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Bachem

Develops and manufactures peptides and oligonucleotides

Chemist 1/2/3

Bioprocess & BiomanufacturingUpdated on Nov 14
Full-timeTorrance, CA, USAIn-person

About the Job

Requirements

  • A bachelor's degree in chemistry or a related field, or 10+ years of relevant experience in lieu of a degree.
  • Experience using general laboratory instrumentation such as HPLC and UV spectrometry.
  • Ability to follow GMP guidelines and housekeeping rules.
  • Written and oral communication skills, with the ability to communicate proactively and keep the direct supervisor aware of potential issues.
  • Ability to work independently and manage time effectively.
  • Ability to organize and multitask in a fast-paced, deadline-driven environment.
  • Detail orientation and ability to troubleshoot and resolve problems.
  • Basic computer knowledge, including Microsoft Word, Excel, and PowerPoint.
  • Ability to work with hazardous materials and chemicals.

Responsibilities

  • Manufacture active pharmaceutical ingredients (APIs) and perform related activities in a cGMP-regulated environment.
  • Install, operate, and maintain equipment for manufacturing and in-process testing, including HPLC/UPLC, lyophilizers, balances, reactors, HF cleavage equipment, diafiltration systems, water purification systems, ovens, and washing systems.
  • Perform solid-phase and liquid-phase synthesis, and deprotect and cleave APIs from resin using chemical cocktails containing HF, TFA, ammonium hydroxide, or other chemicals.
  • Purify products using chromatography, crystallization, and other techniques.
  • Follow approved GMP manufacturing directions, including Master Batch Records, Standard Operating Procedures, Standard Test Procedures, and other procedures, to manufacture GMP materials, perform in-process tests, package products, and carry out related activities.
  • Plan projects and initiate raw-material order requests; receive raw materials, coordinate with QA/QC and Material Management for material release, and monitor raw-material inventories.
  • Follow and maintain the GMP documentation system; investigate deviations and produce reports; initiate document change requests; and assist the quality control and assurance unit in maintaining the equipment calibration program.
  • Maintain and organize work areas, including hoods, benches, floors, and walls, and other designated areas within the manufacturing facility.
  • Write and improve Standard Operating Procedures, Standard Test Procedures, Master Batch Records, and other related GMP documents.
  • Follow procedures to clean GMP-process equipment, maintain equipment cleaning logs, assist with equipment calibration, and dispose of chemical waste generated in manufacturing.
  • Periodically review and sign off on maintenance and cleaning logs to monitor compliance for equipment and instruments used in GMP processes.

Desired Qualifications

  • Experience in GMP manufacturing and basic knowledge of cGMP and FDA regulations.
  • Experience manufacturing peptides and oligonucleotides.

About the Company

Bachem

Develops and manufactures peptides and oligonucleotides

Bachem provides development and manufacturing of peptides and oligonucleotides for research, clinical development, and commercial products. Its offerings include custom synthesis and scale-up production, analytical testing, and related services across the drug development spectrum. Customers work with Bachem by specifying desired sequences and specifications, after which Bachem designs, synthesizes, and quality-controls the peptides or oligonucleotides and delivers them in appropriate scales and formats. The company differentiates itself through more than five decades of experience, a global footprint with sites in Europe, the US, and Asia, and an integrated set of services spanning discovery support to commercial manufacturing. Its goal is to help pharmaceutical and biotechnology companies advance peptide- and oligonucleotide-based therapies by providing reliable, scalable, and well-supported manufacturing and development capabilities.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Bubendorf, Switzerland
Founded
1971

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