Sr. Supervisor, Packaging & Inspection- 2nd Shift

Kindeva; Maryland Heights, Northern (MO, KY); Hybrid; USD 90,000 - 120,000; Full time

Job summary

Kindeva is seeking a Sr. Supervisor of Packaging & Inspection to lead packaging, labeling, serialization, and inspection operations. You will ensure safety, quality, regulatory compliance, and schedule attainment while developing staff.

Responsibilities include leading daily manufacturing, coordinating with Quality, Engineering, Maintenance, Planning, and Supply Chain, and driving continuous improvement. On-site work is required and flexibility for shifts may be needed.

Qualifications

• Required: Associate degree in a scientific, technical, manufacturing, business, engineering, or related field and a minimum of two (2) years of supervisory experience in a manufacturing environment; OR a minimum of ten (10) years of supervisory experience in pharmaceutical operations in lieu of a degree.
• Preferred: Pharmaceutical and/or manufacturing experience, experience in regulated environments, and union leadership experience.
• Effective written and oral communication skills required.
• Demonstrated reading comprehension and writing proficiency. Ability to effectively communicate within a diverse group resulting in desired outcomes.
• Self-starter, team player, with strong interpersonal and coaching skills.
• Proven record of problem-solving, decision-making skills and application of process improvement tools.
• Must have the ability to simultaneously multi-task across multiple capabilities and functions and handle multiple competing priorities and requirements.
• Must have the ability to work effectively under and manage strict production, time and performance deadlines.
• Must be willing and able to work beyond the hours typically defined as a “regular” workday, which may or may not include weekends and holidays.
• Position requires regular onsite attendance.

Responsibilities

• Lead daily manufacturing operations and ensure schedule attainment.
• Lead daily communication meetings and promote accountability, safety, quality, and continuous improvement.
• Ensure compliance with cGMP, SOPs, safety requirements, and regulatory expectations.
• Review production documentation and investigate deviations and quality events.
• Coordinate activities with Quality, Engineering, Maintenance, Planning, and Supply Chain.
• Drive continuous improvement initiatives and operational excellence programs.
• Support audits, inspections, validations, and new product introductions.
• Manage staffing, scheduling, attendance, vacations, and overtime.
• Interview, hire, onboard, coach, and develop employees (supervisors and production colleagues).
• Conduct performance evaluations and administer corrective action when appropriate.
• Ensure employees maintain required qualifications and training.

Skills

Leadership

Team leadership

Communication

Interpersonal skills

Coaching

Problem-solving

Decision-making

Process improvement

Multi-tasking

Time management

Education

Associate degree or higher in science/engineering/related field

10+ years supervisory experience in pharma operations (alternative to degree)

Tools

Microsoft Applications

Kronos

Veeva

Job description

Our Work Matters

At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.

The Impact You Will Make

The Sr. Supervisor of Packaging & Inspection is responsible for supervising packaging, assembly, labeling, serialization, and inspection operations while ensuring safety, compliance, schedule attainment, quality, and employee development. Work week may include time spent on 1st, 2nd, 3rd or split shifts and weekends depending on business need.

Responsibilities

• Lead daily manufacturing operations and ensure schedule attainment.
• Lead daily communication meetings and promote accountability, safety, quality, and continuous improvement.
• Ensure compliance with cGMP, SOPs, safety requirements, and regulatory expectations.
• Review production documentation and investigate deviations and quality events.
• Coordinate activities with Quality, Engineering, Maintenance, Planning, and Supply Chain.
• Drive continuous improvement initiatives and operational excellence programs.
• Support audits, inspections, validations, and new product introductions.
• Manage staffing, scheduling, attendance, vacations, and overtime.
• Interview, hire, onboard, coach, and develop employees (supervisors and production colleagues).
• Conduct performance evaluations and administer corrective action when appropriate.
• Ensure employees maintain required qualifications and training.

Qualifications

• Required: Associate degree in a scientific, technical, manufacturing, business, engineering, or related field and a minimum of two (2) years of supervisory experience in a manufacturing environment; OR a minimum of ten (10) years of supervisory experience in pharmaceutical operations in lieu of a degree.
• Preferred: Pharmaceutical and/or manufacturing experience, experience in regulated environments, and union leadership experience.
• Effective written and oral communication skills required.
• Computer Skills: Microsoft Applications, Kronos, Veeva
• Demonstrated reading comprehension and writing proficiency. Ability to effectively communicate within a diverse group resulting in desired outcomes.
• Self-starter, team player, with strong interpersonal and coaching skills.
• Proven record of problem-solving, decision-making skills and application of process improvement tools.
• Must have the ability to simultaneously multi-task across multiple capabilities and functions and handle multiple competing priorities and requirements.
• Must have the ability to work effectively under and manage strict production, time and performance deadlines.
• Must be willing and able to work beyond the hours typically defined as a “regular” workday, which may or may not include weekends and holidays.
• Position requires regular onsite attendance.