GMP Downstream chemist

MISSION

The GMP downstream chemist will be responsible for handling all GMP downstream peptide purification related processes. The GMP downstream chemist will ensure prioritization, proper documentation, and timely execution of the projects. This individual will work closely with Synthesis department and other areas in production as needed. This position is also responsible for handling the downstream processes in QC department, for raw material testing and release as well as re-testing of final product. The downstream chemist will be responsible for performing analytical testing, according to pre-established specifications, for incoming raw materials and all re-testing activities. The downstream chemist is also responsible in ensuring that the assigned tasks are completed in a timely manner.

General Responsibilities

• Performs large scale peptide purification using reverse phase HPLC methodology.
• Performs sample preparation and analysis using analytical U/HPLC for purity and mass spectrometry for identity.
• Analyses and troubleshoots methods and data obtained from individual projects.
• To provide alternatives and suggestions to improve processes, validity and/or accuracy.
• Maintains and troubleshoots instruments, equipment and general lab areas if needed.
• Maintains detailed records of results which may include collecting, extracting, and entering data via both electronic and paper files (i.e., notebooks, logbooks, batch records, etc.)
• Manage resources according to project priorities.
• Assist is method development practices.
• Train and assist team members. Create an environment knowledge-sharing so everyone on the team learns and grows with the Company.
• Participate actively in joined projects.
• Other duties as assigned by Management.
• Perform quality control testing and release for incoming raw materials and retesting products activities.
• Adhere to strict compliance with written procedures applicable to the job function.
• Create, review, and update of procedures related to job function.
• Provide support and assistance as necessary on tasks and projects as directed by the manager.
• Relies on experience and judgment to plan and accomplish goals. Performs a variety of tasks.
• Ensure continuous improvement of QMS through SOP revision activities.

REQUIREMENTS

• Bachelors in chemistry, organic chemistry, biochemistry or equivalent experience.
• Strong peptide purification and analysis background
• Writing technical SOPs, and technical reports
• Work experience biotech/life science GMP environment preferred
• Good oral and written communication skills.
• Must be organized and detail oriented.
• Able to lift, push and pull up to 40lbs
• Proficient in computer skills (MS Office, data analysis, ChemDraw, others).

AnaSpec, Inc. is an equal opportunity employer offering a competitive compensation and benefits package including medical, dental, vision, flexible spending accounts, life insurance, short-term & long-term disability, 401(k), and other benefits!

Job Type: Full-time

Pay: $75,000.00 - $80,000.00 per year

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Paid time off
• Vision insurance

Ability to Commute:

• Fremont, CA 94555 (Required)

Ability to Relocate:

• Fremont, CA 94555: Relocate before starting work (Required)

Work Location: In person