Senior Process Development Specialist at TriLink BioTechnologies

San Diego, California, United States -

Full Time

Start Date

Immediate

Expiry Date

04 May, 26

Salary

95300.0

Posted On

03 Feb, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

HPLC Purification, Oligo Synthesis, GMP Manufacturing, Standard Operating Procedures, Technical Assistance, Data Analysis, Process Improvement, Scale Up Projects, Wet Chemistry Reactions, Documentation Practices, Training, Troubleshooting, Project Management, Chemical Analysis, Quality Control

Industry

Biotechnology Research

Description

Who we are: Maravai LifeSciences translates extraordinary science into everyday miracles, helping biotech, biopharma, and life sciences companies everywhere deliver novel vaccines, therapeutics, and diagnostics. We are global leaders in providing products and services within the fields of nucleic acid production and biologics safety testing to many of the world's leading biopharma, vaccine, diagnostics, and cell and gene therapy companies. At Maravai, we believe that diverse perspectives are the foundation of innovation. Through an inclusive and equitable culture where every team member is inspired to bring their best selves to work, we cultivate an environment in which we can lead together, providing differentiated value to our customers, and enabling the miracles of science. For over 35 years, Maravai’s portfolio companies have served as a catalyst for innovative, lifesaving technology for humanity. Pioneering nucleotide research since its inception, we are now leading the way in the rapidly expanding mRNA market. Your next role as a Miracle Maker Maravai LifeSciences is seeking a #MiracleMaker to join our custom development team as a Senior Process Development Specialist. The Senior Process Development Specialist will support the transfers of new processes to produce GMP grade oligonucleotides; performing wet chemistry reactions; development work on synthesis, deprotection, purification, salt exchange procedures and in process QC; writes and updates SOPs and work instructions; onboards and trains new technicians. Leads, coordinates and performs process improvement and scale up projects. How you will make an impact: Maintains safe and clean work environment. Keeps equipment operating by following operating instructions; troubleshooting breakdowns; calling for repairs. Identifies bottle necks/process deficiencies and develops and executes projects for improvements Troubleshoots and provides technical assistance with problematic oligo sequences Documents work by accurately completing forms, reports, logs, and records of equipment and batches following good documentation practices. Collects, records and analyzes data Interprets data analysis results and draws inferences and conclusions Plans, develops, organizes, writes and edits operational procedures and GMP batch records Initiates projects based on process improvements and scale up. Initiates characterization assays centered around developmental improvements. Onboards and authors procedures for new equipment and procedures Transfers developmental improvements to manufacturing team through training/technical transfer Oversees training of new processes for GMP manufacturing staff Perform other functions and duties as required The skills and experience that you will bring: Minimum a Bachelor’s of Science in chemistry related field. At least 5 years of relevant manufacturing laboratory experience, HPLC purification, Oligo synthesis, and scale up Experience in GMP Manufacturing following ICH Q7 guidelines in an ISO 7 and/or ISO 8 clean room Experience with Standard Operating Procedures Strong written and verbal skills Self-motivated and able to organize and prioritize multiple tasks Experience in compiling, analyzing and presenting technical data. The anticipated salary range for this position is $95,300 - $95,000. In addition, highly competitive long-term incentives in the form of company equity, bonus participation and company sponsored benefits are provided as part of the total compensation package. The salary offer will depend on multiple factors which may include the successful candidate's skills, experience and other qualifications, as well as the location of the role. #LI-Onsite The benefits of being a #MiracleMaker: You have the potential to change, improve, and save lives around the world. You have the opportunity to be a part owner in Maravai through RSU grants and optional employee stock purchase plans. We offer comprehensive medical plans and HSA/FSA options. Fertility & family planning assistance. A variety of additional optional benefits and insurance options, including pet insurance. Retirement contributions. Holidays & Paid Time Off. Benefits may vary by region and employment type and do not apply to temporary employees or contractors. See a comprehensive list of benefits at our Benefits & growth site at https://www.maravai.com/careers/benefits-and-growth/ To view more opportunities to become a #MiracleMaker, visit our career site at https://www.maravai.com/careers/ Maravai LifeSciences is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation, and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law. Click here to view Maravai LifeSciences Privacy Notice HIRING SCAM ALERT Recently, individuals impersonating Maravai LifeSciences Human Resources members have offered fraudulent interviews and job offers to unsuspecting candidates. To help protect you from these scam artists, please be aware that: Maravai LifeSciences will never interview a candidate over RingCentral, similar messaging apps or social media (e.g. Telegram, Google Hangouts, WhatsApp, Facebook Messenger, etc.) Maravai LifeSciences will never send a company check or ask an applicant to pay a fee or purchase at home work/training materials in connection with an application for employment. Maravai LifeSciences will never provide excess money to an applicant and ask the applicant to write a check for repayment. If you have any doubt about a job offer or any other communication purporting to come from Maravai LifeSciences, please reach out to us directly at taops@maravai.com. If you believe you have been a victim of fraud, you can report this activity at: www.iC3.gov or www.stopfraud.gov.

Responsibilities

The Senior Process Development Specialist will support the transfer of new processes to produce GMP grade oligonucleotides and lead process improvement and scale-up projects. They will also onboard and train new technicians while maintaining a safe and clean work environment.