QC Chemist I MDI

NOTICE: The posting for local applicants only - is not for those applying for a global assignment and/or for employees working outside of Ciplas U.S. Subsidiaries or Affiliates.

Job Title: Quality Control (QC) Chemist

FLSA Classification: Full-Time Exempt Professional

Work Location: Fall River MA

Work Hours: General Shift: 8:30AM 5:00PM (may vary based on business needs)

Reports To: Quality Control Manager

Salary Range:QCChemist I - $66300 - $86000

Purpose:

The job of the Chemist is simply described as an individual contributor who performs testing of samples of various types using various techniques or equipment in the QC laboratory. The job itself may be further modified with respect to the department group etc. as exemplified in the Department on an individual assigned basis to a sometimes-specific testing group. The role may be further modified based upon individual education training experience or a combination of all three.

Generally modifier designation with respect to experience for Chemist are as follows. However combination of education training and special skills will determine the assignment of Level I - III to a specific individual

Duties and Responsibilities

The general duties and responsibilities of the Chemist include but are not limited to the following:

• 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 expect
• Ensure compliance with all good documentation practices.
• Other duties and responsibilities as assigned by the Head of the Department or Section Head

Education and Experience:

• Bachelors 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) is a plus

Working conditions

This role works in a cGMP laboratory or manufacturing environment where personal protective equipment is required which may include uniforms lab coats safety glasses respiratory protective equipment hearing protection etc. Work with or aroundsolvents powders or other materials commonly found in a pharmaceutical laboratory or manufacturing facility is required.

The role may be assigned on a work-shift basis where required (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-to10 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.

GLOBAL COMPANY

Cipla is a leading global pharmaceutical company dedicated to high-quality branded and generic medicines. We are trusted by healthcare professionals and patients across geographies. Over the last eight decades we have strengthened our leadership in Indias pharmaceutical industry and fortified our promise of strengthening our global focus by consolidating and deepening our presence in the key markets of India South Africa the U.S. and other economies of the emerging world.

Cipla employs handpicked professionals not just for their knowledge and experience but for their zeal to make a difference to the world of healthcare. The company believes that our biggest assets are the employees who lead us to prosperity and growth in the future. Driven by the vision none shall be denied Ciplas focus has always been on making affordable world-class medicines with a reputation for uncompromising quality standards across the world.

CIPLA NEW YORK (INVAGEN PHARMACEUTICALS INC.)

About InvaGen Pharmaceuticals a Cipla subsidiary InvaGen Pharmaceuticals Inc. is engaged in the development manufacture marketing and distribution of generic prescription medicines with focus on a range of therapeutic areas including cardiovascular anti-infective CNS anti-inflammatory anti-diabetic and anti-depressants. The company was founded in 2003 and is based in Central Islip and Hauppauge New York. As of February 18 2016 InvaGen Pharmaceuticals Inc. operates as a subsidiary of Cipla (EU) Limited.

EEO Statement

Cipla is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race color age sex sexual orientation gender identity religion national origin genetic information disability or protected veteran status.