GMP QC Lab Associate – ELISA & Data Entry

Actalent; Thousand Oaks (CA); On-site; USD 37,000 - 39,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Onsite onsite facility amenities

Job summary

Actalent is seeking a MCS Associate Quality in Thousand Oaks, CA. You will perform routine GMP-regulated testing across multiple methods, including ELISA, and maintain precise documentation in lab notebooks and electronic systems.

Responsibilities include handling pipetting, weighing, dilutions, data entry, and equipment maintenance, while ensuring compliance with CFRs and cGMPs. This onsite role runs Monday–Friday with standard hours.

Qualifications

• Bachelor’s degree in a scientific discipline or equivalent.
• Prior academic or industry laboratory experience.
• Proficiency with basic laboratory techniques and dilutions.
• Comfort in GMP-regulated environment and GMP testing.
• Strong documentation practices for paper and electronic records.

Responsibilities

• Perform routine laboratory procedures and analyses in GMP environment.
• Execute pipetting, weighing, dilutions, and calculations accurately.
• Document and enter data in lab notebooks and electronic systems.
• Maintain and calibrate laboratory equipment and assist maintenance.
• Support inventory management and ensure supplies are available.
• Comply with cGMPs, CFRs and internal procedures.
• Follow change control processes for document updates.
• Evaluate documentation and data for discrepancies and escalate.
• Contribute to continuous improvement in daily tasks.
• Organize workload, multi-task, and meet deadlines in a fast-paced lab.

Skills

Pipetting

ELISA techniques

GMP environment

Data entry

Documentation

Attention to detail

Communication

Time management

Troubleshooting

Training compliance

Education

Bachelor’s degree in a scientific discipline

Tools

Electronic lab notebooks

LIMS (lab information systems)

Job description

Actalent is seeking a MCS Associate Quality in Thousand Oaks, CA. You will perform routine GMP-regulated testing across multiple methods, including ELISA, and maintain precise documentation in lab notebooks and electronic systems.

Responsibilities include handling pipetting, weighing, dilutions, data entry, and equipment maintenance, while ensuring compliance with CFRs and cGMPs. This onsite role runs Monday–Friday with standard hours.