job summary: As the 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. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you! location: North Billerica, Massachusetts job type: Contract salary: $25 - 30 per hour work hours: 9 to 5 education: Bachelors responsibilities: Perform testing on incoming materials, finished products and stability studies in QC Laboratory. Perform routine QC testing 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, other quality systems.Resolve routine problems by utilizing appropriate resources. Assist in investigations.May assist on special projects as needed. Help with continuous improvement.Train on and maintain knowledge of current regulatory requirements and relevant internal procedures.Team player who can work independently with quality and attention to detail. Good communication skills both oral and written, professional conduct. Effectively and efficiently participate in assigned tasks in a quality manner.Actively promote safety rules and awareness. Reports and takes initiative to correct safety & environmental hazards. Work with potentially hazardous chemical, radiological and/or biological materials on a daily basis. Demonstrate good safety practices at all times including the appropriate use of protective equipment. Actively demonstrates the company values of accountability, communication, customer commitment, entrepreneurial spirit, integrity, safety and teamwork.*In case of absence the "Reports to" Manager above or a peer incumbent will function as a backup for this position. qualifications: Typically requires 1-3 years of previous experience in the pharmaceutical industry, related GMP environment, or equivalent. Previous experience preferred.Requires a BA/BS degree in a related scientific discipline (e.g. chemistry, biology) or equivalent combination of education and experience.Familiar with aseptic techniquePerform routine Environmental Monitoring and utilities testingPerform sterility, microbial limits and Endotoxin testing, identify and trend microorganismsSome non-routine travel may be required.Flexibility with scheduling requirements-may include shifts, overtime, weekends and holiday coverage, including during adverse weather conditions.Must be able to lift 50 lbs. skills: Quality control, SOP, CAPA, GMP (Good Manufacturing Practice), LIMS (Laboratory Information Management System 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.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility). This posting is open for thirty (30) days.