Packaging Supervisor MDI

Are you a Packaging Supervisor MDI looking to join one of the top companies in the Pharmaceutical Industry?

Are you looking to further your career and grow?

Do you have experience in pharmaceutical packaging?

If you answered yes to those three questions, then apply today!

Acara Solutions seeks highly qualified candidates to work ON-SITE with our client in Fall River, MA. Interested?

Here's what you'd do:

• The client is searching for experienced candidates for the position of Packaging Supervisor.
• This person will supervise packaging operators and oversee the production processes in the absence of the Packaging Supervisor.
• The Packaging Supervisor ensures compliance with cGMP's, client, standard operating procedures, and FDA requirements.
• The incumbent will serve as a key resource for conducting product complaints, supporting packaging, and packaging components within approved procedures and regulatory requirements.
• 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.
• 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 (GMP, SOPs).
• 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.

Here's what you'll get:

Pay: $78000 - $99000 / year.

Hours: 40 hrs/Week.

Length: Direct Placement.

Sound like a good fit?

APPLY TODAY

About Acara Solutions

Acara is a premier recruiting and workforce solutions provider-we help companies compete for talent. With a legacy of experience in various industries worldwide, we partner with clients, listen to their needs, and customize visionary talent solutions that drive desired business outcomes. We leverage decades of experience to deliver contingent staffing, direct placement, executive search, and workforce services worldwide.

• High School Diploma or GED.
• Minimum 2 years of experience in pharmaceutical packaging.
• Minimum 2 years of experience in generic pharmaceutical manufacturing and packaging.
• Minimum 2 years of experience in directly managing a team.
• Minimum 2 years of cGMP work experience.
• Minimum 2 years of experience in computer operating and software applications such as Microsoft Office tools, Word and Excel.

• Bachelor's Degree in Pharmaceutical Sciences.
• Knowledge and a understanding of all SOPs and proper use of equipment.
• Good understanding of pharmaceutical packaging machines.
• Technical Knowledge and Computer Systems Skills.
• 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.
• 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.
• Knowledge of good manufacturing practices and good documentation practices.
• Ability to read, write and communicate effectively in English.
• 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.
• Good basic math knowledge and excellent attention to details.

Additional Information:

• Upon offer of employment, the individual will be subject to a background check and a drug screen.
• Be willing and able to work any assigned shift ranging from the first or second shift.
• Be willing to work some weekends based on business needs as needed by management.
• In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire.