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Quality Analyst
| Posted On: Feb 24, 2025
Frederick, MD 21703
12 months, Contingent
On-site
Job Summary
- Job Title:
- Quality Analyst
- Posted Date:
- Feb 24, 2025
- Duration:
- 12 months, Contingent
- Shift(s):
-
09:00 AM - 05:00 PM
- Salary ($):
- 21.39 - 22.76 per Hourly (compensation based on experience and qualifications)
- We care about you! Explore Rangam’s benefits
Skills Needed
Description
SourceAbled is seeking candidates for an exciting opportunity with a Biopharmaceutical company in Frederick, MD for Quality Analyst.
Description
- Performs selected quality control bioassay testing activities,
- Responsible for conducting finished product and stability testing according to standard operating procedures.
- Completes appropriate documentation supporting testing procedures, including data capture forms, equipment logbooks, and inventory forms.
- Enters data evaluated for compliance to specifications and reports abnormalities.
- Maintains laboratory equipment according to standard operating procedures.
- Maintains supply levels to support performance of assigned duties.
- Reads, understands, and follows SOP’s and complies with cGMP’s
- Applies critical thought to solving problems.
- Applies knowledge of good manufacturing practices and good laboratory practices on a daily basis.
- Adheres to Company safety procedures and guidelines on a daily basis.
- Follows all safety regulations as in company Policies and Procedures.
- Maintains training ?95% completed on time, with 100% completed prior performing any related analysis, etc
Education:
- BS/MS in biological or chemical science (chemistry, or biochemistry, etc.).
- BS (0-5years) preferably in pharmaceutical industry.
- Be able to plan and carry out laboratory operations efficiently and effectively.
- Be able to maintain accurate records of all experiments and data.
- Critical thinking and attention to details required.
- Must be a team player and customer oriented.
- Candidate will be working under supervision, but level of independence should increase with time. QC or GMP experience a plus.
- Be able to plan and carry out laboratory operations efficiently and effectively.
- Be able to maintain accurate records of all experiments and data.
- Critical thinking and attention to details required.
- Must be a team player and customer oriented.
- Candidate will be working under supervision, but level of independence should increase with time.
- QC or GMP experience a plus.
Note:
- This one is specific to the bioassay group.
- Someone with cell culture or bioassay experience, but it isn't necessary.
- Also someone with GMP or GLP experience is a plus. No PHD candidates.
- Must have at least a BS in a biological science or chemistry
COVID Vaccination Required
Shift Day Shift 9am - 5pm
M - F