Chemist

Bachem

Bioquímica

Vista, CA - United States

Project Manager Junior / Técnico especialista

Experteer Overview

In this role you will manufacture active pharmaceutical ingredients (APIs) in a cGMP environment and support related processing activities. You’ll operate and maintain manufacturing equipment, conduct solid and liquid phase syntheses, and perform in-process testing and purification. You will follow GMP Master Batch Records, SOPs, and QA/QC coordination for material releases. You’ll write and improve GMP documents and help ensure equipment calibration and cleanability. This is a hands-on, cross-functional role that contributes to compliant production at scale.

Compensaciones / Beneficios

competitive pay
annual performance bonus
comprehensive medical/dental/vision
401(k) with employer contribution
paid vacation
personal and sick days

Responsabilidades

Install, operate and maintain manufacturing equipment (HPLC/UPLC, lyophilizers, reactors, diafiltration, water purification, etc.)
Perform solid and liquid phase synthesis and deprotection/cleavage of APIs
Purify products via chromatography, crystallization and related techniques
Follow GMP documents (MBR, SOPs, STPs) and perform in-process testing and packaging
Plan projects and initiate raw material orders; coordinate material release with QA/QC and Material Management
Maintain GMP documentation system; investigate deviations and initiate change requests
Organize and maintain work areas and write/improve GMP documents (SOPs, STM, MBPR)
Monitor and document cleaning, calibration, and waste disposal procedures for GMP equipment
Ensure compliance with maintenance and cleaning procedures; sign off on logs

Requisitos principales

Bachelor’s degree in chemistry or related field (or 10+ years relevant experience)
Experience with general lab instrumentation (HPLC, UV Spectrometry)
GMP manufacturing experience; knowledge of cGMP and FDA regulations (preferred)
Experience in manufacture of peptides and oligonucleotides (preferred)
Ability to follow GMP guidelines and housekeeping rules
Excellent written and oral communication; Team-oriented and proactive problem solving
Ability to work four 10-hour shifts with early or late start times, including weekends
Ability to work independently, multitask, and operate in a fast-paced environment
Basic computer skills (Word, Excel, PowerPoint)
Ability to handle hazardous materials and chemicals

strong communication team collaboration proactive problem solving HPLC UPLC UV Spectrometry

Descripción del puesto

In this role you will manufacture active pharmaceutical ingredients (APIs) in a cGMP environment and support related processing activities. …

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