QC Cleanroom Analyst
$25 per hourjob summary:
Are you looking to advance your pharmaceutical career with a top-tier global life sciences leader? We are seeking a dedicated Quality Control Analyst to perform vital environmental monitoring across cleanroom environments in Ridgefield, NJ. If you thrive in aseptic manufacturing settings and prioritize cGMP excellence, this is the perfect opportunity to make an impact. location: Ridgefield, New Jersey
job type: Contract
salary: $25 - 30 per hour
work hours: 9 to 5
education: Bachelors responsibilities:
qualifications:
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 View email address on 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.
Are you looking to advance your pharmaceutical career with a top-tier global life sciences leader? We are seeking a dedicated Quality Control Analyst to perform vital environmental monitoring across cleanroom environments in Ridgefield, NJ. If you thrive in aseptic manufacturing settings and prioritize cGMP excellence, this is the perfect opportunity to make an impact. location: Ridgefield, New Jersey
job type: Contract
salary: $25 - 30 per hour
work hours: 9 to 5
education: Bachelors responsibilities:
- Perform daily viable and non-viable environmental monitoring (EM) in Grade A, B, C, and D cleanroom environments.
- Maintain logs and complete contemporaneous batch record documentation following strict ALCOA+ data integrity principles.
- Author and assist with out-of-specification (OOS) and non-conformance EM investigations.
- Review and revise EM Standard Operating Procedures (SOPs) and Batch Production Records (BPRs).
- Prepare daily plates, sanitize EM equipment, and assist manufacturing during periods of inactivity.
qualifications:
- 2+ years of Quality Control experience within a pharmaceutical or biotechnology manufacturing facility.
- Hands-on experience with environmental monitoring in classified cleanroom environments (Grades A-D).
- Strong working knowledge of ALCOA+ principles and cGMP regulatory standards.
- Willingness to work a split shift (Sunday-Saturday) with mandatory overtime to support production schedules.
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 View email address on 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.
Vacancy posted 3 days ago
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