Packaging Supervisor

• 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.

• 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. Bachelors degree 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.
• 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.

• 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.

• 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.

Required Skills:

CGMPWORDGMP