Hikma Pharmaceuticals
Supervisor, Quality Assurance
This job is now closed
Job Description
- Req#: 8732
- Regular and predictable onsite attendance and punctuality.
- Lead ongoing daily departmental activities for areas of direct responsibility including supervision of assigned
- personnel, and when required assist other Quality areas in the successful performance of these activities.
- Manage activities of self and direct reports in achieving defined quality goals in an efficient, accurate and
- timely manner.
- Be directly involved in and where appropriate lead multiple process/product improvement projects which may include, Lean Manufacturing or other focus groups, design of experiments, validation protocols.
- Lead in-plant audit ready status efforts for assigned areas and assist other areas within the facility in understanding FDA, DEA and company quality requirements. Maintain a high level of expertise in current regulatory requirements and serve as a plant resource for compliance to these requirements.
- Lead in the development of customer awareness and understanding activities for areas of direct responsibility, and where appropriate, assist and support such activities throughout the facility.
- Must be a recognized by all levels of the facility as an expert in their area and be able to demonstrate leadership ability.
- Must have the ability to perform the responsibilities of the Quality Section Manager on an as needed basis.
- Assists and writes validations for equipment, product changes and computer systems.
- Assists with vendor audits/assessments and provides ongoing feedback related to quality issues
- Understand scientific strategies and be able to invent new methods or new avenues of investigation
- Good interpersonal/communication/influencing/negation skills
- Good project management skills
- Working knowledge of FDA Regulations, Application of Good Laboratory Practices, and Application of Good Manufacturing Practices
- Lead Auditor training, ISO Lead Assessor training, with 2-3 years’ experience in auditing techniques, interpreting regulations and quality systems
- Computer knowledge of common office applications required
JOB TITLE : SUPERVISOR, QUALITY ASSURANCE
JOB PURPOSE: Supervises a staff of QA analysts, inspectors and technicians to ensure that raw materials in process materials,
finished products and packaging and ensure they are in compliance with chemical, biological, microbiological
and/or physical quality control programs and external regulations.
JOB ACCOUNTABILITIES :
QUALIFICATIONS:
Minimum: College graduate (BS in Chemistry, Biology, Pharmacy or Related science)
EXPERIENCE
Minimum: Up to 3 years experience in the pharmaceutical industry, in the fields of Quality Assurance or
production
Preferred: Supervisory Experience
SKILLS
About the company
Hikma Pharmaceuticals plc is a British multinational pharmaceutical company with headquarters in London, UK that manufactures non-branded generic and in-licensed pharmaceutical products.
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