Seeking a detail-oriented Quality Control professional to manage the QC sample lifecycle. This role is responsible for the timely receipt, distribution, and management of all quality control samples to support our manufacturing operations. Key duties include inventory management of reference standards, stability sample coordination, and ensuring the efficient flow of materials for testing
location: Pennington, New Jersey
job type: Contract
salary: $58.62 - 68.97 per hour
work hours: 9 to 5
education: Bachelors
responsibilities:
- Support establishment of a QC sample management program to ensure timely generation and reporting of test results in support of manufacturing operations.
- Ensure time-sensitive distribution of quality control samples in support of QC-related activities
- Perform routine operations, including but not limited to instrument qualification and maintenance, SOP generation and revision, sample plan generation, sample receipt and distribution, CoA generation, record keeping, etc.
- Manage inventory of reference standards and samples (on-test, retain, reserve, stability) for the QC laboratory.
- Stability sample management.
qualifications:
- Bachelor's Degree or above in Chemistry or Biotechnology related scientific discipline.
- Minimum of 2 years of working experience in an FDA-regulated biotechnology or pharmaceutical company.
- 5+ years of experience preferred with no higher education.
- Working knowledge and experience with analytical testing methods.
- Familiar with USP/EP and cGMP/EU GMP regulations.
- Familiar with instrument and equipment validation.
- Impressive, demonstrable track record and skills/experience gained within a similar position(s), at a similar level.
- Credible and confident communicator (written and verbal) at all levels.
- Strong analytical and problem-solving ability.
- Hands-on approach, with a 'can do' attitude.
- Ability to prioritize, demonstrating good time management skills.
- Excellent attention to detail, with the ability to work accurately in a busy and demanding environment.
- Self-motivated, with the ability to work proactively using own initiative.
- Committed to learning and development.
skills: PCR, FDA, Chemistry, 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.
