Since 1992, the United States Pharmacopeia has
worked cooperatively with the United States Agency for International
Development (USAID) to help developing countries address critical issues
related to poor quality medicines and their appropriate use through the
Promoting the Quality of Medicines (PQM). PQM serves as a primary
mechanism to help ensure the quality, safety, and efficacy of medicines
essential to USAID priority diseases, particularly malaria, HIV/AIDS,
and tuberculosis. USP–USAID collaborative efforts have helped
communities improve drug quality in more than 35 countries.
Supported
by knowledgeable staff and state-of-the-art facilities around the
world, PQM strives to accomplish four key objectives:
· Strengthen quality assurance (QA) and quality control (QC) systems· Increase the supply of quality assured medicines
· Combat the availability of substandard and counterfeit medicines
· Provide technical leadership and global advocacy
USP PQM Indonesia is currently recruiting for the following position: Pharmaceutical Quality Assurance/Quality Control Consultant
The
Pharmaceutical Quality Assurance/Quality Control Consultant will
support the implementation of the USP PQM work plan activities in
Indonesia related to strengthening BPOM central and provincial
laboratories, supporting post-marketing surveillance activities,
providing training support and project reporting. Activities are focused
on quality control of medicines and diagnostics products for
tuberculosis and HIV control programs in Indonesia. The consultant is
expected to provide high-level technical assistance to the Government of
Indonesia and to local manufacturers (as needed) on basic and
compendial testing based on ISO/IEC 17025, GLP requirements for WHO
Prequalification of Quality Control laboratories, ICH (The International
Conference on Harmonisation of Technical Requirements for Registration
of Pharmaceuticals for Human Use), USP, and other relevant standards.
This project is financed under the USAID Indonesia mission in Jakarta,
Indonesia.
MAIN RESPONSIBILITIES:
· Provide
ongoing training and technical assistance support to BPOM and other
quality control laboratories in Indonesia on compendial testing under
the USP PQM program.
· Coordinate activities under GFATM support, including liaising with national TB and AIDS programs, BINFAR, and BPOM
· Support
CoP and USP PQM QA/QC senior management and staff to implement TB and
HIV work plans including conducting sampling and testing of medicines
throughout supply chain.
· Travel to central or provincial BPOM and BBPOM QC labs as needed for training, follow-up, and project implementation.
· Provide
troubleshooting for equipment and systems used in compendial testing of
medicines (HPLC, LC-MS MS, UV, KF titration, dissolution, etc.)
· Other duties, as requested
REQUIRED QUALIFICATIONS:
· Master
degree or higher (PhD preferred) and minimum 8 years of experience in
QA/QC activities in the pharmaceutical industry or regulatory
environments. Preferred Apoteker licensure in Indonesia
· Expertise
with at least three major analytical methods; HPLC, GC, LC-MS, GC-MS, ,
UV, KF titration and dissolution Experience with providing education or
training on advanced compendial testing of medicines
· Experience with developing Quality Management Systems for QC laboratories, ISO/IEC 17025 requirements, SOPs, etc.
· Experience with auditing, monitoring and evaluation
· Work experience in a USAID or other international donor-funded project in Indonesia desirable.
· Fluency in Bahasa Indonesia and proficiency in written and oral English required.
Interested applicants are requested to submit their CV and application to chrispqm@gmail.com by February 28th 2014 at the latest.
Only shortlisted candidates will be notified

No comments:
Post a Comment