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Manufacturing Technician

Actalent
locationVacaville, CA, USA
PublishedPublished: 6/14/2022
Manufacturing
Full Time

Job Description

Job Description

QC Analyst- Pharmaceutical

MUST have at least 1 year experience working in a GMP facility

Opportunity to work with one of California's largest Biotech companies!

Summary

With limited supervision, QC Associate I, is responsible for the performance of direct materials testing in accordance with cGMP regulations. These duties include execution of laboratory testing, trend analysis, documentation review, support of discrepancies (OOS, OOT, OOE) and other laboratory support activities. In conjunction with Quality Control leadership, the QC Associate II works to meet departmental and organizational goals.

Job Responsibilities

● Perform a broad variety of basic and moderately complex tests with documentation according to GMP

● Review data and assess against established acceptance criteria

● Perform technical review of peer-generated data

● Evaluate data to identify trends and/or establish limits

● Identify discrepancies; provide input to design of quality investigations and CAPA (corrective actions preventive actions) initiatives as needed

● Identify and troubleshoot technical problems

● Identify gaps in systems and procedures

● Receive and provide training

● Participate in assay transfer and assay validation

● Perform equipment qualification / maintenance

● Prepare and maintain standards, controls, stocks, cultures, etc. per established procedures

● Support the maintenance and compliance of operational areas

● Assure and apply GMP throughout operations

● Coordinate with customers to support multi-site operational activities

● Support internal and external audits and regulatory inspections

● Works to meet schedules, timelines, deadlines

● Participate in and/or lead group and project teamwork; project and process improvements

● Write protocols and reports under limited supervision

● Meets scheduled performance of 95% on time

● Perform other duties as requested by managers to support Quality activities

Job Requirements

● B.S./B.A. degree and 1-3 years experience or Master’s Degree plus one year experience or an equivalent combination of education and experience. Degrees are preferably in relevant scientific disciplines and experience is in the

pharmaceutical or biopharmaceutical industry.

● Strong verbal and written communication skills, ability to organize and present information both formally and informally.

● Demonstrated ability to apply knowledge of scientific theories, principles, and techniques used in analytical or biological test procedures.

● Routinely exercises sound judgment, reasoning and problem solving.

● Capable of working under limited supervision and determining own short term priorities.

Job Type & Location

This is a Contract position based out of Vacaville, CA.

Pay and Benefits

The pay range for this position is $25.00 - $27.50/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Vacaville,CA.

Application Deadline

This position is anticipated to close on Mar 30, 2026.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through:

  • Hiring diverse talent
  • Maintaining an inclusive environment through persistent self-reflection
  • Building a culture of care, engagement, and recognition with clear outcomes
  • Ensuring growth opportunities for our people

Actalent is an equal opportunity employer.

About Actalent

Actalent is a global leader in engineering and sciences services. For more than 40 years, we’ve helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day.

Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.

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