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Most recent job postings at MDPI
via MDPI UK
schedule_type: Full-timework_from_home: 1
We are seeking editors with a keen eye for detail and outstanding English skills to efficiently edit academic research articles, submitted to our over 300 journals, written by scholars from all over the world. Successful applicants will join our network of remote freelance English Editors and work with a dynamic and fast-paced editing department.
Organisation Overview...
A pioneer in scholarly open access publishing, MDPI has supported academic
We are seeking editors with a keen eye for detail and outstanding English skills to efficiently edit academic research articles, submitted to our over 300 journals, written by scholars from all over the world. Successful applicants will join our network of remote freelance English Editors and work with a dynamic and fast-paced editing department.
Organisation Overview...
A pioneer in scholarly open access publishing, MDPI has supported academic communities since 1996. Based in Basel, Switzerland, MDPI has the mission to foster open scientific exchange in all forms, across all disciplines. Our peer-reviewed, open access journals are supported by more than 80,000 academic editors. We serve scholars from around the world to ensure the latest research is freely available and all content is distributed under a Creative Commons Attribution License (CC BY).
Your Responsibilities
Editors work with short deadlines to accurately edit scholarly articles, making the English clear, consistent, and grammatically correct. You will be familiar with Microsoft Word and be able to work remotely. All editors must complete two editing tests and undergo a brief training period to assess whether this role is a good fit.
Your Experience and Skills
All applicants must have the following:
Advanced knowledge of English.
Experience in editing and writing.
Access to Microsoft Word and antivirus software.
Able to meet short deadlines.
Attention to detail.
Willingness to work remotely as part of an international team.
A strong interest in working with research material.
The following are a benefit:
Previous experience editing scholarly content.
Knowledge of LaTeX.
Familiarity with academic publishing.
What We Offer
Training in editing scholarly content and use of the MDPI style.
The opportunity to develop your editing skills working with a leading academic publishing house Show more details...
Organisation Overview...
A pioneer in scholarly open access publishing, MDPI has supported academic communities since 1996. Based in Basel, Switzerland, MDPI has the mission to foster open scientific exchange in all forms, across all disciplines. Our peer-reviewed, open access journals are supported by more than 80,000 academic editors. We serve scholars from around the world to ensure the latest research is freely available and all content is distributed under a Creative Commons Attribution License (CC BY).
Your Responsibilities
Editors work with short deadlines to accurately edit scholarly articles, making the English clear, consistent, and grammatically correct. You will be familiar with Microsoft Word and be able to work remotely. All editors must complete two editing tests and undergo a brief training period to assess whether this role is a good fit.
Your Experience and Skills
All applicants must have the following:
Advanced knowledge of English.
Experience in editing and writing.
Access to Microsoft Word and antivirus software.
Able to meet short deadlines.
Attention to detail.
Willingness to work remotely as part of an international team.
A strong interest in working with research material.
The following are a benefit:
Previous experience editing scholarly content.
Knowledge of LaTeX.
Familiarity with academic publishing.
What We Offer
Training in editing scholarly content and use of the MDPI style.
The opportunity to develop your editing skills working with a leading academic publishing house Show more details...
via Jooble
posted_at: 27 days agoschedule_type: Full-time
We are seeking editors with a keen eye for detail and outstanding English skills to efficiently edit academic research articles, submitted to our over 300 journals, written by scholars from all over the world. Successful applicants will join our network of remote freelance English Editors and work with a dynamic and fast-paced editing department.
Organisation Overview...
A pioneer in scholarly open access publishing, MDPI has supported academic
We are seeking editors with a keen eye for detail and outstanding English skills to efficiently edit academic research articles, submitted to our over 300 journals, written by scholars from all over the world. Successful applicants will join our network of remote freelance English Editors and work with a dynamic and fast-paced editing department.
Organisation Overview...
A pioneer in scholarly open access publishing, MDPI has supported academic communities since 1996. Based in Basel, Switzerland, MDPI has the mission to foster open scientific exchange in all forms, across all disciplines. Our peer-reviewed, open access journals are supported by more than 80,000 academic editors. We serve scholars from around the world to ensure the latest research is freely available and all content is distributed under a Creative Commons Attribution License (CC BY).
Your Responsibilities
Editors work with short deadlines to accurately edit scholarly articles, making the English clear, consistent, and grammatically correct. You will be familiar with Microsoft Word and be able to work remotely. All editors must complete two editing tests and undergo a brief training period to assess whether this role is a good fit.
Your Experience and Skills
All applicants must have the following:
Advanced knowledge of English.
Experience in editing and writing.
Access to Microsoft Word and antivirus software.
Able to meet short deadlines.
Attention to detail.
Willingness to work remotely as part of an international team.
A strong interest in working with research material.
The following are a benefit:
Previous experience editing scholarly content.
Knowledge of LaTeX.
Familiarity with academic publishing.
What We Offer
Training in editing scholarly content and use of the MDPI style.
The opportunity to develop your editing skills working with a leading academic publishing house Show more details...
Organisation Overview...
A pioneer in scholarly open access publishing, MDPI has supported academic communities since 1996. Based in Basel, Switzerland, MDPI has the mission to foster open scientific exchange in all forms, across all disciplines. Our peer-reviewed, open access journals are supported by more than 80,000 academic editors. We serve scholars from around the world to ensure the latest research is freely available and all content is distributed under a Creative Commons Attribution License (CC BY).
Your Responsibilities
Editors work with short deadlines to accurately edit scholarly articles, making the English clear, consistent, and grammatically correct. You will be familiar with Microsoft Word and be able to work remotely. All editors must complete two editing tests and undergo a brief training period to assess whether this role is a good fit.
Your Experience and Skills
All applicants must have the following:
Advanced knowledge of English.
Experience in editing and writing.
Access to Microsoft Word and antivirus software.
Able to meet short deadlines.
Attention to detail.
Willingness to work remotely as part of an international team.
A strong interest in working with research material.
The following are a benefit:
Previous experience editing scholarly content.
Knowledge of LaTeX.
Familiarity with academic publishing.
What We Offer
Training in editing scholarly content and use of the MDPI style.
The opportunity to develop your editing skills working with a leading academic publishing house Show more details...
via CareerBuilder
posted_at: 20 days agoschedule_type: Full-time
Are you looking for an opportunity to lead the production planning delivery within a production team to achieve the safety, quality, planning and budget and performance in a complex and highly regulated environment? If so, this is the role for you.As a Production Manager Supervisor (First Line Leader) 10-hr, Mon. -Thurs., 2nd shift, 1600 hrs. (4:00pm) - 0230 hrs. (2:30am) you will Supervise... production shift operations to deliver high quality products,
Are you looking for an opportunity to lead the production planning delivery within a production team to achieve the safety, quality, planning and budget and performance in a complex and highly regulated environment? If so, this is the role for you.As a Production Manager Supervisor (First Line Leader) 10-hr, Mon. -Thurs., 2nd shift, 1600 hrs. (4:00pm) - 0230 hrs. (2:30am) you will Supervise... production shift operations to deliver high quality products, manufactured in a safe way to fulfill all requirements of the area and site strategy. Leads shift personnel in the execution of all production related activities. Drives a continuous improvement culture to ensure Zero Accidents, Zero Defects and Zero Waste. You will also manage the day-to-day operations of the manufacturing floor and be the point of contact for internal and external audits.Why GSK?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 organization where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years.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.About the Zebulon Site GSK's Zebulon site is a global supplier of Respiratory and Solid Dose medicines to patients around the globe and the largest GSK Pharmaceutical secondary manufacturing site in North America. The site is located less than 30 minutes from downtown Raleigh, Wendell, Knightdale, Rocky Mount, Wilson, and Wake Forest.
Key differentiators about GSK and Zebulon:
• Our commitment to inclusion and diversity - we see diversity as a critical advantage of ours
• Our focus on cultivating a positive work environment that cares for our employees
• Demonstrated opportunities for continued career growth driven by individual ambition
• Leaders that care about their teams and growth of both individuals and the company
• A priority focus on Safety and Quality
• Clean and GMP compliant work environment
• Onsite cafeteria
• Onsite gym
• Temperature-controlled climate
• Licensed, onsite Health & Wellness clinic
• CDC, local and federal compliant with COVID-19 mandatesIf you have a passion working on life-sustaining products for people who deal with a chronic respiratory or AID/HIV-related illness, please join our team as a Operation Production Supervisor Manufacturing/Packing of Respiratory Dry Powder Inhaler Medicines The production supervisor (First Line Leader) role has responsibilities for leading manufacturing or packing teams; teams are typically between 15 to 25 team members in size. The production supervisor is a key position in succession plans for other leadership roles within GSK including production manager, value stream director and site director roles.If you are ambitious, can effectively partner with supporting groups, and have a passion for developing and leading team that make critical lifesaving medicines each and every day - this role is for you!Key
Responsibilities
Right First TimeLead production shift operations to deliver high quality medicinal products each and every day. Ensure that the focus is always on right first time with respect to safety and quality.Ensure medicines are manufactured in a quality compliant manner and all cGMP (current Good Manufacturing Practices) are adhered to.Represent the value stream during regulatory audits and inspections (internal and external) as directed by line management.Ensure a quality right first-time culture through a robust Self Inspection Audit process.Capability BuildLead the recruitment of team members and then supports their continued development through the establishment of robust development and career progression plans using Workday MyPlans.Provide frequent feedback/coaching as part of our commitment to continually develop team members.Continuous Improvement(Embrace GSK's Production System (GPS; a lean operating system) to drive continuous improvements).Support the tiered accountability process to drive performance management across the balanced scorecard of safety, quality, waste, service and supply.Embed and drive a continuous improvement culture to proactively identify and solve problems.Develop and maintain a robust idea generation process that engages (and recognizes) team members. Focus on the identification and implementation of value adding ideas targeting goals of Zero Accidents, Zero Incidents and Zero Waste.Partnership Ensure robust communication within the department, including daily shift handover process, using visual metrics.Partner with key support teams; technical, quality, scheduling and engineering/maintenance to deliver the weekly schedule at the right time and at the right cost.Why you?
Basic Qualifications:
We are looking for professionals with these required skills to achieve our goals:High School Diploma3 years of experience of pharmaceutical processes, systems, equipment and applicable government regulations
Preferred Qualifications:
If you have the following characteristics, it would be a plus:Associates Degree3+ years of experience and/or Knowledge of pharmaceutical processes, systems, equipment and applicable government regulationsCommunication (written/verbal), conflict resolution, teamwork and leadership skills.Organization skillsKnowledge of manufacturing process and organizationAbility to challenge the production planning and production organization as needed.#LI-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. Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years.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 workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy. We're committed to being more proactive at all levels so that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce.If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at [Phone number shown when applying] (US Toll Free) or [Phone number shown when applying] (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.At GSK, the health and safety of our employees are of paramount importance. As a science-led healthcare company on a mission to get ahead of disease together, we believe that supporting vaccination against COVID-19 is the single best thing we can do in the US to ensure the health and safety of our employees, complementary workers, workplaces, customers, consumers, communities, and the patients we serve. GSK has made the decision to require all US employees to be fully vaccinated against COVID-19, where allowed by state or local law and where vaccine supply is readily available. The only exceptions to this requirement are employees who are approved for an accommodation for religious, medical or disability-related reasons.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.PDN-98542247-38af-4b11-98d2-b6c1ab1624ee
SDL2017 Show more details...
Key differentiators about GSK and Zebulon:
• Our commitment to inclusion and diversity - we see diversity as a critical advantage of ours
• Our focus on cultivating a positive work environment that cares for our employees
• Demonstrated opportunities for continued career growth driven by individual ambition
• Leaders that care about their teams and growth of both individuals and the company
• A priority focus on Safety and Quality
• Clean and GMP compliant work environment
• Onsite cafeteria
• Onsite gym
• Temperature-controlled climate
• Licensed, onsite Health & Wellness clinic
• CDC, local and federal compliant with COVID-19 mandatesIf you have a passion working on life-sustaining products for people who deal with a chronic respiratory or AID/HIV-related illness, please join our team as a Operation Production Supervisor Manufacturing/Packing of Respiratory Dry Powder Inhaler Medicines The production supervisor (First Line Leader) role has responsibilities for leading manufacturing or packing teams; teams are typically between 15 to 25 team members in size. The production supervisor is a key position in succession plans for other leadership roles within GSK including production manager, value stream director and site director roles.If you are ambitious, can effectively partner with supporting groups, and have a passion for developing and leading team that make critical lifesaving medicines each and every day - this role is for you!Key
Responsibilities
Right First TimeLead production shift operations to deliver high quality medicinal products each and every day. Ensure that the focus is always on right first time with respect to safety and quality.Ensure medicines are manufactured in a quality compliant manner and all cGMP (current Good Manufacturing Practices) are adhered to.Represent the value stream during regulatory audits and inspections (internal and external) as directed by line management.Ensure a quality right first-time culture through a robust Self Inspection Audit process.Capability BuildLead the recruitment of team members and then supports their continued development through the establishment of robust development and career progression plans using Workday MyPlans.Provide frequent feedback/coaching as part of our commitment to continually develop team members.Continuous Improvement(Embrace GSK's Production System (GPS; a lean operating system) to drive continuous improvements).Support the tiered accountability process to drive performance management across the balanced scorecard of safety, quality, waste, service and supply.Embed and drive a continuous improvement culture to proactively identify and solve problems.Develop and maintain a robust idea generation process that engages (and recognizes) team members. Focus on the identification and implementation of value adding ideas targeting goals of Zero Accidents, Zero Incidents and Zero Waste.Partnership Ensure robust communication within the department, including daily shift handover process, using visual metrics.Partner with key support teams; technical, quality, scheduling and engineering/maintenance to deliver the weekly schedule at the right time and at the right cost.Why you?
Basic Qualifications:
We are looking for professionals with these required skills to achieve our goals:High School Diploma3 years of experience of pharmaceutical processes, systems, equipment and applicable government regulations
Preferred Qualifications:
If you have the following characteristics, it would be a plus:Associates Degree3+ years of experience and/or Knowledge of pharmaceutical processes, systems, equipment and applicable government regulationsCommunication (written/verbal), conflict resolution, teamwork and leadership skills.Organization skillsKnowledge of manufacturing process and organizationAbility to challenge the production planning and production organization as needed.#LI-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. Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years.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 workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy. We're committed to being more proactive at all levels so that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce.If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at [Phone number shown when applying] (US Toll Free) or [Phone number shown when applying] (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.At GSK, the health and safety of our employees are of paramount importance. As a science-led healthcare company on a mission to get ahead of disease together, we believe that supporting vaccination against COVID-19 is the single best thing we can do in the US to ensure the health and safety of our employees, complementary workers, workplaces, customers, consumers, communities, and the patients we serve. GSK has made the decision to require all US employees to be fully vaccinated against COVID-19, where allowed by state or local law and where vaccine supply is readily available. The only exceptions to this requirement are employees who are approved for an accommodation for religious, medical or disability-related reasons.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.PDN-98542247-38af-4b11-98d2-b6c1ab1624ee
SDL2017 Show more details...
via Jooble
posted_at: 11 days agoschedule_type: Full-time
Job Summary
Are you a native English speaker, interested in supporting scientists and other researchers to publish their latest results? We are looking for full-time English editors to support our scholarly journals from our offices based in Belgrade and Novi Sad, Serbia...
We are looking for meticulous and highly motivated people to join our team of English Editors at MDPI.
Responsibilities:
Editors are expected to accurately edit scholarly articles,
Job Summary
Are you a native English speaker, interested in supporting scientists and other researchers to publish their latest results? We are looking for full-time English editors to support our scholarly journals from our offices based in Belgrade and Novi Sad, Serbia...
We are looking for meticulous and highly motivated people to join our team of English Editors at MDPI.
Responsibilities:
Editors are expected to accurately edit scholarly articles, working to short deadlines and meeting work targets with a high degree of consistency. You may also be asked to edit corporate material (e.g., announcements, flyers, or webpages) and support journal editors with English-related tasks. You will be expected to work full-time from our Serbian offices and be familiar with Microsoft Word. All editors undergo a probation period during which training is provided.
Requirements :
• A Bachelor or Master’s degree in any subject
• English as a first language
• Advanced knowledge of Microsoft Word
• Excellent self-organization, including meeting work targets
• Attention to detail
• Willingness to collaborate as part of an international team
• An interest in scholarly research
• A strong interest in working with research material
The following are a benefit:
• Previous experience editing, writing or publishing scholarly content
• Knowledge of LaTeX
• Experience working in a research environment
• A PhD or equivalent qualification Show more details...
Are you a native English speaker, interested in supporting scientists and other researchers to publish their latest results? We are looking for full-time English editors to support our scholarly journals from our offices based in Belgrade and Novi Sad, Serbia...
We are looking for meticulous and highly motivated people to join our team of English Editors at MDPI.
Responsibilities:
Editors are expected to accurately edit scholarly articles, working to short deadlines and meeting work targets with a high degree of consistency. You may also be asked to edit corporate material (e.g., announcements, flyers, or webpages) and support journal editors with English-related tasks. You will be expected to work full-time from our Serbian offices and be familiar with Microsoft Word. All editors undergo a probation period during which training is provided.
Requirements :
• A Bachelor or Master’s degree in any subject
• English as a first language
• Advanced knowledge of Microsoft Word
• Excellent self-organization, including meeting work targets
• Attention to detail
• Willingness to collaborate as part of an international team
• An interest in scholarly research
• A strong interest in working with research material
The following are a benefit:
• Previous experience editing, writing or publishing scholarly content
• Knowledge of LaTeX
• Experience working in a research environment
• A PhD or equivalent qualification Show more details...
via Jooble
posted_at: 5 days agoschedule_type: Full-time
Job Summary
Once accepted for publication, articles must be prepared to company and industry standards in PDF, XML and HTML formats. This work is carried out by a production team, using custom software developed by MDPI. Training and mentorship will be provided to all new employees...
Responsibilities:
• Supporting the editorial process by formatting the English scientific manuscript (Word or LaTeX files), to ensure that the format meets publishing
Job Summary
Once accepted for publication, articles must be prepared to company and industry standards in PDF, XML and HTML formats. This work is carried out by a production team, using custom software developed by MDPI. Training and mentorship will be provided to all new employees...
Responsibilities:
• Supporting the editorial process by formatting the English scientific manuscript (Word or LaTeX files), to ensure that the format meets publishing requirements
• Converting Word or LaTeX files to XML files
• Converting XML file to new LaTeX file, ensuring that a new PDF file can be generated in high quality
• Working cross-functionally and communicating with editors, to ensure that the publication is done in an accurate and timely manner
• Working independently to meet deadlines while ensuring the high-quality service
Requirements:
• Bachelor’s Degree in any subject
• English level B2 as minimum
• General computer literacy: familiarity with email, Microsoft Office, etc.
• Familiarity with HTML, XHTML or XML
• Good communication and interpersonal skills
• Self-motivated and able to meet deadlines Show more details...
Once accepted for publication, articles must be prepared to company and industry standards in PDF, XML and HTML formats. This work is carried out by a production team, using custom software developed by MDPI. Training and mentorship will be provided to all new employees...
Responsibilities:
• Supporting the editorial process by formatting the English scientific manuscript (Word or LaTeX files), to ensure that the format meets publishing requirements
• Converting Word or LaTeX files to XML files
• Converting XML file to new LaTeX file, ensuring that a new PDF file can be generated in high quality
• Working cross-functionally and communicating with editors, to ensure that the publication is done in an accurate and timely manner
• Working independently to meet deadlines while ensuring the high-quality service
Requirements:
• Bachelor’s Degree in any subject
• English level B2 as minimum
• General computer literacy: familiarity with email, Microsoft Office, etc.
• Familiarity with HTML, XHTML or XML
• Good communication and interpersonal skills
• Self-motivated and able to meet deadlines Show more details...
via Tarta.ai
posted_at: 27 days agoschedule_type: Full-time
Site Name:
USA - North Carolina - ZebulonPosted Date:
Jan 27 2023Are you looking for an opportunity to lead the production planning delivery within a production team to achieve the safety, quality, planning and budget and performance in a complex and highly regulated environment? If so, this is the role for you.As a Production Manager Supervisor (First Line Leader) you will Supervise production... shift operations to deliver high quality products,
Site Name:
USA - North Carolina - ZebulonPosted Date:
Jan 27 2023Are you looking for an opportunity to lead the production planning delivery within a production team to achieve the safety, quality, planning and budget and performance in a complex and highly regulated environment? If so, this is the role for you.As a Production Manager Supervisor (First Line Leader) you will Supervise production... shift operations to deliver high quality products, manufactured in a safe way to fulfill all requirements of the area and site strategy.
Leads shift personnel in the execution of all production related activities.
Drives a continuous improvement culture to ensure Zero Accidents, Zero Defects and Zero Waste.
You will also manage the day-to-day operations of the manufacturing floor and be the point of contact for internal and external audits.Why GSK?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 organization where people can thrive.
Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years.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.About the Zebulon SiteGSK's Zebulon site is a global supplier of Respiratory and Solid Dose medicines to patients around the globe and the largest GSK Pharmaceutical secondary manufacturing site in North America.
The site is located less than 30 minutes from downtown Raleigh, Wendell, Knightdale, Rocky Mount, Wilson, and Wake Forest.Key differentiators about GSK and Zebulon:
Our commitment to inclusion and diversity - we see diversity as a critical advantage of ours
Our focus on cultivating a positive work environment that cares for our employees
Demonstrated opportunities for continued career growth driven by individual ambition
Leaders that care about their teams and growth of both individuals and the company
A priority focus on Safety and Quality
Clean and GMP compliant work environment
Onsite cafeteria
Onsite gym
Temperature-controlled climate
Licensed, onsite Health & Wellness clinic
CDC, local and federal compliant with COVID-19 mandatesIf you have a passion working on life-sustaining products for people who deal with a chronic respiratory or AID/HIV-related illness, please join our team as a Operation Production Supervisor Manufacturing/Packing of Respiratory Dry Powder Inhaler MedicinesThe production supervisor (First Line Leader) role has responsibilities for leading manufacturing or packing teams; teams are typically between 15 to 25 team members in size.
The production supervisor is a key position in succession plans for other leadership roles within GSK including production manager, value stream director and site director roles.If you are ambitious, can effectively partner with supporting groups, and have a passion for developing and leading team that make critical lifesaving medicines each and every day - this role is for you!Key ResponsibilitiesRight First TimeLead production shift operations to deliver high quality medicinal products each and every day.
Ensure that the focus is always on right first time with respect to safety and quality.
Ensure medicines are manufactured in a quality compliant manner and all cGMP (current Good Manufacturing Practices) are adhered to.
Represent the value stream during regulatory audits and inspections (internal and external) as directed by line management.
Ensure a quality right first-time culture through a robust Self Inspection Audit process.Capability Build
Lead the recruitment of team members and then supports their continued development through the establishment of robust development and career progression plans using Workday MyPlans.
Provide frequent feedback/coaching as part of our commitment to continually develop team members.Continuous Improvement
(Embrace GSK's Production System (GPS; a lean operating system) to drive continuous improvements).
Support the tiered accountability process to drive performance management across the balanced scorecard of safety, quality, waste, service and supply.
Embed and drive a continuous improvement culture to proactively identify and solve problems.
Develop and maintain a robust idea generation process that engages (and recognizes) team members.
Focus on the identification and implementation of value adding ideas targeting goals of Zero Accidents, Zero Incidents and Zero Waste.Partnership
Ensure robust communication within the department, including daily shift handover process, using visual metrics.
Partner with key support teams; technical, quality, scheduling and engineering/maintenance to deliver the weekly schedule at the right time and at the right cost.Why you?Basic Qualifications:
We are looking for professionals with these required skills to achieve our goals:
High School Diploma
3 years of experience of pharmaceutical processes, systems, equipment and applicable government regulationsPreferred Qualifications:
If you have the following characteristics, it would be a plus:
Associates Degree
3+ years of experience and/or Knowledge of pharmaceutical processes, systems, equipment and applicable government regulations
Communication (written/verbal), conflict resolution, teamwork and leadership skills.
Organization skills
Knowledge of manufacturing process and organization
Ability to challenge the production planning and production organization as needed.#LI-GSK#GlobalsupplychainGSK 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 want GSK to be a workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy.
We're committed to being more proactive at all levels so that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce.If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-#-# (US Toll Free) or +1 801 # (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 t Show more details...
USA - North Carolina - ZebulonPosted Date:
Jan 27 2023Are you looking for an opportunity to lead the production planning delivery within a production team to achieve the safety, quality, planning and budget and performance in a complex and highly regulated environment? If so, this is the role for you.As a Production Manager Supervisor (First Line Leader) you will Supervise production... shift operations to deliver high quality products, manufactured in a safe way to fulfill all requirements of the area and site strategy.
Leads shift personnel in the execution of all production related activities.
Drives a continuous improvement culture to ensure Zero Accidents, Zero Defects and Zero Waste.
You will also manage the day-to-day operations of the manufacturing floor and be the point of contact for internal and external audits.Why GSK?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 organization where people can thrive.
Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years.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.About the Zebulon SiteGSK's Zebulon site is a global supplier of Respiratory and Solid Dose medicines to patients around the globe and the largest GSK Pharmaceutical secondary manufacturing site in North America.
The site is located less than 30 minutes from downtown Raleigh, Wendell, Knightdale, Rocky Mount, Wilson, and Wake Forest.Key differentiators about GSK and Zebulon:
Our commitment to inclusion and diversity - we see diversity as a critical advantage of ours
Our focus on cultivating a positive work environment that cares for our employees
Demonstrated opportunities for continued career growth driven by individual ambition
Leaders that care about their teams and growth of both individuals and the company
A priority focus on Safety and Quality
Clean and GMP compliant work environment
Onsite cafeteria
Onsite gym
Temperature-controlled climate
Licensed, onsite Health & Wellness clinic
CDC, local and federal compliant with COVID-19 mandatesIf you have a passion working on life-sustaining products for people who deal with a chronic respiratory or AID/HIV-related illness, please join our team as a Operation Production Supervisor Manufacturing/Packing of Respiratory Dry Powder Inhaler MedicinesThe production supervisor (First Line Leader) role has responsibilities for leading manufacturing or packing teams; teams are typically between 15 to 25 team members in size.
The production supervisor is a key position in succession plans for other leadership roles within GSK including production manager, value stream director and site director roles.If you are ambitious, can effectively partner with supporting groups, and have a passion for developing and leading team that make critical lifesaving medicines each and every day - this role is for you!Key ResponsibilitiesRight First TimeLead production shift operations to deliver high quality medicinal products each and every day.
Ensure that the focus is always on right first time with respect to safety and quality.
Ensure medicines are manufactured in a quality compliant manner and all cGMP (current Good Manufacturing Practices) are adhered to.
Represent the value stream during regulatory audits and inspections (internal and external) as directed by line management.
Ensure a quality right first-time culture through a robust Self Inspection Audit process.Capability Build
Lead the recruitment of team members and then supports their continued development through the establishment of robust development and career progression plans using Workday MyPlans.
Provide frequent feedback/coaching as part of our commitment to continually develop team members.Continuous Improvement
(Embrace GSK's Production System (GPS; a lean operating system) to drive continuous improvements).
Support the tiered accountability process to drive performance management across the balanced scorecard of safety, quality, waste, service and supply.
Embed and drive a continuous improvement culture to proactively identify and solve problems.
Develop and maintain a robust idea generation process that engages (and recognizes) team members.
Focus on the identification and implementation of value adding ideas targeting goals of Zero Accidents, Zero Incidents and Zero Waste.Partnership
Ensure robust communication within the department, including daily shift handover process, using visual metrics.
Partner with key support teams; technical, quality, scheduling and engineering/maintenance to deliver the weekly schedule at the right time and at the right cost.Why you?Basic Qualifications:
We are looking for professionals with these required skills to achieve our goals:
High School Diploma
3 years of experience of pharmaceutical processes, systems, equipment and applicable government regulationsPreferred Qualifications:
If you have the following characteristics, it would be a plus:
Associates Degree
3+ years of experience and/or Knowledge of pharmaceutical processes, systems, equipment and applicable government regulations
Communication (written/verbal), conflict resolution, teamwork and leadership skills.
Organization skills
Knowledge of manufacturing process and organization
Ability to challenge the production planning and production organization as needed.#LI-GSK#GlobalsupplychainGSK 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 want GSK to be a workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy.
We're committed to being more proactive at all levels so that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce.If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-#-# (US Toll Free) or +1 801 # (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 t Show more details...
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