QC Scientist I – Environmental Monitoring

Thermo Fisher Scientific•Greenville, NC

1d•Onsite

About The Position

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. As part of the Drug Product Division (DPD), the Greenville, North Carolina site is a multi-purpose pharmaceutical development, manufacturing, and packaging campus. The operation specializes in taking both sterile injectable and oral solid dose drug products from development phase through to commercialization.

Requirements

Must be Legally authorized to work in the United States without sponsorship.
Must be able to pass a comprehensive background check to include drug screening.
An associate's degree in a science related field, preferably Biology, is minimally required.
1+ years related experience performing chemical tests with chromatographic, spectroscopic, or other analytical techniques
Knowledge of MS Excel, Word, and Access and is familiar using each program.
Ability to apply mathematical operations.

Nice To Haves

Bachelor’s degree in a biology/ related science field is preferred.
working knowledge of EMPOWER is a plus.
2 years of experience preferred.
Excellent problem solving and critical thinking skills are a plus when performing this job.
Organization and detailed planning skills are seen as major pros for this job function.
Strong attention to detail and ability to follow standard procedures
a person who enjoys a constantly evolving environment will do well.
Good knowledge of quality and regulatory requirements in the pharmaceutical industry, including pharmaceutical GMPs are a plus.
Good interpersonal and communication skills (both oral and written).

Responsibilities

Perform Environmental Monitoring tasks in support of Steriles production within classified areas.
Perform analyses including instrumental and automated methods using prescribed procedures and techniques.
Generate valid data, report results on appropriate database compared to established specifications while adhering to GMPs.
Compare laboratory results with specifications for acceptability and determine if repetition or OOS is required.
Maintain equipment and troubleshoot instrumentation problems, procedural problems or production problems.
Review and understand SOPs and analytical procedures as needed.
Schedule activities to meet target dates for customer needs.
Follow all job-related safety and other training requirements.
Performs tasks as assigned by area supervision or designee.
Able to withstand extended periods of standing and/or walking and bending.