Purification Associate

We are seeking an independent, organized and energetic Purification Associate to be a key member of our dynamic, fast-paced development and manufacturing team. The successful candidate will primarily be responsible for developing purification processes for therapeutic proteins, including monoclonal antibodies and recombinant proteins; producing purified proteins to support lead generation/optimization and preclinical studies; and producing purified proteins under cGMP standards for production of clinical trial materials. Applicants should include descriptions of their experience with various purification techniques, e.g. chromatography, UF/DF, TFF, etc.

Writing development reports, protocols and batch records as well as participation in technology transfer will be required. Experience with upstream/production processes is a plus. This associate will demonstrate strong scientific/technical and interpersonal skills as well as the ability to communicate effectively. This associate will be self motivated and able to work independently.

Preferred Requirements:
- B.S. in biology/life sciences or related field with 2+ yrs industrial experience in process development and cGMP manufacturing
- Expertise in protein purification. Production experience a plus
- Experience in manufacturing of products following SOPs, batch records and working within a cGMP regulated environment
- Ability to observe technical issues and assist with troubleshooting process and equipment problems as necessary
- Create and review manufacturing and equipment SOPs, BRs, and reports
- Maintain familiarity with regulatory requirements, cGMPs and SOPs
- Work on complex assignments of diverse scope and must exercise judgment within defined procedures and practices to determine appropriate actions
- Excellent record keeping and documentation skills including process records and equipment use and maintenance


To be considered as an applicant, please submit your resume/CV referencing the specific position of interest to careers@pacificgmp.com. In addition, please provide at least 3 professional references, preferably from superiors. Applicants whose qualifications and experience most closely match the requirements of the position will be reviewed. Candidates will only be contacted for evaluative discussions. EOE.