Quality Manager

Ecolab, Purolite Resins, the world leader in resin-based separation, purification and extraction technology, is seeking a Quality Manager at our state-of-the-art manufacturing site in King of Prussia.

We manufacture products which help our customers around the globe, mainly in pharmaceutical and life science sectors, with technology which are critical to safe manufacture of their products. It’s an exciting business which helps make the world cleaner, safer and healthier.

The Quality Manager will oversee the quality control and quality system functions, ensuring compliance with global pharmaceutical regulations and standards, Ecolab and Purolite quality policies, and industrial standards such as ISO 9001.

What’s in it For You:

• The opportunity to take on some of the world’s most meaningful challenges, helping customers achieve clean water, safe food, abundant energy and healthy environments
• The ability to make an impact and shape your career with a company that is passionate about growth
• The support of an organization that believes it is vital to include and engage diverse people, perspectives and ideas to achieve our best

Why choose Ecolab?

• A world-leading international organization, benefitting from a diverse, multinational team
• A fast-paced, dynamic, and rapidly growing environment
• Manufacture of high-quality technical products, developed hand-in-hand with leading minds in the industry
• Entrepreneurial workplace culture with a flat management structure, encouraging new approaches and ideas

What you’ll do:

Main Responsibilities - Quality Control:

• Responsible for all quality control laboratory supervisors, leads, and technicians.
• Is accountable for all incoming, in-progress and final product testing.
• Monitors and communicates non-conformances to department supervisors and senior managers.
• Ensures adequate staffing and resourcing for all functions within the department.
• Recommends measures to improve methods, quality of product.
• Recommends and implements changes in working conditions and use of equipment to increase efficiency of the department.
• Assists company representatives in quality matters Supervises and maintains all lab instrumentation – including PM and calibration schedules.
• Prepares and distributes precise and timely reports as required.
• Oversees maintenance of all quality control records and samples.
• Interprets company policies to department workers and enforces safety regulations.

Main Responsibilities - Quality Systems:

• Management Representative for manufacturing site Quality Management System (QMS).
• Communicates all deviations and non-conformances to plant management and senior leadership as needed.
• Works closely with global quality team.
• Establishes and oversees internal audit process to ensure site is maintained in an audit ready state.
• Communicates with authorities and customers and coordinates the planning and management of audits.
• Analyzes and approves general and operating procedures, work instructions and other quality-related documents.
• Develops and maintains site quality metrics and ensures compliance and identification of trends leading to site/process/product improvements.
• Reviews and approves validation protocols and reports.
• Ensures that quality-related complaints are investigated and resolved as required.
• Oversees process for reviews of completed batch production and laboratory control records of critical process steps before release of the products for distribution.
• Releases or rejects all products. Releases or rejects intermediates for use outside the control of the manufacturing company. Establishes a system to release or reject raw materials, intermediates, packaging, and labeling materials.
• Ensures a robust stability program supporting product, raw materials, QC Reagents and sets retest/expiry dates and storage conditions where appropriate.
• Ensures adherence to professional standards and ethics.
• Provides ad-hoc reports for senior management as required.
• Performs other duties as assigned.

What you’ll need:

• Bachelor of Science in Chemistry, Chemical Engineering, Biology, or another relevant scientific field
• 7 years Quality (QA and/or QC) experience
• 3 years of supervisory or management experience
• 3 years' experience in Quality Systems Management
• Knowledge of quality assurance requirements for pharmaceuticals: 21 CFR Parts 210/211, ISO 9001 standard requirements
• Knowledge of ISO 19011 standard (the principles of auditing, managing an audit program and conducting management system audits, as well as guidance on the evaluation of competence of individuals involved in the audit process)
• Product development and project management experience

• Hands-on analytical laboratory experience
• Experience with performing and hosting audits from regulators and customers
• Proven analytical, evaluative, and root cause analysis abilities

The base salary range for this position is $130,100.00 - $195,100.00. This position is eligible for annual bonus pay based on performance, per plan terms. Many factors are taken into consideration when determining compensation, such as experience, education, training, geography, etc. We comply with all minimum wage and overtime laws.

Ecolab strives to provide comprehensive and market-competitive benefits to meet the needs of our associates and their families. Click here to see our benefits. 

If you are viewing this posting on a site other than our Ecolab Career website, view our benefits at jobs.ecolab.com/working-here.