Job detailsQuality Assurance SpecialistKelly® Science & Clinical is seeking a Quality Assurance Specialist for our client, a top consumer product company, in Fort Washington, PA. If you're passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts. Schedule: On-site Monday through Friday day shiftLength of assignment: 12 monthsPay: $33-35 an hour Depending on experienceThe QA Specialist is responsible for providing daily Quality Assurance support to the manufacturing site to ensure internal and regulatory cGMP and CFR requirements are met. Quality Assurance support areas include but are not limited to Batch Record Review, Product Release, Standard Operating Procedures, Investigations, CAPA, Change Control, Shop Floor Audits. The position will interact with other departments including Manufacturing, Packaging, Quality Laboratories, Quality Systems, Validation, Engineering, Maintenance and other departments as it relates to site Quality Assurance responsibilities.. As a QA Specialist -, you will be accountable for identifying trends and reoccurring issues and suggesting solutions:Key Responsibilities
- Provides daily QA support to warehouse, bulk manufacturing and packaging lines, including work order evaluation.
- Performs or supports activities related to Batch Record Review, Raw Material, Bulk, and Finished Product Review
- Performs or supports activities related Line Audits, Line or Area Cleaning Verifications.
- Participates in design of quality processes and creation/modification/approval of Standard Operating Procedures (SOP's).
- Actively supports Site metrics, compliance improvement and training initiatives.
- Provide support to capturing of site metrics and promote improvement opportunities.
- Prepares APR contributions as needed within schedule.
- Generates and examines documentation regularly for inconsistencies, gaps or errors.
- Performs activities to support Destruct Orders and Shipping Orders.
- Supports to maintain documents retention schedule and file completed documents to the applicable areas.
Required Qualifications
- Bachelor's degree or Equivalent in Science or related field or equivalent experience.
- Minimum of 2 years of experience in pharmaceutical and or OTC management or a related field.
- Strong attention to detail and ability to maintain accuracy in a fast-paced environment.
- Excellent communication and collaboration skills.
- Ability to work independently and manage multiple priorities.
- Strong analytical and problem-solving skills
- Attention to detail to monitor and scrutinize internal and external documents
What happens nextOnce you apply, you'll proceed to the next steps if your skills and experience look like a good fit. But don't worry-even if this position doesn't work out, you're still in our network. That means all of our recruiters will have access to your profile, expanding your opportunities even more.Helping you discover what's next in your career is what we're all about,#19648476