- 214228 - Research Associate II (Microbiologist)
- Industry
- SCI
- Region
- IL-Illinois
- City
- Round Lake
- State
- IL
- Rate
- Up to $44.23 DOE
- Duration
- 18 months
- Description
Chipton Ross is seeking a Research Associate II (Microbiologist) for a contract opportunity in Round Lake, IL.
BASIC QUALIFICATIONS (REQUIRED SKILLS/EXPERIENCE):
1. Basic technical understanding of sterilization (Moist Heat, Aseptic, Irradiation)
2. Basic technical understanding of microbiological method validations (sterility, bioburden and bacterial endotoxin) (specific for the Research Associate II)
3. Ability to write, execute and review validation and qualification protocols and reports.
4. Ability to Evaluate and interpret technical data and test results
5. 2-4 years lab experience preferred
6. Understanding of aseptic technique preferred
7. Ability to conduct experiments with minimal assistance preferred
8. Knowledge and understanding of GxP and related regulations and guidance preferred
POSITION RESPONSIBILITIES:
o Effectively contribute solid technical knowledge to a variety of projects within the sterility assurance discipline with minimal assistance.
o Display basic technical understanding of related sterility assurance disciplines, specifically sterilization modalities and/or microbiological test method validation.
o Without assistance, make sound technical recommendations regarding projects/matters that are more routine than not. Provide some analysis/redesign of key experimental procedures. Independently select techniques and procedures to solve problems within area of responsibility.
o Employ appropriate techniques/methods to successfully and independently execute routine assignments within negotiated deadlines.
o Maintain knowledge of relevant Quality System Regulations and safety requirements while building knowledge of other regulatory requirements related to R&D (product development, design and safety) to ensure compliance in all research, data collection and reporting activities.
o Recommend appropriate designs, techniques and processes for a specified sequence of tasks where needed.
o In-depth knowledge and understanding of GxP and related regulations and guidance.
o Provide support to the Sterility Assurance Focal Point for product development or on change controls.
o Write, execute and review validation and qualification protocols and reports.
o Evaluate and interpret technical data and test results.
o The position requires relevant laboratory skills, writing skills, and computer skills plus teamwork/interpersonal skills.
REQUIRED EDUCATION:
o Bachelor's Degree in a scientific discipline with at least 2-4 years lab experience.
WORK HOURS:
Full time, first shift.
5/40
Employment will be contingent on clearing a drug screen and background check. Both must clear prior to start date.
- Contact
-
Tyler Harrell
tharrell@chiptonross.com
CHIPTON-ROSS, INC.
420 Culver Boulevard
Playa Del Rey, CA 90293
Phone: (310) 414-7800 x307 or (800) 927-9318 x307
Candidates responding to this posting must currently possess the eligibility to work in the United States. No third parties please.
Employment will be contingent on candidate clearing pre-employment drug screen and background check.
Chipton-Ross provides equal employment opportunities to all employees and applicants for employment without regard to race, color, creed, religion, national origin, sex (including pregnancy), age, disability, sexual orientation, gender identity and/or expression, protected veteran status, genetic information, or any other characteristic protected by Federal, State or local law. This policy governs all areas of employment at Chipton-Ross, including recruiting, hiring, training, assignment, promotions, compensation, benefits, discipline, and terminations.