Manufacturing Technician

Randstad Life Sciences US; Pearl River (NY); On-site; USD 45,000 - 60,000; Full time

Job summary

Join a leading company as a Manufacturing Technician I, where you'll support high-quality pharmaceutical production. Your role involves environmental sampling, maintaining cleanliness in a cGMP-compliant facility, and gaining exposure to aseptic techniques. Ideal for candidates with manufacturing experience and a commitment to quality, this position offers a chance to work in a fast-paced environment with a dedicated team.

Benefits

Comprehensive benefits package

Health insurance

401K contribution

Incentive and recognition program

Qualifications

• Minimum 2 years of manufacturing experience in a cGMP-regulated environment.
• Fluent in English (written and spoken).

Responsibilities

• Perform routine aseptic sampling and environmental monitoring.
• Maintain accurate records and documentation in compliance with cGMP standards.
• Collaborate with cross-functional teams to resolve quality-related issues.

Skills

SOP

GMP

Teamwork

Attention to Detail

Education

High school diploma or equivalent

Tools

SAP

MS-WORD

MS-EXCEL

MS-Powerpoint

Job description

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Job Summary

Step into a critical role as a Manufacturing Technician I, where your attention to detail and hands-on experience will directly support high-quality pharmaceutical production. You'll be responsible for performing environmental and utility sampling, preparing materials like glassware and transfer assemblies, and maintaining cleanliness in a cGMP-compliant facility. Working closely with a dedicated team, you'll gain valuable exposure to aseptic techniques, autoclaving, and documentation practices that are essential to regulated manufacturing environments.

This opportunity is perfect for individuals with at least two years of manufacturing experience and familiarity with Good Manufacturing Practices (GMP). If you're eager to contribute to a mission-driven team, work with precision in both hot and cold environments, and expand your skills in a fast-paced, high-impact setting, we encourage you to apply today.

Location: Pearl River, New York

Responsibilities

• Perform routine aseptic sampling, including environmental monitoring and sampling of purified water, clean steam, and WFI (Water for Injection).
• Prepare materials for manufacturing processes, such as glassware washing, transfer assembly preparation, and autoclaving.
• Maintain accurate records and documentation in compliance with cGMP and GDP standards.
• Support cleaning and sanitization of the cGMP manufacturing facility using chemical solutions and detergents.
• Collaborate with cross-functional teams to resolve manufacturing or quality-related issues as they arise.
• Follow standard operating procedures (SOPs) and promptly report any deviations or irregularities.
• Work a flexible schedule, including overtime and holidays, as needed to support production demands.

Qualifications

Required Skills & Qualifications:

• Minimum 2 years of manufacturing experience, preferably in a cGMP-regulated environment
• Familiarity with GMP (Good Manufacturing Practices) and GDP (Good Documentation Practices)
• Ability to follow Standard Operating Procedures (SOPs) for sampling and material prep
• Comfortable working in hot (autoclave) and cold room environments daily
• Capable of frequent lifting (up to 35 pounds), including totes and carts
• Experience working within a team environment (team of ~7 people)
• Willingness to work overtime and holidays, as required
• Ability to handle chemical cleaning agents, such as ISO alcohol, spore cleanse, and germicidal detergents
• High school diploma or equivalent
• Fluent in English (written and spoken)
• Candidates must be authorized to work in the U.S. without current or future visa sponsorship (including but not limited to OPT, STEM OPT, or H-1B).

Preferred (Nice-to-Have) Skills:

• SAP experience or familiarity with enterprise systems
• Aseptic technique sampling experience in a GMP environment
• Prior experience with environmental or water sampling

Skills: SOP, MS-WORD, MS-EXCEL, MS-Powerpoint, 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 [e-mail].

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.