General Application

PR, Puerto Rico
Full Time
PR Operations
Mid Level

We are always looking for Scientists and Engineers to support clients’ needs in the pharmaceutical, biological, and medical devices industry.

General responsibilities:

  •  Applies mastery of in-depth regulatory and process knowledge in one job family or broader expertise in most areas of a job function.
  • Develops solutions to complex problems that require the regular use of ingenuity and creativity. Ensures that solutions are consistent with organization objectives.
  • Work is performed without appreciable direction. Exercises considerable latitude in determining deliverables of assignment.
  • Completed work is reviewed from a relatively long-term perspective, for desired results.  May provide guidance about work activities to colleagues.
  • Contributes to defining the direction for new products, processes, standards, or operational plans based on business strategy with a significant impact on work group results.
  • Frequent interaction with internal or external contacts at various organizational levels concerning ongoing operations or changes relating to processes or programs. Leads briefings with internal and external contacts.
  • Complies with all the requirements in the operational procedures at the area of responsibility to meet the requirements of all applicable regulations.
  • Conducts activities in support of their assigned project.
  • Prepares well documented documents for all processes in compliance with corporate guidelines, procedures, regulations, and industry current practices.
  • Executes successful and timely activities as per established documents. Executes activities according to the schedule developed by the client.
  • Analyzes data and generates conclusions based on test results. Reports the results in an accurate and timely manner.
  • Delivers successful and on time resolution of incidents and deviations related to exercises.
  • Pursues completion of exercises in a timely manner in alignment with the client’s timetable.
  • Assures the accuracy and correctness of documentation used during activities.
  • Other duties as business needs require ensuring that company operates to adequate levels of performance, compliance, and profitability.

Minimum Requirements:

  • Bachelor’s in Engineering or Science or Chemistry or any other related science.
  • 5 years of experience in Health Care (Biotechnology, Pharmaceutical and Medical Devices) industry with one (1) core competencies (Commissioning and Qualifications, Validations, Quality and/or Regulatory)

 

It is the policy of PharmaLex not to discriminate against any applicant for employment, or any employee because of age, sex, gender, sexual orientation, disability, national origin, race, religion, or veteran status.

We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, creed, national origin, ancestry, sex, age, handicap or disability, marital status, sexual orientation, gender identity or expression, pregnancy or pregnancy-related condition, genetic information, veteran status, immigration or citizenship status, military obligations, status as a domestic violence victim or a victim of sexual assault or stalking, participation in discrimination complaint-related activities, or any other status protected under applicable federal, state or local law.

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