Oligo Manufacturing Technician I

LGC Group•Petaluma, CA

23d•$21 - $35

About The Position

Oligo Manufacturing Technician I Company Description LGC Biosearch Technologies locations Petaluma and Novato, CA, as well as our sister site in Denmark, represent a focused, collaborative culture of producing mission-critical genomics components, primarily oligonucleotides and supporting reagents, for our diverse customer base. We believe in Science for a Safer World and have embodied our mission by supporting first responders during the COVID-19 pandemic where our Biosearch Technologies portfolio has been and continues to be enabling millions of PCR tests worldwide. We are currently seeking candidates who are up for the challenge of operating in a high-growth, purpose-driven organization. Job Description Position Summary 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) (ISO 13485), 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. This is a 6-month contract role. Roles and Responsibilities Conscientiously learn requirements of the ISO 9001 and/or ISO 13485 quality management system and diligently follow the Quality Policy, which describes the relevance and importance of the employee’s work to the achievement of LGC’s quality objectives.

Requirements

Bachelor's degree in a related field or 1 year of equivalent industry experience and/or demonstration of ability to meet the requirements of an Oligo Manufacturing Technician I.
Proficiency in Microsoft Office (Word, Excel, Outlook) and web-based applications.
Demonstrates LGC’s core values: Passion, Curiosity, Integrity, Brilliance, and Respect
Self-motivated and capable of working independently as well as collaboratively in team settings
Takes ownership of tasks, meets deadlines, follows through on commitments
Executes tasks with meticulous attention to detail, consistently applying a structured and methodical approach to ensure accuracy, consistency and compliance with established protocols.
Demonstrates the ability to deliver and receive constructive and appreciative feedback, while accepting personal accountability when appropriate
Strong attention to detail and a methodical, organized approach to tasks
Effective communication and problem-solving skills
Ability to multi-task and perform efficiently in a fast-paced, regulated environment
Strong computer literacy and ability to learn new systems quickly
Maintains a professional presence and upholds the organization’s values through appearance, behavior, and attitude, fostering trust and respect across teams

Nice To Haves

Experience or familiarity working in a laboratory and cGMP regulated environment
Experience or familiarity with laboratory equipment such as HPLC, mass spectrometry (MS), IR, SpectraMax, SpeedVacs, liquid handlers, Tangential Flow Filtration (TFF) systems, and pipettes
Familiarity with laboratory software platforms such as Unicorn, Empower, LabSolutions, Chromeleon, MassLynx, Softmax Pro, Evoware and Filemaker Pro.

Responsibilities

Perform oligonucleotide manufacturing activities in accordance with written protocols and under the direction of departmental leadership.
Maintain accurate and complete batch records, equipment logs, and other production documentation in compliance with GDP (Good Documentation Practices) and company procedures.
Perform basic laboratory tasks and analytical measurements using various instruments to support product quality.
Assist with and/or perform basic troubleshooting, routine maintenance and calibration of laboratory equipment and instruments, documenting and reporting results. Initiate support tickets as needed.
Maintain a clean, safe, and organized laboratory environment, PPE (Personal Protection Equipment) policies, and where applicable, adhering to cGMP and ISO 13485; Report safety hazards or incidents to supervisors or designated safety personnel.
Ensure proper labeling and storage of buffers and reagents in accordance with Environmental, Health and Safety (EHS) policy, and dispose of laboratory debris and hazardous waste in compliance with EHS guidelines.
Participate in team meetings, training sessions, and continuous improvement initiatives.
Collaborate with team members and support groups to ensure timely and compliant production, report/escalate any delays or deviations with team supervisors.
Support inventory management by stocking consumables and communicating shortages or out-of-stock items.
Maintain up-to-date training while actively engaging in learning and development opportunities.
Adhere to scheduled work hours with flexibility for overtime as required and approved.

Benefits

Competitive compensation with 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 meeting onsite/virtual, Cheer program where employees are recognized for outstanding work, Company wide social events, frequent catered lunches and much more!