Quality Assurance Supervisor (Packaging/Printing in Pharma) - Onsite in Windsor, NJ

BravoTECH

Robbinsville Township (NJ)

On-site

USD 80,000 - 100,000

Full time

14 days+

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Job summary

A leading company in pharmaceutical packaging is seeking a Quality Assurance Supervisor to oversee quality management systems and ensure compliance with industry standards. This role involves leading quality initiatives, conducting audits, and fostering a culture of continuous improvement. Ideal candidates will have a Bachelor's degree and experience in quality management within the pharmaceutical or packaging sectors.

Qualifications

Minimum 2 years of experience in quality management in printing, packaging, or pharmaceutical industries.
Expertise in ISO 9001 and ISO 15378 standards.
Lean Six Sigma certification is a plus.

Responsibilities

Develop and manage the site Quality Management System (QMS).
Lead quality improvement initiatives and ensure compliance with quality standards.
Conduct audits and analyze quality performance data.

Skills

Analytical skills

Communication

Leadership

Education

Bachelor's degree in Quality Management, Engineering, or Business Administration

Tools

QCBD Software

Job description

Quality Assurance Supervisor (Pharmaceutical Packaging) - Onsite in Windsor, NJ

This range is provided by BravoTECH. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$80,000.00/yr - $100,000.00/yr

Additional compensation types

Annual Bonus

Direct message the job poster from BravoTECH

Technical Recruiting Executive at BravoTECH

Quality Assurance Supervisor - Pharmaceutical Packaging

Overview:

Our client leads the way in providing innovative packaging solutions to the Healthcare market. Our client provides a one-stop shop for all pharmaceutical packaging needs including labels, folding cartons and boxes, inserts, outserts, IFUs and DFUs, Med Guides, and physician support literature. Their industry-best lead times are made possible by their coast-to-coast manufacturing footprint and their dedicated team of packaging specialists with a passion for quality and service. They are currently seeking a highly motivated and experienced Quality Assurance Supervisor to lead their commitment to quality, operational efficiency, and excellence at in Windsor, NJ. As the QA Supervisor, you will be responsible for developing, implementing, and maintaining a comprehensive Quality Management System and will play a key role in fostering a culture of quality, efficiency, and continuous improvement at the facility.

Responsibilities:

Develop, implement, and manage the site Quality Management System (QMS) that aligns with industry standards and organizational objectives.
Facilitate quality and continuous improvement initiatives to enhance operational efficiency, customer satisfaction, and overall performance.
Lead all quality efforts at the plant to ensure that our products consistently meet or exceed defined quality standards and customer expectations.
Collaborate with cross-functional teams to identify and implement quality improvements, drive process optimization, and achieve cost-effectiveness.
Ensure timely resolution and closure of Corrective and Preventive Action (CAPA) plans.
Conduct regular audits and assessments to evaluate the effectiveness of the QMS and processes, identifying areas for improvement.
Analyze quality performance data and metrics to identify trends, develop insights, and drive data-driven decision-making.
Establish and monitor key performance indicators (KPIs) to track the effectiveness and efficiency of quality processes and continuous improvement initiatives.
Ensure site adheres to local regulations and industry standards for pharmaceutical packaging and printing.
Ensure timely and accurate reporting of safety concerns, incidents, and near misses.
Oversee housekeeping walkthroughs and address all safety issues with Plant Management.
Conduct monthly trainings and safety meetings to reinforce safe work practices and company policies.
Oversee monthly 5S projects to improve workplace organization, cleanliness, and efficiency. Work with teams to ensure compliance with 5S principles.
Provide training and mentorship to employees to enhance their understanding of quality principles, practices, and methodologies.
Oversee supplier quality management, including supplier evaluations and audits, to ensure the quality of incoming materials and components.
Represent the facility in dealings with external stakeholders related to quality and continuous improvement.
Assist plant Management in driving a culture of quality excellence, continuous improvement, and accountability.
This role will have supervisory responsibilities over the Quality Department, and it is expected that this individual will have previous experience leading successful teams.
Other duties as assigned.

Qualifications:

Bachelor's degree in a related field (e.g., Quality Management, Engineering, Business Administration) is preferred.
Minimum of 2 years of experience in quality management within the printing, packaging or pharmaceutical industries, with a proven track record of improving quality standards and processes.
Expertise in ISO 9001 (Quality Management Systems) and ISO 15378 (Primary Packaging Materials for Medicinal Products) standards
Expertise with FSC, SFI and PEFC environmental certifications and system maintenance
Prior experience managing direct reports and leading teams to drive quality improvements and standardization efforts.
Understanding of pharmaceutical industry regulations, including cGMP, FDA, and international quality standards.
Strong analytical skills with the ability to analyze data, identify trends, and implement effective solutions.
Excellent communication and interpersonal skills to lead and collaborate with cross-functional teams, direct reports, and stakeholders.
Proficiency in quality management systems, data analysis tools, and software applications.
QCBD Software Experience is a plus
Relevant certifications such as Certified Quality Manager (CQM) or Certified Quality Auditor (CQA) are advantageous.
Lean Six Sigma certification is a plus

Additional Notes:

Hands-on working experience with QA techs on the floor and having a regular presence
4 direct reports at full capacity. 2 currently with 1 temp to perm and 1 open role
60 total employees sit at the site
Product is held at a nearby facility and may go there on occasion to review the product

Seniority level