity protections, please view the Equal Employment Opportunity is THE LAW Poster, EEO is the Law Poster Supplement, and Pay Transparency Non-Discrimination Provision.
3rd Party Non-Solicitation Policy:
By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor, or by failing to comply with the Avantor recruitment process, you forfeit any fee on the submitted candidates, regardless of your usual terms and conditions. Avantor works with a preferred supplier list and will take the initiative to engage with recruitment agencies based on its needs and will not be accepting any form of solicitation.
Education: Bachelor’s degree in Chemistry, Biology, Biochemistry or science related field
Experience: 5 years of related/applicable lab experience; minimum 1 year of supervisory experience
Familiarity with MS Office (Word, Excel, Access)
Strong interpersonal and organizational skills
Ability to work in a team environment
Ability to identify and resolve issues
Strong decision making skills
Ability to lead a team and provide guidance
Strong attention to detail
Strong communication skills
Benefits
Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor
Responsibilities
Responsible for providing supervision of inspection process and staff
Ensure staffing levels and work assignments meet facility requirements
Assist in the administration of the Quality Assurance (QA) and Quality Control (QC) programs and ensure compliance with the Quality Manual as well as all applicable regulations and standards for which Therapak/VWR is certified to
Perform acceptance activities as required to ensure Company objectives are met
May provide oversight to lower-level supervisor(s)
This position reports into the Sr
Quality Control Manager and sits at our Solon, OH location
Directly supervises the quality control staff, monitor individual skills and abilities for most efficient operation; follow progress of work; anticipate or investigate delays or inadequate performance; take corrective action within limits of established practice; provide assistance to other departments as needed
Provides on the floor and technical support to quality control associates
Support and enforce the quality system, regulatory policies and work instructions
Maintain quality and quantity of output; arrange for equipment, materials and supplies to be available for work assignments; see that equipment is given proper care; troubleshoot faulty operations to determine cause and arrange for required repair and maintenance
Provide or arranges for training and cross training to employees in the performance of duties; assist and instruct personnel as necessary to insure proper flow of work through department
Provide guidance to all level Technicians including test methods, analytical technique, good laboratory practice, paperwork completion, equipment, schedule interpretation, and LIMS support
Review and approval of controlled Quality Control documents including but not limited to: specifications, procedures, work instructions, validation protocols and validation reports
Ensure department documents and procedures are up to date and reflect current practice; revising procedures & processes when needed
Performs investigations for laboratory out of specification results, safety related incidents and/or processes related to the QC laboratory
Work with customers, regulatory agents and vendors during audits and site visits
Understands regulatory requirements for 21 CFR820, GLP, GMP including USP/EP general practices and procedures
Proactively maintains current industry and regulatory knowledge for medical devices, , GMP principles and current analytical technology
Assist in determining priority of urgent items and appropriate action plan to effectuate priority
Approve rejections and rework actions as recommended by Quality Control Technicians
Enforce prescribed safety rules and regulations; insure that work areas are maintained in a neat and orderly condition; perform safety and security procedures to open and close buildings and facilities
Performs other duties as assigned
Environmental Working Conditions & Physical Effort
Typically works in a lab environment with adequate lighting and ventilation and a normal range of temperature and noise level
At times, may be exposed to a variety of different chemicals including flammables, corrosives, oxidizers and others
It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle
It enables medical devices that help a little boy hear his mom's voice for the first time
Job description
The Opportunity:
At Avantor, people are the most important part of our success because they drive our global performance. That’s why our Operations, Lab Services, Sales, and many other Avantor teams rely on our talent acquisition initiatives to attract, engage and hire the right talent. Avantor’s Quality Assurance & Quality Systems vertical is a crucial part of this mix, enabling all our internal teams worldwide to grow beyond their limits.
Responsible for providing supervision of inspection process and staff. Ensure staffing levels and work assignments meet facility requirements. Assist in the administration of the Quality Assurance (QA) and Quality Control (QC) programs and ensure compliance with the Quality Manual as well as all applicable regulations and standards for which Therapak/VWR is certified to. Perform acceptance activities as required to ensure Company objectives are met. May provide oversight to lower-level supervisor(s).
This position reports into the Sr. Quality Control Manager and sits at our Solon, OH location.
What we’re looking for:
• Education: Bachelor’s degree in Chemistry, Biology, Biochemistry or science related field
• Experience: 5 years of related/applicable lab experience; minimum 1 year of supervisory experience
• Familiarity with MS Office (Word, Excel, Access)
Who you are
• Strong interpersonal and organizational skills
• Ability to work in a team environment
• Ability to identify and resolve issues
• Strong decision making skills
• Ability to lead a team and provide guidance
• Strong attention to detail
• Strong communication skills
How you will create an impact
• Directly supervises the quality control staff, monitor individual skills and abilities for most efficient operation; follow progress of work; anticipate or investigate delays or inadequate performance; take corrective action within limits of established practice; provide assistance to other departments as needed.
• Provides on the floor and technical support to quality control associates
• Support and enforce the quality system, regulatory policies and work instructions.
• Maintain quality and quantity of output; arrange for equipment, materials and supplies to be available for work assignments; see that equipment is given proper care; troubleshoot faulty operations to determine cause and arrange for required repair and maintenance.
• Provide or arranges for training and cross training to employees in the performance of duties; assist and instruct personnel as necessary to insure proper flow of work through department.
• Provide guidance to all level Technicians including test methods, analytical technique, good laboratory practice, paperwork completion, equipment, schedule interpretation, and LIMS support.
• Review and approval of controlled Quality Control documents including but not limited to: specifications, procedures, work instructions, validation protocols and validation reports.
• Ensure department documents and procedures are up to date and reflect current practice; revising procedures & processes when needed.
• Performs investigations for laboratory out of specification results, safety related incidents and/or processes related to the QC laboratory.
• Work with customers, regulatory agents and vendors during audits and site visits.
• Understands regulatory requirements for 21 CFR820, GLP, GMP including USP/EP general practices and procedures.
• Proactively maintains current industry and regulatory knowledge for medical devices, , GMP principles and current analytical technology.
• Assist in determining priority of urgent items and appropriate action plan to effectuate priority.
• Approve rejections and rework actions as recommended by Quality Control Technicians.
• Enforce prescribed safety rules and regulations; insure that work areas are maintained in a neat and orderly condition; perform safety and security procedures to open and close buildings and facilities.
• Performs other duties as assigned.
Environmental Working Conditions & Physical Effort
• Typically works in a lab environment with adequate lighting and ventilation and a normal range of temperature and noise level.
• At times, may be exposed to a variety of different chemicals including flammables, corrosives, oxidizers and others.
Disclaimer:
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer.
Why Avantor?
Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science.
The work we do changes people's lives for the better. It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor.
We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world. Apply today!
EEO Statement:
We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, ****** orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law.
If you need a reasonable accommodation for any part of the employment process, please contact us by email at [email protected] and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address.
For more information about equal employment opportunity protections, please view the Equal Employment Opportunity is THE LAW Poster, EEO is the Law Poster Supplement, and Pay Transparency Non-Discrimination Provision.
3rd Party Non-Solicitation Policy:
By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor, or by failing to comply with the Avantor recruitment process, you forfeit any fee on the submitted candidates, regardless of your usual terms and conditions. Avantor works with a preferred supplier list and will take the initiative to engage with recruitment agencies based on its needs and will not be accepting any form of solicitation.
💡 Quick Summary
Seeking a career-building opportunity? The Quality Control Supervisor position is now open for candidates interested in the Helper Jobs sector. This role in Solon offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in Helper Jobs is a plus.
