Manufacturing Technician (Upstream/Downstream)
USA-Manufacturing Technician I (Manufacturing/Quality) 1st Shift
7am - 3:30pm: Mon-Fri (OT and Holidays as needed)
Free parking onsite, Open candidates willing to relocate at their own expense Possibility of extension Exposure to cold room
Ability to lift up to 30 pounds Exposure to chemicals: hypochlorite, bleach, isopropyl alcohol Face mask is required when sampling, however no respirators are required for this role
Must have:
2+ years of hands-on experience in GMP environment similar role
Previous Biotech or pharma required
Must have combination of skills/ experience related to environmental monitoring, water sampling, glass wear prep, autoclave (not all required, however strongest candidates will have experience will most/ all of these skills)
Will accept candidates with more than 2+ years of experience or bachelor’s degree or higher – they will not be considered overqualified
SAP experience a plus
MS Office Work Outlook
Must be open to OT, holidays and possible weekends if needed, not a frequent occurrence, however as required due to business need.
Description:
This position is responsible for ensuring all sampling are collected within the required frequency.
Sampling includes environmental monitoring and utilities sampling in cGMP areas.
The position is also responsible for preparing all the material needed for the manufacturing process.
Preparation includes Glassware washing, Transfer Assembly preparation and Autoclaving.
Responsibilities:
Execute standard operating procedures (SOPs) in routine/non-routine sampling process in areas of the cGMP manufacturing facility.
Perform aseptic sampling (Environmental monitoring sampling, WFI (water injection), PUW (Purified Water) and Clean Steam Sampling)
Prepare material for manufacturing process (Glassware washing, Transfer Assembly preparation and, Autoclaving)
Perform routine cleaning of the cGMP facility.
Interact with other departmental personnel to assist in resolving manufacturing quality issues.
Maintain records and documentation in accordance with a cGMP environment
Work a flexible work schedule, weekends and holidays as required.
Follows instructions on notification of deviations as they occur and provides information during investigations.
Must be able to support additional manufacturing activities as needed.
Requisite Education/Skills:
Education: High School degree with at least two years of experience or training in a cGMP manufacturing environment
Aseptic technique sampling experience in GMP environment is preferred
Strong content knowledge in cGMP/regulatory compliance.
English fluent, both written and spoken
Good communication and social skills
Job Type: Contract
Pay: $27.00 - $28.00 per hour
Benefits:
Health insurance
Education:
High school or equivalent (Preferred)
Experience:
CGMP: 2 years (Preferred)
Pharma or biotech industry: 2 years (Preferred)
upstream/downstream process: 2 years (Preferred)
AKTA: 2 years (Preferred)
Ability to Commute:
Pearl River, NY 10965 (Preferred)
Work Location: In person