What are the responsibilities and job description for the QC Scientist II position at myGwork - LGBTQ Business Community?
This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ business community. Please do not contact the recruiter directly.
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description
When you’re part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you’ll be supported in achieving your career goals.
Location/Division Specific Information
St. Louis, MO
How will you make an impact?
As a QC Scientist II, you will engage in valuable work that makes a real-world impact. Your efforts will help in developing treatments for cancer, safeguarding the environment, and ensuring food safety.
What will you do?
Education
BS/BA in biology, biochemistry, chemistry, or a related science field, or a four-year degree with meaningful experience.
Experience
Apply today! http://jobs.thermofisher.com
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description
When you’re part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you’ll be supported in achieving your career goals.
Location/Division Specific Information
St. Louis, MO
How will you make an impact?
As a QC Scientist II, you will engage in valuable work that makes a real-world impact. Your efforts will help in developing treatments for cancer, safeguarding the environment, and ensuring food safety.
What will you do?
- Build QC Raw Materials (QCRM) specification documents in accordance with internal SOPs and external regulations.
- Review batch records, process validation protocols/reports, technical transfer documents, and product specifications with high attention to detail and assess the impact of changes on the testing laboratory
- Collaborate with QCM laboratory scientists to support laboratory needs and questions.
- Review Raw Data for the QC Microbiology (QCM) laboratory
- Generate Certificates of Testing for bioburden and endotoxin results
- Support QCM testing by providing matrices, SOPs, and other testing protocols
Education
BS/BA in biology, biochemistry, chemistry, or a related science field, or a four-year degree with meaningful experience.
Experience
- Minimum of two (2) years of experience in cGMP or another highly regulated industry.
- Experience with bioburden and/or endotoxin assays
- Knowledge of cGMP regulations and international health authority guidelines.
- Knowledge of compendial requirements for raw material testing is desired
- Proficient in Microsoft Office (Word and Excel).
- Experience with Smartsheet and Trackwise systems is desired
- Benefits & Total Rewards | Thermo Fisher Scientific
- Medical, Dental, & Vision benefits-effective Day 1
- Paid Time Off & Designated Paid Holidays
- Retirement Savings Plan
- Tuition Reimbursement
- Relocation assistance is NOT provided
- Must be legally authorized to work in the United States now and in the future, without sponsorship.
- Must be able to pass a comprehensive background check, which includes a drug screening
Apply today! http://jobs.thermofisher.com