What are the responsibilities and job description for the GMP/QC Quality Analyst (Onsite) position at Jobs via Dice?
Dice is the leading career destination for tech experts at every stage of their careers. Our client, NetSource, Inc., is seeking the following. Apply via Dice today!
Please note that this is a 12-18 months contract position, onsite.
Qualifications:
The world's most revolutionary biopharma companies are partnering to advance the next frontier of medicine. The company continues to invest in capacity and expansion of its Colorado operations. Join a team of professionals dedicated to the development and commercialization of nucleic acid therapeutics for life-changing, lifesaving medicines.
Candidates must provide their phone number. Job reference number is A5186.
Please note that this is a 12-18 months contract position, onsite.
Qualifications:
- Bachelor's degree or equivalent
- Generally requires minimal to no prior relevant work experience
- Demonstrated knowledge of analytical equipment and instrumentation and working in a GMP environment is helpful
- Proven skills in coordinating and leading day-to-day tasks and working in collaboration to accomplish deadlines and objectives
- First shift hours: Mon-Friday, 8am - 4pm
- Conduct routine preparations for stability, raw materials, in-process, microbiology/cleaning validation program, and other requested testing according to Standard Operating Procedures (SOP) and Analytical Methods in accordance with current Good Manufacturing Practices (cGMPs) and regulatory requirements
- Complete projects with supervision and have a clear understanding of Good Laboratory Practices (GLPs), cGMPs, and other regulatory requirements
- Ability to exercise judgment and appropriately raise issues to QC management
- Key focus will be preparing solutions (mobile phase, diluent, etc.) and standard/sample preparations
- Outstanding interpersonal skills, both written and oral, and encouraged to collaborate with other analysts and management
- Ensure equipment is performing well and communicate and take appropriate action as necessary
- Required to follow good documentation practices
- Work cross-functionally to complete projects and testing
The world's most revolutionary biopharma companies are partnering to advance the next frontier of medicine. The company continues to invest in capacity and expansion of its Colorado operations. Join a team of professionals dedicated to the development and commercialization of nucleic acid therapeutics for life-changing, lifesaving medicines.
Candidates must provide their phone number. Job reference number is A5186.