QC Technician II
at Thermo Fisher Scientific
Rockville, MD 20850, USA -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 25 Jan, 2025 | USD 27 Hourly | 26 Oct, 2024 | 1 year(s) or above | Adherence,Digital Literacy,Ppe,Documentation | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
JOB DESCRIPTION
At Thermo Fisher Scientific Inc., our Rockville, MD site, part of the BioServices Team, focuses on managing critical product and biological materials. We support advancements in cell therapy, high-value biologics, and public health research through customized end-to-end chain-of-custody solutions, ensuring the integrity and efficacy of materials from manufacturer to bedside.
EDUCATION:
- High school diploma or equivalent required.
EXPERIENCE:
- Minimum of 1 year of experience in QA, QC, or a related field required.
- Experience in a cGMP environment preferred.
KNOWLEDGE, SKILLS, ABILITIES:
To succeed in this role, you should have:
- Strong attention to detail and adherence to standard operating procedures (SOPs).
- Proven skills in documentation, communication, and digital literacy.
- High ethical standards with a commitment to maintaining quality requirements.
PHYSICAL REQUIREMENTS / WORK ENVIRONMENT:
- Use Personal Protective Equipment (PPE) and follow chemical hygiene protocols.
- Occasionally lift and manipulate up to 50 pounds unassisted.
- Stand and move around, including reaching, bending, stooping, and grasping.
Responsibilities:
In this role, you will:
- Inspect components, in-process packaging, and finished products to ensure they meet quality standards.
- Collect and analyze data from quality control review logs to identify trends and potential issues.
- Maintain accurate quality assurance documentation, including inspection reports.
- Collaborate with team members to address quality concerns and implement corrective actions.
- Assist in training QC Technicians on procedures and work with Operations staff to resolve issues
To succeed in this role, you should have:
- Strong attention to detail and adherence to standard operating procedures (SOPs).
- Proven skills in documentation, communication, and digital literacy.
- High ethical standards with a commitment to maintaining quality requirements
REQUIREMENT SUMMARY
Min:1.0Max:6.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Diploma
Proficient
1
Rockville, MD 20850, USA