LGC
Oligo Manufacturing Technician I/II/III - Swing Shift
LGC, Petaluma, California, United States, 94954
We are looking for an Oligo Manufacturing Technician I to work in our Petaluma, CA facility or our sister site in Denmark. Our team produces mission‑critical genomics components such as oligonucleotides and supporting reagents for a diverse customer base, including high‑throughput diagnostic testing.
Job Description The Oligo Manufacturing Technician I is responsible for supporting Molecular Biology conversion manufacturing in an ISO 9001 (Custom RUO) and/or ISO 13485 (DxGMP) regulated environment. This position performs production procedures in compliance with current Good Manufacturing Practices (cGMP), Standard Operating Procedures (SOPs) and applicable regulatory standards. The technician will work closely with cross‑functional teams to deliver high‑quality oligonucleotide products for research or diagnostic applications.
Swing Shift:
Monday‑Thursday, 4 × 10 hours, 13:00‑23:30
Learn ISO 9001 and/or ISO 13485 quality management system requirements and follow the Quality Policy.
Perform oligonucleotide manufacturing activities in accordance with written protocols and under the direction of departmental leadership.
Maintain accurate batch records, equipment logs and other documentation in compliance with GDP and company procedures. Perform basic laboratory tasks and analytical measurements.
Assist with or perform troubleshooting, routine maintenance and calibration of laboratory equipment, documenting results and initiating support tickets as needed.
Maintain a clean, safe, and organized laboratory environment, adhere to PPE policies and cGMP/ISO 13485 requirements, and report safety hazards or incidents.
Ensure proper labeling and storage of buffers and reagents per EHS policy and dispose of hazardous waste in compliance with guidelines.
Participate in team meetings, training sessions and continuous improvement initiatives.
Collaborate with team members and support groups to ensure timely and compliant production, reporting delays or deviations.
Support inventory management by stocking consumables and communicating shortages.
Maintain up‑to‑date training and engage in learning opportunities.
Adhere to scheduled work hours with flexibility for overtime as required.
Qualifications
Minimum Qualifications:
Bachelor’s degree in a related field or 1 year of equivalent industry experience.
Proficiency in Microsoft Office (Word, Excel, Outlook) and web‑based applications.
Preferred Qualifications:
Experience in a laboratory and cGMP regulated environment.
Familiarity with laboratory equipment such as HPLC, mass spectrometry, IR, SpectraMax, SpeedVac, liquid handlers, TFF systems and pipettes.
Familiarity with laboratory software platforms such as Unicorn, Empower, LabSolutions, Chromeleon, MassLynx, Softmax Pro, Evoware and Filemaker Pro.
Competencies and Behaviors
Demonstrates LGC’s core values: Passion, Curiosity, Integrity, Brilliance, and Respect.
Self‑motivated, works independently and collaboratively.
Takes ownership of tasks, meets deadlines and follows through.
Executes tasks with meticulous attention to detail, following a structured approach.
Receives and provides constructive feedback and accepts accountability.
Strong attention to detail and organized approach.
Effective communication and problem‑solving skills.
Ability to multi‑task in a fast‑paced, regulated environment.
Strong computer literacy and ability to learn new systems quickly.
Maintains a professional presence and upholds organizational values.
Additional Information The typical pay range for this role is: Minimum: $20.91/hr Maximum: $34.86/hr This range represents the low and high end of the anticipated salary range for the California‑based position.
What we offer (US‑based employees)
Competitive compensation with a strong bonus program
Comprehensive medical, dental, and vision benefits for employees and dependents
FSA/HSA pre‑tax savings plans for health care, childcare, and elder care
Deductible buffer insurance and critical illness insurance
401(k) retirement plan with matching employer contribution
Company‑paid short‑ and long‑term disability, life insurance, and employee assistance program
Flexible work options
Pet insurance for our furry friends
Enhanced parental leave of 8 additional weeks
PTO that begins immediately
Town Hall monthly meetings, cheer program for employee recognition, company‑wide social events, frequent catered lunches, and more!
About LGC LGC is a leading, global life science tools company, providing mission‑critical components and solutions across human healthcare and applied markets. Our high‑quality product portfolio supports NGS workflows and quality assurance applications.
Our Values
PASSION
CURIOSITY
INTEGRITY
BRILLIANCE
RESPECT
Equal Opportunities LGC strongly believes that every job applicant and employee should be valued for their individual talents regardless of age, disability, race, color, ethnic or national origin, sex, sexual orientation, gender reassignment, marital or civil partnership, pregnancy or maternity, religion, or belief. Shortlisting, interviewing and selection will always be carried out without regard to gender, sexual orientation, marital status, color, race, nationality, ethnic or national origins, religion or belief, age, or trade union membership.
Seniority Level Entry level
Employment type Full‑time
Job function Production
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Job Description The Oligo Manufacturing Technician I is responsible for supporting Molecular Biology conversion manufacturing in an ISO 9001 (Custom RUO) and/or ISO 13485 (DxGMP) regulated environment. This position performs production procedures in compliance with current Good Manufacturing Practices (cGMP), Standard Operating Procedures (SOPs) and applicable regulatory standards. The technician will work closely with cross‑functional teams to deliver high‑quality oligonucleotide products for research or diagnostic applications.
Swing Shift:
Monday‑Thursday, 4 × 10 hours, 13:00‑23:30
Learn ISO 9001 and/or ISO 13485 quality management system requirements and follow the Quality Policy.
Perform oligonucleotide manufacturing activities in accordance with written protocols and under the direction of departmental leadership.
Maintain accurate batch records, equipment logs and other documentation in compliance with GDP and company procedures. Perform basic laboratory tasks and analytical measurements.
Assist with or perform troubleshooting, routine maintenance and calibration of laboratory equipment, documenting results and initiating support tickets as needed.
Maintain a clean, safe, and organized laboratory environment, adhere to PPE policies and cGMP/ISO 13485 requirements, and report safety hazards or incidents.
Ensure proper labeling and storage of buffers and reagents per EHS policy and dispose of hazardous waste in compliance with guidelines.
Participate in team meetings, training sessions and continuous improvement initiatives.
Collaborate with team members and support groups to ensure timely and compliant production, reporting delays or deviations.
Support inventory management by stocking consumables and communicating shortages.
Maintain up‑to‑date training and engage in learning opportunities.
Adhere to scheduled work hours with flexibility for overtime as required.
Qualifications
Minimum Qualifications:
Bachelor’s degree in a related field or 1 year of equivalent industry experience.
Proficiency in Microsoft Office (Word, Excel, Outlook) and web‑based applications.
Preferred Qualifications:
Experience in a laboratory and cGMP regulated environment.
Familiarity with laboratory equipment such as HPLC, mass spectrometry, IR, SpectraMax, SpeedVac, liquid handlers, TFF systems and pipettes.
Familiarity with laboratory software platforms such as Unicorn, Empower, LabSolutions, Chromeleon, MassLynx, Softmax Pro, Evoware and Filemaker Pro.
Competencies and Behaviors
Demonstrates LGC’s core values: Passion, Curiosity, Integrity, Brilliance, and Respect.
Self‑motivated, works independently and collaboratively.
Takes ownership of tasks, meets deadlines and follows through.
Executes tasks with meticulous attention to detail, following a structured approach.
Receives and provides constructive feedback and accepts accountability.
Strong attention to detail and organized approach.
Effective communication and problem‑solving skills.
Ability to multi‑task in a fast‑paced, regulated environment.
Strong computer literacy and ability to learn new systems quickly.
Maintains a professional presence and upholds organizational values.
Additional Information The typical pay range for this role is: Minimum: $20.91/hr Maximum: $34.86/hr This range represents the low and high end of the anticipated salary range for the California‑based position.
What we offer (US‑based employees)
Competitive compensation with a strong bonus program
Comprehensive medical, dental, and vision benefits for employees and dependents
FSA/HSA pre‑tax savings plans for health care, childcare, and elder care
Deductible buffer insurance and critical illness insurance
401(k) retirement plan with matching employer contribution
Company‑paid short‑ and long‑term disability, life insurance, and employee assistance program
Flexible work options
Pet insurance for our furry friends
Enhanced parental leave of 8 additional weeks
PTO that begins immediately
Town Hall monthly meetings, cheer program for employee recognition, company‑wide social events, frequent catered lunches, and more!
About LGC LGC is a leading, global life science tools company, providing mission‑critical components and solutions across human healthcare and applied markets. Our high‑quality product portfolio supports NGS workflows and quality assurance applications.
Our Values
PASSION
CURIOSITY
INTEGRITY
BRILLIANCE
RESPECT
Equal Opportunities LGC strongly believes that every job applicant and employee should be valued for their individual talents regardless of age, disability, race, color, ethnic or national origin, sex, sexual orientation, gender reassignment, marital or civil partnership, pregnancy or maternity, religion, or belief. Shortlisting, interviewing and selection will always be carried out without regard to gender, sexual orientation, marital status, color, race, nationality, ethnic or national origins, religion or belief, age, or trade union membership.
Seniority Level Entry level
Employment type Full‑time
Job function Production
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