Supervisor, Packaging

International Vitamin Corporation; Greenville (SC); On-site; USD 60,000 - 90,000; Full time

Job summary

International Vitamin Corporation is seeking a Manufacturing Supervisor to maintain GMP quality standards, plant safety, and productivity across the department. You will understand equipment setups, adjustments, and repairs per manuals and specs, guiding on-shift staff and ensuring compliance with SOPs.

The role requires 1–3 years in GMP environments, strong communication, and leadership, with Lean Six Sigma familiarity.

Qualifications

• Associates degree or equivalent experience.
• 1-3 years of experience in related field.
• Experience in GMP environment (preferably in pharmaceutical industry).

Responsibilities

• Monitors operators and equipment to ensure SOPs are followed and documents violations.
• Directs machine operators and service staff on daily schedules and SOP requirements.
• Maintains production schedule by adjusting equipment for optimal performance.
• Sets up equipment for material, size, and product changes and inspects quality after changeover.
• Checks product for defects and records conformity to quality specs.
• Promotes continuous improvement in quality, efficiency, and safety.
• Assists with interviewing, evaluating, promoting, and developing direct reports.
• Conducts CAPA analysis to prevent recurrence and mitigates risks.
• Communicates objectives across the organization and helps drive performance.
• Promotes teamwork and safe work environment; enforces safety procedures.

Skills

Team player

Problem solver

Strong communication

LEAN Six Sigma

Organizational skills

Analytical skills

Leadership

Interpersonal skills

Education

Associates degree or equivalent

1-3 years experience

GMP environment experience

Tools

MS Word

Excel

PowerPoint

Job description

Overview

Position Overview

Responsible for maintaining GMP quality standards, plant safety, and manufacturing productivity throughout the department. Requires in-depth knowledge and understanding of equipment to support set-ups, adjustments, repairs, andmaintainingall equipmentin accordance withdiagrams, sketches, operation manuals, and manufacturer's specifications. Direct reports include all on-shift department staff.

Responsibilities

Specific Responsibilities

• Monitors operators and equipment throughout each shift to ensure allSOPsare properly followed and executed.Coachesoperators on proper operation andaddressesviolations with proper documentation.

• Directs machine operators and service personnel indetailsof daily schedule, operational goals and standard operating procedures and requirements.

• Ensures production schedule ismaintainedby making necessary corrections and adjustments to equipment tomaintainmaximum performance. Reports issues that may result in schedule not beingmaintainedto management immediately.

• Oversees process parameters and makes changes by setting up assigned equipment for change in material, size, and product.Inspects and monitors equipment for quality of operation when changeover is completed.

• Routinely checks product for defects and imperfections. Examines finished product for conformity with quality specifications and records.

• Fosters a continuous improvement environment by evaluating and recommending on-going quality and efficiency improvements as it relates to

• process/engineering/formulation changes, machinery, documentation, machineutilization, and safety best practices.

• Assistswith interviewing,selection, evaluating, promoting and dismissal of direct reports. Rewards,coachesand provides clear,meaningfuland constructive feedback to direct reports tofacilitateindividual development.

• Appraisers employees’ productivity, efficiency and performance for probationary reviews and annual merit reviews.

• Develops andmaintainsa capable, flexible, and motivated workforce by continuous education, cross-training, compliancetrainingand maximizing employee effectiveness.

• Mentors Manufacturing Trainers, and Operation Specialists to help drive business performance.

• Communicates to all levels of the organization so that all employees understand company and departmentalobjectivesand have clear expectations of performance.

• Evaluates machines/processes andutilizesroot causes analysis to generatenew ideasand creative solutions to improveutilization, effectiveness, and productivity rates.

• Promotes an environment of teamwork with all departments to ensure effective and efficient company operations.

• Responds to audit observations by correcting deficiencies and performingdetailedCAPA analysis to prevent future occurrences.

• Promotes a safe work environment by ensuring proper and effective safety procedures are in place and enforced. Documents all safety incidents and near misses accurately andtimely.

General Responsibilities

• Poses no direct threat to the health or safety of himself/herself, of others, or to property. Defined as a significant risk of substantial harm that cannot be eliminated or reduced to an acceptable level by reasonable accommodation.

• Requires regular attendance to perform essentialelementascontainedhereinbetween the assigned start and end times for work.

• Performs such individual assignments as management may direct.

• Other duties as assigned.

Qualifications

TheCandidate

Education,Experience, and Licenses:

• Associates degree or equivalent experience

• 1-3 yearsofexperiencein related field

• Experience in GMP environment (Preferably in Pharmaceutical Industry)

Knowledge, Skills, and Abilities

• Strong teamplayer and motivated problem solver.

• Clear and concise communication skills, both written and verbal.

• Proficiencyin computer software applications: MS Word,Exceland PowerPoint.

• Ability to constructively interact with others to resolve issues and improve the operation.

• Continuous LEAN Six Sigma training (i.e.5S) is highly desirable.

• Strong organizational, communication, and analytical skills.

• Team building skills and leadership qualities.

• Mustmaintaina positive attitude and a willingness to learn and develop skills.

• Ability to interact with otherdepartmentTechnicians, Schedulers, Productdevelopmentand Information Services.

• The ability to workindependently,within a production team and without supervision.

• Ability to work flexible workschedule.

• Job requires the ability to stand forlong periodsof time

• Requires the ability to lift 50lbs.

International Vitamin Corporation (IVC) Is an Equal Opportunity Employer. Our organizationremainssteadfast in our commitment to fostering an inclusive and non-discriminatory work environment that welcomes individuals from all backgrounds. We firmlymaintainthe belief that every individual ought to be treated with respect and dignity, regardless of their race, color, religion, sex, sexual orientation, gender identity or expression, age, national origin, disability, veteran status, marital status, genetic information, or any other protected characteristic, as defined by the law. We pledge that all eligible job applicants shall receive an impartial and unbiased evaluation during the recruitment process, without any form of discrimination based on any of the protectedclass. Our dedication to promoting diversity and inclusivityremainsunwavening, and we take immense pride in cultivating a workplace culture that values and celebrates differences. Our efforts towards creating an environment that is free from prejudice and discrimination are an integral part of our organizational philosophy, and we stand committed to upholding theseprincipl