Documentation Specialist Job
Company Name:
Arca24.com
Salary period: Annual
Documentation Specialist needed for a contract opportunity with Yoh's client located in Hillsboro, OR
The Big Picture - Top Skills You Should Possess:
- cGMP
- GMP-regulated industry
What You'll Be Doing:
- The successful candidate will be responsible for scanning GMP documents using FileNet.
- Other duties include shelving documents and labeling QA file room contents, performing document audits, and generating reports at requested intervals.
- Effectively follow SOPs, policies, and cGMPs.
- Adhere to and enforce Genentech policies and procedures related to document control.
- Attend cGMP training per department policy.
- Complete SOP and on-the job training per department policy.
What You Need to Bring to the Table:
- Must have ability to take initiative and work with little supervision.
- High level of professionalism and the ability to interact with personnel at all levels
- High degree of skill and comfort with computer applications
- Demonstrate ability to work accurately, follow instructions, and handle multiple priorities
- Very strong organizational and communication skills
Bonus Points! Otherwise Known As Preferred
Qualifications:
- Knowledge of cGMP regulations and concepts preferred, particularly in good documentation practices.
- Experience in pharmaceutical/biotech or other GMP-regulated industry preferred.
- Candidates must have at least AA/AS Degree and one to two (1 - 2) years-related work experience.
Recruiter: Mary Nguyen
Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer, M/F/D/V. Click here to contact us if you are an individual with a disability and require accommodation in the application process.
J2W: CLINICAL; J2W: SCIENTIFIC
MONJOB
J2WPACNW
Ref:
SFSF: LSEstimated Salary: $20 to $28 per hour based on qualifications.
Arca24.com
Salary period: Annual
Documentation Specialist needed for a contract opportunity with Yoh's client located in Hillsboro, OR
The Big Picture - Top Skills You Should Possess:
- cGMP
- GMP-regulated industry
What You'll Be Doing:
- The successful candidate will be responsible for scanning GMP documents using FileNet.
- Other duties include shelving documents and labeling QA file room contents, performing document audits, and generating reports at requested intervals.
- Effectively follow SOPs, policies, and cGMPs.
- Adhere to and enforce Genentech policies and procedures related to document control.
- Attend cGMP training per department policy.
- Complete SOP and on-the job training per department policy.
What You Need to Bring to the Table:
- Must have ability to take initiative and work with little supervision.
- High level of professionalism and the ability to interact with personnel at all levels
- High degree of skill and comfort with computer applications
- Demonstrate ability to work accurately, follow instructions, and handle multiple priorities
- Very strong organizational and communication skills
Bonus Points! Otherwise Known As Preferred
Qualifications:
- Knowledge of cGMP regulations and concepts preferred, particularly in good documentation practices.
- Experience in pharmaceutical/biotech or other GMP-regulated industry preferred.
- Candidates must have at least AA/AS Degree and one to two (1 - 2) years-related work experience.
Recruiter: Mary Nguyen
Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer, M/F/D/V. Click here to contact us if you are an individual with a disability and require accommodation in the application process.
J2W: CLINICAL; J2W: SCIENTIFIC
MONJOB
J2WPACNW
Ref:
SFSF: LSEstimated Salary: $20 to $28 per hour based on qualifications.
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