Biotech and Pharmaceutical, Cleanroom, Customer Support/Service, Detail Oriented, Documentation, English Language, Environmental Work, GMP (Good Manufacturing Practices), Laboratory Management, MPI, Maintain Compliance, Manufacturing, Manufacturing Assembly, Manufacturing Operations, Material Process Control, Mathematics, Medical Equipment, Medical Office Administration, Process Management, Product Control, Production Support, State Laws and Regulations, Team Player, Warehousing
A leading Biotechnology company is looking for a Manufacturing Technician to join the team for an initial 3 months starting ASAP. You will support the medical device manufacturing operations, with primary focus on downstream production activities e.g. product inspection, kit assembly, packaging, material handling, documentation and general production support.Client DetailsOur client is a groundbreaking Biotechnology company making waves in their specialized field. This is a fast-paced work environment with a strong team of dedicated and driven Manufacturing professionals.DescriptionPerform manual kit assembly, packaging, sealing, and labeling activities in accordance with approved procedures and batch documentation. Inspect components, labels, containers, and finished kits for accuracy, completeness, appearance, and proper configuration. Verify product identity, quantity, labeling, lot information, and packaging configuration against applicable work instructions and production records. Prepare, assemble, and package finished product kits using defined process steps and controlled materials. Operate basic production and packaging equipment such as labelers, sealers, shrink-wrap equipment, torque tools, scanners, scales, or other equipment as required. Complete production records, logbooks, forms, and electronic transactions accurately, legibly, and contemporaneously. Follow line clearance, segregation, and product status control requirements to prevent mix-ups and maintain GMP compliance. Identify and escalate discrepancies, damaged materials, documentation errors, equipment issues, or process concerns to supervision. Maintain cleanliness, organization, and GMP readiness of the work area.ProfileHigh school diploma, GED, or equivalent. Prior experience in GMP, medical device, pharmaceutical, biotechnology, diagnostics, food, or other regulated manufacturing environment. Experience with packaging, kitting, labeling, inspection, assembly, or production documentation. Familiarity with Good Manufacturing Practices, Good Documentation Practices, line clearance, material reconciliation, or batch record execution. Experience using electronic documentation, ERP, inventory, or production tracking systems. Basic understanding of metric units and material/component traceability. Ability to read, understand, and follow written procedures, batch records, and work instructions.Strong attention to detail and ability to perform repetitive manual tasks accurately.Ability to speak, read, and write English sufficiently to complete GMP documentation and follow safety instructions.Basic math skills, including ability to count, reconcile quantities, and understanding units of measure.Ability to work in a controlled manufacturing, laboratory, warehouse, or cleanroom-adjacent environment.Job OfferHourly rate $20-$25.On site in Irvine/Santa Ana, California.2nd shift 1pm - 9:30pm.Quick interview process.2 week training period with pass or fail.MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.M
Michael Page International
Michael Page is one of the world's leading professional recruitment consultancies, specializing in the placement of candidates in permanent, contract, temporary and interim positions with clients around the world.
Our business was established in Canada in 2005 when we opened our Toronto office. Our role is to work with employers and job seekers to facilitate a successful match. This can range from advising a global company on a candidate sourcing strategy to helping a job seeker find their dream job.
In Canada, we focus on recruiting for the following areas:
Banking and financial services
Digital and e-commerce
Engineering and manufacturing
Finance and accounting
Human resources
Information technology
Marketing
Oil and gas
Procurement and supply chain
Property and construction
Sales
An Established Brand
The Group has established a leading presence in many of the key markets for professional recruitment around the world and has positioned itself in certain other markets, which offer the opportunity for future growth. Within its current largest markets, Michael Page has also built a regional presence, including in the UK, France and Australia. Consequently, the Michael Page brand is among the most widely recognized brands in the professional recruitment industry.
A Market Leader
The role of a recruitment consultancy is to act as an intermediary, identifying and sourcing suitably qualified candidates on behalf of its clients. Candidates are recruited either for permanent or contract positions (typically for a fixed term) or on a temporary basis. Within the overall recruitment industry, the market for professional recruitment services is a specialist sector which has developed more recently. Michael Page is widely recognized as leading the development of this market around the world.
Learn the benefits of working with Michael Page yourself. Submit your resume or contact a Michael Page recruitment consultant today.
10,000 employees or more
Staffing/Employment Agencies
https://www.michaelpage.ca/