Packaging Supervisor, Metered-Dose Inhaler

Aequor; Fall River (MA); On-site; USD 65,000 - 90,000; Full time

Job summary

Aequor is seeking a Packaging Supervisor for the MDI line in Fall River, MA. This full-time role requires overseeing packaging operators on all shifts and ensuring production runs smoothly in the Packaging Manager’s absence.

Candidates should have automated packaging line experience in pharma, food, or cosmetics, plus 2+ years of cGMP work and team leadership. Relocation assistance is provided onsite.

Qualifications

• Bachelor's degree in Pharmaceutical Sciences or related field required.
• 2–4 years direct experience in pharmaceutical packaging.
• 2 years direct experience managing a team.
• Must have cGMP work experience.

Responsibilities

• Supervise packaging operators and oversee production in the absence of the Packaging Manager.
• Maintain cGMP practices and comply with SOPs and regulatory requirements.
• Work with SAP and the Systech serialization system.
• Train and coach employees; maintain documentation and records.

Skills

Team leadership

cGMP knowledge

Data analysis

English communication

Education

Bachelor's degree in Pharmaceutical Sciences

Tools

SAP

Microsoft Office

Job description

Packaging Supervisor, MDI (Metered-Dose Inhaler)

1st Shift = 7am to 3:30pm or 8:30am to 5:00pm - 2nd Shift = 3pm to 11:30pm - 3rd Shift = 11pm to 7:30am

Onsite in Fall River, MA (partial relocation assistance provided)

Full-Time

Required: automated packaging line experience at a pharmaceutical, food, or cosmetic company as well as cGMP experience. Each shift will be managing fifteen people (direct reports).

Our 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 Manager.

The Packaging Supervisor ensures compliance with cGMP’s, company policies, 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.

The job duties for this position include but are not limited to the following

• 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.
• 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.

Education and Experience

• Bachelor’s degree in Pharmaceutical Sciences or related field of study from an accredited college/university required.
• Required: automated packaging line experience in a pharmaceutical, food, or cosmetic company.
• 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.
• Must have 2 years’ experience 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 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.

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.