Breaking News

Tuesday, August 9, 2016

Openings at Gilead Pharmaceutical Limited


Gilead Pharmaceutical Limited, is recruiting suitably qualified candidates to fill the position below:


Job Title: Territory Sales Representative


Job Description
The Territory Sales Representative is responsible for the following:


  • Generate prescriptions in line with territory sales quota

  • Maintain sample inventories, distribute samples, comply with sample accountability policies and procedures, and comply with Prescription Drug Marketing Act

  • Make complete, accurate and timely submission of all call activity, sample activity and expense reports

  • Compliance with all applicable state and federal laws pertaining to promotion of prescription products.

  • Keep current with product and market knowledge as well as competing products.

  • Participate in all training, sales meetings and conventions

  • Under guidance of sales management, plan and organize territory call plan to meet sales and call targets

  • Make sales presentations to physicians, nurses and pharmacists

Requirements


  • Two years successful pharmaceutical sales experience, preferably in a small to mid-size company

  • Demonstrated success in outside sales

  • Understanding of product marketing, messaging and promotion

  • Ability to manage a sales territory comprised of physician offices and pharmacies

Education and Experience


  • Bachelor’s degree

  • 2 or more years of documented, successful pharmaceutical sales experience

  • Strong working knowledge of Microsoft Office programs

Compensation & Benefits


  • Competitive base salary plus uncapped bonus structure

  • Enrollment in the company’s employee share option plan on hire with opportunity for bonus performance-based options

  • Company-provided vehicle (includes company-paid fuel and all maintenance)

  • 22 Paid Days off/full year

 


Job Title: Quality Assurance Officer


Job Description


  • Review/perform daily compliance verification, document results, and report to the MD.

  • Environmental monitoring and documentation e.g. personnel monitoring, air bioburden, surface bioburden, temperature, and particle counts

  • Collect Environmental Monitoring samples as necessary

  • New staff training

  • Sterility tests, aseptic technique qualifications, and media fill process validations.

  • Prepare/revise operating procedures and specifications

  • Review/approve routine change control requests as designated

  • Verify that raw materials meet specification limits

  • Verify that all documentation is complete

  • Document non-compliance and evaluate if further investigation is needed

  • Submit samples to the appropriate labs for chemical assay and microbial tests

  • Track vendor equipment calibration and maintenance records and assess for deviations

  • Enter test results or summaries into the pharmacy specific monthly and quarterly Quality Assurance report template

  • Document results of deviation and complaint investigations, causal analysis, corrective actions and preventive actions

  • Develop method validations and lead stability studies

  • Maintain quality records (equipment calibration and maintenance, training, deviation and complaint investigation, environmental monitoring, Certificate of Analysis, clean room certification etc.).

  • Control of product labeling/label accountability

  • Recommend and/or implement improvements in streamlining processes and procedures in the areas of compounding, validation, change control, laboratory, and risk assessments

  • Lead root cause analysis and corrective and preventive actions for audit observations, product complaints, product non-conformances, in-process deviations issues related to process controls

  • Direct the investigation of excursions in manufacturing or other related operations, resolve the nature of the cause, impact on product quality, disposition and corrective actions

  • Perform final review of test data/reports to ensure conformance to the established specifications and standard operating procedures, perform final disposition of batch.

  • Ensure products are released on time and within specification

  • Verify that product test results meet specification limits

Qualifications


  • BS degree in Technical or Scientific discipline preferably Microbiology

  • Effective communication skills, both written and verbal

  • Leadership skills and the ability to facilitate the work activities of others

  • Good organizational and time management skills

  • Preferred minimum of 2 years of related experience preferably in the pharmaceutical industries

  • Ability to work autonomously within established procedures and practices

  • Working knowledge of Pharmaceutical Regulations

Additional Benefits:


  • Cell phone reimbursement allowance

  • Gym membership reimbursement allowance

  • Full medical benefits

How To Apply
Applicants should forward their CVs/Applications to: [email protected]


Note: Only shortlisted applicants will be contacted


Application Deadline: October 10th, 2016




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