Packaging Jobs

Responsible for package engineering projects and specification development in one or more manufacturing areas. The focus is on package design through identification of opportunities and recommending solutions.

Work as a team member to ensure that packages are properly designed, that production schedules are met, products are delivered to the market on time, cost is contained, and tasks are performed in accordance with our company mission, vision, values and business objectives.

Job Responsibilities

Perform a wide variety of tasks and operations in GMP, aseptic and controlled environments that are required to support and execute production. This includes formulating bulk product and culture media, performing cleaning and sterilization of equipment, setting-up and operating filling equipment, staging and loading components and bulks, setting-up and operating inspection equipment, setting-up and operating the nitrogen tunnels for freezing, completing lyo cabinet operations, staging and loading packaging components, setting-up and operating packaging equipment, and completing associated batch record and log-book documentation.
Operate and maintain assigned equipment in SPO by performing mechanical, electronic, electrical, and pneumatic/hydraulic troubleshooting and repairs.
Complete preventative maintenance and repairs as assigned for the equipment and facilities within Sterile and Packaging Operations.

Bachelor's Degree in relevant Packaging discipline plus some experience in Packaging Development or 5 years experience in a Packaging function. Experience in an associated area to Packaging Development eg. Marketing, Sales, manufacturing is an advantage.
Accountable for interacting and working with outsourced contractors in design and development of packaging.
High level packaging development knowledge and skills including legal requirements of packaging.
Strong operational knowledge or experience of analyzing the packaging requirements of a brand and ability to identify new packaging opportunities.
Strong operational knowledge or experience of monitoring industry trends, both traditional and other, and competitor developments.
Demonstrated effectiveness as a team member with superior interpersonal/communication skills.
Ability to work globally across matrix organization, integrating complex multi-functional efforts crossing multiple business areas.

Performs specific assignments to ensure that equipment in various manufacturing, packaging and related areas operate properly and is maintained. Operates, maintains, troubleshoots and repairs equipment associated with the packaging of pharmaceutical products. Performs routine preventive maintenance, equipment changeovers, equipment cleaning and set-up. Performs duties with advanced skill on many different types of equipment. Applies advanced working knowledge and experience to independently improve maintenance techniques and operations.

Job Responsibilities

•Adheres strictly to all cGMP’s, PPG’s, regulatory and safety standards and procedures to ensure the quality and integrity of products and safety of employees

•Keeps working area in a clean and orderly condition according to PPG’s and 5S principles

Perform a wide variety of tasks and operations in GMP, aseptic and controlled environments that are required to support and execute production. This includes formulating bulk product and culture media, performing cleaning and sterilization of equipment, setting-up and operating filling equipment, staging and loading components and bulks, setting-up and operating inspection equipment, setting-up and operating the nitrogen tunnels for freezing, completing lyo cabinet operations, staging and loading packaging components, setting-up and operating packaging equipment, and completing associated batch record and log-book documentation.
Operate and maintain assigned equipment in SPO by performing mechanical, electronic, electrical, and pneumatic/hydraulic troubleshooting and repairs.
Complete preventative maintenance and repairs as assigned for the equipment and facilities within Sterile and Packaging Operations.

This position will assist with revising and tracking Pharmaceutical Packaging Procedures and Pharmaceutical Packaging Specifications in support of area requirements.

RESPONSIBILITIES:
•Initiate Change Controls and compile supporting documentation.
•Backup support for Tracking and maintaining vacation, personal time off and sick time for Bargaining Unit personnel
•Entering new/revised Production Models into Prism
•Performing general administrative duties to support Riverside Operations.
•Assisting with PowerPoint Presentations as requested.

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• develop business case justifications, which should include robust market research data, complete equipment engineering evaluation, and financial justification.
• specify processes relating to packaging materials, molds, tooling, components and functional testing
• provide NPS documentation support and team leadership with the completion of the CIDD, PIDD, Pack Brochures, and graphic logo and pack designs.
• provide critical documentation including Package Component Specifications, General Specifications, and PAO/PRFs.
• provide technical/project management support to all USA Manufacturing locations (UMO, Bristol, Zebulon)
• improve production and procurement efficiencies through development and implementation of cost effective packaging technologies
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• develop business case justifications, which should include robust market research data, complete equipment engineering evaluation, and financial justification.
• specify processes relating to packaging materials, molds, tooling, components and functional testing
• provide NPS documentation support and team leadership with the completion of the CIDD, PIDD, Pack Brochures, and graphic logo and pack designs.
• provide critical documentation including Package Component Specifications, General Specifications, and PAO/PRFs.
• provide technical/project management support to all USA Manufacturing locations (UMO, Bristol, Zebulon)
• improve production and procurement efficiencies through development and implementation of cost effective packaging technologies

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• Supervises the day to day activities of the associates performing packaging, material handling and cold chain operations.
• Develops Validation Master Plan for packaging operations in partnership with validation.
• Drives the PQ Master Plan process for packaging operations and manages PQ activities for the function including, developing PQ protocols, executing PQ protocols and writing PQ summary reports.
• Leads core cross functional team to launch commercial packaging operations according to established timelines.
• Implements and conceives operational strategies to optimize process, production and maintenance systems.
• Manages packaging resources to meet production scheduling ensuring the availability of equipment and personnel resources to meet demand.
• Manages processes and equipment to ensure quality operations. Participates in audits and investigations and recommends solutions to resolve problems.

• develop business case justifications, which should include robust market research data, complete equipment engineering evaluation, and financial justification.
• specify processes relating to packaging materials, molds, tooling, components and functional testing
• provide NPS documentation support and team leadership with the completion of the CIDD, PIDD, Pack Brochures, and graphic logo and pack designs.
• provide critical documentation including Package Component Specifications, General Specifications, and PAO/PRFs.
• provide technical/project management support to all USA Manufacturing locations (UMO, Bristol, Zebulon)
• improve production and procurement efficiencies through development and implementation of cost effective packaging technologies

Click Here For More Information