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Process Development Sr Associate Scientist
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Process Development ....
QRC Group, LLC
drjobs Process Development Sr Associate Scientist العربية

Process Development Sr Associate Scientist

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1 Vacancy
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Jobs by Experience

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3 years

Job Location

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Juncos - Puerto Rico

Monthly Salary

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Not Disclosed

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Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Req ID : 1433416

Process Development Sr. Associate Scientist:


  • Identify raw material and container components (glass/polymer) defects.
  • Knowledge regarding primary container components defects andclassifications.
  • Perform experiments, records, organize data and analyze results under minimal
  • supervision.
  • Understands and interprets raw materials and primary components specifications
  • and methods.
  • Follow established experimental design and protocols and performs routine tasksand studies to obtain reproducible and reliable results.
  • Perform assignments that have clear and specific objectives and requireinvestigation of limited number of variables.
  • Assist activities and investigation of deviations, CAPAs, including local or corporateaudits.
  • Build and maintain effective cross-functional collaborations with peers fromacross the network.
  • Write and/or review standard operating procedures, protocols, raw materialspecifications, and reports.
  • Ensures that studies are conducted in compliance with the respective protocol andapplicable guidelines and regulations.
  • Monitor and maintain inventory of supplies and sample inventory.


Requirements


  • Doctorate degree or Master s degree and 1 years experience in GMP regulated industry orBachelor s degree and 3 years experience in GMP regulated industry.
  • Excellent communication skills: oral and written. Interacts effectively with variety
    of communication and working styles. (Bilingual)
  • Demonstrated problem solving and conflict resolution
  • Computer literacy (Windows environment: Word, Excel, Power Point, Minitab)
  • Ability to interpret and apply GLPs and GMPs.
  • Working hours are regular 8:00 am to 5:00 pm the candidate need the flexibility to support non- standard shift operations in a 7/24 format including extended hours and/orweekends as needed.


Doctorate degree or Master s degree and 1 years experience in GMP regulated industry or Bachelor s degree and 3 years experience in GMP regulated industry. Excellent communication skills: oral and written. Interacts effectively with variety of communication and working styles. (Bilingual) Demonstrated problem solving and conflict resolution Computer literacy (Windows environment: Word, Excel, Power Point, Minitab) Ability to interpret and apply GLP's and GMPs. Working hours are regular 8:00 am to 5:00 pm the candidate need the flexibility to support non- standard shift operations in a 7/24 format including extended hours and/or weekends as needed.

Employment Type

Full Time

Company Industry

About Company

0-50 employees
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