AnaSpec, EGT Group is a leading provider of integrated proteomics and genomics solutions for worldwide life science research. As a subsidiary of Eurogentec, AnaSpec offers expertise in peptides, fluorescent dyes, antibodies, assay kits, oligonucleotides, and qPCR kits. AnaSpec carries a broad product line of biochemicals and reagents for basic research, high-throughput screening and drug discovery. Our expertise in these complementary fields translates into both premium quality products and cutting-edge innovation.
Our employees perform ground-breaking, and rewarding work. In return, we offer a compensation package that includes:
Medical, Dental, and Vision insurance
Company Paid life Insurance, Short-term and Long-Term Disability
Employee Assistance Program
Paid Time Off and Sick Days
We proudly support our employees' contribution to life science research in its efforts to improve global health. If youre interested in becoming part of our team, please submit your resume to email@example.com
QC Analyst I
This position is responsible for performing analytical testing to insure that raw materials and finished products are evaluated in a timely manner and meet all procedural requirements. This position is responsible for review of data for accuracy and completeness and the review of manufacturing records.
Perform quality control testing of AnaSpec products and incoming raw materials including Mass Spectroscopy (MALDI & ESI), Amino Acid Analysis, HPLC, Karl Fischer, Polarimeter and TLC.
Perform peer review of analytical data.
Review completed manufacturing records against procedural requirements and specifications.
Adhere to strict compliance with written procedures applicable to the job function.
Trend data as needed including data for nonconforming products.
Assess validity of quality related complaints by customers by performing investigations.
Create, review, and update of procedures related to job function.
Provide support and assistance as necessary on tasks and projects as directed by the manager including method and process validation support.
Must have attention to detail
Flexibility and interest in learning new techniques and skills
Ability to prioritize work
Must have excellent communication skills
Must be a team player and self-motivated
IVD/RUO Fill and Finish Associate
To contribute to the pursuit of the companys mission (conception, manufacture and supply of reliable products and services to the life sciences community) by:
Ensuring the effective operation of all stages of fill-and-finish
Contributing to the cost-effectiveness of products and services
Optimizing the satisfaction of the customers
Perform all procedures according to the work instructions and in a manner compliant with ISO 13485 and cGMP regulations
Bachelors Degree in Chemistry, Biology, or a life science related degree
Record production data into the batch record documents
Perform final desalting of products by G25 and ethanol precipitation
Perform UV quantitation of in-process and final product
Coordinate transfer of samples from IVD Production to QC
Prepare final samples per specifications for customers
Create certificate of analysis for final products
Coordinate shipment of final product with the shipping department
Maintain in-house retain samples
Manage the tracking file for each project
Oversee the filing of the batch record documentations during production
Coordinate completion of all batch records with the Quality Assurance manager and Quality Control manager
Inform the Production Leader of any problems and issues occurring in Production at all times to avoid late orders and remakes
Ensure full collaboration between all sections of oligonucleotide production by the effective communication of all information in relation to orders
Write and revise work instructions and checklists
Train on IVD and RUO production processes as needed
Train fellow employees in Fill & Finish responsibilities
Assist in synthesis and purification
Assist in document control for Quality Assurance department
Proven ability to work well in a multi-disciplinary project team environment
Excellent oral and written communication skills
Possess a strong work ethic
Must be capable of thinking and acting independently, accepting supervision by Eurogentec SA and working quickly and accurately in a fast-paced environment
Proven ability to author, understand and follow complex written procedures
Solid organizational, time management, problem-solving, decision-making, judgment, and interpersonal skills are critical
What We Offer:
To be part of a company well recognized in the Biotech sector and constantly looking for development opportunities
A motivating job with direct impact on companys results
A competitive compensation and benefits package
A team spirit organization
Who We Are: Eurogentec North America, Inc.
Eurogentec is always seeking talented and motivated employees to help the company grow. Join us for an exciting career in a young and growing team. We provide opportunities for professional development and advancement.
Eurogentec was founded in 1985 as a spin-off of the University of Liθge (Belgium). Its mission is to design and deliver reliable and innovative services and products for the Life-Science community. As a leading supplier for genomic and proteomic research, Eurogentec is able to offer its customers integrated solutions, whether they use DNA, antibodies, peptides or proteins as research tools. Eurogentec also offers research and development services for the biopharmaceutical industry. In this area of activities the services provided to customers are manufacturing process transfer and development to support the GMP manufacturing of new drugs and vaccines mainly for use in clinical trials. Eurogentec's headquarters are located in the LIEGE Science Park. The Company has subsidiaries in France, Germany, the UK, the Netherlands and a branch office in Switzerland. Eurogentec has also offices and manufacturing centers in the USA, Japan and Singapore. The EGT Group currently employs around 400, including 40 PhDs. Our success over the last 20 years is largely attributed to our employees working together towards a common set of goals, which are:
To serve our customers efficiently and effectively by providing an innovative quality product and service at a competitive price
To foster an environment that encourages creativity & innovation and promotes superior performance
To value and respect our people by encouraging diversity, transparency, trust and openness within the organization
Senior Chemist (Peptide Department)
Synthesize peptides both in solution phase and solid phase
Synthesize peptides on automation mode and manual mode
Synthesize peptides in multi-gram or kilo production scale
Synthesize protected amino acid derivatives, and resin modification
Synthesize dye conjugated amino acids
Perform different peptide conjugation, including dye-labeled, FRET, and others
Design peptide production strategies, and design of experiment (DOE)
Perform peptide or other molecule analysis using MALDI-MS, LC-MS, HPLC, TLC, -UV-Vis, and NMR
Perform peptide purification using Prep-HPLC, recrystallization, and others
Perform peptide production process development and improvement
Perform methodology studies (R&D) on peptide synthesis and peptide purification
Be able to work independently
BS and/or MS degree or higher in chemistry
Strong Organic background, perform multi-step synthesis
Strong peptide synthesis using SPPS and solution phase method
Writing technical SOPs and technical reports
Experience in peptide modification and peptidomimetic
Five year peptide production (synthesis, purification, and analysis) experience
More than five year working experience in industry or biotech environment
Experience in instrumentation (analytical and synthesis)
Good oral and written communication skills
Must be organized and detail oriented
Experience working in a global atmosphere is a plus
Proficient in computer skills (MS Office, data analysis, ChemDraw, others)
Please send your resume and cover letter to:
Attn: Human Resources Dept.
34801 Campus Drive
Fremont, CA 94555