Process Development Sr Associate Scientist at BioPharma Consulting JAD Group
Juncos, , Puerto Rico -
Full Time


Start Date

Immediate

Expiry Date

09 Jan, 26

Salary

0.0

Posted On

11 Oct, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Advanced Scientific Analysis, Troubleshooting, Laboratory Techniques, Instrumentation Expertise, Verbal Communication, Written Communication, Technical Writing, Project Management, Negotiation, Conflict Resolution, Supervision, Motivation, Adaptability, Change Management, Computer Literacy, Creative Problem-Solving

Industry

Biotechnology Research

Description
This role is ideal for candidates with a strong foundation in engineering or physics, and hands-on experience in inspection, packaging, or primary container evaluation. The successful candidate will design and execute experiments, analyze data, and contribute to cross-functional initiatives with minimal supervision. Key Responsibilities Plan, conduct, and monitor laboratory experiments with limited oversight. Record, organize, and interpret scientific data to support project goals. Develop and implement new protocols and methods to enhance lab efficiency. Ensure compliance with protocols, cGMPs, and regulatory guidelines. Author technical reports, presentations, regulatory documents, and patent submissions. Serve as a departmental representative in cross-functional teams and committees. Provide scientific input and recommendations to improve processes and instrumentation. Mentor peers and contribute to team-wide initiatives such as safety and recruitment. Competencies & Skills Advanced scientific analysis and troubleshooting Strong laboratory techniques and instrumentation expertise Excellent verbal and written communication, including technical writing Project management, negotiation, and conflict resolution Ability to supervise and motivate others Adaptability and change management Computer literacy and data organization Creative problem-solving and experimental design Strong knowledge of cGMPs Qualifications Doctorate degree OR Master’s degree with 2+ years of directly related experience OR Bachelor’s degree with 4+ years of directly related experience Preferred fields: Engineering or Physics Fully bilingual (English/Spanish) Preferred Experience Inspection processes (manual and automated) Packaging operations and incoming material evaluation (e.g., primary containers) Comfortable working in a Process Development laboratory environment 9-months contract with possible extension Administrative Shift
Responsibilities
The successful candidate will plan, conduct, and monitor laboratory experiments with limited oversight while ensuring compliance with protocols and regulatory guidelines. They will also develop and implement new protocols to enhance lab efficiency and contribute to cross-functional initiatives.
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