Lead Associate, Manufacturing (A Shift Pack)

Holly Springs, MS - USA

Monthly Salary: Not Disclosed

Posted on: Yesterday

Vacancies: 1 Vacancy

Job Summary

Reporting to the Supervisor you will work onsite on the shop floor employee in manufacturing operations. You will provide the technical skill-sets necessary to manufacture high quality biologicals safely in a compliant efficient and cost-effective manner and help lead a team of associates.

Shift: Day
Hours: 5:45AM-5:45PM
Follow 2-2-3 schedule

Responsibilities:

Provide production support setting up production procedures and labels
Review and maintain GMP production support documentation /departmental databases and spreadsheets
Assist with investigations; reviews operational and process discrepancies in manufacturing
Complete process steps according to defined SOPs and BPRs.

Qualifications:

High School Diploma or equivalent vocational or technical education
Expert knowledge of cGMP requirements required
Experience completing SOPs and documenting work required
5 years production experience
Experience completing SOPs and documenting work
Basic mechanical aptitude or knowledge of electronic / mechanical equipment preferred.
Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.

About CSL Seqirus

CSL Seqirus is part ofCSL. As one of the largest influenza vaccine providers in the world CSL Seqirusis a major contributor to the prevention of influenza globally and a transcontinental partner in pandemic preparedness. With state-of-the-art production facilities in the U.S. the U.K. and Australia CSL Seqirus utilizes egg cell and adjuvant technologies to offer a broad portfolio of differentiated influenza vaccines in more than 20 countries around the world.

To learn more about CSL CSL Behring CSL Seqirus and CSL Vifor visit and CSL Plasma at Benefits

For more information on CSL benefits visit How CSL Supports Your Well-being CSL.

You Belong at CSL

At CSL Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy we are able to better understand and connect with our patients and donors foster strong relationships with our stakeholders and sustain a diverse workforce that will move our company and industry into the future.

To learn more about inclusion and belonging visit Opportunity Employer

CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process please visit our On the Front Line video to learn more about CSL Seqirus

Required Experience:

Shift: Day
Hours: 5:45AM-5:45PM
Follow 2-2-3 schedule

Responsibilities:

Provide production support setting up production procedures and labels
Review and maintain GMP production support documentation /departmental databases and spreadsheets
Assist with investigations; reviews operational and process discrepancies in manufacturing
Complete process steps according to defined SOPs and BPRs.

Qualifications:

High School Diploma or equivalent vocational or technical education
Expert knowledge of cGMP requirements required
Experience completing SOPs and documenting work required
5 years production experience
Experience completing SOPs and documenting work
Basic mechanical aptitude or knowledge of electronic / mechanical equipment preferred.
Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.