Easter Seals Jobs

associate i, quality control, raw materials.

• norwood , massachusetts

• posted 5 days ago

job details

summary

• $25 - $34.67 per hour

• contract

• bachelor degree

• category life, physical, and social science occupations

• reference48877

job details

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: Norwood, Massachusetts

job type: Contract

salary: $25.00 - 34.67 per hour

work hours: 9 to 5

education: Bachelors

responsibilities:

Reporting to the Supervisor of Quality Control, Seeking a Quality Control Raw Materials Associate I, Sampler based at their Norwood, MA site. The individual in this role will perform QC Raw Material activities in support of GMP Manufacturing and further support special projects as assigned.

• Requesting, sampling, and shipping of raw materials

• Sample coordination including cross functional collaboration with internal and external labs

• Supporting domestic and international sample shipments

• Supporting testing for methods including pH, conductivity, TruScan RM spectroscopy, appearance, and dimensional verification

• Inspect product and raw material retain samples.

• LIMS (LabVantage) sample logging and result entry

• Raw material and consumable component inspection and release

• Clean room gowning and aseptic techniques.

• Managing/stocking of QC lab supplies and routine lab cleaning.

• Complete and maintain cGMP documentation for work performed.

• Maintain a safe laboratory working environment.

• Foster a positive and inclusive work culture that promotes collaboration, innovation, and continuous improvement.

• Follow all relevant GxP regulations, guidelines, and company policies to ensure compliance with regulatory and internal requirements.

• Execute tasks precisely as defined in internal guiding documents including but not limited to standard operating procedures (SOPs) and work instructions.

• Follow Good Documentation Practices and Data Integrity requirements to ensure data, documentation, and records are completed and maintained for use by the business and available to support audits or inspections.

• Complete training in assigned required learning plan according to the defined timing and the prescribed requalification cadence.

qualifications:

• BA/BS in a relevant scientific discipline

• 0-2 years or 3+ years in a GMP QC laboratory setting

• • Demonstrated aptitude or ability to learn in order to gain a strong understanding of GxP regulations.

skills: Quality control, 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.