Quality Control Associate

Job Description

* Must have experience working at a GMP facility (bio-tech or pharma regulated industry)*

Job Details:

• Under general supervision, this position will perform routine procedures and testing in support of the Environmental and Clean Utility Microbiological Monitoring programs.
• Specific responsibilities include performing routine laboratory procedures, such as sample testing, compendial (Membrane Filtration and Pour Plate Analysis) and non-compendial test methods and environmental monitoring and sampling (Laser Particle Counter/ Slit-to-Agar Sampler/ Contact Plates).
• 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.

Skills:

Lab experience

* Must have GMP Experience*

Strong Aseptic experience preferred

Looking for 1-3 years of work experience within the industry (internship exp. counts)

Skills:

Lab experience

* Must have GMP Experience*

Strong Aseptic experience preferred

Looking for 1-3 years of work experience within the industry (internship exp. counts)

All your information will be kept confidential according to EEO guidelines.