programmer numerical control salaries in boston, massachusetts

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 find 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. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you!   location: Cambridge, Massachusetts job type: Contract salary: $42.95 - 50.53 per hour work hours: 9 to 5 education: Bachelors   responsibilities: This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation. The Analyst, Cell Therapies QC Laboratory is responsible for the performance of testing of cell therapy manufacturing facilities (CTMF) utilized in Takeda studies. Aid with inventory, documentation, and organization of the QC Lab.This position supports internal QC testing as well as assistance with management of contract testing laboratories.This position is responsible to assist in all QC related activities needed in the in-house GMP cell therapies production of investigational new drugs from development, transfer, (re-)qualification, (re-)validation to routine performance.Perform incoming component/raw material inspection/testing, in-process testing, and product release testing to support the manufacturing of advanced therapy drug products manufactured in the internal GMP facility.Assists with work with contract testing laboratories associated with QC testing for the advanced therapy drug products manufactured at the internal GMP facility.Assist in prepare certificate of analysis of the products manufactured at the internal GMP facility.Ensure that testing is performed on time and as needed.Assist in stability testing as needed.Assist in reserve/retention sample and reference sample management.Author, edit, and review SOPs, job aids, reports etc. as assigned.Assist in maintain data integrity and ensure compliance with company SOPs, specifications and cGMP regulations.Assist in the investigation into any non-conformance, OOS, OOT, instrument malfunction, accident or other abnormal occurrence per SOPs.Assist in method transfer and method validation as needed.Assist in testing, managing, data trending and report writing related to stability as needed.Assist in maintenance, calibration, validation and cleaning of QC equipment and instruments as needed.Initiate and own deviations, Lab Investigations, CAPAs and change controls within the electronic Quality Management SystemAssist in diverse qualification activities (facility, cleaning, software etc) as needed.Assist in the Microbiology laboratory as needed.Keep the QC lab clean, safe and tidy all the times.Work closely and collaboratively with cross-functional team members from QA, QC, production, facility and development.Help with inventory activities, receive and create materials in electronic system.Support the lab with stock and maintain all the materials in stock.Help with ordering activities.Experience with aseptic gowning techniques.Additional duties as assigned.  qualifications: Bachelor's or Master's Degree in related Life Sciences field.PhD Degree desirable.Experience with Flow Cytometry, PCR, ELISA, Cell Culture is desirable.Previous industry experience in a regulated environment desirable.Ability to handle multiple tasks concurrently, and in a timely fashion.Must have basic understanding of laboratory instrumentation.Must be able to communicate effectively with supervisors and peers.Must be able to read, write and converse in English.Must be computer literate. Able to navigate, conduct searches, and complete online forms on Personal Computer for the purposes of training, performance management, and self service applications.Good interpersonal skills and be able to work effectively and efficiently in a team environment.Knowledge of cGMP manufacturing preferred.Knowledge of basic chemical and biological safety procedures.Must display eagerness to learn and continuously improve.Must have the following personal attributes: integrity and trust, work ethic, sound judgment, intellectual honesty, pragmatism, courage and conviction.In general, the position requires a combination of sedentary work and standing for extended periods of time in the Quality Control labs.In general, the position requires a standing for extended periods of time in the Quality Control laboratory. This role supports pharmaceutical production operations therefore the work environment includes exposure to production and cell processing facilities, packaging, component printing and analytical laboratories (this list is not exhaustive).  skills: Quality control, SOP, CAPA, 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 find 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. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you!   location: Cambridge, Massachusetts job type: Contract salary: $60.00 - 67.38 per hour work hours: 9 to 5 education: Bachelors   responsibilities: This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation. The Analyst, Cell Therapies QC Laboratory is responsible for the performance of testing of cell therapy manufacturing facilities (CTMF) utilized in Takeda studies. Aid with inventory, documentation, and organization of the QC Lab.This position supports internal QC testing as well as assistance with management of contract testing laboratories.This position is responsible to assist in all QC related activities needed in the in-house GMP cell therapies production of investigational new drugs from development, transfer, (re-)qualification, (re-)validation to routine performance.Perform incoming component/raw material inspection/testing, in-process testing, and product release testing to support the manufacturing of advanced therapy drug products manufactured in the internal GMP facility.Assists with work with contract testing laboratories associated with QC testing for the advanced therapy drug products manufactured at the internal GMP facility.Assist in prepare certificate of analysis of the products manufactured at the internal GMP facility.Ensure that testing is performed on time and as needed.Assist in stability testing as needed.Assist in reserve/retention sample and reference sample management.Author, edit, and review SOPs, job aids, reports etc. as assigned.Assist in maintain data integrity and ensure compliance with company SOPs, specifications and cGMP regulations.Assist in the investigation into any non-conformance, OOS, OOT, instrument malfunction, accident or other abnormal occurrence per SOPs.Assist in method transfer and method validation as needed.Assist in testing, managing, data trending and report writing related to stability as needed.Assist in maintenance, calibration, validation and cleaning of QC equipment and instruments as needed.Initiate and own deviations, Lab Investigations, CAPAs and change controls within the electronic Quality Management SystemAssist in diverse qualification activities (facility, cleaning, software etc) as needed.Assist in the Microbiology laboratory as needed.Keep the QC lab clean, safe and tidy all the times.Work closely and collaboratively with cross-functional team members from QA, QC, production, facility and development.Help with inventory activities, receive and create materials in electronic system.Support the lab with stock and maintain all the materials in stock.Help with ordering activities.Experience with aseptic gowning techniques.Additional duties as assigned.  qualifications: Bachelor's or Master's Degree in related Life Sciences field and minimum of 3 years of relevant experience.PhD Degree desirable.Previous industry experience in a regulated environment highly desired.Ability to handle multiple tasks concurrently, and in a timely fashion.Must have basic understanding of laboratory instrumentation.Must be able to communicate effectively with supervisors and peers.Must be able to read, write and converse in English.Must be computer literate. Able to navigate, conduct searches, and complete online forms on Personal Computer for the purposes of training, performance management, and self service applications.Good interpersonal skills and be able to work effectively and efficiently in a team environment.Knowledge of cGMP manufacturing preferred.Knowledge of basic chemical and biological safety procedures.Must display eagerness to learn and continuously improve.Must have the following personal attributes: integrity and trust, work ethic, sound judgment, intellectual honesty, pragmatism, courage and conviction.In general, the position requires a combination of sedentary work and standing for extended periods of time in the Quality Control labs.In general, the position requires a standing for extended periods of time in the Quality Control laboratory. This role supports pharmaceutical production operations therefore the work environment includes exposure to production and cell processing facilities, packaging, component printing and analytical laboratories (this list is not exhaustive).  skills: Quality control, SOP, CAPA, 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.