Senior Manufacturing Process Technician

Tandem Diabetes Care; San Diego (CA); On-site; USD 35,000 - 43,000; Full time

Job description

A Day In The Life

Performs functions associated with all manufacturing operations. Works with engineers in set-up and development of support processes. Assists in the development and execution of protocols and test runs. Design, implement and maintain production support processes. Assess manufacturing processes for compliance with written policies and procedures including QSR’s and cGMP practices. Assembles and initiates documentation change order packages. Proactively communicates notifications on problems and issues.

Manufacturing Engineering Technician II's at Tandem are also responsible for:

• Maintains, operates and develops processes in support of manufacturing operations.
• Performs assessments of procedures within the manufacturing environment, identifying non-conformances, recommending and implementing corrective and preventative actions.
• Performs all manufacturing assignments in accordance with established safety procedures and applicable regulatory requirements.
• Contributes to and develops equipment operating procedures (EOPs) and preventative maintenance (PMs) plans as requested.
• Develops and releases written and picture-based work instructions.
• Participates in continual process improvement activities designed to optimize quality, compliance, process efficiency, and lead times.
• Executes process validation and qualification protocols and documents results and findings as required.
• Provides training, as required, to production personnel on procedure, and process changes.
• Assists in the implementation Lean Manufacturing and 6 sigma techniques.
• Other duties as assigned.

When & Where You’ll Work

Onsite: This position is fully onsite and open to candidates located in San Diego, California. Equipment for the role will be provided and training will occur onsite.

Schedule

This position will work Monday - Thursday from 2:30 PM - 1:45 AM PST.

What You’ll Need

• Knowledge, skills & abilities:
• Knowledgeable with QSRs.
• Must have strong cGMP documentation skills.
• Working knowledge of small scale electromechanical device assembly operation,
• Ability to effectively share information regarding issues in written or verbal form and making recommendations in a clear and concise manner.
• Skilled at promoting team cooperation and a commitment to team success.
• Demonstrated ability to effectively prioritize and handle multiple priorities and complete assignments on time and with minimal errors.
• Proficient with Microsoft Office and Internet.
• Minimum certifications/educational level:
• Associate degree in a technical discipline, or applicable job experience and education.
• Minimum experience:
• 4+ years of experience in Instrumentation or Biomedical Industries, or Consumer Electronics.
• Experience in FDA/GMP/ISO environment.
• Lean Manufacturing experience desirable.

Compensation

The starting base pay range for this position is $25.19 to $31.47 per hour. Base pay will vary based on job-related knowledge, skills, experience and may also fluctuate depending on candidate’s location and the overall job market.

Benefits

Please note that is a temporary position. As a temporary employee you will be employed through a staff agency partner. Benefits during your temporary assignment may be provided by the staffing agency. Access to Tandem sponsored benefits is contingent upon conversion from temporary to regular full-time status. Conversion is determined based upon business need and job performance.

Background Check and Other Compliance

Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable state and local Fair Chance laws and regulations. A conditional offer of employment from Tandem is contingent upon successful completion of a pre-employment screening process comprising a drug test (excluding marijuana) and background check, which includes a review of criminal history information. Tandem has good cause to conduct a review of criminal history information of candidates for this position, as this role may involve access to proprietary, sensitive and/or confidential information, including customer protected health information. This review is required to ensure that individuals in such roles uphold high standards of trust and integrity so as to protect the interests of our customers, employees, and stakeholders.

SpONSORSHIP

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

Equal Opportunity Employer

Tandem is firmly committed to being an equal opportunity employer and does not discriminate on the basis of age, disability, sex, race, religion or belief, gender identity or expression, marriage/civil partnership, pregnancy/maternity, or sexual orientation. We are an inclusive organization, and we welcome applications from a wide range of candidates. Selection for roles will be based on individual merit alone.