job summary :
As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena.
Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions.
We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!
responsibilities :
This position will perform in a cGMP environment following FDA and ICH
guidelines.
Duties include but are not limited to : method development;
method and instrument validation; testing in accordance with cGMP
regulations, regulatory filings, and approved procedures for products
including, but not limited to : raw materials, drug substance, finished product
and stability.
Responsibilities :
60%) Perform analytical testing
15%) Prepare and maintain reagents and reference standards
10%) Operate and maintain equipment
10%) Record, report, and verify data
5%) Participate in special projects, as necessary
Weekend work is possible but not expected
qualifications : Education :
Education :
Bachelor of Science in Chemistry or related scientific discipline
Competencies :
- Ability to work and prioritize independently;
- Strong computer and organizational skills;
- Excellent oral and written communication in English;
- Self-motivated;
- Adaptable to changing priorities;
- Positive attitude;
- Quick learner;
- Familiar with Good Documentation Practices (GDP).
Experience :
0 3 years in a laboratory, GMP preferred
Physical Demands : Able to lift 25 - 50 lbs; able to stand 3 - 4 hours at a time
skills :
MS-WORD, MS-EXCEL, MS-Powerpoint, Chemistry, GMP (Good Manufacturing Practice)
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