Negotiable
Undetermined
Remote
Remote
Summary: The Quality Assurance Associate role involves verifying and validating medical device barcodes, assisting with artwork reviews, and managing recall communications. Candidates should possess knowledge of FDA regulations and demonstrate effective communication skills, along with the ability to handle multiple projects under pressure. A background in science and some experience in Quality/Regulatory within the pharmaceutical or medical device industry is preferred.
Key Responsibilities:
- Verify and Validate medical device barcodes using a barcode scanner.
- Assist with artwork review and approvals.
- Assist with recall communication work.
- Follow written SOPs and formal procedural documents.
- Perform clerical functions, including but not limited to copying, filing, scanning, faxing, etc.
- Process large volumes of administrative forms efficiently with high accuracy.
- Interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
- Perform moderate troubleshooting with minimal supervision.
- Participate in continuous improvement activities.
Key Skills:
- Effective verbal and written communication skills.
- Excellent customer service background.
- Data entry experience.
- Knowledge of FDA regulations.
- Ability to multi-task and handle multiple projects under pressure.
- Attention to detail and compliance with procedures.
- Ability to embrace change.
- 4-year college degree in a science-related field preferred.
- 0-1 year Quality/Regulatory experience in the pharmaceutical or medical device industry preferred.
Salary (Rate): £20 hourly
City: undetermined
Country: undetermined
Working Arrangements: remote
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Other
Location: Remote
Duration: 8 Months
Description:
- Verify and Validate medical device barcodes using a barcode scanner.
- Assist with artwork review and approvals.
- Assist with recall communication work.
- Knowledge of FDA and able to work independently.
- Effective verbal and written communication skills, excellent customer service background, data entry experienced.
- Prefer 4-year college degree in science related field with 0-1 year Quality/Regulatory experience in the pharmaceutical or medical device industry.
- Able to follow written SOPs and formal procedural documents.
- Able to multi-task and handle multiple projects under pressure.
- Able to quickly process large volumes of administrative forms in an efficient manner with a high degree of accuracy and quality.
- Able to be flexible and change directions as necessary.
- Performs clerical functions, including but not limited to copying, filing, scanning, faxing, etc.
- Ability to follow instructions, superb attention to detail and, verbatim compliance to procedure
- Ability to interpret a variety of instructions furnished in written, oral, diagram or schedule form.
- Perform moderate trouble shooting with minimal supervision.
- Ability to embrace change and participate in continuous improvement activity.