17003 PD Scientist

TITLE:           PD Scientist

LOCATION:  Frederick, MD 

REQ#:             17-003

Company Overview: Jecho Laboratories, Inc. (Jecho) is a biopharmaceutical company developing innovative therapeutic biologics, including therapeutic monoclonal antibodies, cytokines, immunotoxins, and vaccines to address a broad range of infectious diseases as well as treatment of cancer. The company headquarter is located in Frederick Maryland, USA.


We are seeking a Process Development Scientist to join our R&D in Frederick, MD. Qualified individuals will play an important role in upstream process development for bio-therapeutics. The candidate must work independently on experiment design, data analysis, summary and report. The candidate is expected to be well organized, multi-functional and self-motivated.



Ø  Perform literature search and design experiment with sound scientific rational and logics.

Ø  Independently design and conduct experiment for upstream process development.  

Ø  Design and conduct assays including but not limited to SDS-PAGE, Western blot, ELISA, HPLC and other assays.  

Ø  Assist tech transfer activity such as providing operation parameters, writing technical report and perform tech transfer.

Ø  Generate, evaluate, and maintain critical data in a highly organized manner.

Ø  Collaborate and coordinate with colleagues in other departments for developing a robust, high purity/yield, economic and scalable recombinant production process.

Ø  Write scientific proposal, progress report to support the corporate goal.


Minimum Requirements:

Ø  Ph.D. in biological science, biotech/bioengineering or other related areas. 1-2 years’ experience in pharmaceutical or biotechnology field.

Ø  Strong hands on experience of recombinant biologic products expression in mammalian cell culture, cloning and scale up in bioreactor.

Ø  Diverse knowledge and experience in various relevant areas, including but not limited to molecular/cell biology, biochemistry, neuroscience, immunology, and others.

Ø  Capable of performing multiple functions in a fast paced environment. Strong technical protocol/report writing and good presentation skills are required.

Ø  Excellent record keeping abilities to adequately record and to keep documents in support of drug development and approval.

Ø  GMP experience is a plus. Aware of general FDA regulatory requirements associated with biological approval for human use.

Ø  Skillful on basic computer software including Excel, Word and PowerPoint.




Jecho offers a competitive salary and excellent benefits package.

Jecho is an equal opportunity employer.

Please submit resumes to This email address is being protected from spambots. You need JavaScript enabled to view it. .