drjobs Process Development Sr. Associate Scientist- 34495

Process Development Sr. Associate Scientist- 34495

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1 Vacancy
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Job Location drjobs

Juncos - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Description:
  • To perform experiments organize data and analyze results with minimal review.
  • Plans conducts or monitors experiments records and organizes data analyzes and interprets results.
  • Provides input to new processes to generate robust and reliable data and/or ensures that studies are conducted in compliance with the respective protocol and applicable guidelines and regulations.
  • Designs monitors or conducts and interprets laboratory experiments with general oversight of supervisor.
  • Performs data analysis provides interpretation and integrates results into the context of a project. Introduces new or improved methods into the lab.
  • Develops and implements new protocols with minimal review. May serve as a representative to cross-functional teams or as a lead on department teams with guidance.
  • Recommends decisions regarding scientific-related issues.
  • Demonstrates skills in problem solving at the project level.
  • Demonstrates expertise and is responsible for making improvements in one or more major laboratory instruments/techniques.
  • Acts as a resource in area of expertise.
  • Authors complex technical documents reports presentations regulatory documents invention disclosure submissions and/or patents clearly and concisely with minimal revision.
  • Assumes influential role in department-wide support efforts such as safety recruiting and committees.
  • Under general direction has overall responsibility for a program or project of limited scope.
  • Provides constructive criticism suggestions and interpretation of results to co-workers.
Education Requirement:
  • Masters degree and 2 years of experience.
  • Bachelors degree and 4 years of experience.
  • Preference: Engineering area and Physics.
Preferred Qualifications:
  • Educational background in Engineering and/or Sciences.
  • Knowledge in Material Sciences (glass/polymers).
  • Knowledge of the practical application of engineering sciences and technology. This includes applying principles techniques procedures and equipment to the design and production of various goods and services.
  • Knowledge of arithmetic algebra geometry calculus statistics and their applications.
  • Knowledge of the chemical composition structure and properties of substances and of the chemical processes and transformations that they undergo. This includes uses of chemicals and their interactions danger signs production techniques and disposal methods.
  • Knowledge and prediction of physical principles laws interrelationships and applications to understanding fluid material and atmospheric dynamics and mechanical electrical atomic and sub- atomic structures and processes.
  • Understanding of equipment commissioning and qualification validation and documentation processes in a highly regulated environment.
  • Familiarity with Biopharmaceutical Environment.
  • Knowledge in Primary Packaging Components (vials syringes cartridges etc.).
  • Knowledge in Secondary Packaging Components (labels dispensing cartons blisters etc.).
  • Knowledge in Glass/Polymer Forensics.
Skills:
  • Advanced scientific analysis and troubleshooting skills.
  • Advanced laboratory work skills.
  • Ability to motivate and/or supervise the activities of others.
  • Must be well organized have multi-task project experience and be able to communicate and work well with other departments.
  • Must have demonstrated skills and competencies in the following areas: Verbal communication. Written communication including technical writing skills negotiation and conflict resolution analytical problem solving and project management.
  • Ability to be flexible and manage change.
  • Computer literacy.
  • Skills requiring the application of scientific theory.
  • Creative skills in the design and performance of scientific experiments and interpretation of results.
  • Strong knowledge of cGMPs.
  • Fully bilingual (English/Spanish).

Work Methodology:

  • 100%-On Site
  • 11 months (1st Contract)
  • Administrative Shift(weekends and overtime may also be required).
  • Professional Service Contract

Required Experience:

Senior IC

Employment Type

Full Time

Company Industry

About Company

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