Manufacturing Associate Nights

Lonza, Inc. Newington , NH 03801

Posted 1 week ago

At Lonza, we invest in great people. We encourage our employees to challenge themselves and we offer an environment that fosters creativity and success.

Headquartered in Basel, Switzerland, we operate production, R&D, and business sites around the world, including Europe, North America, and Asia. Our vision: We strive to be the leading supplier using science and technology to improve the quality of life.

Our mission: We work with passion, using advanced technologies, to transform life science into new possibilities for our customers. Do you want to help us as we shape the future of this great organization?

Job Description Summary The Manufacturing Associate is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials.

Key Accountabilities and Duties: Set up, operate equipment, and monitor production processes, including clean-in-place (CIP) and steam-in-place (SIP) operations and report production in written and electronic documents in accordance with good documentation procedures (GDPs), review documentation as appropriate Attain qualification for all assigned tasks and maintain individual training plan Perform basic laboratory tasks, such as monitor pH, conductivity, test product samples, etc. Perform material movements, transfer raw materials, chemicals into, out of, across the production areas.

Maintain facility and equipment through routine cleaning and sanitization, support 6S programs Office tasks attending shift exchange, meetings, sending/receiving emails, participating in projects Perform other duties as assigned. Minimum Required Qualifications/

Skills:
High School Diploma or Equivalent minimum; AS/BS preferred Preferred area of study:

Science related discipline Some prior experience in a manufacturing setting preferred. Proven logic and decision making abilities, critical thinking skills Strong written and verbal communication skills are required The employee is living the cultural beliefs with the flexibility to adapt to changing business priorities. Is open to and actively seeks out feedback on their performance and translates that feedback into action.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law. Lonza. The place to Go, Stay and Grow.

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VIEW JOBS 10/18/2018 12:00:00 AM 2019-01-16T00:00 At Lonza, we invest in great people. We encourage our employees to challenge themselves and we offer an environment that fosters creativity and success. Headquartered in Basel, Switzerland, we operate production, R&D, and business sites around the world, including Europe, North America, and Asia. Our vision: We strive to be the leading supplier using science and technology to improve the quality of life. Our mission: We work with passion, using advanced technologies, to transform life science into new possibilities for our customers. Do you want to help us as we shape the future of this great organization? Job Description Summary The Manufacturing Associate is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Level I associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials. Key Accountabilities and Duties: Set up, operate equipment, and monitor production processes, including clean-in-place (CIP) and steam-in-place (SIP) operations and report production in written and electronic documents in accordance with good documentation procedures (GDPs), review documentation as appropriate Attain qualification for all assigned tasks and maintain individual training plan Perform basic laboratory tasks, such as monitor pH, conductivity, test product samples, etc. Perform material movements, transfer raw materials, chemicals into, out of, across the production areas. Maintain facility and equipment through routine cleaning and sanitization, support 6S programs Office tasks – attending shift exchange, meetings, sending/receiving emails, participating in projects Perform other duties as assigned. Minimum Required Qualifications/Skills: High School Diploma or Equivalent minimum; AS/BS preferred Preferred area of study: Science related discipline Some prior experience in a manufacturing or leadership setting preferred. Proven logic and decision making abilities, critical thinking skills Strong written and verbal communication skills are required The employee is living the cultural beliefs with the flexibility to adapt to changing business priorities. Is open to and actively seeks out feedback on their performance and translates that feedback into action. Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law. Lonza. The place to Go, Stay and Grow. Lonza, Inc. Newington NH

Manufacturing Associate Nights

Lonza, Inc.