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Quality Manager, Pharmaceutical And Medical Device Finished Products by GENO: 8:45am On Sep 18, 2015 |
NOSDOC Diagnostics was founded in 2013, it is
located in Katampe Ext district of Abuja, in Nigeria.
Katampe Ext district is famous for been
surrounded with rocks and mountains which
stretch far and wide. Katampe Ext is a developing
area which is sure to attract customers and
businesslike minds from all over the world. This
attribute encourages the rapid growth for start-up
businesses and well established firms and
corporations.
We are recruiting to fill the position of:
Job Title: Quality Manager, Pharmaceutical and
Medical Device Finished Products
Location: Abuja Branch Nigeria
Department: Production
Reports to: CEO
Job Objective:
Liaising with external bodies and agencies on
healthcare and medical matters.
Responsibilities:
Maintains a working knowledge of QA inspection
requirements for components, raw materials, in-
process/bulk and finished goods.
Ensures that review of in-process activities in both
Manufacturing and
Assembly areas is conducted by QA inspectors for
conformance to specifications; follow up on out-of-
specifications including non-conformances.
Develop, implement, manage, audit and maintain
GXP quality systems to support commercial and
development activities for a virtual pharmaceutical
and biologics company with sales in multiple
countries
Participates in In-process Quality in-house and
outside training program.
Conducts periodic analysis of In-process
Inspection program and makes recommendations.
Assist in interpreting and/or developing of
customer specifications and requirements for
assembly/packaging specifications.
Assists in establishing production and assembly
inspection information sheets and documentation
as required.
Maintains and updates ERP System, maintains
repository of batch records/documents, and other
Mfg. & Assembly in-process Specifications.
Develop, manage and maintain a GXP compliant
document control system
Reviews of batch records, work sheets, and
Inspection documentation for completeness and
correctness.
Conduct non-conformance resolutions, complaint
investigations, and associated corrective and
preventative actions.
Ensure that cGMP requirements and quality
standards are recognized, understood and
maintained across the Company
Reviews of QA Inspection reports daily for
correctness and completeness.
Facilitates on site customer inspections,
coordinating availability of product and
communication of disposition to Quality and
Inventory Control.
Interfaces with customer distribution operations
where needed.
Maintains awareness and compliance with safety
regulations in performing job duties.
Reviews Production and in-process related
information on batch records/documents.
Ensure that finished goods, bulk, raw materials,
components are maintained correctly in the
warehouse and other holding areas.
Assist in the review and release of finished
products.
Perform supplier and vendor audits, as well as,
Mock recall and internal audits
Any additional duties of assignments as directed
by the Head of Quality.
Job Requirements
Qualifications:
Minimum of Bachelor Degree (Biochemistry, Life
Sciences, Engineering, related profession).
3 years minimum in industry or related experience
in cosmetic, device, food, or pharma.
Previous inspecting, auditing or manufacturing
experience.
Computer literate and effective communication
skills.
Application Closing Date:
8th October, 2015.
Method of Application:
Interested and qualified candidates should send
their CVs to recruitment@nosdoc-dt.com |
(1) (Reply)
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