QC Biochemistry Supervisor
GSK is currently looking for QC Biochemistry Supervisor to join our team in Upper Merion, PA.
The QC Biochemistry Supervisor provides first line supervision to QC analysts, who are responsible for in-process and BDS samples for release and stability testing.
The Supervisor also serves as a leader outside of their immediate role in regard to testing and system optimization, driving continuous improvement, and participating in cross functional and cross business collaboration and teamwork.
Key
Responsibilities:
Supervise a team of front-line QC Scientists.
Performs administrative duties, i.
e.
hiring, performance management and supporting your team s development goalsSchedules and assures adherence to schedule for the performance of analytical testing for biochemical analysis, so that all testing to support the production and release of product lots is performed in compliance with internal procedures and standards and external regulatory standards.
Reviews and approves investigations, change controls, protocols, validation reports.
May review and approve biochemistry test results.
Writes, updates, reviews, and approves Laboratory Standard Operating Procedures and Analytical MethodsEvaluates new equipment for purchase.
Serves as point of contact for internal and external customers for analytical testingAssures that laboratory equipment is calibrated and in good working condition, purchases supplies and equipment.
Utilizes GPS tools and processes to continuously improve efficiencies and leads problem solving for laboratory test problems.
Responsible for ensuring laboratories are operated in a state of control with regards to current LSOP s, GMP s and regulations and may serve as Biochemistry SME for internal and external regulatory audits and inspections.
Why you?Basic
Qualifications:
We are looking for professionals with these required skills to achieve our goals:
BS/BA degreeMinimum of 5 years pharmaceutical experience in a GMP regulated environmentPreferred
Qualifications:
If you have the following characteristics, it would be a plus:
Demonstrated supervisory and leadership skills with ability to hold team accountable.
Strong interpersonal and leadership skills.
Solid team player able to function within team based organization.
Strong verbal and written communication skills.
Able to interact with peers, subordinate and senior personnel in multidisciplinary environment including engineering, facility operations, validation, production and QA.
Able to prioritize and decide appropriate course of actions.
Effective at implementing decision.
Fully versed in cGXP, ICH guidelines, FDA, USP/EP/JP and data integrity guidelines and regulations for analytical testing and stabilityBiopharmaceutical testing experience is preferred, ability to learn biopharmaceutical testing techniques.
Assays include (but not limited to) CGE, ELISA, CiEF, Bioassay, SEC, SPR, Protein Concentration, HPLC/UPLC, PCR, automated liquid handlingSystem experience preferred SAP/ERP, LES, Webstatistica, EmpowerExperience with MS Excel, Word, PowerPoint.
Strong organizational skills and task management skills.
Strong understanding of analytical methods.
Strong data analysis, trending, technical writing, and communication (verbal and written) skills.
Ability to solve problems.
#LI-GSKPlease visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.
Why GSK? Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a special purpose to unite science, technology and talent to get ahead of disease together so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns as an organisation where people can thrive.
We prevent and treat disease with vaccines, specialty and general medicines.
We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).
Our success absolutely depends on our people.
While getting ahead of disease together is about our ambition for patients and shareholders, it s also about making GSK a place where people can thrive.
We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be.
A place where they can be themselves feeling welcome, valued, and included.
Where they can keep growing and look after their wellbeing.
So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.
If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US).
GSK is an Equal Opportunity Employer and, in the US, we adhere to Affirmative Action principles.
This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.
Important notice to Employment businesses/ AgenciesGSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site.
All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK.
The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK.
In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK.
GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment.
This capture of applicable transfers of value is necessary to ensure GSK s compliance to all federal and state US Transparency requirements.
For more information, please visit GSK s Transparency Reporting For the Record site.
SummaryLocation:
USA - Pennsylvania - King of PrussiaType:
Full time.
Estimated Salary: $20 to $28 per hour based on qualifications.
The QC Biochemistry Supervisor provides first line supervision to QC analysts, who are responsible for in-process and BDS samples for release and stability testing.
The Supervisor also serves as a leader outside of their immediate role in regard to testing and system optimization, driving continuous improvement, and participating in cross functional and cross business collaboration and teamwork.
Key
Responsibilities:
Supervise a team of front-line QC Scientists.
Performs administrative duties, i.
e.
hiring, performance management and supporting your team s development goalsSchedules and assures adherence to schedule for the performance of analytical testing for biochemical analysis, so that all testing to support the production and release of product lots is performed in compliance with internal procedures and standards and external regulatory standards.
Reviews and approves investigations, change controls, protocols, validation reports.
May review and approve biochemistry test results.
Writes, updates, reviews, and approves Laboratory Standard Operating Procedures and Analytical MethodsEvaluates new equipment for purchase.
Serves as point of contact for internal and external customers for analytical testingAssures that laboratory equipment is calibrated and in good working condition, purchases supplies and equipment.
Utilizes GPS tools and processes to continuously improve efficiencies and leads problem solving for laboratory test problems.
Responsible for ensuring laboratories are operated in a state of control with regards to current LSOP s, GMP s and regulations and may serve as Biochemistry SME for internal and external regulatory audits and inspections.
Why you?Basic
Qualifications:
We are looking for professionals with these required skills to achieve our goals:
BS/BA degreeMinimum of 5 years pharmaceutical experience in a GMP regulated environmentPreferred
Qualifications:
If you have the following characteristics, it would be a plus:
Demonstrated supervisory and leadership skills with ability to hold team accountable.
Strong interpersonal and leadership skills.
Solid team player able to function within team based organization.
Strong verbal and written communication skills.
Able to interact with peers, subordinate and senior personnel in multidisciplinary environment including engineering, facility operations, validation, production and QA.
Able to prioritize and decide appropriate course of actions.
Effective at implementing decision.
Fully versed in cGXP, ICH guidelines, FDA, USP/EP/JP and data integrity guidelines and regulations for analytical testing and stabilityBiopharmaceutical testing experience is preferred, ability to learn biopharmaceutical testing techniques.
Assays include (but not limited to) CGE, ELISA, CiEF, Bioassay, SEC, SPR, Protein Concentration, HPLC/UPLC, PCR, automated liquid handlingSystem experience preferred SAP/ERP, LES, Webstatistica, EmpowerExperience with MS Excel, Word, PowerPoint.
Strong organizational skills and task management skills.
Strong understanding of analytical methods.
Strong data analysis, trending, technical writing, and communication (verbal and written) skills.
Ability to solve problems.
#LI-GSKPlease visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.
Why GSK? Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a special purpose to unite science, technology and talent to get ahead of disease together so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns as an organisation where people can thrive.
We prevent and treat disease with vaccines, specialty and general medicines.
We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).
Our success absolutely depends on our people.
While getting ahead of disease together is about our ambition for patients and shareholders, it s also about making GSK a place where people can thrive.
We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be.
A place where they can be themselves feeling welcome, valued, and included.
Where they can keep growing and look after their wellbeing.
So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.
If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US).
GSK is an Equal Opportunity Employer and, in the US, we adhere to Affirmative Action principles.
This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.
Important notice to Employment businesses/ AgenciesGSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site.
All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK.
The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK.
In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK.
GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment.
This capture of applicable transfers of value is necessary to ensure GSK s compliance to all federal and state US Transparency requirements.
For more information, please visit GSK s Transparency Reporting For the Record site.
SummaryLocation:
USA - Pennsylvania - King of PrussiaType:
Full time.
Estimated Salary: $20 to $28 per hour based on qualifications.
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