Secondary Packaging Supervisor Shift 3 (6pm-6:30am)

NEPHRON SC, LLC•West Columbia, SC

6h•Onsite

About The Position

The Secondary Packaging Supervisor is responsible for overseeing production lines, ensuring adherence to GMP requirements, managing personnel, and performing administrative duties. This role also involves monitoring compliance with cGMP, SOPs, and safety regulations, assisting in problem-solving within quality assurance, and communicating quality-related issues to management. The supervisor must stay updated on FDA requirements and ensure compliance through SOPs.

Requirements

Bachelor’s degree or 5+ years equivalent experience
Previous manufacturing / production work experience preferred.
Previous experience with B/F/S or Packaging equipment a plus
Detail oriented, ability to work independently as a self-starter, dependable.
Ability to supervise and motivate up to twenty to seventy employees.
Previous supervisory training preferred.
The ability and willingness to change direction and focus to meet shifting organizational and business demands.
The ability to create and contribute to an environment that values people, encourages trust, teamwork, and open communication, and provides participation, learning, feedback and recognition.
The ability to effectively manage one self, demonstrates integrity, be productive under pressure, and achieve development goals.
The ability to take strategic objectives and accept accountability, motivate and influence others, thinks globally and leverages diversity.
The ability to manage a multitude of resources and to be accurate and current with data and information.
Reaching (waist to overhead)
Bending (waist to floor)
Climbing (floor to ceiling)
Lifting (up to 20 lbs)
Vision (20/20)
Good hearing
Standing (30% of shift time)

Nice To Haves

Previous experience with B/F/S or Packaging equipment

Responsibilities

Communicate with peers via production log book and face-to-face with on-coming/off-going supervisor.
Ensure product lines are running within time guidelines for changeovers, with correct lot# and expiration date, formulations, clean in place and product transfer.
Verify all Batch Records and Lot Records are complete to meet GMP requirements to include all required signatures and or initials.
Ensure training of new hires and any personnel involved in cross training.
Monitor employee attendance/tardiness and provide guidance and discipline when appropriate.
Monitor timecards, vacations, personal time, etc., to ensure production lines are staffed to meet production requirements.
Perform administrative duties to include personnel roster, personnel scheduling, and monitoring production line.
Assist with monitoring all production areas and personnel for adherence to all cGMP, SOPs, and safety regulations.
Assist with development of solutions for chronic problems within quality assurance.
Communicate quality-related observations, issues, problems, discrepancies and any violations of company policies or procedures to Quality Management.
Stay abreast of current FDA requirements and ensure compliance by familiarity with important department Standard Operating Procedures (SOPs) and routine observance of procedures being performed.
Assist in other activities (as needed) for Quality Assurance management.