Inactive
L

LGC Group

Sells oligos, probes, primers, viral materials

Oligo Manufacturing Lead - Swing shift

Bioprocess & BiomanufacturingPosted on Oct 22
Full-timePetaluma, CA, USA

About the Job

Requirements

  • A bachelor's degree in a related field, or 2+ years of equivalent industry experience and training and/or demonstrated ability to meet the requirements of a GMP Technician.
  • Experience or knowledge with instrumentation such as HPLC, mass spectrometry, purifiers, SpectraMax, SpeedVacs, liquid handlers, TFF, and pipettes is preferred.
  • Ability to perform basic arithmetic using whole numbers, common fractions, and decimals.
  • Computer skills including Microsoft Office, Outlook, Word, Excel, and web browsers; knowledge of Unicorn and Empower is a plus.
  • Technical proficiency to execute documented procedures effectively.
  • Demonstrated experience with common computer software packages, including Windows and Microsoft Office.
  • Ability to work independently and on teams, multitask in a fast-paced environment, and use a methodical, detail-oriented approach.
  • Strong communication and problem-solving abilities.
  • Ability to meet the normal physical demands of a laboratory environment, with reasonable accommodations where applicable.

Responsibilities

  • Work with the departmental Supervisor and Manager to ensure departmental functions in the GMP Manufacturing Lab comply with company procedures and external regulatory requirements.
  • Learn and follow the ISO 13485 quality management system and the terms of the quality contract, including the relevance of the employee’s work to the company’s quality objectives.
  • Perform or support departmental tasks for GMP oligonucleotides according to established procedures.
  • Operate instruments in the immediate work area to manufacture product.
  • Make decisions guided by policies and procedures that affect the group’s ability to meet performance objectives.
  • Use tracking and reporting systems to drive performance and ensure timely completion of product and process quality activities.
  • Recognize equipment or documentation issues and take appropriate corrective action within the role’s scope.
  • Lead and oversee training activities and adherence to standard operating procedures.
  • Provide technical guidance to team members.
  • Assist in creating and reviewing manufacturing procedures and documentation used in the GMP manufacturing lab.
  • Initiate and execute quality-system documentation, including deviation and nonconformance reports, customer notifications, and change request records.
  • Use hazardous chemicals safely in the manufacturing environment and comply with the company’s personal protective equipment policy.
  • Keep training up to date.
  • Work the schedule and core hours determined by the production lab and shift; overtime may be required based on workload with manager pre-approval.
  • Travel is not required.

Desired Qualifications

  • Experience or knowledge with instrumentation such as HPLC, mass spectrometry, purifiers, SpectraMax, SpeedVacs, liquid handlers, TFF, and pipettes.
  • Knowledge of Unicorn and Empower.

About the Company

LGC Group

Sells oligos, probes, primers, viral materials

LGC Group provides life sciences tools and solutions, including oligo components, probes, primers, and recombinant viral materials, plus proficiency-testing schemes for areas like food safety. Its products support detection and development in healthcare through mass spectrometry, immunoassays, and nucleic acid chemistry for vaccines, diagnostics, and therapies. The company differentiates itself with a broad portfolio and global testing services that help customers from diagnostics to vaccine development. Its goal is to improve healthcare outcomes and public safety by enabling accurate testing and high-quality scientific tools.

Company size
1,001-5,000
Company stage
Not listed
Total funding
Not listed
Headquarters
London, United Kingdom
Founded
1841

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