QC Chemists (Multiple Levels) - Fall Riv

Job Title: Quality Control (QC) Chemist
FLSA Classification: Full-Time, Exempt Professional
Work Location: Fall River, MA
Work Hours: General Shift: 8 AM - 5 PM (may vary based on business needs)
Reports To: Quality Control Manager
Pay Range: $65,000 - 90,000 (Annually)

InvaGen pharmaceuticals is looking for talent in the following areas at ourmanufacturing sitein Fall River, MA.

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 to a specific individual:

Level 1: 0 to 3 years
Level 2: 3 to 5 years
Level 3: 5 to 10 years
Senior: more than 10 years
Level 2 or above is strongly preferred.

Summary of Responsibilities:

Conduct routine testing or other analysis in a specific group or department setting
Conduct advanced testing and/or critical testing, as required.
Ensures QC Analysts receive proper training.
Attends meetings to keep informed of manufacturing priorities.
Ensures that safety standards are maintained.
Operate specialized equipment or conduct specialized skill testing.
Participate in investigation activities.
Ensure compliance to all data integrity and cGMP practices, procedures, and expect ensuring compliance with all good documentation practices.
Other duties and responsibilities as assigned by the Head of the Department or Section Head.

Educational, Skills & Experience Requirements and Preferences:

Bachelor's degree (BS or BA), inChemistry, Biology, Pharmaceutical Sciences, or related field, and a preferred 1-year experience in the pharmaceutical or biotechnology industries preferred.
Must have current Good Manufacturing Practices (cGMP)
Good Laboratory Practice (GLP) knowledge

Professional and Behavioral Competencies
Proficiently speak, communicate, and understand (read and write) scientific work in English.
Have excellent organization, learning and teaching skills required to work in teams.
You enjoy working in a fast-paced environment and are flexible to changing requirements.
Working knowledge of raw materials and finished product testing and instruments and techniques such as GC, High-Performance... For full info follow application link.

Cipla USA and its US Affiliates 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.