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Quality Assurance Supervisor opening with a new and quickly expanding
healthcare and consumer packaging printer in Bristol, PA. This position will be a key role in this company reporting to the VP of Quality Assurance and has the potential for advancement opportunities. Relocation assistance is available. Preference for experience within packaging and pharmaceuticals.

You will manage, plan, organize, direct, and evaluate all activities and QA staff to ensure that Quality support is present on the production floor. Necessary and critical functions include but are not limited to documentation review and issuance along with prompt resolution and Quality oversight over production ensuring compliance with site and corporate standards. You will support to improve safety, customer satisfaction, employee development, continuous improvement, and financial performance consistent with Plant goals. You will make important decisions in ensuring the deviations are investigated, alerts resolved, complaints examined, and product dispositioned promptly. You will report to the Vice President, Quality Assurance.

How you will contribute:

Comply with all company safety rules and workplace requirements
Will provide strong leadership, project and people management skills, and ability to make critical decisions.
Willing to learn new aspects of the business.
Hire and retain great talent, develop, and provide challenging work for team members; support the career development of their employees. Manage people performance, maintain performance records, and development.
Assure a safe and non-discriminatory working environment for employees.
Ensure compliance with manufacturing, specifications, and company policies. Ensure the departmental SOPs are current and staff trained on activities being performed
Manages the supplier quality program to ensure cGMP compliance over vendors that provide materials/services for the site
Ensures GMP compliance of quality systems/tools used at the site including a quality manual, policies, procedures, and work instruction documentation that make up the hierarchy of the Document Control system
Maintains metrics program with measurables that achieve continuous improvements of processes and procedures
Prepare the department for both internal and external authorities during audits ensuring facility is always audit ready
Provide necessary floor support to the production teams and help in resolving compliance concerns.
Responsible for change control activities/documentation in QMS. Required to perform review of submission documents.
Maintain Supplier Qualification program
Ensure deviations and non-conformances are initiated, investigated, and closed.
Support generation and approval of manufacturing documents (SOP's/WI, Forms)
Participate / lead teams which impact production, increase efficiency, solve problems, create cost savings, improve quality, and provide new product support.
Manage relationship with Third Party Testing Labs, Vendors of Equipment and Calibration, suppliers
Performs other job duties as assigned
Education and Background

Bachelors Degree in science preferred or combination of education and working knowledge
5 + Years experience in pharmaceutical, packaging, or similar regulated industry
2+ years direct/indirect supervisory experience and/or leading a team or process
Working knowledge of cGMPs, ISO standards and production processes.
Ability to work autonomously applying strong problem-solving skills
Strong communication skills are needed to manage support personnel.
Can navigate through CERM (ERP) and QISS (QMS)
Must be able to lift, push, pull and carry up to 35 lbs
In general, you will do a combination of sedentary work and walking around observing conditions in the facility
5% travel
Must be able to work with and around inks, solvents, and other chemicals
Willingness to work overtime when needed, including weekends
Ability to work well with others and in a diverse workforce environment
Must be eligible to work in the United States without restriction