associate scientist ii.

job summary: Quality Control Microbiology (QCM) is responsible for testing intermediate production samples, final product samples, and environmental samples to demonstrate that all products meet the standard requirements for CGMP operations.Additional functions include raw material testing, stability testing, assay transfers, and qualification of instrumentation.Quality Control is also responsible for assisting in site wide studies and projects.This position is responsible for performing routine and complex testing of in-process samples and final products in accordance with SOPs and relevant procedures for method development, qualification, validation, method transfer, product release, stability, and process validation and investigations. As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Framingham, Massachusetts job type: Contract salary: $30.00 - 35.71 per hour work hours: 8 to 4 education: Bachelors   responsibilities: Perform laboratory assays in support of method development, qualification, validation, method transfer, product release, stability, and process validation and investigations.Perform maintenance on complex laboratory equipment.Review data for compliance to procedures and specifications.Calculate and evaluate results.Make detailed observations in support of Alert, Action and OOS result investigations.Participate in writing and revising SOPs.Assists in the qualification of new controls, standards and reagentsEffectively demonstrate an understanding of and work in compliance with CGMPs.Practice safe work habits and adhere to Genzyme's safety procedures and guidelines.Actively participate in problem solving meetings with senior staff members and suggest process improvements.Independently work under supervision and direction.  qualifications: Leadership Qualifications: An ongoing commitment to conducting our global business according to the highest legal and ethical standards, and to continually pursue excellence in the development and delivery of all of our products and services. This includes:Being a Subject Matter Expert (SME)/Trainer/Coach to other analysts within the laboratory.Constantly striving to make Genzyme a great place to work, and a company respected for the quality of its people and products.Acting as role models for our fellow employees by acting responsibly, fairly, and honestly in our dealings and exercising sound judgment in performing our jobs. Basic Qualifications:Bachelor's degree or equivalent and 2 + years laboratory experience.Master's degree or equivalent and 0-1 year experience.Basic knowledge (i.e. 1-2 years experience) in the required method platform (e.g. Bioburden, TOC, Endotoxin, Water Chemistry, ELISA).Attention to detail, and able to maintain accurate records with excellent proofreading skillsAble to communicate effectively with othersAble to work effectively both independently and as a member of a teamProficient with Microsoft Office tools such as: Word, Excel & Powerpoint. Preferred Qualifications:Experience in GMP lab environment.Experience with lab based data management systems.Experience in a quality control lab. Special Working Conditions:Work in a laboratory with minimal use of chemicals.Ability to lift 10 lbs.  skills: MS-WORD, MS-EXCEL, MS-Powerpoint, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.

job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Worcester, Massachusetts job type: Contract salary: $28.00 - 30.43 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Performs test methods validations for clinical and commercial projects.Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements.Understands, implements and maintains cGMP with respect to laboratory records, procedures and systems in accordance with procedural requirements.Performs a multitude of laboratory techniques for which they are trained.Accepts responsibility to complete assigned tasks within required timelines and works with others to accomplish business objectives.Authors validation protocols and reports as well as corresponding test methods.Support laboratory investigations in a timely manner.Support a variety of testing techniques upon completion of training.  qualifications: BA/BS in Chemistry, Biochemistry, Medical Technology, Biology or equivalent science degree and 2+ years of related work experience.CE-SDS, HPLC or ELISA existing experience and troubleshooting experienceEmpower or Softmax / PLA software experience  skills: Quality control, HPLC, Phase iii, Chemistry, GLP (Good Laboratory Practice), GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.

job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Worcester, Massachusetts job type: Contract salary: $20.00 - 26.48 per hour work hours: 9 to 5 education: Bachelors   responsibilities: The Cell and Protein Sciences (CPS) group, located at the Company's Bioresearch Center in Worcester, MA, is seeking a motivated individual to join its Cell, Gene and Protein Engineering (CGPE) team as a contractor.Our department designs and generates a diverse array of purified protein reagents and engineered cell lines to enable discovery campaigns across the organization.The contractor will be responsible for generating stable and clonal cell-lines for antibody discovery and assay development across multiple therapeutic areas (Immunology, virology, neurobiology, aesthetics).The individual will work with immortalized cell-lines and generate recombinant cell-lines by using transfection and viral transduction methods.They will also have an opportunity to attend project team meetings and learn more about biologics drug discovery across multiple therapeutic areas, while also presenting their findings to the team.  qualifications: Bachelor's or Masters Degree Mammalian cell culture - adherent, suspension cell culture Basic laboratory techniques Research book keeping Communication skills - written and presentation Microsoft office   skills: Molecular Biology, Cell Biology, Flow Cytometry, Cell Cultures, GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.