Join a high-energy production team at the forefront of vaccine manufacturing, where your work directly contributes to the creation of life-saving drug substances. This role offers an immersive experience in a state-of-the-art commercial manufacturing facility, focusing on the critical preparation of media, buffers, and solutions essential for high-quality pharmaceutical production.
Located in a modern, cGMP-compliant campus in Pearl River, this site serves as a hub for innovation and technical excellence in biotechnology. You will work alongside industry experts in an environment that prioritizes safety, precision, and professional growth within the biopharmaceutical sector.
location: Pearl River, New York
job type: Contract
salary: $20 - 26 per hour
work hours: 8 to 4
education: High School
responsibilities:
- Formulate Solutions: Execute all aspects of media, buffer, and solution formulation, including the precise weighing and dispensing of raw materials and intermediate solutions.
- Operate Equipment: Manage and maintain specialized equipment such as stainless-steel mix tanks, pH/conductivity meters, osmometers, tube welders, and peristaltic pumps.
- Maintain Cleanliness: Perform Clean-in-Place (CIP) and Steam-in-Place (SIP) procedures for equipment, and participate in facility sanitization in accordance with SOPs.
- Ensure Compliance: Uphold strict Good Documentation Practices (GDP) while reviewing production records and following established SOPs for material and personnel flow.
- Test Integrity: Perform filter integrity testing and material sampling for analytical testing to ensure all products meet rigorous quality standards.
- Troubleshoot & Analyze: Assist in troubleshooting manufacturing issues and manage manufacturing data to improve process efficiency.
qualifications:
Required Skills:
- High School Diploma or equivalent.
- Minimum of 2 years of work experience or specialized training within a cGMP manufacturing environment.
- General knowledge of Current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), and Standard Operating Procedures (SOPs).
- Proficiency in aseptic techniques and the operation of in-process testing equipment (pH meters, osmometers).
- Ability to work a flexible schedule, including weekends and holidays as needed.
- Basic understanding of the Baculovirus Expression Vector System (BEVS) manufacturing process.
- Experience with CIP/SIP (Clean-in-Place/Steam-in-Place) systems.
- Strong social and communication skills for departmental collaboration.
skills: SOP Development, Good Manufacturing Practices (GMP), Corrective and Preventive Actions (CAPA), Good Documentation Practices (GDP)
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.
