Packaging Supervisor

Lifelancer•Fall River, MA

7d•Onsite

About The Position

InvaGen Pharmaceuticals, Inc., a Cipla subsidiary, is seeking experienced Packaging Supervisors to support the production of their newly launched inhalation product. The Packaging Supervisor manages packaging operators and oversees production processes in the absence of the Packaging Manager. This role ensures compliance with cGMP, company policies, standard operating procedures, and FDA requirements. The supervisor serves as a key resource for conducting product complaints and supporting packaging operations within approved procedures and regulatory guidelines.

Requirements

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
Strong understanding of pharmaceutical or fully automated packaging machines
Capable of conducting trouble-shootings packaging machines
Capable of handling and participating in compliance and regulatory audits at the local and federal levels
Proficiently speak English as a first or second language
Ability to understand and analyze complex data sets
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
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

Nice To Haves

Experience using SAP business systems and applications is a plus
Knowledge of statistical packages is a plus
Knowledge of good manufacturing practices and good documentation practices preferred

Responsibilities

Managing shifts and controls activities
Supervising activities and work performed on the shop floor
Maintaining proper cGMP practices across all work areas
Working in all areas such as Pre-check and office duties
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
Serving as a point of contact for questions regarding procedures and expectations for employees
Serving as a leader and coach
Contributing to Standard Operating Procedure (SOP) writing in the technical area
Understanding and operating all necessary equipment and instrumentation to perform activities
Maintaining documentation in accordance with internal procedures and regulatory requirements (i.e., GMP, SOPs etc.)
Following strict internal protocols and Standard Operating Procedures (SOPs) as well as following current Good Manufacturing Practices (cGMP)
Complying with legal regulations, monitoring the environment
Performing other duties as assigned