Actalent
QA Supervisor
Actalent, Verona, Wisconsin, United States, 53593
Job Title: Quality Assurance Supervisor
Job Description
We are seeking a dynamic QA Supervisor to join our team. In this role, you will ensure compliance and manage non-conformance issues related to raw materials and finished products. You will focus on assessing the release of products and addressing any deviations by collaborating with production and QC teams. You will write food safety plans for a multi-product facility that includes pharmaceutical, dietary, and food products. Additionally, you will provide PCQI training and support the Master Control system, eventually becoming an expert. Responsibilities include editing and approving SOPs, overseeing shipment releases, and supervising a growing QA team.
Qualifications
B.S. chemistry, biochemistry, biology or related life science field with 7 years of GMP experience in the pharmaceutical/biotech industry OR Masters with 5 years of GMP experience
2 years of supervisory experience
Software validation experience is a plus
Experience with making decisions on releasing of raw materials and finished products (QC writes OOS but QA decides if they agree)
QC lab/chemistry experience is a plus (equipment review experience)
PCQI certified- most preferred- but they can provide certification (8-16 hour training)
SQF certified- nice to have
Candidate who wants to be in QA long term- future opportunities within the next 5 years (people retiring)
Experience within contract manufacturing companies. A lot of moving parts compared to contract labs.
Culture fit: Patient, self-motivated, positive, mentor other employees
Job Type
This is a permanent position.
Work Site
This is a fully on-site position in Verona, Wisconsin.
Work Environment
Your immediate team includes the Director of QA, QA Manager, QA personnel in production, and a QA Specialist.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.
Job Description
We are seeking a dynamic QA Supervisor to join our team. In this role, you will ensure compliance and manage non-conformance issues related to raw materials and finished products. You will focus on assessing the release of products and addressing any deviations by collaborating with production and QC teams. You will write food safety plans for a multi-product facility that includes pharmaceutical, dietary, and food products. Additionally, you will provide PCQI training and support the Master Control system, eventually becoming an expert. Responsibilities include editing and approving SOPs, overseeing shipment releases, and supervising a growing QA team.
Qualifications
B.S. chemistry, biochemistry, biology or related life science field with 7 years of GMP experience in the pharmaceutical/biotech industry OR Masters with 5 years of GMP experience
2 years of supervisory experience
Software validation experience is a plus
Experience with making decisions on releasing of raw materials and finished products (QC writes OOS but QA decides if they agree)
QC lab/chemistry experience is a plus (equipment review experience)
PCQI certified- most preferred- but they can provide certification (8-16 hour training)
SQF certified- nice to have
Candidate who wants to be in QA long term- future opportunities within the next 5 years (people retiring)
Experience within contract manufacturing companies. A lot of moving parts compared to contract labs.
Culture fit: Patient, self-motivated, positive, mentor other employees
Job Type
This is a permanent position.
Work Site
This is a fully on-site position in Verona, Wisconsin.
Work Environment
Your immediate team includes the Director of QA, QA Manager, QA personnel in production, and a QA Specialist.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.