... oligonucleotide field or similar field. * Proficiency of organic synthesis and purification ... Excellent full time benefits including comprehensive medical coverage, dental, and vision options
... oligonucleotide field or similar field. * Proficiency of organic synthesis and purification ... Excellent full time benefits including comprehensive medical coverage, dental, and vision options
... oligonucleotide field or similar field. * Proficiency of organic synthesis and purification ... Excellent full time benefits including comprehensive medical coverage, dental, and vision options
... oligonucleotide field or similar field. * Proficiency of organic synthesis and purification ... Excellent full time benefits including comprehensive medical coverage, dental, and vision options
Senior Manager, Process Development
Verona, WI · On-site
$150K - $165K/yr
... synthesis, and manage outsourced manufacturing relationships with contract manufacturing ... This role is full-time onsite, 5 days a week in Verona, WI. Responsibilities * Define and defend ...
Senior Manager, Process Development
Verona, WI · On-site
$150K - $165K/yr
... synthesis, and manage outsourced manufacturing relationships with contract manufacturing ... This role is full-time onsite, 5 days a week in Verona, WI. Responsibilities * Define and defend ...
Senior Manager, Process Development
Madison, WI · On-site
$150K - $165K/yr
... synthesis, and manage outsourced manufacturing relationships with contract manufacturing ... This role is full-time onsite, 5 days a week in Verona, WI. Responsibilities * Define and defend ...
Quick apply
Senior Manager, Process Development
Madison, WI · On-site
$150K - $165K/yr
... synthesis, and manage outsourced manufacturing relationships with contract manufacturing ... This role is full-time onsite, 5 days a week in Verona, WI. Responsibilities * Define and defend ...
... oligonucleotide field or similar field. * Proficiency of organic synthesis and purification ... Excellent full time benefits including comprehensive medical coverage, dental, and vision options
... oligonucleotide field or similar field. * Proficiency of organic synthesis and purification ... Excellent full time benefits including comprehensive medical coverage, dental, and vision options
This is a full-time training position of up to three years in duration. Research Opportunity: We ... Rich experience in synthetic/medicinal chemistry Demonstrated record of scientific achievement ...
This is a full-time training position of up to three years in duration. Research Opportunity: We ... Rich experience in synthetic/medicinal chemistry Demonstrated record of scientific achievement ...
Innovation Postdoctoral Fellow, Peptide or LMW Delivery of New Drug Modality
San Diego, CA · On-site
$52K - $70K/yr
This is a full-time training position of up to three years in duration. Research Opportunity: We ... Rich experience in synthetic/medicinal chemistry Demonstrated record of scientific achievement ...
Innovation Postdoctoral Fellow, Peptide or LMW Delivery of New Drug Modality
San Diego, CA · On-site
$52K - $70K/yr
This is a full-time training position of up to three years in duration. Research Opportunity: We ... Rich experience in synthetic/medicinal chemistry Demonstrated record of scientific achievement ...
Develop appropriate laboratory-scale models for key process steps in synthesis and/or purification ... Demonstrated experience and proficiency in the areas of protein, oligonucleotide, and peptide ...
Develop appropriate laboratory-scale models for key process steps in synthesis and/or purification ... Demonstrated experience and proficiency in the areas of protein, oligonucleotide, and peptide ...
Develop appropriate laboratory-scale models for key process steps in synthesis and/or purification ... Demonstrated experience and proficiency in the areas of protein, oligonucleotide, and peptide ...
Develop appropriate laboratory-scale models for key process steps in synthesis and/or purification ... Demonstrated experience and proficiency in the areas of protein, oligonucleotide, and peptide ...
Full Time Oligonucleotide Synthesis information
What is a full time oligonucleotide synthesis?
A Full Time Oligonucleotide Synthesis job involves the production and purification of short strands of DNA or RNA, known as oligonucleotides, in a laboratory setting. Professionals in this role use specialized equipment and chemical processes to synthesize oligos for research, diagnostics, or therapeutics. The position typically requires attention to detail, adherence to safety protocols, and maintaining accurate records. Full-time roles often also include responsibilities like quality control, troubleshooting instruments, and collaborating with other scientists.
What are the key skills and qualifications needed to thrive as a full time oligonucleotide synthesis specialist?
To thrive as a Full Time Oligonucleotide Synthesis Specialist, you need a strong background in chemistry, molecular biology, and laboratory techniques, typically supported by a relevant bachelor's degree or higher. Familiarity with DNA/RNA synthesizers, HPLC, mass spectrometry, and laboratory information management systems (LIMS) is essential, along with any industry-standard certifications. Attention to detail, problem-solving abilities, and effective communication are standout soft skills in this role. These skills and qualifications ensure the accurate, efficient, and high-quality production of oligonucleotides critical for research and diagnostic applications.
What are some common challenges faced in a full time oligonucleotide synthesis role and how can they be managed?
A key challenge in full-time oligonucleotide synthesis is ensuring the precision and quality of each batch, as even minor errors can affect downstream research or clinical applications. Technicians often encounter issues such as instrument calibration, reagent purity, and troubleshooting failed syntheses. Staying organized, adhering to strict protocols, and maintaining detailed documentation are essential for managing these challenges. Collaboration with quality control teams and regular training on new synthesis technologies can also help mitigate common problems and improve overall workflow.
What is the difference between Full Time Oligonucleotide Synthesis vs Oligonucleotide Synthesis Technician?
| Aspect | Full Time Oligonucleotide Synthesis | Oligonucleotide Synthesis Technician |
|---|---|---|
| Credentials | Typically requires a degree in chemistry, biochemistry, or related field | Usually requires a diploma or associate degree in a relevant science |
| Work Environment | Laboratory setting, often in biotech or pharmaceutical companies | Laboratory or manufacturing environment, often in research labs |
| Job Responsibilities | Design, synthesize, and analyze oligonucleotides; oversee synthesis processes | Prepare and execute oligonucleotide synthesis; operate synthesis equipment |
Full Time Oligonucleotide Synthesis roles generally involve more responsibility, including process oversight and design, while Oligonucleotide Synthesis Technicians focus on hands-on synthesis tasks. Both roles are essential in biotech labs, but Full Time positions often require more advanced education and experience.
What is the most common method of full time oligonucleotide synthesis?
Full time oligonucleotide synthesis typically uses solid-phase synthesis, where nucleotides are added sequentially to a growing chain attached to a solid support. This method allows for automation, high throughput, and precise control, making it the standard approach in the industry.
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Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 5 days ago
Eurofins rating
7.5
Based on 181 frontline employees who took The Breakroom Quiz
63rd of 120 rated laboratories
Job description
Company Description
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
Job Description
The Project Management Associate of Oligo Production is responsible for the oligonucleotide manufacturing operation and implementation of key customer projects to meet production goals, quality, and cost objectives. Perform activities in concordance with FDA-QMS/QSR and ISO-9001 standards; ensure compliance with environmental, health and safety regulations. Select, develop, and evaluates personnel to ensure the efficient operation of the function. Plan and administer procedures and budget, serve as a manufacturing representative and technical expert. This position is full time onsite in Louisville KY, Monday to Friday.
RESPONSIBILITIES:
- Leads the teams and manages individual contributors (Supervisor, Team Leads, Production Chemists, Lab Technicians, contractors).
- Coordinates the activities of project(s) with responsibility for results in terms of timelines, cost, process implementation and employees.
- Manages Red Folder/ VIP customer list projects
- Works on problems of diverse scope including multiple projects and/or objectives.
- Develops and administers schedules and monitors progress (KPI) against objectives. Safety/Quality/TAT/5S
- Prepares KPI reports and communicate regularly with other managers, upper management, and other designated contacts within the organization.
- Coaches subordinate(s) on job performance and development.
- Leads validation activities of new projects and equipment.
- Leads Kaizen and other improvement projects within department.
- Ensures BOMs and manufacturing documents are current, effective and maintained properly in electronic document management system.
- Reviews weekly KPI reports
- Coordinates weekly safety training and recruitment process within department.
- Ensures and adheres to GMP compliance and maintain a clean/ traceable work environment.
- Production Schedule Alignment (Outline deadline requirements for Production, and follow up with schedule to make sure deadlines are met)
- Point of contact for QC questions regarding RF/VIP projects (reviewing MS/HPLC traces before passing to next production step)
- Provide updates/ Delays on RF projects (Tracking for RF and VIP projects)
- Perform activities in concordance with FDA-QMS/QSR and ISO-9001 standards
Qualifications
- A minimum of a Bachelor's degree in engineering, chemistry, biochemistry, or similar field.
- A minimum of 1 years of experience in manufacturing or oligonucleotide field or similar field.
- Proficiency of organic synthesis and purification techniques.
- Effective organization and planning skills.
- Working knowledge of GMP, ISO, and QSR regulations.
- Experience in documenting and analyzing experimental data
- Strong computer, scientific, and organization skills
- Excellent communication (oral and written), and attention to detail
Additional Information
Schedule:
- Monday-Friday 8am-5pm
What we offer:
- Excellent full time benefits including comprehensive medical coverage, dental, and vision options
- Life and disability insurance
- 401(k) with company match
- Paid vacation and holidays
Eurofins USA Genomic Services is a Disabled and Veteran Equal Employment Opportunity employer.
About Eurofins
Sourced by ZipRecruiter
Industry
Scientific research and development services, biotechnology research and development and environmental consulting services
Company size
10,000+ Employees
Headquarters location
Leacock, PA, US