controls and instrument technician.

job summary: A Quality Control Documentation Specialist is needed for a leader in developing and providing healthcare in the Lexington, MA area. The ideal candidate will possess strong interpersonal communication skills, the ability to work well in a team setting, as well as independently. This individual must be detail oriented and able to meet deadlines while working with limited oversight.   location: Lexington, Massachusetts job type: Contract salary: $20.57 - 32.05 per hour work hours: 8am to 5pm education: Bachelors   responsibilities: Primary Duties of this position will focus on creation and maintenance of documents to support the operations of the QC Raw Materials laboratory.Documents created and maintained may include protocols, risk assessments, reports, standard operating procedures, and methods.This position is expected to maintain operational and GMP readiness of the QC areas. In addition, the individual may participate in more complex projects, operational excellence initiatives, laboratory operation activities and quality systems with supervision. Education/Experience: Normally requires a Bachelor's degree in the field; 3 - 5 years of experience   qualifications: Experience level: ExperiencedEducation: Bachelors  skills: QualityPharmaceutical 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.

Onsite in Billerica, MA. Great entry level Quality Analyst position for someone with a recent Biology degree or GMP experience.   Perform testing on incoming materials, finished products and stability studies in QC Laboratory. Work in both lab and warehouse areas.  Testing also includes visual inspections, dimensional verifications and analytical testing. 1-3 years of previous experience in the pharmaceutical industry, related GMP environment, or equivalent. Previous experience preferred. BA/BS degree in a related scientific discipline (e.g. chemistry, biology) or equivalent combination of education and experience.salary: $26 - $32 per hourshift: Firstwork hours: 8 AM - 4 PMeducation: BachelorResponsibilitiesPerform routine QC testing and Visual Inspection in accordance with SOPs and cGMP guidelines. Some supervision required. ·       Perform verification of data to ensure accuracy.  Perform approval upon discretion of supervisor. ·       Assist with audit readiness of laboratory area and calibration and maintenance of laboratory equipment. ·       Utilize a range of electronic systems such as LIMS and document/equipment management software. ·       Author SOP changes; participate in change controls, CAPAs and other quality systems.SkillsQuality AssuranceQualificationsYears of experience: 0 yearsExperience level: Entry LevelRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. 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: 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.