Job Description
Ensure customer satisfaction and cost savings by managing batch records in compliance with cGMP regulations and Quality Assurance Systems.
ResponsibilitiesReview and integrate batch records into the Quality Assurance System.Ensure records are complete, accurate, and meet specifications.Create certificates of analysis and manufacturing.Document and justify deviations and CAPAs.Process alerts, deviations, customer complaints, CAPAs, Change Controls/Orders, and Annual Product Reviews.Monitor and ensure timely completion of quality system actions.Prepare investigations and respond to customer needs accurately and promptly.Analyze monthly data to identify trends.Implement and maintain lean standards and processes.Use lean tools to eliminate waste and improve efficiency.Institutionalize 5-S (Sort, Straighten, Shine, Standardize, Sustain).Perform additional tasks as assigned.Additional Skills & QualificationsBachelor's degree in sciences discipline (Chemistry, Biology, Biochemistry, etc.)2+ years of industry quality experience within a GMP environmentWorking knowledge of batch record reviewingExperience in creating or maintaining COAsPrevious investigation and deviation documentation experienceWorking experience with CAPAs\"Certified Quality Auditor\" (CQA) Certification (preferred)
Pay Rate: $29-32/hr
Pay and BenefitsThe pay range for this position is $29.00 - $32.00
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 Eden Prairie,MN.
Application Deadline
This position will be accepting applications until Dec 30, 2024.
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.