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Production Supervisors- 2nd Shift 3:00pm-11:30pm

Company: Harrow Health, Inc.
Location: Ledgewood
Posted on: June 12, 2021

Job Description:

About Imprimis Rx

At ImprimisRx we are working hard to help our customers navigate the realities of the healthcare market by providing innovative medications that address both clinical and economic needs. To get there, we need exceptionally talented, bright, and driven people. If you would like to help us build a quality culture organization trusted by healthcare professionals from across the US, this is your chance to join us. We are looking for a dynamic, organized self-starter to lead our Production initiatives for our Ledgewood, New Jersey Site.

Job Summary

The Production Supervisor directly leads the activities of the Operations in the Production area and is responsible for leading direct reports. The Production Supervisor ensures manufacturing, filling, inspection, packaging and labeling jobs are executed accurately with the highest quality, meet applicable cGMP requirements, and are completed on time per the production schedule. The Production Supervisor works with the highest degree of accountability and customer service to ensure client needs are met in a timely manner.

Position Type and Expected Hours of Work

This is a full-time position that will start out on first shift Monday - Friday 7am - 3:30pm for 2-3 months then transition to 2nd shift. 2nd shift schedule will provide site coverage from 3:00pm - 11:30pm (Monday to Friday). Occasional Saturday coverage may be required.

Position Responsibilities:

  • Provides overall Leadership to the Sterile Production Team structured around:
  • Leads Production team members by providing them strategic vision and direction aligned with Organization's core values.
  • Integrates and drives collaboration within the Sterile Production area to achieve highest levels of quality.
  • Fosters and drives collaboration within the production area for improvements which will result in high quality products and customer satisfaction.
  • Drives, implements and sustains changes to attain highest standards of performance.
  • Facilitates communication and drives accountability.
  • Provides a work environment that fosters positive energy, creativity and team work.

  • Must be able to review and approve production batch records in a timely manner.
  • Must be gown qualified to supervise production in the clean room.
  • Supervise a one-shift operation by spending at least 50% of available time interfacing with employees to ensure that all batches are of high quality and exceed all the Company's current Good Manufacturing Practices (CGMPs) and follow all safety guidelines.
  • Ensure that production schedule is met by distributing workload in accordance with changing priorities by working in collaboration with Quality, Supply Chain, Engineering, Product Development and Maintenance departments.
  • Ensure sterile production operations are properly controlled and regulatory compliance requirements are met by ensuring batch documentation is accurate, Standard Operating Procedures (SOP's) are accurate and personnel training is current, critical documentation templates are accurate, equipment is in good repair and current calibration, and high standards of housekeeping are maintained in all areas of responsibility.
  • Provide feedback for continuous improvement. Assist with hiring and disciplining staff, as required. Support the Company's safety program to maximize safety awareness and provide a safe work environment.
  • Evaluate /solve production problems by reviewing the area of concern, developing potential solutions, technically evaluating or testing the solutions, and preparing summary reports/recommendations for management.
  • Supports continuous improvement by completing work on time, identifying potential issues, and driving to improve work processes and procedures relative to manufacturing and/or filling and packaging equipment.
  • Write investigations and CAPA's for non-conformances and deviations generated by the production departments. Write and maintain SOPs and other manufacturing specifications.
  • Develop and Monitor KPI's to improve department metrics including scrap, non-conformance, batch record errors and plant efficiencies.
  • Other additional duties as assigned.

Experience

Requirements and Qualifications:

High School diploma required; Bachelor's degree, preferred.

  • Must have 3 - 5 years' leadership experience in a cGMP regulated environment and have worked in a pharmaceutical, Biotechnology or medical device manufacturing facility.
  • Minimum of 3 - 5 years' previous experience in a pharmaceutical manufacturing or medical device preferably in sterile environment.
  • Ability and willingness to work and participate effectively in a team environment.
  • Ability and willingness to maintain accurate and factual hard copy and electronic records.
  • Attention to detail, safety, quality and customer requirements.
  • Ability to effectively communicate verbally and in writing to subordinates, peers and management.
  • Ability to read information and apply what is described in the reading material to situations that may contain several details or describe processes involving several steps.
  • Demonstrate high level of personal motivation and initiative.

We offer competitive salary and excellent company benefits including 401K plan.

Work Environment and Physical Demands

While performing the responsibilities of the job, the work environment characteristics are representative of the environment the job holder will encounter, and the physical demands are representative of the physical requirements necessary for an employee to successfully perform the essential functions of the job. Reasonable accommodation can be made to enable people with disabilities to perform the described essential functions.

  • The employee may frequently be required to sit and Communicate effectively.
  • The employee is occasionally required to stand; walk; use hands to finger, handle, or feel; reach with hands and arms; climb or balance; stoop, kneel, crouch.
  • The employee must occasionally lift and/or move up to 50 pounds.
  • May work with hazardous materials and chemicals.

Travel

No travel is expected for this position.

AAP/EEO Statement

ImprimisRx believes in creating long-term relationships by being responsive and relevant and by consistently delivering value to our community of customers. Specifically, with our employees, we focus on attracting, developing and retaining the best talent for our business, challenging our people, demonstrating a "can-do" attitude and fostering a collaborative and mutually supportive environment.

Diversity creates a healthier atmosphere: All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, protected veteran status, or disability status.

ImprimisRx is a drug-free workplace. Candidates are required to pass a drug test before beginning employment. In addition, employees in certain positions are subject to random drug testing.

Other Duties

Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time, with or without notice.

Keywords: Harrow Health, Inc., Newark , Production Supervisors- 2nd Shift 3:00pm-11:30pm, Other , Ledgewood, New Jersey

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