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Kindeva Drug Delivery
Simi Valley, CA | Full Time
$45k-60k (estimate)
3 Days Ago
Production Documentation Reviewer
Kindeva Drug Delivery Simi Valley, CA
$45k-60k (estimate)
Full Time | Medical Technology 3 Days Ago
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Kindeva Drug Delivery is Hiring a Production Documentation Reviewer Near Simi Valley, CA

Kindeva is a leading global contract developer and manufacturer (CDMO) with delivery platform expertise in Autoinjector, Inhalation, Transdermal/Intradermal Patch Technologies. We partner with our customers to improve patient outcomes around the world. Together, as One Team, we will manufacture many more tomorrows.
3rd Shift Opening - 9 PM-5:30 AM M-F
SummaryTo check production manufacturing documents, such as manufacturing orders (M.O.) and shop orders (S.O.) for completeness, accuracy, and adherence to good documentation practices before M.O. and S.O. are submitted to QA.
Must be able to perform the essential functions of the job, as listed in the Essential Function Analysis Form, with or without a reasonable accommodation.
The essential functions and physical demands of this job can be found on the Essential Function Analysis Form for this position.
ResponsibilitiesCore Job Duties:
  • Review each M.O., batch record and other production documents for accuracy & completeness.
  • Correct errors by seeking out responsible individuals.
  • Ensure & verify in-process product quality audits completed & documented as required by MO instructions.
  • Ensure shop order documentation of components are properly entered (i.e. receiver lot numbers, locations, quantities, initials).
  • Check accuracy of shop order calculations.
  • Deliver reviewed M.O.s to the shift supervisor for approval signatures.
  • Deliver M.O. to the production planning tech for posting.
  • Responsible for notifying the supervisor of QIR for OOS.
  • Assist QSAs to resolve documentation issues.
  • Attend weekly FOT meetings or review FOT meeting minutes to understand MO due dates.
  • Close out batch records for all processes in dept.
  • Must be proficient in serialization process.
Secondary Job Responsibilities
  • Become familiar with all processes in the department.
  • Recognizes and suggests quality improvement procedures that apply to area.
  • Gives and accepts constructive feedback.
  • Knows & uses good safety practices and takes ownership for running of a safe operation.
  • Performs general housekeeping and cleaning of the assigned work area.
  • Takes the initiative to help when required or needed with the total production operation.
  • Performs other duties as requested.
Qualifications
  • Good understanding of batch record documentation requirements.
  • Good attention to details.
  • Basic math skills.
  • Become proficient in the use of a calculator.

Job Summary

JOB TYPE

Full Time

INDUSTRY

Medical Technology

SALARY

$45k-60k (estimate)

POST DATE

06/24/2024

EXPIRATION DATE

07/14/2024

WEBSITE

kindevadd.com

HEADQUARTERS

SAINT PAUL, MN

SIZE

500 - 1,000

FOUNDED

2020

TYPE

Private

CEO

AARON MANN

REVENUE

$50M - $200M

INDUSTRY

Medical Technology

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