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Packaging Supervisor

Job in Fall River, Bristol County, Massachusetts, 02720, USA
Listing for: Orison
Full Time position
Listed on 2026-06-03
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing
Job Description & How to Apply Below
Overview:

The job duties for this position include but are not limited to the following:
  • 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.
  • 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.
  • Serve as a leader and coach.
  • Contribute to Standard Operating Procedure (SOP) writing in the technical area.
  • Understand and operates all necessary equipment and instrumentation to perform activities.
  • Maintains documentation in accordance with internal procedures and regulatory requirements (i.e., GMP, SOPs etc.).
  • 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.
  • Perform other duties as assigned.
Education and Experience
  • Two (2) to four (4) years of direct work experience in pharmaceutical packaging.
  • Preference will be given to candidates with experience in generic pharmaceutical manufacturing and packaging.
  • At least two years directly managing a team.
  • High School Diploma or GED is required. Bachelor's degree in Pharmaceutical Sciences or related field of study from an accredited college/university preferred.
  • Must have 2 years' cGMP work experience.
Technical Knowledge and Computer Systems Skills
  • Strong understanding of pharmaceutical packaging machines.
  • Capable of conducting trouble-shootings.
  • Capable of handling and participating in compliance and regulatory audits at the local and federal levels.
  • Experience using SAP business systems and applications is a plus
  • Must have 2 years' cGMP work experience.
  • Must be proficient in computer skills and software applications such as Microsoft Office tools.
Professional and Behavioral Competencies
  • Proficiently speak English as a first or second language
  • 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.
  • Ability to read, write and communicate effectively.
  • Self-motivated, with the ability to work in a fast-paced manufacturing environment and handle multiple tasks simultaneously.
  • Excellent organizational skills with the ability to focus on details.
  • Basic computer skills (Word and Excel) - Intermediate
  • Good basic math knowledge and excellent attention to details.
Work Schedule and Other Position Information
  • Must be willing to work in a pharmaceutical packaging setting.
  • Must be willing and able to work any assigned shift ranging from the first or second shift. The work schedule may be Monday to Friday.
  • Must be willing to work some weekends based on business needs as required by management.
  • No remote work is available.
Skills:

CGMP,WORD,GMP
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