Job description

Position is Onsite

Description

This is an associate scientist position, we do want someone with a science background as future growth in this role will be geared toward a science background. However, the role is strictly documentation and updating documentation around diagnostic products. There is no lab work associated with this position. Activities, would be updating data/information associated to Client products.

Education:

• BS in molecular biology, biochemistry, or related field with at 2-4 years relevant experience.
• Knowledge of GMP, ISO, and FDA regulations and audits a plus.

Top 5 skills/requirements:

• Computer system adaptability- This role is entirely computer based and it requires the employee to learn/work in multiple systems
• Critical reading- This role has a significant amount of training associated to it which is based on operating procedures, having someone who is able to read and understand an operating procedure is a big plus
• Critical thinking- When the answer is not obvious or ambiguous it is important to be able to understand when to ask questions and when to challenge a perceived truth
• Attention to detail- We are dealing with a moderate amount of data that has impact to final product so errors need to be minimized and caught ahead of implementation
• Self-Driven- The workflow here is a person is assigned a product and all the activities associated to that product should be driven by them, meaning following up with different groups to get their portion done and elevating to management when that is not the case.
• Good organization- We update a lot of trackers so good organization and ability to follow the routine is important.

Job Type: Contract

Salary: $16.13 - $24.00 per hour

Benefits:

• Health insurance

Schedule:

• 8 hour shift
• Day shift
• Monday to Friday

Ability to commute/relocate:

• North Chicago, IL 60064: Reliably commute or planning to relocate before starting work (Required)

Education:

• Bachelor's (Preferred)

Experience:

• documentation: 1 year (Preferred)
• updating documentation around diagnostic products.: 1 year (Preferred)
• GMP, ISO, and FDA regulations: 1 year (Preferred)
• medical device: 1 year (Preferred)

Work Location: One location

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