MV01-102324 Sr. Process Development Scientist at Validation Engineering Group
Juncos, PR 00777, USA -
Full Time


Start Date

Immediate

Expiry Date

19 Nov, 25

Salary

0.0

Posted On

20 Aug, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Pharmaceuticals, Raw Materials, Middle Management, Gxp, Technical Reports, Medical Operations, Schedules, Organization Skills, Communication Skills, Emotional Intelligence, Technology Transfer, Manufacturing, Analytical Skills, Biotechnology, Medical Devices

Industry

Pharmaceuticals

Description

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

  • Sr. Process Development Scientist

Summary:
To independently conceive, design, implement and advance scientific experiments, which contribute to the successful completion of goals and/or projects. Interprets experimental strategies or leads these activities.
Provides input to new processes to generate robust and reliable data. Functions as a lead scientific / technical resource or as a project leader.

Preferred Qualifications:

  • Proficient in Automatic Visual Inspection Machines.
  • Able to work under pressure.
  • Good organization skills and team worker.
  • Proficient in the preparation of technical reports and business/scientific presentations.
  • Knowledge in raw materials, in-process controls, packaging material, labeling, and finished product variables.
  • Fully Bilingual.
  • Provide group technical guidance.
  • Participate in global cross-functional teams, working effectively in a highly matrixed team environment to advance programs.
  • Acts as an advisor to staff members to meet schedules.
  • Able to develop solutions to routine technical problems of limited scope.
  • Experience in Technology Transfer, pharmaceutical, medical devices, and biotechnology in manufacturing, inspection, and packaging processes.
  • Meticulous, Committed, Skilled, Proactive, Risk-Taking, Structured, Excellent Interpersonal Skill, Energetic, Solution Oriented.
  • Provides analytical skills and ability to understand the big picture in complex environment.
  • Working cross functionally and building collaborative working relationships.
  • Ability to manage, development, implementation, and adherence to processes.
  • Strong verbal and written communication skills, emotional intelligence, and decision maker.
  • Knowledge of GXP for Pharmaceuticals, Biotechnology, and Medical Operations.
  • Knowledge in Pharmaceutical and Biotechnology equipment.
  • Interface with Upper and Middle Management.
  • Determines and pursues courses of action necessary to obtain desired functional results.
  • Knowledge in pharmaceutical product commercialization and lifecycle management.

Education:

  • Doctorate degree and 2 years of Scientific experience OR Master’s degree and 6 years of Scientific experience OR Bachelor’s degree and 8 years of directly related experience.

How To Apply:

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Responsibilities

Please refer the Job description for details

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