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Packaging Operations Manager

2 months ago


Fall River, Massachusetts, United States Cipla Full time
About the Role

We are seeking a highly skilled and experienced Packaging Supervisor to join our team at Cipla. As a key member of our packaging operations, you will be responsible for ensuring compliance with cGMPs, company policies, and regulatory requirements.

Key Responsibilities
  • Manage shifts and control activities in the absence of the Packaging Manager.
  • Supervise activities and work performed on the floor.
  • Support Line Leaders and other employees as needed.
  • Maintain proper cGMP practices across all work areas.
  • Responsible for working in all areas, including Pre-check and office duties.
  • Responsible for working with Systech serialization system and SAP.
  • Reduce time spent preparing lines for the next products.
  • Train and educate employees as needed.
  • Record In-process entries into respective documents.
  • Check the Cleanliness of machines prior to or after use.
  • Perform daily routine checkups and ensure safety measures are in place.
  • Reduce time spent during changeovers.
  • Enforce cGMP.
  • Maintain 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.
  • 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.
Requirements
  • One (1) to three (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. 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 application is a plus.
  • Must have 2 years cGMP work experience.
  • Must be proficient in computer skills and software applications such as Microsoft Office tools.
  • Bilingual in Spanish is preferred.
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.