Top 89 Chemical engineer Jobs in Korea Pr

Process Development Scientist
Weil Group, Inc —Juncos, PR
- Temporary
- Background check
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- Computer literacy
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Weil Group, Inc —Juncos, PR
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CMM Validation & Engineering Solutions, LLC. —Juncos, PR
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Process Development Scientist ID 35500
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InnovaWorkforce Inc. —Juncos, PR
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Process Development Scientist ID 35470
Inteldot —Municipio de Juncos, PR
- Full-time
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7d
Engineer
Flexible & Integrated Technical Services, LLC —Carolina, PR
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JT388 - ENGINEER
Quality Consulting Group —Juncos, PR
- Extended hours
- Spanish
- English
- Mid-level
1d

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Process Development Scientist

Weil Group, Inc
Juncos, PR

Quick Apply

Job Details

Temporary | Full-time
7 days ago

Qualifications

Computer operation
Teamwork
Content creation for technical audiences
Technical documentation
English
Production validation processes
Bachelor's degree
Conflict management
Desktop applications
Data-driven problem-solving
Managing projects
Productivity software
Manufacturing
Cross-functional collaboration
Negotiation in dispute resolution

Full Job Description

Temporary Job - initially for 6 months - Administrative Shift

What attributes (i.e. - preferred qualifications) would make this candidate stand out? Experience in drug product manufacturing. Process Validation Writing technical protocols or reports

Job Description

To conceive, design, implement and execute specific scientific experiments, which contribute to the successful completion of goals and/or projects under general guidance of supervisor. Under general guidance of supervisor, Conceives and designs, executes or evaluates, and interprets experimental strategies. Provides input to new processes to generate robust and reliable data. Ensures that studies are conducted in compliance with the respective protocol and applicable guidelines and regulations. Designs, monitors or conducts experimental strategies with general guidance from supervisor. Provides data analysis and interpretation and assesses impact of the data on the project. Keeps current in field of scientific expertise and areas relevant to their function. Monitors field of expertise, including literature and technology development, and communicates relevant observations. May introduce advanced scientific methods. Develops and implements new and novel protocols to address specific issues. May represent the department on project teams under supervision of a senior scientific staff member. May initiate productive collaborations within and outside of the department or company. Advises or assists others in experimental design and/or interpretation/diagnosis of data and implementing innovative remedies. Independently authors scientific reports, summary documents, complex regulatory documents, invention disclosure submissions and/or patents. Participates in external scientific community. May assume lead role in department-wide support efforts such as safety, recruiting and committees. May develop supervisory and mentoring skills.
Develops and follows timelines for completing project teamwork.

EDUCATION
Bachelors + 4 years of Scientific experience

EXPERIENCE
Previous experience in process validation is required.

COMPETENCIES/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 Project management Ability to be flexible and manage change. Computer literacy (Windows environment: Word, Excel, Power Point). Skills requiring the application of scientific theory. Creative skills in the design and performance of scientific experiments and interpretation of results. Strong knowledge of cGMP’s. Fully bilingual (English/Spanish).

*Weil Group is proud to be an Equal Employment Opportunity Employer.*

#IND2

Job Types: Full-time, Temporary

Education:

Bachelor's (Required)

Experience:

Process Validation: 3 years (Preferred)
Writing technical protocols or reports: 3 years (Preferred)
drug product manufacturing: 3 years (Preferred)

Language:

Bilingual (Preferred)

Work Location: In person

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