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Packaging Supervisor

2 months ago

Fall River, United States Nesco Resource Full time

A major client of ours in the Pharmaceutical Industry has a need for a Packaging Supervisor. This is a permanent position in Fall River, MA. This is a second shift working from 12pm - 8pm.


Responsibilities

  • Ensures compliance with cGMP's, company policies, standard operating procedures, and FDA requirements
  • Conducts product complaints, supporting packaging, and packaging components within approved procedures and regulatory requirements.
  • Managing shifts and controls activities in the absence of the Packaging Manager.
  • Supervising activities and work performed on the floor.
  • Supporting Line Leaders and other employees when necessary.
  • Maintaining proper cGMP practices across all work areas.
  • Responsible for working in all areas such as Pre-check and office duties.
  • Responsible for working with Systech serialization system and SAP.
  • Follow strict internal protocols and Standard Operating Procedures (SOPs) as well as follow current Good Manufacturing Practices (cGMP), comply with legal regulations, monitoring the environment
  • Reducing time spent preparing lines for the next products.
  • Training and educating employees when necessary.
  • Recording In-process entries into respective documents.
  • Checking the Cleanliness of machines prior to or after use.
  • Performing daily routine checkups and ensuring safety measures are in place.
  • Reducing time spent during changeovers.
  • Enforcing cGMP.
  • Maintaining full knowledge and a strong understanding of all SOPs and proper use of equipment.
  • Be a point of contact for questions regarding procedures and expectations for employees.
  • Contribute to Standard Operating Procedure (SOP) writing in the technical area.
  • Understand and operate all necessary equipment and instrumentation to perform activities.
  • Maintains documentation in accordance with internal procedures and regulatory requirements (i.e., GMP, SOPs etc.).


Requirements

  • 1-3 years of direct work experience in pharmaceutical packaging. Preference will be given to candidates with experience in generic pharmaceutical manufacturing and packaging.
  • High School Diploma or GED is required. BS in Pharmaceutical Sciences or related field of study from an accredited college/university preferred.
  • Must have 2 years cGMP work experience.
  • Strong understanding of pharmaceutical packaging machines.
  • Capable of conducting trouble-shootings.
  • Ability to understand and analyze complex data sets.
  • Knowledge of statistical packages is a plus.
  • Knowledge of good manufacturing practices and good documentation practices preferred.
  • Capable of handling and participating in compliance and regulatory audits at the local and federal levels.
  • Experience using SAP business systems and application is a plus
  • Must be proficient in computer skills and software applications such as Microsoft Office tools.
  • Bilingual in Spanish is preferred.