Overview
QA Auditor II Jobs in Whitehouse, NJ at Intertek
QA Auditor II – Whitehouse, NJ
Intertek is searching for a QA Auditor II to join our Chemicals & Pharmaceuticals team in our Whitehouse, NJ office. This is a fantastic opportunity to grow a versatile career in Quality Assurance.
Intertek’s Chemical & Pharmaceuticals team brings quality and safety to life through regulatory guidance and supply chain assurance to support your unique pharmaceutical or biopharmaceutical outsourcing requirements. Over the last 20 years, our network of laboratories and regulatory experts have provided high quality custom pharmaceutical services ensuring Total Quality Assurance for some of the world’s largest and most innovative pharmaceutical companies. Intertek is continually innovating and evolving to reduce risk for consumers, brands and organizations in every sector and industry around the world. We go beyond Testing, Inspection and Certification of products: we are a Total Quality Assurance Provider to industries worldwide. Our Purpose: Bringing quality, safety, and sustainability to life.
What are we looking for?
The QA Auditor II is responsible for ensuring that analytical data generated meets company standards and regulatory requirements (US FDA, US DEA and EMA regulations).
Salary & Benefits Information
The base wage or salary range for this position is $70,000-$95,000. Individual compensation packages are based on a variety of factors unique to each candidate including skill set, experience, qualifications, and other job-related reasons. This position is bonus eligible.
In addition to competitive compensation packages, when working with Intertek you can expect benefits including medical, dental, vision, life, disability, 401(k) with company match, generous vacation / sick time (PTO), tuition reimbursement and more.
What you’ll do:
- Review all tests results, raw data including electronic data generated in support client sample testing, utilizing but not limited to the following industry technologies.
-
Review/approval of GMP Analytical Reports and associated electronic and hard copy data, audit trails and notebooks to ensure:
- Accuracy and completeness of data including system suitability
- Reagents, standards, and equipment used are within the acceptance range.
- The correct samples were run and methods were performed as intended.
- Calculations are correct
- Electronic data audit trails and instrument logs on cGMP instrumentation and equipment are reviewed for accuracy and approved for data release.
- Review and release of cGMP reports including validation, transfer, method development/optimization, release, and stability reports.
- Ensure analyst follow all SOPs, good documentation practices (GDP) and cGMP requirements.
- Ensure project notebooks and data are reviewed promptly, in accordance with SOPs.
- Work with analysts for document corrections and provide guidance accordingly. on SOP and good documentation practices (GDP) requirements.
- Review/approval of internal records such as: Instrument calibration and maintenance, Training records, Laboratory investigations OOS/OOT, NCRs, Complaints, Change Control, and Internal audits
- Review of root cause analyses, risk assessments and analyses, corrective and preventive actions (CAPA), and effectiveness checks
- Ensure compliance with US FDA, US DEA and EMA regulations
- Follow all SOPs and Safety Guidelines to ensure compliance with a cGMP environment and Safety Practices.
- Assists and support with internal, client, vendor and regulatory audits
- Assists and support with policy and procedure development
- Assists and support for Corrective Actions Preventative Actions (CAPA)
- Assists and support for DEA activities
- Assist and support with monitoring and managing KPIs.
- Perform additional tasks as assigned by the QA Director
This position outline is a general guideline and does not represent all encompassing details. The position assumes that the incumbent has both the mental and physical requirements to carry out the above defined duties.
Minimum Requirements & Qualifications:
- BA/BS Chemistry, Biology or related scientific degree
- Minimum of 4 years of related industry experience (ATIC) in a related analytical laboratory (pharmaceutical or medical device)
- Knowledge of laboratory safety precautions and protocols for safe handling and the disposal of hazardous agents/ reagents, chemicals and materials
- Organization, communication, and analytical skills
- Ability to understand and effectively communicate technical and business information, both oral and written to others, including co-workers, supervisors, subordinates, clients, and vendors
- Ability to define problems, collect data, establish facts, and draw valid conclusions
- Intermediate mathematical skills
- Be aware of, and adhere to, safety practices and policies to ensure your own safety, as well as the safety of others who may be affected by your actions at work
- Ability to work in fast-paced, multi-tasking environment with shifting priorities and demanding deadlines
- Must be detailed-oriented and able to effectively prioritize and organize workload, with efficient time management
- Ability to communicate and interact effectively in verbal written and presentation formats
- Must possess the fundamental technical and administrative skills required to perform the job duties
- Must be customer focused and quality driven
Ability to travel as business needs dictate
Preferred Requirements and Qualifications:
- Previous experience using and or reviewing data from analytical instrumentation, and including: HPLC, LC-MS, GC, GC-MS, ICP, ICP-MS, UV
Intertek: Total Quality. Assured.
Intertek is a world leader in the Quality Assurance market, with a proven, high-quality business model and a global network of customer-focused operations and highly engaged subject matter experts. With passion, pace, and precision we work to exceed our customers’ expectations, while engaging with our employees to be 10X in their performance and professional growth.
Intertek is a drug-free workplace. As a condition of employment, certain positions may be required to pass a pre-employment drug test based on the type of work that will be performed.
We Value Diversity
Intertek’s network of phenomenal people are our greatest assets, and the diversity they bring fuels our success. Intertek is an Equal Employment Opportunity Employer that values inclusion and diversity. We take affirmative action to ensure all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other legally protected characteristics.
For individuals with disabilities who would like to request accommodation, or who need assistance applying, please email [email protected] or call 1-877-694-8543 (option #5) to speak with a member of the HR Department.
#LI-JC1
- Intertek does not accept unsolicited approaches from agencies and will not pay a fee for any placement resulting from the receipt of an unsolicited resume
Intertek’s Chemicals & Pharmaceuticals team serves the chemical and pharmaceutical industries with a diverse range of services. Our chemical experts provide testing, consultancy, inspection, to ensure a variety of chemicals are produced efficiently and in compliance to regulatory standards. Our pharmaceutical specialists support drug development and products through contract laboratory services, regulatory guidance, and supply chain assurance.Intertek is a leading Total Quality Assurance provider to industries worldwide. Our network of more than 1,000 laboratories and offices in more than 100 countries, delivers innovative and bespoke Assurance, Testing, Inspection and Certification (ATIC) solutions for our customers’ operations and supply chains. Working at Intertek means joining a global network of state-of-the-art facilities and passionate people who deliver superior customer service with a purpose of bringing quality, safety, and sustainability to life.
Title: QA Auditor II
Company: Intertek
Location: Whitehouse, NJ
Category:
