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Quality Control Senior Associate

West Greenwich, RI
Top 3 Must Have Skill Sets:
    
• Strong Analytical Skills – Ideal candidate will have at least 4 years of experience
performing analytical testing
• Attention to Detail – Ideal candidate will be thorough and deliver polished work
product.
• Can Do Attitude – Ideal Candidate will have a positive attitude and be willing to
participate in lean initiatives on site

Description:

Requires all staff, staff augmentation external workers, and certain other external workers, in the United States and Puerto Rico to be vaccinated from COVID 19 as a condition of assignment. In accordance with applicable law,  will provide reasonable accommodations to staff augmentation external workers who qualify on the basis of a medical reason or a sincerely held religious belief, practice, or observance. Such accommodation may not pose an undue hardship to its operations, or its staff.”


***On-site in Rhode Island***

This is a true mid-level role and not suitable for Ph.D. candidates or recent graduates.

Job Details: Under general supervision, this position will perform routine procedures and HPLC/UPLC testing in support of routine and stability samples for multiple drug substance programs. Specific responsibilities include performing routine laboratory procedures, such as performing analytical testing and review for HPLC/UPLC assays, troubleshooting, solving problems and communicating with stakeholders. Will also be responsible for documenting, computing, compiling, interpreting, reviewing, and entering data. Additional responsibilities include providing and communicating results, maintaining/operating specialized equipment, and initiating and/or implementing changes in controlled documents. Must learn and comply with safety guidelines, GLP, and cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, laboratory notebooks, written procedures, building monitoring systems and laboratory log books.

Preferred Qualifications:
• 4-6 years of experience in performing HPLC/UPLC assays.
• Demonstrated experience in investigations and QC processes
• Self-motivated, strong organizational skills and ability to manage multiple tasks at one
time with minimal supervision
• Strong communication skills (both written and oral), facilitation and presentation skills
• Understanding and application of principles, concepts, theories and standards of GMP
QC analytical laboratories.
• Understanding of biopharmaceuticals process and related unit operations
• Strong analytical skills with the ability to collect, organize, analyze, and disseminate
significant amounts of information with attention to detail and accuracy
• Independent, self-motivated, organized, able to multi-task in time-sensitive
environments.

"This posting is for Contingent Worker, not an FTE"
 

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