QC Scientist I
About The Position
TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to clients worldwide. The job opportunity below is with one of our clients specializing in biotechnology product development services. The client is dedicated to supplying laboratory equipment, chemicals, supplies, and services essential in healthcare, scientific research, safety, and education. As a global leader in serving the scientific community, the organization generates approximately $40 billion in annual revenue and is committed to making the world healthier, cleaner, and safer. Their global team delivers innovative technologies, convenient procurement solutions, and pharmaceutical services through industry-leading brands.
Requirements
- Bachelor's degree required; Chemistry, Biology, Biochemistry, or related field preferred.
- No prior experience required.
- Knowledge of GMP regulations, documentation practices, and pharmaceutical quality standards.
- Strong attention to detail and commitment to data integrity.
- Strong scientific problem-solving and analytical skills.
- Proficiency with Microsoft Office and laboratory information systems.
- Strong written and verbal communication skills.
- Ability to work independently and collaboratively.
- Ability to work in cleanroom environments with required PPE.
- Ability to stand/walk for extended periods and lift up to 50 lbs.
- Good manual dexterity and ability to perform laboratory activities safely.
Nice To Haves
- Experience with microbiological identification, testing, environmental monitoring, and aseptic techniques preferred.
- Pharmaceutical or regulated-environment experience preferred.
Responsibilities
- Perform microbiological and bioanalytical testing, including: Sterility testing, Bacterial testing, Endotoxin testing, Particulate matter, Membrane filtration, TOC, Conductivity
- Document testing procedures and results according to cGMP requirements.
- Compare laboratory results with specifications and determine acceptability.
- Work with QA and management on repeat testing and OOS investigations.
- Maintain laboratory equipment and cleanliness.
- Report equipment or laboratory issues to supervisors.
- Complete assigned activities within required timelines.
- Collaborate with cross-functional teams to solve problems and improve quality.
- Follow SOPs, GMP, GLP, and safety procedures.
- Maintain required compliance and data integrity.
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What This Job Offers
Career Level
Entry Level
