Immediate need for a talented Manufacturing Technician III (Manufacturing/Quality) 1st Shift. This is a 05+ Months contract opportunity with long-term potential and is located in Pearl River, NY (Onsite). Please review the job description below and contact me ASAP if you are interested.
Job ID: 24-19759
Pay Range: $25 - $37/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).
Key Responsibilities:
- Interacts with other departmental personnel to assist in resolving manufacturing quality issues.
- Ability to present and explain techniques and results of manufacturing processes with outside departmental personnel.
- Responsible for identifying required training and training on, understanding, and following documented procedures that apply to their departments that support the Quality System.
- Maintains records and documentation in accordance with a cGMP environment and improves as necessary.
- Participates in the cleaning of the cGMP facility in accordance with sanitary maintenance SOP.
- Cross training as a support operator as required.
- Follows established SOPs for the flow of materials, personnel and equipment in and out of the cGMP facility
- Work a flexible work schedule, weekends and holidays as required (estimated 1 weekend per month). Potential to switch to second shift or weekend shift.
- Follows instructions on notification of deviations as they occur and provides information during investigations.
- Position may work OT and occasional weekends
- Primary responsibility is large scale recombinant protein production operations for commercial production through execution of SOPs, Batch Records, and all associated cGMP activities in the manufacturing facility.
- Duties include operation, maintenance, cleaning (CIP) and sterilization (SIP) of large scale cell culture bioreactors and associated operations such as media preparation, infection and harvest.
- The incumbent is capable of identifying, troubleshooting and leading the resolution of operational and equipment problems as they arise in the large-scale Bioreactor and Media Preparation areas with minimum supervision and effective communication to management.
Key Requirements and Technology Experience:
- Onsite The role has exposure to cleaning chemicals: CP200 & CP310 No heavy lifting - however will require pushing portable tanks or buffers;
- The role may enter cold rooms OT (asked to stay later) and May Work Occasional weekends Open to candidates willing to relocate at their own expense, must be able to start asap.
- Education: High School degree with at least seven of experience or training in a cGMP
- manufacturing environment OR
- BS degree with three years of experience OR
- MS degree with one year of experience
- Knowledge of cGMP
- English fluent, both written and spoken
- Good communication and social skills
- Minimum HS Diploma.
- Minimum of 4+ years of experience.
- GMP manufacturing environment.
- Pharma Experience is required.
- Experience with bioreactors, fermenters, and automated control systems.
- Cytiva & Allen Bradley (or similar automation exp).
- Strong communication skills, ability to work cross-functionally as a team.
- Bioreactor & cell culture experience.
- More than 4 years of experience
Our client is a leading Pharmaceutical organization and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration.
Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, colour, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.