Packaging Supervisor - MDI

Umanist Staffing LLC

Fall River, MA, USA

Published: 6/14/2022

Full Time

Job Description

Job Title: Packaging Supervisor – 2nd Shift
Job Location: Fall River, MA
Work Schedule: Monday to Friday; must be available for 1st or 2nd shift and occasional weekends as per business needs

Purpose:

A leading pharmaceutical manufacturer is seeking an experienced Packaging Supervisor to join their team on the 2nd Shift. This position plays a crucial role in ensuring packaging operations comply with current Good Manufacturing Practices (cGMP), company policies, SOPs, and regulatory requirements. The Packaging Supervisor will lead shift operations, train staff, and ensure efficient and compliant production.

Key Responsibilities:

Supervise packaging operations on the production floor during assigned shift.
Act as the shift lead in the absence of the Packaging Manager.
Ensure proper cGMP practices are followed in all areas of packaging.
Support line leaders and coordinate team performance to maintain efficiency.
Participate in troubleshooting and resolving production or equipment issues.
Oversee cleanliness inspections and changeovers of packaging machinery.
Manage and execute daily documentation, including in-process checks and logs.
Enforce company procedures and safety protocols across the department.
Train and mentor new and existing staff in packaging SOPs, equipment use, and cGMP compliance.
Operate and support serialization systems (e.g., Systech) and enterprise systems (e.g., SAP).
Contribute to the development and revision of SOPs and technical documentation.
Serve as a point of contact for questions regarding procedures and production expectations.
Support audits and inspections by regulatory bodies as needed.
Maintain a clean, organized, and safe work environment.

Education Experience Requirements:

High School Diploma or GED required.
Bachelor’s degree in Pharmaceutical Sciences or related field preferred.
1–3 years of direct experience in pharmaceutical packaging (non-biotech).
Minimum 2 years of cGMP work experience is required.
Prior experience in generic pharmaceutical packaging is strongly preferred.

Technical Skills:

Proficient in operating and troubleshooting pharmaceutical packaging machines.
Experience with serialization systems (Systech) and ERP systems (SAP preferred).
Strong computer skills, including Microsoft Office (Word, Excel, Outlook).
Understanding of compliance and regulatory audit processes.
Familiarity with documentation practices under FDA and cGMP requirements.

Preferred Qualifications:

Bilingual in English and Spanish.
Knowledge of statistical tools and data analysis is a plus.
Strong understanding of SOPs, quality assurance processes, and manufacturing documentation.

Professional Competencies:

Strong verbal and written communication skills in English.
Exceptional attention to detail and ability to follow complex procedures.
Self-motivated and capable of managing multiple priorities in a fast-paced environment.
Excellent leadership and coaching abilities.
Strong organizational and time management skills.
Good interpersonal skills and ability to work collaboratively across departments.

Additional Requirements:

Must be a U.S. Citizen or Green Card Holder.
Must have a background in Chemistry.
Will be required to pass pre-employment drug screening.
Must be willing to work any assigned shift and weekends as needed.