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Sector:
Research and Development, Technology
Role:
Senior Manager
Contract Type:
Permanent
Hours:
Full Time
Site Name:
UK - Essex - Harlow Posted Date:
Jan 13 2025
We have a new opportunity for an R&D Supply QA Senior Manager to join our team at the GSK Harlow site.
As an R&D Supply QA Senior Manager within Quality R&D, you will lead a team of Quality professionals overseeing clinical packaging and distribution activities who support the R&D clinical supply chain to get our products to the patient.
In this role you will:
Develop strategy, policy, group objectives, and processes in product Quality R&D and with business partners.
Lead projects, continuous improvement programs or team activities which may include GxP.
Direct the activities of one or more direct reports or lead a matrix team or business process.
Manage resource (may include budgets), priorities, schedules and/or projects to assure delivery of group objectives.
Contribute to an environment that optimizes employee productivity and adds value.
Develop group skill sets and knowledge base to meet the needs of a changing environment.
Develop internal/external networks and communicate with key stakeholders at various levels.
Engage with the business in strategic/operational decisions on behalf of the group.
Provide input into the development of strategy, policy, group objectives and processes in R&D Supply QA and with business partners.
Assure products meet regulatory requirements and that they conform to regulatory submissions.
Conduct review of completed batch and/or packaging records.
Initiation and maintenance of Quality Assurance Agreements.
Participate in investigations, such as Quality Investigations, customer complaints and vendor complaints and make recommendations for corrective and preventative actions.
Represent the group as a business contact or on a quality forum/council.
Contribute to Tech projects supporting business processes improvements.
Basic Qualifications & Skills:
Experience on a manufacturing site in the Pharmaceutical Industry.
Strong experience in GMP related to manufacture/testing or Packing activities preferably related to IMPs.
Experience in line management or managing/leading a multidisciplined project or matrix team in a GMP environment.
Proven experience in problem resolution and continuous improvement. Experience with cGMP regulations and Quality Systems.
Ability to lead and motivate a team in a matrix organization.
Preferred Qualifications & Skills:
Extensive knowledge of cGMP regulations and R&D supply chains and processes.
Experience working with internal/external partners connected with GMP.
Project management and internal/external inspection experience.
Closing Date for Applications:
Wednesday 22nd January 2025 (COB)
Please take a copy of the Job Description, as this will not be available post closure of the advert.
When applying for this role, please use the 'cover letter' of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above.
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.
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. 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.
As an Equal Opportunity Employer, we are open to all talent.
We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.
#J-18808-Ljbffr
Sector:
Research and Development, Technology
Role:
Senior Manager
Contract Type:
Permanent
Hours:
Full Time
Site Name:
UK - Essex - Harlow Posted Date:
Jan 13 2025
We have a new opportunity for an R&D Supply QA Senior Manager to join our team at the GSK Harlow site.
As an R&D Supply QA Senior Manager within Quality R&D, you will lead a team of Quality professionals overseeing clinical packaging and distribution activities who support the R&D clinical supply chain to get our products to the patient.
In this role you will:
Develop strategy, policy, group objectives, and processes in product Quality R&D and with business partners.
Lead projects, continuous improvement programs or team activities which may include GxP.
Direct the activities of one or more direct reports or lead a matrix team or business process.
Manage resource (may include budgets), priorities, schedules and/or projects to assure delivery of group objectives.
Contribute to an environment that optimizes employee productivity and adds value.
Develop group skill sets and knowledge base to meet the needs of a changing environment.
Develop internal/external networks and communicate with key stakeholders at various levels.
Engage with the business in strategic/operational decisions on behalf of the group.
Provide input into the development of strategy, policy, group objectives and processes in R&D Supply QA and with business partners.
Assure products meet regulatory requirements and that they conform to regulatory submissions.
Conduct review of completed batch and/or packaging records.
Initiation and maintenance of Quality Assurance Agreements.
Participate in investigations, such as Quality Investigations, customer complaints and vendor complaints and make recommendations for corrective and preventative actions.
Represent the group as a business contact or on a quality forum/council.
Contribute to Tech projects supporting business processes improvements.
Basic Qualifications & Skills:
Experience on a manufacturing site in the Pharmaceutical Industry.
Strong experience in GMP related to manufacture/testing or Packing activities preferably related to IMPs.
Experience in line management or managing/leading a multidisciplined project or matrix team in a GMP environment.
Proven experience in problem resolution and continuous improvement. Experience with cGMP regulations and Quality Systems.
Ability to lead and motivate a team in a matrix organization.
Preferred Qualifications & Skills:
Extensive knowledge of cGMP regulations and R&D supply chains and processes.
Experience working with internal/external partners connected with GMP.
Project management and internal/external inspection experience.
Closing Date for Applications:
Wednesday 22nd January 2025 (COB)
Please take a copy of the Job Description, as this will not be available post closure of the advert.
When applying for this role, please use the 'cover letter' of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above.
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.
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. 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.
As an Equal Opportunity Employer, we are open to all talent.
We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.
#J-18808-Ljbffr
