Job Description
We are seeking a dedicated and experienced QC Document Control professional to join our team. The ideal candidate will be responsible for overseeing documentation, reviewing SOPs, logbooks, worksheets, and assay validation plans. This role involves cross-functional collaboration with QC, QA, and Manufacturing teams.
ResponsibilitiesManage documentation processesReview Standard Operating Procedures (SOPs), logbooks, and worksheetsDevelop and review assay validation plans, including PCR and SDS-PageCollaborate cross-functionally with QC, QA, and Manufacturing teamsValidate assays and manage change controlsOversee a team of 4-6 peopleProvide documentation support to the QC teamRun reports and validation plansEssential SkillsExperience in validation and documentation processesProficiency with assays, including PCR and SDS-PageStrong organizational and management skillsAbility to oversee and manage a teamBachelor's degree in a science-related fieldAdditional Skills & QualificationsExperience with cross-functional collaborationAbility to develop and review complex documentationStrong analytical and problem-solving skillsWork Environment
You will be working in both an office and lab setting. This role is critical as we prepare to start phase 3 of clinical trials, making it an exciting time for our manufacturing and testing teams.
Pay and Benefits
The pay range for this position is $35.00 - $45.00
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 Los Angeles,CA.
Application Deadline
This position will be accepting applications until Jan 25, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & InclusionAt Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are 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 peopleThe company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.