Document Control Administrator
at Thermo Fisher Scientific
Frederick, MD 21704, USA -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 18 Jul, 2024 | Not Specified | 19 Apr, 2024 | 2 year(s) or above | Instructions,Teams,Teamwork,E1,Production Schedules,Biology,Microsoft Outlook,Computer Skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
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OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
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Contract – W2 | C2H Independent |
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Contract to Hire – Corp 2 Corp |
Description:
JOB DESCRIPTION
When you’re part of the team at Thermo Fisher Scientific, you’ll do important work. And you’ll have the opportunity for continual growth and learning in a culture that empowers your development. With revenues of more than $40 billion and the largest investment in R&D in the industry, we give our people the resources and opportunities to make significant contributions to the world.
EDUCATION
- High school diploma or equivalent required.
EXPERIENCE
- Minimum of 0-2 years related experience
- Experience in a life science company preferred
- Batch records knowledge and experience preferred
KNOWLEDGE, SKILLS, ABILITIES
- Proven ability to follow policies and procedures, instructions, and to meet production schedules consistently and independently.
- Ability to work in a fast-paced environment with changing priorities.
- Computer skills such as proficiency with Microsoft Outlook, Teams, and E1 to support the operation in its daily functions.
- Strong quality-minded individual with prior experience working within a fast-paced cGMP manufacturing environment.
- Experience in an administrative setting with strong organizational skills and high attention to detail.
- Possess a positive and professional demeanor.
- Places a strong importance on teamwork and peer collaboration.
- Possess strong communication abilities, verbally and written.
- Biology or chemistry background (preferred but not required)
PHYSICAL REQUIREMENTS / WORK ENVIRONMENT
Ability to lift up to 40 pounds.
Work in a GMP manufacturing environment. Must follow PPE requirements specified within the Manufacturing area including: Wear company provided hairnet, beard net (if applicable), lab coat, safety glasses. Must wear closed shoes (no open heel/top/toe areas), maintain no exposed skin other than neck, face and hands.
As a documentation review team member you’ll be working mostly with computers and documents.
Responsibilities:
- Review manufacturing records with strong emphasis on Good Documentation Practices (GDP)
- Daily interaction and collaboration between production and quality team members to assist with timely resolution of quality issues and improve current documentation practices.
- Work in standard laboratory environment while adhering to room specific PPE requirements.
- Satisfactorily complete Thermo Fisher Scientific training requirements on time and operate within all ISO and FDA standards pertaining to Frederick site Manufacturing.
- Have excellent attention to detail of alpha and numerical text as well as symbols.
- Ability to peer review team members’ work to catch errors and collaborate with the appropriate party to resolve.
- Must perform with high accuracy in performing all functions of this position as errors in work could cause customers to receive a non-conforming product.
- This position requires the individual to be ready to start work on-time daily and maintain strong attendance.
- Training will be provided through one-on-one instruction following process specific on-the-job-training until the operator is proficient to work individually.
- The incumbent normally receives general instruction on routine work and detailed instruction on new assignments.
Keys to Success:
REQUIREMENT SUMMARY
Min:2.0Max:7.0 year(s)
Information Technology/IT
Pharma / Biotech / Healthcare / Medical / R&D
Other
Diploma
Proficient
1
Frederick, MD 21704, USA