- 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. With therapeutic areas that include Oncology, Vaccines, and Rare Diseases, our partner aims to make treatments streamlined, easily accessible, and globally produced. If you share their goal of approaching healthcare in a novel way, look no further - apply for your dream job now!
location: Andover, Massachusetts
job type: Contract
salary: $21.13 - 47.88 per hour
work hours: 9 to 5
education: Bachelors
responsibilities:
- The QA Specialist Demonstrates sufficient depth of knowledge within own work area in order to perform hands-on routine QA tasks.
- This role supports Operations including batch record, investigation, and document review, and disposition activities.
- Resolve routine quality issues related to product manufacture and testing with guidance/coaching.
- Project work, as needed, will also be expected. Other essential duties and responsibilities in quality assurance include:
- Provide Quality Assurance expertise to colleagues on and off the Manufacturing floor as required.
- Identify continuous improvement opportunities based on metrics and drive consistency through the process to align with company standard processes and quality systems.
- Conduct regular Production areas walkthroughs (Area product clearances, GMP and compliance walkthroughs)
- Conduct On floor QA review of executed batch records and Logbooks to assure compliance with regulatory standards and regulatory filing.
- Assist Quality Operations
- Deviations and Product Floor Support for all planned and unplanned manufacturing deviations.
- Escalate issues as appropriate to the Quality Assurance Management in a timely manner.
- Maintain regulatory compliance in accordance with current Good Manufacturing Practices.
- Accurately communicate Supply/Operational needs/perspectives as well as Quality Operations (QO) perspectives.
- Quality Assurance approval of SOPs, Campaigns start up Form and QA validation protocols and reports.
- Maintains inspection readiness and supports internal/external audits as needed. Interface with
- Regulatory Agencies in audits.
- Ability to work in a fast-paced environment and be able and willing to juggle priorities as required.
qualifications:
Required:
- Bachelor's degree
- 1+ years of experience in GMP pharmaceutical manufacturing environment
skills: SOP, 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.
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: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
This posting is open for thirty (30) days.
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
