Production Technician (biopharmaceutical)
at Next Level Group
Charlottetown, PE, Canada -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 02 Dec, 2024 | Not Specified | 04 Sep, 2024 | 1 year(s) or above | Training,Writing,Regulatory Requirements,Deviations,Interpersonal Skills,Computer Skills,Excel | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
MINIMUM QUALIFICATIONS (EDUCATION, EXPERIENCE AND/OR TRAINING, REQUIRED CERTIFICATIONS):
Biotechnology diploma would be an asset. High School (Grade 12) diploma is a must.
1-2 years of pharmaceutical/biological manufacturing experience in GMP environment is preferred.
1-2 years of experience in aseptic techniques or cell culture experience is preferred.
Excellent interpersonal skills, both communications and written.
Outlines of Production, cGMP guidelines, and HSE regulations.
Experience performing investigations and writing deviations.
Intermediate/Expert computer skills using MS Office (Word, Excel, Power Point).
Thorough technical understanding of quality systems and regulatory requirements.
Responsibilities:
- Adhere to the principles of “safety first, quality always”.
- Perform sterile manipulations in both a biosafety hood and isolator.
- Maintain a cell line completing media changes and cell passages.
- Operate and maintain production instruments and equipment, such as pH meters, conductivity meters, microscopes, lyophilized, peristaltic pumps and other production equipment.
- Perform sterile cell culture and viral infection processes.
- Write and review batch records, SOPs, qualification documents for viral/Renogen operations.
- Complete timely SAP postings and maintain department inventory.
- Comply with safety requirements, cGMP, SOP, and manufacturing documentation.
- Collaborate with other departments involved in GMP manufacturing for planning production, testing and product release in a timely manner resulting in successful completion of projects.
- Work as a cross functional team with different manufacturing groups to provide resources as needed.
- Perform tasks under minimal supervision, and within tight timelines to meet production schedules.
- Assist in maintaining production equipment in good condition as per manufacturer’s specifications.
- Maintain the cleanliness of the production areas and follow disinfection procedure of clean rooms.
- Responsibilities include cleaning, preparing and sterilizing items in autoclaves.
- Other duties as required.
REQUIREMENT SUMMARY
Min:1.0Max:2.0 year(s)
Pharmaceuticals
Production / Maintenance / Quality
Clinical Pharmacy
Diploma
Proficient
1
Charlottetown, PE, Canada