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Pharmacy Quality

Location:
Toronto, ON, Canada
Salary:
Negotiable
Posted:
February 11, 2021

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Resume:

PROFESSIONAL PROFILE

Extensive hands on supervisory and technical experience in multinational and generic pharmaceutical manufacturing industry

Well disciplined with proven multi tasking ability to manage multiple assignments efficiently under extreme pressure while meeting tight deadlines.

Self-starter with strong initiative and drive, flexibility to adapt to new environments, dedicated team player with a positive attitude.

Well organized and adapt well to new situations

Proven ability to effectively train, supervise and motivate employees to achieving organizational goals

Highly motivated, self-starter, dedicated team player with

EMPLOYMENT EXPERIENCE

Albion Martin Grove Pharmacy

Pharmacy Assistant – Feb 2013 – Continue

Performs quarterly and annual internal audit, and work with Pharmacist to ensure follows up and corrective actions are completed.

Tracks document requests and ensure completion of outstanding items

Assist in audit and review data for accuracy, completeness and regulatory compliance

Assists the Pharmacist in the preparation of prescriptions

Helps in the management of dispensary inventories, through the ordering, receiving and rotating of stock and supplies, returning outdated and unsalable product, and assisting in the perpetual inventory processes

Maintains of pharmacy stock through inventory control systems

General OTC enquiries from patients and referral to Pharmacist where required and necessary

Perform special assignment as per management

Apotex Inc., Toronto, ON

AGO-QA Production Reviewer – Sep. 2007 – Oct. 2011

Worked and helped with AGO-QA Production Review Group for Critical In-Process Parameters data collection for Annual Product Quality Reviews

Audited and reviewed parameters with specification limits, results, filling and populating excel spreadsheets and creating control charts

Prepared and review Standard Operating Procedures (SOPs)

Coordinated in develop, implement and update QA Manual, QA Supplement Manual and standard operating procedures

Reviewed Quality Control documentation made actions to improve accuracy, GMP compliance.

Coordinated documentation activities to ensure compliance with GLP and GMP

Assured method development records are reviewed as per SGS SOP and rechecked calculations and documented information such as reagent expiry, instrument calibration, logbook entries, control charts etc are present and complete and accurate.

Reviewed internal logbooks for incoming samples, standards and equipment etc.

Audit and inspect laboratory equipment daily use logbooks

Trained departmental staff on documentation and regulatory issues

Delivered documents to associates for further investigation as per GDP requirements

Managed the GMP Documentation, Change Control, CAPS, OOT, OOS, Training Record systems

Reviewed and approve CoA and other quality documentation

Delivered documents to associates for further investigation as per GDP requirements

Reviewed validation activities

Performed timely data review with a high focus on data quality to ensure accuracy and completeness of analytical testing documentation.

Issue and reconcile Quality Control laboratory workbooks and other GMP documentation

Assisted in implement Quality Policies and Procedures for on-site test activities

Assisted in develop, implement and update QA Manual, QA Supplement Manual and standard operating procedures

Coordinated in the review and approval of GMP documents

Coordinated in support training initiatives by implementing training program and ensure training records are compliant

Performed other tasks assigned by the senior management

Compounding Technician PO5/Team Lead - Oct. 2001 - Aug. 2007

Coordinated with other support groups to maximize the production results and complete production schedule on time while ensuring quality compliance

Dealt with process related problems/troubleshooting

Responsible for dealing with process deviations (Q-notes), writing deviation reports and follow-up on conclusion and long term tasks

Ensured each process stage complied with GMP, SOP and Health and Safety standards

Worked effectively on SAP production related system

Closely reviewed reliability sheets for each shift in order to help manager process optimization in achieving reliability targets

Investigated all Quality and safety incidences and making sure all the corrective action and long term tasks completed

Worked actively as a member of class A MRP II team for inventory control management.

Maintained discipline and administration with respect to scheduled tea/lunch break times, arrival/departure

Vita Pharm Windsor, Windsor, ON - Aug. 1998 - Feb. 2001

QA Documentation Technician (Production)

Checked formula after completion of blending, including dispensing tags against formula

Ensured all the calculations and cleaning sheets were accurately recorded on process documentation

Checked compression documents with all weight variation sheets

Verified with the attachments on the documents to sign for completion

Reviewed Certificate of Analysis (C of A) to make sure that it was within the limits of the MMD

Accurately prepared the Document Review sheets for each batch processed

Conducted investigation for any errors in the logbooks and forwarded the recommendations to QA director for review

Abbott Labs Pak Ltd.,

Supervisor Production - Mar 1994 - Jun. 1998

Responsible for production operation in granulation and compression department

Involved in manufacturing of various solid dosage forms

Involved in process by using FITZ GRANUMILL, MATRIX MIXER, and TRAY DRYER and high sheer mix

Responsible for following weekly schedule prepared by production control department, preparation of production reports and monitoring production equipment and processes

Coordinated with production maintenance for issuance of work orders and for completion of repairs

Ensured proper use of plant and machinery, fault, breakdowns or service be brought to the notice of the maintenance department and higher management

Maintained discipline and administration in respect of scheduled break times, arrival, departure, overtime and leave of personnel in department

Made all necessary efforts through personal interest and experience to boost the production/productivity activities to a maximum

Took steps and efforts to control process deviation and anomalies

Maintained inventory of machines, fixtures, equipments and tools in the section

Glaxo Welcome Pak Ltd

Store Officer/Supervisor Warehouse - Oct 1990 – Sep 1994

Organizing daily raw material issuance plan, handling with 19 workers

Coordinating with production area for timely raw material and packaging material issuance

Effectively coordinated with production department for raw material and packaging material sampling and issuance

Abbott Labs Pak Ltd.,

Jr. Supervisor Production - Feb. 1987 - Jun. 1990

Responsible for production operations in Ware House for issuance and dispensing raw materials. Also Coordinating with production area for timely raw material and packaging material issuance

Effectively coordinated with production department for raw material and packaging material sampling and issuance. Maintained discipline and administration in respect of scheduled break times, arrival, departure, overtime and leave of personnel in department

Made all necessary efforts through personal interest and experience to boost the production/productivity activities to a maximum

Ensured each process stage complied with GMP, SOP and Health and Safety standards

Profession Development & Education

Apotex In-House training in MESH, Warehouse, Production, Packaging and Quality Assurance, SAP

Bachelor of Pharmacy (University of Toronto equivalent 4 years Degree)

Karachi University, Pakistan

COMPUTER SKILLS

Working knowledge of SAP, AS400, Microsoft Office

References: Available upon request.



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