Job Description
The primary purpose of this position is to provide quality control functions, including technical and analytical support for all areas of the facility. Additionally, personnel in this position will support the continuous development of Quality Assurance systems in manufacturing and packaging areas.
ResponsibilitiesProvide accurate and timely testing of raw materials, bulk formulations, and finished goods in accordance with established procedures and work instructions, as well as FDA and GLP guidelines.Maintain records and documentation in accordance with GLP, FDA, and established standards.Assure inspection and control of incoming raw materials and components, as well as finished goods.Verify line end-of-shift and end-of-run reconciliation.Assemble and verify all batch records.Support the implementation of Quality Systems to ensure compliance with FDA regulations.Coordinate with lines to identify and document nonconformities, and report results as required.Perform routine verification of instrument calibration and preventive maintenance on laboratory equipment.Support calibration and verification programs for testing equipment on lines.Assist with training of line personnel, batching personnel, and office staff as required.Perform routine environmental microbiological testing.Ensure laboratory supplies are current and that all required supplies and chemicals are sufficiently stocked.Accurately prepare and document the preparation of standards, standard solutions, and other reagents.Champion quality both in the lab and in the plant.Maintain an effective and efficient laboratory that processes samples accurately and precisely.Promote a team environment where people feel free to seek support and advice on quality matters.Assure compliance with FDA regulations regarding inspection and testing.Interpret and report analytical data.Product release/rejection with approval from QC Supervisor/QA Specialist.Essential SkillsQuality assuranceWet chemistryAnalytical chemistryQuality controlLab experienceOperation and maintenance of FTIR, HPLC, and GCKnowledge of GMP and GLP standardsBS in Chemistry or similar lab sciencesGood computer skills with Microsoft Office (Word, Excel, PowerPoint, and Access)Good verbal and written communication skillsAbility to work in a team environmentAdditional Skills & QualificationsExperience in a QC lab environmentExperience in Pharma or cosmetic labMicrobiological experienceA.S with a couple of years of lab experiencePay and Benefits
The pay range for this position is $20.00 - $22.00/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 Sidney,OH.
Application Deadline
This position is anticipated to close on Feb 14, 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.