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Randstad Compliance Specialist II in Framingham, Massachusetts

Compliance Specialist II

job details:

  • location:Framingham, MA

  • salary:$30.81 - $36.25 per hour

  • date posted:Tuesday, September 1, 2020

  • experience:3 Years

  • job type:Contract

  • industry:Professional, Scientific, and Technical Services

  • reference:32948

job description

Compliance Specialist II

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. 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, !

location: Framingham, Massachusetts

job type: Contract

salary: $30.81 - 36.25 per hour

work hours: 9 to 5

education: Bachelors


The Quality Assurance (QA) Operations department is responsible for quality oversight of operations. QA's main responsibility is to ensure adherence to CGMPs during manufacturing operations through partnership with the site and direct engagement with daily operations activities. Quality Assurance Operations is responsible for providing support and guidance to the Operations function in order to protect the safety, quality and efficacy of company products, thereby ensuring the availability of compliant and safe products for our patients and assuring the security of the company's business and global markets.

The Senior Compliance Specialist is responsible for providing quality support and direction to Manufacturing, Quality Control, and support functions to ensure continued compliance to CGMPs as well as being responsible for providing technical support serving as a Subject Matter Expert (SME) to the QA team.

  • Actively supports the QA Operations team by providing technical support

  • Completes Phenix/Trackwise Laboratory Investigations/Deviations/CAPA/Change Controls

  • Ensure all safety requirements are being met

  • Performs batch record and logbook review

  • Performs review of column packing and qualification records

  • Review and approve CRs related to EBRs

  • Function as SME on challenges related to production requiring quality input

  • Provide on the floor (OTF) support to the operations department, including OTF support for critical operations steps

  • Issue action notices and conduct affiliated provisional release

  • Conduct log book audits against compliance requirements

  • Review CV related documentation against specification

  • Perform media / buffer and intermediate release

  • Perform release of Cell Banks for forward processing (as applicable)

  • Support cross-functional internal audit activities and conduct walkthrough inspections

  • Execute containment activities

  • Provide expertise during procedure/SOP revision process and function as DCR approver for department related SOPs and PRs

  • Maintain a high level of personal compliance to the required standards

  • Partner with manufacturing and support operations to ensure a culture of continuous compliance


Basic Qualifications:

  • Master's Degree & 2 years of experience or Bachelor's Degree and 4 years of experience in a Quality and /or other cGMP related field.

  • Knowledge in external agency regulations (FDA, EMA, etc.)

  • Strong computer, verbal and written communication skills.

  • Experience in quality systems.

  • Experience with Trackwise or equivalent system.

  • Proficient in Microsoft Office

Preferred Qualifications :

  • Operations experience in one of the following areas: Quality Assurance, Quality Control, Manufacturing Technical Support, Facilities Engineering, or Automation.

  • Experience with Manufacturing System (SMS) or comparable continuous improvement systems.

  • Experience with root cause analysis tools.

  • Demonstrated experience with change control, CAPA and deviation quality systems.

  • Experience in a Quality Assurance role.

  • Strong technical writing skills.

  • Effective time management, attention to detail, organizational skills, teamwork and collaboration.

  • Significant capability in problem solving methodology.

  • Experience training and technically developing employees.

  • Experience participating in external agency inspections.

  • Knowledge of regulatory enforcement trends.

  • Ability to work independently

Special Working Conditions:

  • Ability to gown and gain entry to manufacturing and Quality Control areas.

  • Ability to work a 12-hour rotating shift and every other weekend, including holidays.

  • Ability to lift 10 lbs.

skills: SOP, FDA, CAPA, MS-Project, 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.