Quality Control Technician

Are you passionate about quality control in a dynamic manufacturing environment? A pharmaceutical company in Ridgefield, NJ is seeking a Quality Control Technician I for a 1st shift, onsite role. This is a high-priority opportunity with immediate openings, supporting environmental monitoring (EM), deviation writing, and microbiology tasks in a GMP-regulated setting.

Ideal candidates will bring at least two years of industry experience, an AA or Bachelor's in Microbiology, and the ability to work both collaboratively and independently. Strong computer skills and confidence in writing deviations without assistance are essential. If you have experience with aseptic gowning, or in a micro or chem lab, this could be an excellent match. Be prepared for occasional overtime or weekend work-this is a fast-moving opportunity on a critical team, so apply today!

location: Ridgefield, New Jersey
job type: Contract
salary: $28.00 - 30.57 per hour
work hours: 9 to 5
education: Bachelors

responsibilities:

• Conduct daily viable and non-viable environmental monitoring within the production facility.
• Prepare media plates and maintain necessary supplies for environmental monitoring activities.
• Write and investigate environmental monitoring deviations independently.
• Perform product sampling and assist in routine manufacturing operations as needed.
• Maintain accurate and compliant documentation, including batch records and monitoring logs.
• Clean and sanitize production equipment and classified cleanroom spaces.
• Support team operations while working independently in a fast-paced GMP environment.

qualifications:
Required Skills & Qualifications

• Associate's or Bachelor's degree in Microbiology or a related scientific field.
• Minimum of 2 years of relevant industry experience in manufacturing or microbiology.
• Must be able to write deviations without assistance.
• Must have strong computer skills.
• Must be able to work both independently and collaboratively within a team environment.
• Experience performing environmental monitoring (viable and non-viable) in a GMP-regulated setting.
• Strong attention to detail and documentation accuracy.
• Must be authorized to work in the United States without current or future need for employment sponsorship (no OPT, STEM OPT, or other visa sponsorships will be considered).

Preferred Skills & Experience

• Experience with aseptic gowning and working in cleanroom or classified environments.
• Background in microbiology or chemistry lab procedures.
• Familiarity with deviation investigation and GMP documentation processes.

#LI-ST1

skills: MS-WORD, MS-EXCEL, MS-Powerpoint, Chemistry, GLP (Good Laboratory Practice), Microbiology, 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 ....

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.