Pilot Plant QC Chemist II

Purpose

Individual contributor who performs testing of samples of various types using various techniques or equipment in the QC laboratory.

Scope

General description of the nature and level of work as well as a basic understanding of the role, responsibilities, and expectations. May be modified with respect to department, group, and on an individually assigned basis. Consideration of education, relevant training, and experience or a combination may result in modification of the role.

Duties And Responsibilities

• Conduct routine testing or other analysis in a specific group or department setting
• Conduct advanced testing and/or critical testing, as required
• Operate specialized equipment or conduct specialized skill testing
• Working knowledge of raw materials testing and release
• Working knowledge of instruments such as Karl Fisher, HPLC, GC, Particle size, ICP
• Lead investigation activities
• Ensure compliance to all data integrity and cGMP practices, procedures, and expectations
• Ensure compliance with all good documentation practices
• HPLC/GC knowledge and handling experience
• SAP knowledge and handling
• MDI testing experience
• Other duties and responsibilities as assigned by the Head of the Department or Section Head

Education And Experience

• Bachelor's degree (BS or BA), physical sciences preferred
• Proficiently speak English as a first or second language
• Proficiently communicate and understand (read and write) scientific work in English
• Have excellent organization, learning and teaching skills required to work in teams
• Ability to understand and analyze complex data sets
• Working knowledge of Microsoft Office programs and other scientific based software
• Experience in Inhalation products MDI/DPI

Working Conditions

• Works in a cGMP laboratory or manufacturing environment, where personal protective equipment is required (uniforms, lab coats, safety glasses, respiratory protective equipment, hearing protection, etc.)
• Work with or around solvents, powders, or other materials commonly found in a pharmaceutical laboratory or manufacturing facility
• May be assigned on a work-shift basis (Day, Evening, Night)
• Weekend or Holiday work may be requested or required

Physical Requirements

• Work standing or walking unassisted for 75% or greater of an 8-hour period
• Unassisted lifting up to 10 kg, may be required
• Able to wear appropriate personal protective equipment at all times, when required
• Sitting at a desk and/or working at a computer or other "screen" 75% or greater of an 8-hour period

Professional and Behavioral Competencies

• Must be willing to work in a pharmaceutical packaging setting
• Must be willing and able to work any assigned shift ranging from first or second shift
• Work schedule may be Monday to Friday
• Must be willing to work some weekends based on business needs as required by management
• No remote work available
• No employment sponsorship or work visas

About Cipla

Cipla is a leading global pharmaceutical company, dedicated to high-quality, branded and generic medicines. Trusted by healthcare professionals and patients across geographies. Over the last eight decades, strengthened leadership in India's pharmaceutical industry and consolidated presence in key markets of India, South Africa, the U.S., and other economies of the emerging world. Cipla employs professionals for their knowledge, experience, and zeal to make a difference to healthcare. Driven by the vision that none shall be denied, Cipla's focus has always been on making affordable, world-class medicines with a reputation for uncompromising quality standards across the world.

About InvaGen Pharmaceuticals (a Cipla subsidiary)

Engaged in the development, manufacture, marketing, and distribution of generic prescription medicines with focus on cardiovascular, anti-infective, CNS, anti-inflammatory, anti-diabetic, and anti-depressants. Founded in 2003 and based in Central Islip and Hauppauge, New York. Operates as a subsidiary of Cipla (EU) Limited since February 18, 2016.