Specialist QA at Biopharma Consulting Services
Juncos, PR 00777, USA -
Full Time


Start Date

Immediate

Expiry Date

06 Dec, 25

Salary

35.0

Posted On

07 Sep, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Commissioning, Change Control, Deviations, Technical Writing, Addition, Validation Reports

Industry

Other Industry

Description

SUMMARY

Perform one or more of the following duties and responsibilities in support Quality Assurance program under minimal supervision.

EDUCATION/LICENSES

  • Doctorate degree or Master’s degree and 3 years of directly related experience or Bachelor’s degree and 5 years of directly related experience or Associate’s degree and 10 years of directly related experience or High school diploma / GED and 12 years of directly related experience.

REQUIREMENTS

Quality Professional with Validations and Commissioning & Qualifications of manufacturing equipment and laboratory bench equipment experience (IOQ, PQ, Functional Test). In addition to Technical Writing, Quality Systems (Deviations, Change Control) and Maintenance (PM, Work Orders, Job Plans review and approval) knowledge. Technical Documents review (Validation Reports, Procedures, Forms).
Job Type: Full-time
Pay: From $35.00 per hour
Work Location: In perso

How To Apply:

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Responsibilities

Please refer the Job description for details

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