BioSpace
Supervisor - Aseptic Filling (Day Shift)
BioSpace, Concord, North Carolina, United States, 28027
Supervisor - Aseptic Filling (Day Shift)
Lilly
is a global healthcare leader headquartered in Indianapolis, Indiana. We are investing over $1 Billion in a new, environmentally conscious campus in Concord, NC, to expand our parenteral (injectable) medicine manufacturing capacity.
We are looking for a supervisor to lead the aseptic filling team for the new site. The role supports start‑up activities, builds and maintains a high‑performing team, and ensures compliance with safety and quality standards while driving continuous improvement.
Key Objectives / Deliverables
Lead by example with a safety first, quality always mindset and enforce “Stop Work Authority” for unsafe conditions.
Maintain a safe work environment, support HSE goals, and demonstrate compliance with quality systems.
Act as an administrator and technical leader for operations, teaching procedures and ensuring compliance.
Collaborate with other supervisors to ensure high standards of communication, best practice sharing, and consistency across shifts.
Drive shop‑floor execution (cGMP conformance, Operational Standards for Manufacturing Excellence) and continuous improvement initiatives.
Ensure adequate trained personnel are staffed to meet production goals, reviewing training plans as needed.
Develop and maintain area documentation (procedures, work instructions, job aids) to support start‑up, training, and operation.
Investigate deviations and operational quality issues, support root cause analysis and implement corrective actions.
Support building a diverse, empowered team; manage direct reports across multiple lines; coach and evaluate operators; communicate cross‑functionally with support team.
Requirements (Education & Experience)
High School Diploma or equivalent.
Prior supervisory experience.
Basic computer skills (MS Office).
Experience in operations or manufacturing (pharma, food, clean‑room, etc.).
Excellent interpersonal, written, and oral communication skills.
Strong organizational skills and the ability to handle multiple requests.
Strong technical aptitude and ability to train and mentor others.
Valid driver’s license.
Time Commitments & Work Authorization
Ability to work overtime as required; willing to work a 12‑hour day shift (6 am–6 pm) on a 2‑2‑3 schedule.
Ability to wear safety equipment and work in a cleanroom environment (Grade C, ISO 8).
The position may require short‑term assignments of 3‑12 months domestically or internationally, and occasional short travel for equipment testing.
Candidate must be legally authorized to be employed in the United States; Lilly does not anticipate providing visa sponsorship.
Preferred Attributes
4+ years in manufacturing/operations, with 2+ years in a supervisory role.
Knowledge of cGMP standards and FDA (or other industry) guidelines.
STEM degree or certification.
Experience with aseptic filling, single‑use assemblies, isolator technology.
Experience with automated and semi‑automated inspection systems.
Experience using MES/SAP or other electronic business systems.
Lean/Six Sigma or other continuous improvement methodology; root cause analysis.
Strong team organization and motivation skills.
Compensation & Benefits Salary: $35.33 – $51.83 per hour (estimated). Full‑time employees are eligible for company bonus, 401(k), pension, vacation, medical, dental, vision, prescription drug, flexible benefits, life insurance, and well‑being programs.
Equal Employment Opportunity Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. We also offer accommodations for applicants with disabilities.
#J-18808-Ljbffr
is a global healthcare leader headquartered in Indianapolis, Indiana. We are investing over $1 Billion in a new, environmentally conscious campus in Concord, NC, to expand our parenteral (injectable) medicine manufacturing capacity.
We are looking for a supervisor to lead the aseptic filling team for the new site. The role supports start‑up activities, builds and maintains a high‑performing team, and ensures compliance with safety and quality standards while driving continuous improvement.
Key Objectives / Deliverables
Lead by example with a safety first, quality always mindset and enforce “Stop Work Authority” for unsafe conditions.
Maintain a safe work environment, support HSE goals, and demonstrate compliance with quality systems.
Act as an administrator and technical leader for operations, teaching procedures and ensuring compliance.
Collaborate with other supervisors to ensure high standards of communication, best practice sharing, and consistency across shifts.
Drive shop‑floor execution (cGMP conformance, Operational Standards for Manufacturing Excellence) and continuous improvement initiatives.
Ensure adequate trained personnel are staffed to meet production goals, reviewing training plans as needed.
Develop and maintain area documentation (procedures, work instructions, job aids) to support start‑up, training, and operation.
Investigate deviations and operational quality issues, support root cause analysis and implement corrective actions.
Support building a diverse, empowered team; manage direct reports across multiple lines; coach and evaluate operators; communicate cross‑functionally with support team.
Requirements (Education & Experience)
High School Diploma or equivalent.
Prior supervisory experience.
Basic computer skills (MS Office).
Experience in operations or manufacturing (pharma, food, clean‑room, etc.).
Excellent interpersonal, written, and oral communication skills.
Strong organizational skills and the ability to handle multiple requests.
Strong technical aptitude and ability to train and mentor others.
Valid driver’s license.
Time Commitments & Work Authorization
Ability to work overtime as required; willing to work a 12‑hour day shift (6 am–6 pm) on a 2‑2‑3 schedule.
Ability to wear safety equipment and work in a cleanroom environment (Grade C, ISO 8).
The position may require short‑term assignments of 3‑12 months domestically or internationally, and occasional short travel for equipment testing.
Candidate must be legally authorized to be employed in the United States; Lilly does not anticipate providing visa sponsorship.
Preferred Attributes
4+ years in manufacturing/operations, with 2+ years in a supervisory role.
Knowledge of cGMP standards and FDA (or other industry) guidelines.
STEM degree or certification.
Experience with aseptic filling, single‑use assemblies, isolator technology.
Experience with automated and semi‑automated inspection systems.
Experience using MES/SAP or other electronic business systems.
Lean/Six Sigma or other continuous improvement methodology; root cause analysis.
Strong team organization and motivation skills.
Compensation & Benefits Salary: $35.33 – $51.83 per hour (estimated). Full‑time employees are eligible for company bonus, 401(k), pension, vacation, medical, dental, vision, prescription drug, flexible benefits, life insurance, and well‑being programs.
Equal Employment Opportunity Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. We also offer accommodations for applicants with disabilities.
#J-18808-Ljbffr