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Packaging Line Supervisor

Job in Fall River, Bristol County, Massachusetts, 02720, USA
Listing for: Merck & Co.
Full Time position
Listed on 2026-07-18
Job specializations:
  • Manufacturing / Production
    Packaging Engineer, Production Manager, Pharmaceutical Manufacturing
Salary/Wage Range or Industry Benchmark: 76000 - 120000 USD Yearly USD 76000.00 120000.00 YEAR
Job Description & How to Apply Below

Title: Packaging Supervisor

Work Location: Fall River, MA (relocation benefits available)

Shifts Available:

  • 1st Shift: 7:00 AM - 3:30 PM
  • 2nd Shift: 3:00 PM - 11:30 PM
  • 3rd Shift: 11:00 PM - 7:30 AM

Pay Range: $76,000 - $120,000

Responsibilities

Inva Gen Pharmaceuticals, Inc., a Cipla subsidiary, is searching for experienced Packaging Supervisors to support the production of our newly launched inhalation product. The Packaging Supervisor manages packaging operators and oversees the production processes in the absence of the Packaging Manager. The Packaging Supervisor ensures compliance with cGMP, company policies, standard operating procedures, and FDA requirements, serving as a key resource for conducting product complaints, supporting packaging, and packaging components within approved procedures and regulatory requirements.

  • Managing shifts and controlling activities
  • Supervising activities and work performed on the shop floor
  • 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 operate all necessary equipment and instrumentation to perform activities
  • Maintain 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 current Good Manufacturing Practices (cGMP), comply with legal regulations, monitoring the environment
  • Perform other duties as assigned
Education and Experience
  • Bachelor's degree in Pharmaceutical Sciences, Packaging, or related field of study from an accredited college/university required
  • Minimum of two years of experience in pharmaceutical or fully automated packaging lines
  • At least two years directly managing/supervising/leading a team
  • 2 years' experience cGMP work experience
Technical Knowledge and Computer Systems Skills
  • Strong understanding of pharmaceutical or fully automated packaging machines
  • Capable of conducting trouble‑shooting packaging machines
  • 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
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
EEO Statement

Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, sex, sexual orientation, gender identity, religion, national origin, genetic information, disability, or protected veteran status.

At Cipla, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact c

Pre-employment Process

Applicants who receive a conditional offer must satisfactorily complete pre-employment drug testing.

Disclaimer on Pay Ranges

About the Salary/Pay Range:
The salary range mentioned above is an anticipated base salary range for this position. Exact salary depends on several factors such as experience, skills, education, and budget. Salary range may vary based on geographic location. In addition to base salary, this position may be eligible for benefits and participation in a bonus program based on performance and company results.

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