{"id":13964,"date":"2013-09-02T11:28:07","date_gmt":"2013-09-02T09:28:07","guid":{"rendered":"https:\/\/joblistsouthafrica.com\/?p=13964"},"modified":"2016-11-10T10:49:32","modified_gmt":"2016-11-10T08:49:32","slug":"adcock-ingram-quality-assurance-validation-officer","status":"publish","type":"post","link":"https:\/\/joblistsouthafrica.com\/adcock-ingram-quality-assurance-validation-officer.html","title":{"rendered":"Adcock Ingram: Quality Assurance – Validation Officer"},"content":{"rendered":"
Job Grade:\u00a0CL<\/div>\n

Reporting to:\u00a0Validation Coordinator<\/p>\n

Job Purpose<\/strong><\/p>\n

Ensure that all required documentation for all validation is compiled and approved to meet regulatory requirements. Effective. Responsible liaising with different departments to ensure all input is compliant and submitted timeously. Implementation, maintenance and periodic reviews of the Quality Management System including self-inspections. Assist with projects on an on-going basis.<\/p>\n

Required Learning<\/strong><\/div>\n

\u2022 BSc Chemistry, ND Analytical Chemistry or equivalent
\n\u2022 Minimum of 6 years pharmaceutical experience or R&D environment.
\n\u2022 In depth knowledge of Quality Assurance, relevant Medicine Regulatory Authority Guidelines
\n\u2022 Thorough knowledge of MCC and all relevant ICH Guidelines and Pharmacopoeias
\n\u2022 Experience in the manufacture of various dosage forms e.g tablets, capsules, syrups and steriles
\n\u2022 Good knowledge\/experience of analytical and formulation equipment processes. and qualification procedures
\n\u2022 Experience in validations and advantage<\/p>\n

Key Job Outputs<\/strong><\/div>\n

\u2022 Preparation of documentation of new and reformulated products in accordance with in-house and regulatory requirements.
\n\u2022 Preparation of documentation of new and existing equipment, instrumentation and utilities in accordance with in-house and regulatory requirements and\u00a0maintenance of the calibration schedule.
\n\u2022 Perform validation of equipment\/ manufacturing processes including reports.
\n\u2022 Evaluation of formulation and analytical reports.
\n\u2022 Ensure all auditing of documentation is co-ordinated to meet deadlines.
\n\u2022 Development, maintenance and continual improvement of the QMS.
\n\u2022 Compliance of procedures and facility with Total Quality Management, Good Manufacturing and Good Documentation Practices.
\n\u2022 Handle ad-hoc requests for data and other related tasks.<\/p>\n

Core Competencies<\/strong><\/div>\n

\u2022 Ability to work as part of a team and on own initiative
\n\u2022 Excellent decision making and problem solving skills
\n\u2022 Excellent planning and organising skills
\n\u2022 Excellent verbal and written skills
\n\u2022 Strong analytical and problem solving ability
\n\u2022 Excellent inter-personal and communication skills
\n\u2022 Good time management skills
\n\u2022 Excellent leadership skills
\n\u2022 Proficient computer skills (MS Office, MS Excel)<\/p>\n

 <\/p>\n

How to Apply<\/strong><\/p>\n

Click on this link to apply online<\/a><\/p>\n

Closing Date for Applications<\/b><\/div>\n

Saturday, 14 September 2013<\/p>\n

 <\/p>\n","protected":false},"excerpt":{"rendered":"

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