What are the responsibilities and job description for the Engineer i, cqv, laboratory compliance, clinical biomarker laboratory position at Randstad?
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 : $45.00 - 50.32 per hour
work hours : 9 to 5
education : Bachelors
responsibilities :
The Engineer I, CQV (Commissioning, Qualification, and Validation) will be responsible for delivering commissioning, qualification, and validation activities ensuring equipment and systems remain in a qualified operational state of compliance within a GCLP / GLP Laboratory environment. This individual will collaborate closely with Lab Operations, Lab Compliance and R&D Quality to complete qualification activities. Applicants should enjoy working in a fast-paced, dynamic, and innovative environment. This role will report to the Associate Director, Laboratory Compliance, Clinical Biomarker Laboratory. This is a non-remote position.
- Execute commissioning, qualification, and validation activities to maintain compliance with GCLP guidelines and GLP regulations.
- Author and execute design, commissioning, qualification, and validation documentation and support records to certify compliance with specifications and procedures.
- Ensure timely resolution of documentation compliance and quality system issues.
- Investigate deviations related to qualification and validation activities
- Participate in cross-functional teams to meet project timelines and business needs while adhering to regulatory requirements.
- Ensure Standard Operating Procedures (SOPs) and procedures are created, understood, and followed.
- Participate in Moderna training to support CQV requirements.
qualifications :
skills : SOP, MS-Powerpoint, MS-Project, GLP (Good Laboratory Practice), GCP (Good Clinical 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 health, an incentive and recognition program, and 401K contribution (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.
Salary : $45 - $50
