The Quality Assurance (QA) Manager will serve as the QA leader of the Companys operational site in Alexandria MN dedicated to the successful delivery of site quality goals and objectives. This individual leads the daily operations of a team of QA staff responsible for confirming satisfactory product design verification validation and transfer; documentation control for release of commercialized product; suitability of local quality management system (QMS); change and risk management; corrective and preventive actions; complaint resolution and root cause investigation; monitoring and reporting of relevant data and metrics. As directed by leadership this individual may direct QA operations for more than one operational site. This role is expected to serve as the primary QA business partner to site-focused teams within the Manufacturing Supply Chain EH&S Commercial Product Management R&D and Customer Service functions among others.
In partnership with respective HR operational leadership and cross-functional stakeholders this individual is expected to foster a positive work environment and a culture of ownership continuous improvement and accountability.
To perform this job successfully an individual must be able to perform each of the following essential functions satisfactorily:
- Provide daily leadership to a team of direct reports in the areas of safety efficiency quality control cost resources and engagement in support of the organizations commercial and operational activities
- Responsible for personnel activities of direct reports including business objective setting staffing resource planning training performance management and staff development and effectiveness
- Ensure effectiveness of local quality management system (QMS) while also ensuring the highest standard of product quality and site compliance with applicable regulatory and customer requirements
- In partnership with QA leadership support the development implementation and scaling of global and local QMS in alignment with best practices and business needs across the site functions
- Serve as Quality Management Representative for operational site(s) under direct remit including hosting third-party inspections and audits and chairing periodic management reviews of the QMS
- In partnership with site and functional leadership develop and implement key performance indicators (KPIs) relevant to the site QMS and QA function; oversee the regular review analysis and reporting on KPIs for team(s) and area(s) under direct remit
- Ensure high-quality data delivery and effective communication to customers internal or external
- In partnership with direct management develop execute and review strategies to improve the effectiveness of local QA procedures processes training and business reporting
- Ensure effective delivery of and timely resolutions resulting from local operational processes which include document and change control; corrective and preventive actions (CAPAs); manufacturing non-conformance; risk management and business continuity; complaint resolution; root cause investigations; quality standard certification and maintenance; product design verification validation and transfer
- Oversee the effective delivery of QA and QMS training needs and activities across the site
- Serve as business partner with the relevant subject matter expertise to local leaders and functional stakeholders
- Support deployment of global practices and platforms; may lead global projects as directed
- Perform other duties as required to meet business needs
Qualifications :
Minimum Qualifications:
- Bachelors degree in an engineering mathematics business or scientific disciplineor equivalent combination of applicable education and relevant work experience
- Prior experience managing the quality assurance function or a related product quality function and delivery of associated operational processes within an ISO-certified quality management system and manufacturing environment
- Proven success managing and developing business staff with the demonstrated ability to effectively manage and direct a team in a dynamic working environment
- Proven expert knowledge and understanding of the ISO 9001 standard or a relevant ISO quality standard
- Demonstrated experience performing risk analyses (e.g. FMEA FTA Risk Ranking/Filtering) and cross-functional root cause investigations throughout the product manufacturing lifecycle
- Proven success directing and chairing large-group engagements such as customer or supplier audits ISO (re)certifications and company management reviews
- Proficient computer skills including working knowledge of Microsoft Office suite of products particularly Word Excel and PowerPoint
Preferred Qualifications:
- Prior experience in the medical device biotechnology or biopharma industry
- Prior experience in an FDA-certified manufacturing environment
- Demonstrated experience with electronic platforms for quality management systems
Competencies & Behaviours:
- Unwavering commitment to business quality and continuous improvement
- Proven emotional resilience to lead through influence and direct line management
- Clear strategic thinker with proven critical relationship development skills
- Demonstrated attention to detail and planning and organizational skills
- Demonstrated verbal and written communication skills with the ability to communicate to external and internal audiences at all levels of an organization
- Ability to work effectively in a team environment possess an ability to adapt to change in the environment and have proven ability to exert influence in a directive and positive manner
- Demonstrated autonomy: ability to self-start and drive whilst recognising the appropriate time for stakeholder engagement
- Extensive problem-solving skills with the ability to analyze data and develop dynamic solutions that produce deliverables and meet business objectives
- Adaptable and willing to take on multiple new tasks and responsibilities while managing and prioritizing multiple tasks within a dynamic work environment
- Assertive and decisive consistent and fair demonstrating self-confidence and emotional strength
- Results-driven and process-oriented ensuring targets are met on time and on budget
- Demonstrated integrity and judicious discretion with business data personnel matters and confidential information
- Resonate and operate in line with LGCs core value behaviours: Passion Curiosity Integrity Brilliance and Respect
Additional Information :
What we offer (US based-employees):
- Competitive compensation with strong bonus program
- Comprehensive medical dental and vision benefits for employees and dependents
- FSA/HSA Pre-tax savings plans for health care childcare and elder care
- Deductible Buffer Insurance and Critical Illness Insurance
- 401(k) retirement plan with matching employer contribution
- Company-paid short- and long- term disability life insurance and employee assistance program
- Flexible work options
- Pet Insurance for our furry friends
- Enhanced Parental leave of 8 additional weeks
- PTO that begins immediately
- Town Hall monthly meeting onsite/virtual Cheer program where employees are recognized for outstanding work Company wide social events frequent catered lunches and much more!
LGC strongly believes that every job applicant and employee should be valued for their individual talents regardless of age disability race color ethnic or national origin sex sexual orientation gender reassignment marital or civil partnership pregnancy or maternity religion or belief. Short listing interviewing and selection will always be carried out without regard to gender sexual orientation marital status color race nationality ethnic or national origins religion or belief age or trade union membership.
Remote Work :
No
Employment Type :
Full-time
The Quality Assurance (QA) Manager will serve as the QA leader of the Companys operational site in Alexandria MN dedicated to the successful delivery of site quality goals and objectives. This individual leads the daily operations of a team of QA staff responsible for confirming satisfactory product...
The Quality Assurance (QA) Manager will serve as the QA leader of the Companys operational site in Alexandria MN dedicated to the successful delivery of site quality goals and objectives. This individual leads the daily operations of a team of QA staff responsible for confirming satisfactory product design verification validation and transfer; documentation control for release of commercialized product; suitability of local quality management system (QMS); change and risk management; corrective and preventive actions; complaint resolution and root cause investigation; monitoring and reporting of relevant data and metrics. As directed by leadership this individual may direct QA operations for more than one operational site. This role is expected to serve as the primary QA business partner to site-focused teams within the Manufacturing Supply Chain EH&S Commercial Product Management R&D and Customer Service functions among others.
In partnership with respective HR operational leadership and cross-functional stakeholders this individual is expected to foster a positive work environment and a culture of ownership continuous improvement and accountability.
To perform this job successfully an individual must be able to perform each of the following essential functions satisfactorily:
- Provide daily leadership to a team of direct reports in the areas of safety efficiency quality control cost resources and engagement in support of the organizations commercial and operational activities
- Responsible for personnel activities of direct reports including business objective setting staffing resource planning training performance management and staff development and effectiveness
- Ensure effectiveness of local quality management system (QMS) while also ensuring the highest standard of product quality and site compliance with applicable regulatory and customer requirements
- In partnership with QA leadership support the development implementation and scaling of global and local QMS in alignment with best practices and business needs across the site functions
- Serve as Quality Management Representative for operational site(s) under direct remit including hosting third-party inspections and audits and chairing periodic management reviews of the QMS
- In partnership with site and functional leadership develop and implement key performance indicators (KPIs) relevant to the site QMS and QA function; oversee the regular review analysis and reporting on KPIs for team(s) and area(s) under direct remit
- Ensure high-quality data delivery and effective communication to customers internal or external
- In partnership with direct management develop execute and review strategies to improve the effectiveness of local QA procedures processes training and business reporting
- Ensure effective delivery of and timely resolutions resulting from local operational processes which include document and change control; corrective and preventive actions (CAPAs); manufacturing non-conformance; risk management and business continuity; complaint resolution; root cause investigations; quality standard certification and maintenance; product design verification validation and transfer
- Oversee the effective delivery of QA and QMS training needs and activities across the site
- Serve as business partner with the relevant subject matter expertise to local leaders and functional stakeholders
- Support deployment of global practices and platforms; may lead global projects as directed
- Perform other duties as required to meet business needs
Qualifications :
Minimum Qualifications:
- Bachelors degree in an engineering mathematics business or scientific disciplineor equivalent combination of applicable education and relevant work experience
- Prior experience managing the quality assurance function or a related product quality function and delivery of associated operational processes within an ISO-certified quality management system and manufacturing environment
- Proven success managing and developing business staff with the demonstrated ability to effectively manage and direct a team in a dynamic working environment
- Proven expert knowledge and understanding of the ISO 9001 standard or a relevant ISO quality standard
- Demonstrated experience performing risk analyses (e.g. FMEA FTA Risk Ranking/Filtering) and cross-functional root cause investigations throughout the product manufacturing lifecycle
- Proven success directing and chairing large-group engagements such as customer or supplier audits ISO (re)certifications and company management reviews
- Proficient computer skills including working knowledge of Microsoft Office suite of products particularly Word Excel and PowerPoint
Preferred Qualifications:
- Prior experience in the medical device biotechnology or biopharma industry
- Prior experience in an FDA-certified manufacturing environment
- Demonstrated experience with electronic platforms for quality management systems
Competencies & Behaviours:
- Unwavering commitment to business quality and continuous improvement
- Proven emotional resilience to lead through influence and direct line management
- Clear strategic thinker with proven critical relationship development skills
- Demonstrated attention to detail and planning and organizational skills
- Demonstrated verbal and written communication skills with the ability to communicate to external and internal audiences at all levels of an organization
- Ability to work effectively in a team environment possess an ability to adapt to change in the environment and have proven ability to exert influence in a directive and positive manner
- Demonstrated autonomy: ability to self-start and drive whilst recognising the appropriate time for stakeholder engagement
- Extensive problem-solving skills with the ability to analyze data and develop dynamic solutions that produce deliverables and meet business objectives
- Adaptable and willing to take on multiple new tasks and responsibilities while managing and prioritizing multiple tasks within a dynamic work environment
- Assertive and decisive consistent and fair demonstrating self-confidence and emotional strength
- Results-driven and process-oriented ensuring targets are met on time and on budget
- Demonstrated integrity and judicious discretion with business data personnel matters and confidential information
- Resonate and operate in line with LGCs core value behaviours: Passion Curiosity Integrity Brilliance and Respect
Additional Information :
What we offer (US based-employees):
- Competitive compensation with strong bonus program
- Comprehensive medical dental and vision benefits for employees and dependents
- FSA/HSA Pre-tax savings plans for health care childcare and elder care
- Deductible Buffer Insurance and Critical Illness Insurance
- 401(k) retirement plan with matching employer contribution
- Company-paid short- and long- term disability life insurance and employee assistance program
- Flexible work options
- Pet Insurance for our furry friends
- Enhanced Parental leave of 8 additional weeks
- PTO that begins immediately
- Town Hall monthly meeting onsite/virtual Cheer program where employees are recognized for outstanding work Company wide social events frequent catered lunches and much more!
LGC strongly believes that every job applicant and employee should be valued for their individual talents regardless of age disability race color ethnic or national origin sex sexual orientation gender reassignment marital or civil partnership pregnancy or maternity religion or belief. Short listing interviewing and selection will always be carried out without regard to gender sexual orientation marital status color race nationality ethnic or national origins religion or belief age or trade union membership.
Remote Work :
No
Employment Type :
Full-time
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